Mouse Cell Surface Antigens: Nomenclature and
Immunophenotyping
This information is current as
of November 23, 2015.
Subscriptions
Permissions
Email Alerts
J Immunol 1998; 160:3861-3868; ;
http://www.jimmunol.org/content/160/8/3861
This article cites 54 articles, 28 of which you can access for free at:
http://www.jimmunol.org/content/160/8/3861.full#ref-list-1
Information about subscribing to The Journal of Immunology is online at:
http://jimmunol.org/subscriptions
Submit copyright permission requests at:
http://www.aai.org/ji/copyright.html
Receive free email-alerts when new articles cite this article. Sign up at:
http://jimmunol.org/cgi/alerts/etoc
The Journal of Immunology is published twice each month by
The American Association of Immunologists, Inc.,
9650 Rockville Pike, Bethesda, MD 20814-3994.
Copyright © 1998 by The American Association of
Immunologists All rights reserved.
Print ISSN: 0022-1767 Online ISSN: 1550-6606.
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
References
Lily Lai, Noosheen Alaverdi, Lois Maltais and Herbert C. Morse
III
Mouse Cell Surface Antigens: Nomenclature and
Immunophenotyping1
Lily Lai,* Noosheen Alaverdi,* Lois Maltais,† and Herbert C. Morse III2‡
This paper reviews cell surface Ags expressed on mouse hemopoietic and nonhemopoietic cells. The review will cover molecules
included in the cluster of differentiation (CD) from CD1 to CD166 and lymphocyte Ag (Ly) series from Ly-1 to Ly-81 as well as
some new Ags without current CD or Ly assignments. In addition to an update on mouse nomenclature, there will be a discussion
of some known functions of the molecules and brief comments on the use of particular Ags for immunophenotyping of cell subsets.
Several novel markers mentioned may prove useful in mouse immunology research. The Journal of Immunology, 1998, 160:
3861–3868.
*PharMingen, San Diego, CA 92121; †Nomenclature Coordinator/Mouse Genome,
The Jackson Laboratory, Bar Harbor, ME 04609; and ‡Laboratory of Immunopathology, National Institute of Allergy and Infectious Diseases, National Institutes of
Health, Bethesda, MD 20892
Received for publication September 26, 1997. Accepted for publication December
24, 1997.
The costs of publication of this article were defrayed in part by the payment of page
charges. This article must therefore be hereby marked advertisement in accordance
with 18 U.S.C. Section 1734 solely to indicate this fact.
1
The Mouse Genome Database Project is supported by National Institutes of Health
Grant HG00330.
2
Address correspondence and reprint requests to Dr. Dr. Herbert C. Morse III, Laboratory of Immunopathology, National Institute of Allergy and Infectious Diseases,
Building 7, Room 304, National Institutes of Health, Bethesda, MD 20892– 0760.
ceptor, and blind (multilineage panels). More information can be
obtained from the HLDA website (http://mol.genes.nig.ac.jp/hlda)
or Protein Reviews on the worldwide web (http://www.ncbi.nlm.
nih.gov/prow).
Over the years, the Committee on Standardized Genetic Nomenclature for Mice has continued to assign new Ly and CD names to
novel genes and Ags. Since the last update (2), many new Ly
designations have been assigned; for example, the F4/80 Ag,
whose gene has recently been cloned, was given the designation
Ly-71. (See Table I for an update of the Ly nomenclature.) The
human homologues of a number of mouse Ags or genes, including
members of the Ly-6 and Ly-49 families, have not yet been definitively identified. When a mouse Ly Ag is identified as a human
CD homologue, the Ly number for the molecule is withdrawn and
reassigned the appropriate CD number. If the mouse molecule was
encoded by a gene that is assigned a Ly number, that gene name is
withdrawn and reassigned a Cd number, unless another gene name
was agreed on by the human and mouse nomenclature groups. As
one example, the Ly-5 molecule of the mouse, encoded by Ly5,
was assigned CD45 in the human nomenclature for Ags and the
gene name CD45. The mouse designations were changed to CD45
for the Ag and, initially, Cd45 for the gene. More recently, the
human and mouse nomenclature committees adopted the gene Ptprc for the genes encoding CD45 in both species.
Multiple studies, including biochemical analysis, cloning, functional, and immunologic assays, are necessary to confirm homologues between species. In addition to differences in DNA sequence, evolutionary divergence between mice and humans may
also be manifested in Ag distribution. Notable examples include
CD2, CD90 (Thy-1), and perhaps CD34. Table II reflects several
novel mouse CD homologues that have been identified via cloning,
Abs, or protein probes, such as the use of ligand-Ig fusion proteins.
Some molecules are particularly useful as phenotyping markers
for different cell subpopulations. The large number of well-characterized mAbs has facilitated identifying cell types based on their
surface phenotypes. For additional reference, a review of mAbs to
human and murine CD Ags has been made available (4). It should
be noted that only a few Ags have restricted lineage distributions;
most cell surface molecules exhibit a broader distribution than initially reported. Multiparameter immunoanalysis, therefore, is required to isolate different cell types. Below is a summary of relevant Ags associated with cell lineages.
B cells
3
Abbreviations used in this paper: CD, cluster of differentiation; Ly, lymphocyte
antigen; HLDA, human leukocyte differentiation antigen; KIR, killing inhibitory receptor; DC, dendritic cell.
Copyright © 1998 by The American Association of Immunologists
In the mouse, one of the most commonly used pan-B cell markers
is identified by the mAb RA3-6B2 (CD45R/B220); however, this
0022-1767/98/$02.00
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
M
olecules on the surface of hemopoietic cells play important roles in the development and function of these
cells and have permitted us to understand the immune
system in increasingly great depth. In recent years, it has become
clear that there is a considerable amount of cross-talk between
cells of the hemopoietic system and nonhemopoietic cells, with
much of this interplay mediated by cell surface molecules. This
review includes a discussion of cell surface Ags expressed on both
hemopoietic and nonhemopoietic cells. In addition to an update on
nomenclature, there will be a discussion of functions of the molecules, when known, and brief comments on the use of particular
Ags for immunophenotyping cell subsets. The review will cover
molecules included in the cluster of differentiation (CD)3 and lymphocyte Ag (Ly) series as well as some new Ags without current
CD or Ly assignments.
As discussed in previous reviews (1, 2), there is a need for
unifying mouse and human nomenclature to facilitate communication between researchers studying these species. For mice, the
Ly nomenclature was originally devised to classify genes identified
through serologic studies of inbred strains; for humans, the CD
nomenclature originates from mAb reactivity to human Ags. Human leukocyte differentiation Ag (HLDA) workshops assign each
CD based on the same reactivity to one human Ag by at least two
mAbs; provisional CDw are sometimes given to clusters not well
characterized or represented by only one mAb (3). The Sixth
HLDA Workshop, which took place in 1996, resulted in the assignment of novel CDs with new designations spanning CD131 to
CD166. mAb submitted to the workshop are tested by laboratories
participating in the following sections: T cell, B cell, NK cell,
adhesion, endothelial, myeloid, nonlineage, platelet, cytokine re-
3862
MOUSE CELL SURFACE Ags
Table I. Mouse Ly molecules a
Status
Ly-1
Ly-2
Ly-3
Ly-4
Ly-5
Ly-6A
Ly-6B
Ly-6C
Ly-6D
Ly-6E
Ly-6F
Ly-6G
Ly-7
Ly-8
Ly-9
Ly-10
Ly-11
Ly-12
Ly-13
Ly-14
Ly-15
Ly-16
Ly-17
Ly-18
Ly-19
Ly-20
Ly-21
Ly-22
Ly-23
Ly-24
Ly-25
Ly-26
Ly-27
Ly-28
Ly-29
Ly-30
Ly-31
Ly-32
Ly-33
Ly-34
Ly-35
Ly-36
Ly-37
Ly-38
Ly-39
Ly-40
Ly-41
Ly-42
Ly-43
Ly-44
Ly-45
Ly-46
Ly-47
Ly-48
Ly-49A
Ly-49B
Ly-49C
Ly-49D
Ly-49E
Ly-49F
Ly-49G
Ly-49H
Ly-49I
Ly-50
Ly-51
Ly-52
Ly-53
Ly-54
Ly-55
Ly-56
Ly-57
Ly-58
Ly-59
Ly-60
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Current CD
CD5
Cd8a
CD8b
CD4
CD45
Previous Designation
Gene Symbol
Chromosome
Ly-35
Cd5
Cd8a
CD8b
CD4
Ptprc
Ly6a
Ly6b
Ly6c
Ly6d
Ly6e
Ly6f
Ly6g
Ly7
Ly8
Ly9
CD98
Ly11
Cd5
Ly13
Ly14
Itgal
Ly16
Fcgr2b
Ly18
Cd72
Ly20
Itgal
Sell
Ly23
CD44
Ly25
Ly26
Ly6
Ly28
Ly29
Ly30
Ly31
Cd72
Ly33
Ly34
Cd8a
Ly36
Cd2
Cd1d
Ly39
Itgam
Npps
Fcer2a
IL2ra
Cd20
Ly45
Ly46
Icam1
Spn
Klra1
Klra2
Klra3
Klra4
Klra5
Klra6
Klra7
Klra8
Klra9
Fcer1g
Enpep
Cd24a
Cd80
Cd79a
Klrb1
Cd152
Ly57
CD86
Klrb3
Icam2
19
6
6
6
1
15
15
15
15
15
15
15
16
Unknown
1
19
2
19
Unknown
7
7
12
1
12
4
4
7
1
2
2
2
Unknown
15
13
4
Unknown
4
4
1
13
6
6
3
3
17
Unknown
10
8
2
19
Unknown
Unknown
9
7
6
6
6
6
6
6
6
6
6
1
3
10
16
7
6
1
19
16
6
11
TAP, Sca-1, Ly-6D
ThB, Ly-61
TSA-1, Sca-2, Ly-67
Withdrawn
CD98
Withdrawn
CD5
Withdrawn
CD11a
Withdrawn
CD16/32
Withdrawn
CD72
Withdrawn
Withdrawn
CD11a
CD62L
Withdrawn
CD44
Withdrawn
Allele of Ly-1
LFA-1
Ly-18
Ly-m18
Ly-m19, Lyb-2
Ly-22a
Allele of Ly-15, LFA-1
L-selectin, MEL-14
Pgp-1
Ly-6
Withdrawn
CD72
Lyb-2
Withdrawn
CD8a
Allele of Ly-2
Withdrawn
Withdrawn
CD2
CD1d
Withdrawn
CD11b
Mac-1
Withdrawn
Withdrawn
Withdrawn
CD23
CD25
CD20
FceRIIa
IL-2Ra
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
CD54
CD43
ICAM-1
leukosialin
A1
5E 6
LGL-1
Withdrawn
Withdrawn
Withdrawn
Withdrawn
Withdrawn
CD24a
CD80
CD79a
CD161
CD152
Withdrawn
Withdrawn
Withdrawn
CD86
CD102
FceRI, high affinity
6C3/BP-1
HSA
B7-1
mb-1, lga
NKR-P1A
CTLA-4
Lyw-57
B7-2
NK1.1, NKR-P1C
ICAM-2
Continued
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
Ly
The Journal of Immunology
3863
Table I. continued
Status
Ly-61
Ly-62
Ly-63
Ly-63L
Ly-64
Ly-65
Ly-66
Ly-67
Ly-68
Ly-69
Ly-70
Ly-70L
Ly-71
Ly-72
Ly-72L
Ly-73
Ly-74
Ly-75
Ly-76
Ly-77
Ly-78
Ly-79
Ly-80
Ly-81
Lyb-2
Lyb-3
Lyb-4
Lyb-5
Lyb-6
Lyb-7
Lyb-8
Withdrawn
Withdrawn
Withdrawn
CD154
CD136
Withdrawn
CD157
a
Current CD
Previous Designation
Withdrawn
Withdrawn
CD134
Withdrawn
CD135
Withdrawn
CD72
Withdrawn
CD22
ThB
gp39
4-1BB
4-1BB ligand
14/A10
BP-3
LAG3
TSA-1, Sca-2
AA4.1
Ly-69
OX-40
OX-40L
F4/80
Flk-2/Flt3
Flt3 L
Flk-1
Ep-CAM
DEC-205
TER-119
GL7
RP-105
33D1
Ly32
Gene Symbol
Ly6d
Cd401
Cd136
Ly631
Ly64
Bp3
Lag3
Ly6e
Ly68
Itgb7
Txgp1
Txgp1l
Emr1
Flt3
Flt3l
Flk1
Ly74
Ly75
Ly76
Ly77
Ly78
Ly79
Mir
Trail
CD72
Lyb3
Lyb4
Lyb5
Lyb6
Lyb7
Cd22
Chromosome
15
X
4
17
13
5
6
15
Unknown
15
4
1
17
5
7
5
Unknown
Unknown
Unknown
Unknown
Unknown
Unknown
Unknown
Unknown
4
Unknown
4
Unknown
4
12
7
References for all Ly molecules have been entered into the Mouse Genome Database (http://www.informatics.jax.org).
epitope is also expressed on activated T and NK cells (5) and NK
cell progenitors (6). The CD19 Ag appears to be more restricted to
the B cell lineage and is not expressed by NK progenitor cells (6)
or by LAK cells (N. Alaverdi, unpublished observation). Hence,
Abs to mouse CD19 may be used more reliably to identify B cells.
Although the mouse CD20 gene has been cloned (7), no mAb has
been reported. While surface IgM and IgD are expressed by both
conventional (B-2) and unconventional (B-1) B cells, the expression of CD23 (8), CD5, and CD11b (9) can be used to distinguish
these subsets. Other markers identifying the B cell lineage and its
subsets include CD138 (Syndecan-1) (10), CD157 (BP-3) (11, 12),
CD35 and CD21 (13), CD40 (14), CD72 (15), CD22 (16), Ly-68
(AA4.1) (17), and Ly-78 (RP-105) (18, 19). CD86 (B7-2) and
CD80 (B7-1), although broadly expressed on APCs other than B
cells, are useful markers for activated B cells.
T cells
While mAbs to Thy-1 (CD90) and TCR complex Ags have commonly been used as pan-T cell markers in mice, Thy-1 is not restricted to T cells, while CD3e expression is correlated with T cell
maturation, similar to CD27 (20) and CD28 (21). In humans, CD2,
CD5, and CD7 are preferred pan-T cell markers, although they are
also expressed on subsets of other cell types (3). The mouse CD7
gene has been cloned recently (22); its Ag distribution remains to
be determined. The CD8 and CD4 molecules are generally used for
identification of mainstream helper and cytotoxic T cells, respectively. A third class of T cells with both helper and cytotoxic
properties has been identified using the CD161c (NK1.1, previously Ly-59 or NKR-P1C) (23). Reported memory T cell markers
include CD44 (24), CD62L (25), and CD45RB (26). Activated T
cell markers include CD26, CD27, CD30, CDw137 (4-1BB),
CD152 (CTLA-4), CD154 (gp39), CD134 (OX-40), CD95L (Fas
ligand), CD45R/B220, and Ly-6E (TSA, sca-2) (27).
NK cells
The official mouse and human genetic nomenclature for a substantial number of the surface molecules expressed by NK cells will,
most likely, soon be changed by consensus of those expert in the
field. The provisional symbol for both the mouse and human nomenclature relating to the lectin-like molecules would be Klr, for
killer cell lectin-like receptor. This will be followed by the letters
a through e to designate five distinct families and then a number to
specify each member of that family: Klra# will be used for the
Ly49 family, Klrb# for the NKR-P1 family, Klrc# for the NKG2
family, klrd# for CD94 and related genes, and klre# for the MKAP
family. The Klra and Klre families have no human members
to date.
The CD161c (NK1.1 Ly-59, NKR-P1C) Ag is the most widely
used pan-NK marker in mice. Since its expression is restricted to
CE, New Zealand Black, and C57BL/6-related strains, many commonly used strains do not express the Ag. In addition, like many
NK cell markers, CD161c is also expressed on a subset of T cells
(23). Although CD56 (NCAM (neural cell adhesion molecule)) is
used as the human NK cell marker, several existing Abs to mouse
CD56 did not react with mouse NK cells (3); however, a novel
mAb, DX5, exhibits similar reactivity to anti-CD161c Ab but reacts with NK cells in all strains of mice tested, including NK1.1negative strains (L. Lanier, unpublished observation). CD122
(IL-2R b-chain), which is constitutively expressed on NK cells and
a subset of T cells, can also be used to identify NK cells (V.
Kumar, unpublished observation). A multitude of genes encoding
NK receptors, such as the newly cloned mouse gene CD94 (L.
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
Ly
3864
MOUSE CELL SURFACE Ags
Table II. Mouse CD moleculesa
CD/Other name
Chromosome
CD1d
CD2/LFA-2
CD3d
CD3e
CD3g
CD3z
CD4/L3T4/Ly-4
CD5/Ly-1
CD6
CD7
CD8a/Ly-2
CD8b/Ly-3
CD9
CD10/CALLA, NEP
CD11a/Ly-15, LFA-1 a-chain
CD11b/Ly-40, Mac-1 a-chain
CD11c/integrin aX
CD12
CD13
CD14
CD15
CD16/FcgR III
CD17
CD18/integrin b2
CD19
CD20/Ly-44
CD21/complement receptor-2
CD22/Lyb-8
CD23/Ly-42
CD24a/HSA
CD24b
CD24c
CD25/p55, IL-2Ra chain
Cd1d
Cd2
Cd3d
Cd3e
Cd3g
Cd3z
Cd4
Cd5
Cd6
Cd7
Cd8a
Cd8b
Cd9
Mme
Itgal
Itgam
Itgax
Not defined
Lap1
Cd14
Not defined
Fcgr3
Not defined
Itgb2
Cd19
Cd20
Cr2
Cd22
Fcer2a
Cd24a
Cd24b
Cd24c
Il2ra
3
3
9
9
9
1
6
19
19
11
6
6
6
3
7
Unknown
Unknown
CD26/THAM
CD27
CD28
CD29/integrin b1, gplla
CD30/Ki
CD31/PECAM-1
CD32/Ly-17/Fcg receptor II
CD33
CD34
CD35/complement receptor-1
CD36
CD37
CD38
CD39
CD40
Dpp4
Cd27
Cd28
Itgb1
Cd30
Pecam
Fcgr2
Cd33
Cd34
Cr1
Cd36
Cd37
Cd38
Not defined
Cd40
CD41/integrin allb
CD42
CD43/leukosialin, Ly-48
CD44/Pgp-1, Ly-24
Itga2b
Not defined
Spn
Cd44
CD45/LCA, Ly-5
CD45RA
Ptprc
Ptprc
CD45RB
Ptprc
CD45RC
Ptprc
CD45RO
Ptprc
CD45R/B220
Ptprc
CD46
CD47/integrin-associated protein
(IAP)
CD48/Sgp-60, BCM-1, BLAST-1
CD49a/integrin a1
CD49b/integrin a2
CD49c/integrin a3
Not defined
Itgp
Cd48
Itga1
Itga2
Itga3
9
18
1
10
7
19
1
7
8
10
8
14
2
Comments
Associates with b2m, Ag presentation, ligand for NK11 T cells
Ig superfamily, CD49 counter-receptor, adhesion, T cell activation
TCR subunit, receptor complex assembly/traffic, signal transduction
TCR subunit, receptor complex assembly/traffic, signal transduction
TCR subunit, receptor complex assembly/traffic, signal transduction
TCR subunit, receptor complex assembly/traffic, signal transduction
TCR coreceptor, MHC class II receptor, signal transduction
CD72 counter-receptor, regulation of cellular activation
T cell activation, thymic development, CD166 counterreceptor
Early T cell marker (human)
TCR coreceptor, MHC class I receptor, signal transduction
TCR coreceptor, MHC class I receptor, signal transduction
TM4 superfamily, T cell costimulation
Ectoenzyme, neutral endopeptidase, B cell development
Associates with CD18, ICAM-1, and ICAM-2 counterreceptor
Associates with CD18, fibrinogen, and C3bi counterreceptor
Associates with CD18
Type II transmembrane protein, aminopeptidase N
GPI-linked protein, LPS/LBP complex receptor
Carbohydrate determinant: Lewis X (human); binds CD62E, CD62L, CD62P
Low-affinity binding to IgG, ADCC
Carbohydrate determinant: lactosylceramide (human)
Adhesion, associates with CD11a, CD11b, CD11c
BCR co-receptor, signal transduction, pan B marker
B cell activation/differentiation, Type III transmembrane protein
Cd 3 receptor, complex with BCR
Adhesion, B cell activation
Low-affinity receptor for IgE
T cell costimulation, adhesion, CD62P counterreceptor
Low-affinity binding to IL-2 by itself, associates with CD122 and CD132,
lymphocyte differentiation and activation
2
Ectoenzyme, dipeptidyl peptidase, cellular activation
6
TNFR superfamily, T cell costimulation, CD70 counterreceptor
1
T cell costimulation, CD80 and CD86 counterreceptor
Unknown VLAb, associates with CD49a, b, c, d, e, or f, adhesion
4
TNFR superfamily, T cell activation/regulation
6
Adhesion, signal transduction; counterreceptor to CD38
1
Low-affinity binding to IgG, ADCC
7
1
Multiple isoforms, CD62L counterreceptor (90 kD), hemopoiesis (human)
1
C3b receptor, phagocytosis
5
Thrombospondin receptor; oxidixed LDL receptor; collagen receptor
7
5
Ectoenzyme, cyclase/hydrolase, cellular activation, CD31 counterreceptor (human)
2
11
TNFR superfamily, B cell activation/differentiation/survival
CD154 (gp39) counterreceptor
Associates with integrin b3, adhesion; platelet marker
7
2
Two isoforms; adhesion, signal transduction, binding to CD54
Receptor for hyaluronate, adhesion, homing, metastasis, T cell activation,
marker for memory T cells
1
Cellular differentiation/activation, tyrosine phosphatase pan-leukocyte marker
1
Cellular differentiation/activation, tyrosine phosphatase restricted expression,
exon A dependent
1
Cellular differentiation/activation, tyrosine phosphatase restricted expression,
exon B dependent
1
Cellular differentiation/activation, tyrosine phosphatase restricted expression,
exon C dependent
1
Cellular differentiation/activation, tyrosine phosphatase, marker for naive T cells;
restricted expression
1
Cellular differentiation/activation, tyrosine phosphatase, marker for B cells
and activated T and NK (LAK) cells
Membrane cofactor protein (MCP)
Unknown Activation and extravasation of PMN; Ig superfamily
1
13
13
11
GPI-linked protein, T cell costimulation, adhesion, CD2 counterreceptor
Associates with CD29, laminin/collagen receptor
Associates with CD29, laminin/collagen/fibronectin receptor
Associates with CD29, laminin/collagen/fibronectin receptor
Continued
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
Mouse Gene Symbol
The Journal of Immunology
3865
Table II. continued
CD/Other name
Mouse Gene Symbol
Chromosome
CD49d/integrin a4
CD49e/integrin a5
CD49f/integrin a6
CD50/ICAM-3
CD51/integrin aV
CD52
CD53
CD54/ICAM-1, Ly-47
CD55
CD56/NCAM-1
CD57
CD58
CD59
CD60
CD61/integrin b3
CD62E/E-selectin, ELAM
CD62L/L-selectin, LECAM-1
Itga4
Itga5
Itga6
Icam3
Itgav
Not defined
Cd53
Icam1
Daf1
Ncam
Not defined
Not defined
Cd59
Not defined
Itgb3
Sele
Sell
2
15
2
Unknown
2
CD62P/P-selectin, PADGEM
CD63
CD64/FcgRI
CD65
Selp
Cd63
Fcgr1
Not defined
1
18
3
CD66
CD67
CD68/macrosialin
CD69/very early activation Ag
CD70
CD71/transferrin receptor
CD72/Lyb-2
CD73
CD74/invariant chain
CD75
CD76
CD77
CD78
CD79a/Iga
CD79b/Igb
CD80/B7-1
CD81/TAPA-1
CD82/KAI1
CD83
CD84
CD85
CD86/B7-2
CD87
CD88
CD89
CD90/Thy-1
CD91/a2 macroglobulin receptor
CD92
CD93
CD94
CD95/Fas
CD96
CD97
CD98/4F2, Ly-10
CD99
CD100
CD101
CD102/ICAM-2
CD103/integrin aIEL
CD104/integrin b4
CD105/endoglin
CD106/VCAM-1
CD107a/LAMP-1
CD107b/LAMP-2
CDw108
CDw109
CD110
CD111
CD112
CD113
CD114
Not defined
3
9
1
9
Comments
Associates with CD29
Associates with CD29, fibronectin/laminin receptor
Associates with CD29, laminin receptor
Adhesion/signaling
Associates with b integrins, vitronectin and fibronectin receptor
Campath (human)
Adhesion, T cell costimulation, CD11a, CD11b, and CD43 counterreceptor
Adhesion, nervous system
HNK1 (human)
LFA-3 (human)
2
11
1
1
Ceremide dodecasaccharide (human)
Cd68
Cd69
Cd70
Trfr
Cd72
Nt5
Ii
Not defined
Not defined
Not defined
Not defined
Cd79a
Cd79b
Cd80
CD81
Cd82
Cd83
Not defined
Not defined
Cd86
Not defined
Not defined
Not defined
Thy1
Lrp
Not defined
Not defined
Not defined
Fas
Not defined
Not defined
Cd98
Not defined
Not defined
Not defined
Icam2
Itgae
Itgb4
Eng
Vcam1
Lamp1
Lamp2
Not defined
Withdrawn, now CD66b
Unknown Type I transmembrane, lysosomal-associated protein
6
Leukocyte activation; early lymphocyte activation marker
CD27 counter-receptor
Unknown Type II transmembrane protein, activation, iron metabolism
4
Cd5 counter-receptor, B cell costimulation
Ecto-59 nucleotidase; B and T cell subsets (human)
18
MCH class II folding/trafficking, Ag presentation
7
Unknown
16
7
2
Unknown
Ig superfamily, signal transduction
Ig superfamily, signal transduction
B cell costimulation, T/B interaction CD28 and CE152 counterreceptor
TM4 superfamily, signal transduction, T cell costimulation
TM4 superfamily, signal transduction, T cell costimulation
Marker for dendritic and activated T and B (human; mouse cloned, no mAb)
16
B cell costimulation, T/B interactions, CD28 and CD152 counterreceptor
9
15
C5a receptor (human)
Receptor for IgA
GPI-linked transmembrane protein, signal transduction, T cell activation
Lipoprotein metabolism
19
NK cell receptor for HLA-class I molecules
TNFR superfamily apoptosis, T cell costimulation, lpr mutation
Ig superfamily, T cell activation, increased late expression
19
Cellular activation, calcium flux
11
Unknown
11
2
3
8
X
V7 glycoprotein, Ig superfamily, CD3-dependent T cell activation (human)
Ig superfamily, adhesion to CD11a
Associates with integrin b7, adhesion
Associates with integrin a6, adhesion
Adhesion, ligand for TGF-b
Signaling, adhesion to CD49d/CD29 (VLA-4)
Lysosomal-associated membrane protein, adhesion/metastasis
Lysosomal-associated membrane protein, adhesion/metastasis
Sialomucin
Reserved
Reserved
Reserved
Reserved
Not defined
Continued
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
Associates with CD41 and CD51, extracellular adhesion
Adhesion, leukocyte rolling/migration, binds to sialyl Lewis X (CD15)
Adhseion, leukocyte rolling/migration, binds to sialyl Lewis X (CD15)
CD34 counterreceptor
Adhesion, leukocyte rolling/migration, binds to CD15 and CD24
Platelet activation Ag (TM4 superfamily)
High-affinity binding to IgG, ADCC
3866
MOUSE CELL SURFACE Ags
Table II. continued
Mouse Gene Symbol
Chromosome
CD115/M-CSFR, CSF-1R
CD116
CD117/c-KIT, steel factor receptor
CD118/IFN-ab receptor
Csfmr
Csfgmra
Kit
Ifnar
18
19
5
16
Ifngr 1
Tnfr1
Thfr2
Il1r1
IL1r2
Il2rb
13
6
4
1
1
15
II3ra
Il4ra
Il5ra
Il6ra
Il7ra
Cmkar2
Reserved
Il6st
II3rb 1/II3rb2
Il2rg
14
7
6
3
15
1
CD119/IFN-g receptor
CD120a/TNF receptor a-chain
CD120b/TNF receptor b-chain
CD121a/IL-1 receptor a-chain
CD121b/IL-1 receptor b-chain
CD122/IL-2 receptor b-chain
CD123/IL-3 receptor a-chain
CD124/IL-4 receptor a-chain
CD125/IL-5 receptor a-chain
CD126/IL-6 receptor a-chain
CD127/IL-7 receptor a-chain
CD128/IL-8 receptor a-chain
CD129
CD130/gp 130
CDw131/common b-chain
CD132/common g-chain
CD133
CD134/OX-40, Ly-70
CD135/Flk-1/flt3, Ly-72
CD136/4-1BB, Ly-63
CD137/MSPR, RON
CD138/syndecan-1
CD139
CD140a/PDGF-R a-chain
CD140b/PDGF-R b-chain
CD141/thrombomodulin
CD142
CD143
CD144/VE-cadherin
CDw145
CD146/MUC 18/s-endo
CD147/neurothelin, basigin
CD148/M4, M56
CD149/MEM-133
CDw 150/IPO-3; SLAM
CD151/PETA
CD152/CTLA-4, Ly-56
CD153/CD30 ligand
CD154/CD40 ligand (gp39), Ly-62
CD155
CD156/ADAM8
CD157/BST-1, Mo-5, Ly-65
CD158a/p58.1
CD159b/p58.2
CD160
CD161a
CD161b
CD161c
CD162/PSGL-1
CD163
CD164/MGC-24, A115, A25
Reserved
Txgp2
Flt3
Cd136
Not defined
Synd-1
Not defined
Pdgfra
Pdgfrb
Thbd
Not defined
Ace
Cdh5
CD165/Ad2/gp37
CD166/ALCAM
Not defined
Cd166
a
Not defined
Bsg
Not defined
Not defined
Not defined
Not defined
Cd152
Cd153
Cd154
Not defined
Cd156
Bp3
Not defined
Not defined
Reserved
Klrb1
Klrb3
Cd162
Not defined
Not defined
Comments
Tyrosine kinase receptor family, signal transduction, cell differentiation
Receptor for GM-CSF, associates with CDw131
Tyrosine kinase receptor family, signal transduction, cell differentiation,
Wr mutation
IFN-ab receptor, signal transduction
High-affinity binding to IFN-g, signal transduction
Type I, TNFR superfamily, signal transduction, apoptosis
Type II, TNFR superfamily, signal transduction, apoptosis
Ig superfamily, IL-1 binding, signal transduction
Ig superfamily, IL-1 binding
Associates with CD25 and CD132 for high-affinity binding to IL-2, signal
transduction
Low-affinity binding to IL-3, associates with CDw131 for high-affinity binding
Associates with CD132 for high-affinity binding to IL-4
Low-affinity binding to IL-5, associates with CDw131 for high-affinity binding
Low-affinity binding to IL-6, associates with CD130 for high-affinity binding
Associates with CD132 for high-affinity binding to IL-7
Binding to mouse MIP-2
Unknown Signal transduction, common b chain of IL-6R, IL-11R, LIFR, OSMR
15
Signal transduction, member of IL-3R, IL-5R, and GM-CSFR complexes
X
Signal transduction, member of IL-2R, IL-4R, IL-7R, IL-13R, and IL-15R
complexes
4
5
4
12
5
18
2
Unknown
11
8
10
1
4
X
7
5
6
TNFR superfamily, T cell costimulation
Tyrosine kinase receptor family myeloid and lymphoid progenitor development
TNFR superfamily, T cell costimulation
Receptor for macrophage-stimulating protein (MSP) (human)
B cell development/differentiation
Tyrosine kinase receptor family, binds to PDGF a and b, signal transduction
Tyrosine kinase receptor family, binds only to PDGF b, signal transduction
Tissue factor, receptor for cofactor VII (human)
Angiotesin converting enzyme
Adhesion
Pan endothelial marker (defined by mAbs E036, E037)
Ig superfamily, blood-brain barrier, expressed on activated leukocytes
Ig superfamily, T cell stimulation (human)
TM4 family; signaling
T cell activation/regulation, CD80 and CD86 counter-receptor
TNF family, activated lymphocytes, CD30 counter-receptor
TNF family, T cell activation, transient expression
Poliovirus receptor (human)
Ectoenzyme, B and T cell development
NK receptor (human)
NK receptor (human)
NK cell activation/regulation; NKR-P1A
Mouse NK1.1, pan NK marker; NKR-P1C
P-selectin ligand protein one P11, P12 (human)
CD6 counter-receptor, activated leukocyte-cell adhesion molecule,
thymic development, T/B interaction, nervous system (human)
CD1-CD130 are cited in ref. 4; references for CD131–CD166 have been entered into the Mouse Genome Database (http://www.informatics.jax.org).
Lanier, unpublished observation), CD161a, and the Klra family
members, have been characterized (28). The MHC class I ligands
of these NK receptors and their inhibitory or activating functions
are being elucidated. To date, no mouse homologues of the killing
inhibitory receptor (KIR) and killing-activating receptor (KAR) Ig
superfamily members have been discovered, although two mouse
genes related to human KIR, gp49A and gp49B (B1 and B2), have
been cloned from mouse mast cells (29). The available data sug-
gest that gp49 is unlikely to be the mouse equivalent of human
KIR (29). It is likely that Klra family members serve as KIR and
KAR functional equivalents in mice (28).
Macrophages/monocytes
The anti-Ly-71 (F4/80) mAb has been used extensively in determining the distribution and function of mouse tissue macrophages
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
CD/Other name
The Journal of Immunology
(30), although eosinophils and dendritic cells (DC) have been reported to react with this mAb (31, 32). To date, no human homologue of Ly-71 (F4/80) has been reported. CD11b (Mac-1), another commonly used marker for the monocyte/macrophage
lineage, is expressed on NK cells, granulocytes, a T cell subset,
and peritoneal B-1 B cells. CD14 is widely perceived as the best
marker for the human macrophage/monocyte population. In mice,
the level of CD14, as recognized by an anti-CD14 mAb, rmC5–3,
was low or undetectable on resting blood monocytes. It remains to
be determined whether other newly generated Abs to mouse CD14
will recognize a distribution similar to that in humans. Other mAbs
used for identification of macrophage/monocyte subsets are
MOMA-1, MOMA-2 (33), Mac-2, Mac-3, and the macrophage
scavenger receptor.
Dendritic cells
Granulocytes
Expression of Ly-6G is reported to be primarily limited to granulocytes; mAbs specific to this molecule, also known as the Gr-1
Ag, have been used successfully to separate mouse granulocyte
lineage cells (40).
Erythroid cells
The Ly-76 Ag detected by the mAb TER-119 has been used to
identify cells of the erythroid lineage (41, 42).
Endothelial cells
MECA-32 appears to be most restricted marker for endothelium
(43). Other Ags expressed by endothelial cells include CD106
(vascular cell adhesion molecule-1), CD31, CD34, Ly-73 (Flk-1),
and CD105. CD62E is expressed by activated endothelial
cells (27, 44).
Platelets
CD41 (integrin aIIb) is the best marker for platelets; other surface
proteins expressed by platelets include CD61 (integrin b3) (45)
and CD9 (46). Activated platelets express CD62P (27).
Progenitor cells
The classic method for identifying mouse stem/pluripotent cells in
total bone marrow cells has included the use of a combination of
Abs; cells negative for lineage markers CD4, CD8, CD11b (Mac1), CD45/B220, Ly-6G (Gr-1), and Ly-76 (Ter-119) and positive
for CD117 (c-kit), and Ly-6A (Sca-1), which are greatly enriched
for capacity to reconstitute hemopoiesis (47, 48). Polyclonal and
monoclonal Abs to mouse CD34 (49 –50) have demonstrated that
CD34 is expressed on a small subset of bone marrow cells. In
humans, the stem cell populations are identified by the expression
of CD34. A recent report with one anti-mouse CD34 mAb, 49E8
(RAM34), however, suggests that primitive hemopoietic stem cells
capable of long term repopulation are contained in the CD34-negative/low fraction, whereas the CD34-positive cells are committed
progenitor cells lacking self-renewal capability (51). Other relevant Ags expressed by progenitor cells include CD25, CD90 (Thy1), ER-MP12 (52), CD135 (Flk-2/Flt-3) (53), Ly-6E (TSA-1,
Sca-2) (54), Ly-51 (BP-1, 6C3), and CD157 (BP-3).
Activation Ags
An important feature of cellular activation is the de novo expression of surface molecules or up-regulation of the Ags expressed
constitutively. The mode of stimulation, kinetics, and expression
pattern of any given marker may imply its role in the immune
response. Surface molecules, including CD71 (transferrin receptor), CD98 (4F2), and CD69, are expressed by a wide range of
activated cell types, reflecting their general role in cellular proliferation. CD69 is useful as a lymphocyte activation marker because
of its expression in the very early stage of activation (55). It is
noteworthy that although some markers were initially defined to be
restricted to specific types of activated cells, their distributions
were subsequently found to be more general. For example, CD25
(IL-2R a-chain), often used as a T cell activation marker, is
present on activated T, B, and NK cells and is expressed during
ontogeny on pre-B and pre-T cells. CD80 and CD86, initially reported as B cell activation markers, are constitutively expressed by
macrophages, DCs, and fibroblasts and can be induced on activated T cells (56, 57). Further, sensitivity of the detection method
may be a limiting factor when studying low density Ags. Other
molecules reported to be expressed by activated lymphocytes include CD152 (CTLA-4), CDw137 (4-1BB), CD134 (OX-40),
DATK44 Ag (TABS), Ly-77 (GL7), CD45R (B220), CD30, CD95
ligand, CD43, Ly-6 family members, CD106, cytokine receptors,
and the family of very late Ag adhesion molecules.
In this communication, we provide an update on mouse cell
surface molecules, including lists of surface markers that, in combination with multiparameter flow cytometric analysis, can be used
to trace cell lineages and activation state. Several novel markers
mentioned here may prove useful in mouse immunology research.
Most of the reported mAbs and their respective Ags are compiled
in the CD and Ly charts. Undoubtedly, many molecules have not
been included here. Scientists are encouraged to contact the authors and the Committee on Standardized Genetic Nomenclature
for Mice to submit novel molecules for their inclusion in the future
reports. In addition to this communication, information on the
mouse genome and genetic markers is available on the worldwide
web. The Mouse Genome Database can be accessed via http://
www.informatics.jax.org. Information on germ-line disruptions of
Ly/CD-encoding loci can be obtained at www.bioscience.org/
knockout/knochome.htm or TBASE at www.gdb.org/dan/tbase.html.
Acknowledgments
We thank M. A. Reyes and Drs. C. Shih, K. Holmes, and V. Kumar for
their helpful assistance with this manuscript, and B. R. Marshall for excellent editorial assistance.
References
1. Holmes, K. L., and H. C. Morse III. 1988. Cell surface antigen expression in
murine hematopoietic cell differentiation. Immunol. Today 9:355.
2. Morse, H. C., III. 1992. Genetic nomenclature for loci controlling surface antigens of mouse hemopoietic cells. J. Immunol. 149:3129.
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
DC display surface phenotype heterogeneity depending on their
microenvironment and state of activation. Their ill-defined surface
phenotypes in addition to their low numbers in tissues have made
the isolation of these cells rather cumbersome. DC express many
adhesion and costimulatory molecules and myeloid lineage markers (32). Although several Ags have been reported to be expressed
specifically by DC, mAb to these Ags often react with other cell
types or only recognize subsets of DC. For separation of DC from
other cell types, multicolor analysis or prior enrichment protocols
such as plastic adherence methods are necessary. The Ly-75
(DEC-205) Ag (34) and CD11c (35) have proved to be more restricted markers for DC, although they may not be expressed on all
DC, and they may also be expressed on other cell types. In humans, CD83 and the Ag identified by mAb CRMF-44 have recently been identified as novel markers for DC (3, 36). Other Abs
useful for the identification of DCs include Ly-79 (33D1) (37), 4F7
(38), and Ly-74 (Ep-CAM, gp40), a homologue of human epithelial growth factor (39).
3867
3868
31. McGarry, M. P., and C. C. Stewart. 1991. Murine eosinophil granulocytes bind
the murine macrophage-monocyte specific monoclonal antibody F4/80. J. Leukocyte Biol. 50:471.
32. Peters, J. H., R. Gieseler, B. Thiele, and F. Steinbach. 1996. Dendritic cells: from
ontogenetic orphans to meylomonocytic descendants. Immunol. Today 17:273.
33. Leenen, P. J. M., M. F. T. R. deBruijn, J. S. A. Voerman, P. A. Campbell, and
W. van Ewijk. 1994. Markers of mouse macrophage development detected by
monoclonal antibodies. J. Immunol. Methods 174:5.
34. Jiang, W., W. J. Swiggard, C. Heufler, M. Peng, A. Mirza, R. M. Steinman, and
M. C. Nussenzweig. 1995. The receptor DEC-205 expressed by dendritic cells
and thymic epithelial cells is involved in antigen processing. Nature 375:151.
35. Metlay, J. P., M. D. Witmer-Pack, R. Agger, M. T. Crowley, D. Lawless, and
R. M. Steinman. 1990. The distinct leukocyte integrins of mouse spleen dendritic
cells as identified with new hamster monoclonal antibodies. J. Exp. Med. 171:
1753.
36. Summers, K. L., P. B. Daniel, J. L. O’Donnel, and D. N. J. Hart. 1995. Dendritic
cells in synovial fluid of chronic inflammatory arthritis lack CD80 surface expression. Clin. Exp. Immunol. 100:81.
37. Crowley, M., K. Inaba, M. Witmer-Pack, and R. M. Steinman. 1989. The cell
surface of mouse dendritic cells: FACS analyses of dendritic cells from different
tissues including thymus. Cell. Immunol. 118:108.
38. Mohamadzadeh, M., H. Jonuleit, G. Kolde, A. Pavlidou, E. Schmitt, and J. Knop.
1993. Functional and morphological characterization of 4F71 spleen accessory
dendritic cells. Int. Immunol. 5:615.
39. Borkowski, T. A., A. J. Nelson, A. G. Farr, and M. C. Udey. 1996. Expression
of gp40, the murine homologue of human epithelial cell adhesion molecule (EpCAM), by murine dendritic cells. Eur. J. Immunol. 26:110.
40. Fleming, T. J., M. L. Fleming, and T. R. Malek. 1993. Selective expression of
Ly-6G on myeloid lineage cells in mouse bone marrow. RB6 – 8C5 mAb to granulocyte-differentiation antigen (Gr-1) detects members of the Ly-6 family. J. Immunol. 151:2399.
41. Ikuta, K., T. Kina, I. MacNeil, N. Uchida, B. Peault, Y.-H. Chien, and
I. L. Weissman. 1990. A developmental switch in thymic lymphocyte maturation
potential occurs at the level of hematopoietic stem cells. Cell 62:863.
42. Okada, S., H. Nakauchi, K. Nagayoshi, S. Nishikawa, S. Nishikawa, Y. Miura,
and T. Suda. 1991. Enrichment and characterization of murine hematopoietic
stem cells that express c-kit molecule. Blood 78:1706.
43. Hallmann, R., D. N. Mayer, E. L. Berg, R. Broermann, and E. C. Butcher. 1995.
Novel mouse endothelial cell surface marker is suppressed during differentiation
of the blood brain barrier. Dev. Dyn. 202:325.
44. Becker-Andre, A. M., R. H. van Huijsduijnen, C. Losberger, J. Whelan, and
J. F. Delamarter. 1992. Murine endothelial leukocyte-adhesion molecule 1 is a
close structural and functional homologue of the human protein. Eur. J. Biochem.
206:401.
45. Cieutat, A. M., J. P. Rosa, F. Letourneur, M. Poncz, and S. Rifat. 1993. A comparative analysis of cDNA-derived sequences for rat and mouse b3 integrins
(GPIIIA) with their human counterpart. Biochem. Biophys. Res. Commun. 193:
771.
46. Rubinstein, E., M. Billard, S. Plaisance, M. Prenant, and C. Boucheix. 1993.
Molecular cloning of the mouse equivalent of CD9 antigen. Thromb. Res. 71:377.
47. Spangrude, G. J., S. Heimfeld, and I. L. Weissman. 1988. Purification and characterization of mouse hematopoietic stem cells. Science 241:58.
48. Spangrude, G. J., and R. Scollay. 1990. A simplified method for enrichment of
mouse hematopoietic stem cells. Exp. Hematol. 18:920.
49. Krause, D. S., T. Ito, M. J. Fackler, O. M. Smith, M. I. Collector, S. J. Sharkis,
and W. S. May. 1994. Characterization of murine CD34, a marker for hematopoietic progenitor and stem cells. Blood 84:691.
50. Lin, G., E. Finger, and J. C. Gutierrez-Ramos. 1995. Expression of CD34 in
endothelial cells, hematopoietic progenitors, and nervous cells in fetal and adult
mouse tissues. Eur. J. Immunol. 25:1508.
51. Osawa, M., K. Hanada, H. Hamada, and H. Nakauchi. 1996. Long-term lymphohematopoietic reconstitution by a single CD34-low/negative hematopoietic stem
cell. Science 273:242.
52. van der Loo, J. C., W. A. Slieker, and R. E. Ploemacher. 1995. Use of ER-MP12
as a positive marker for the isolation of murine long-term in vitro repopulating
stem cells. Exp. Hematol. 23:1002.
53. Zeigler, F. C., B. D. Bennett, C. T. Jordan, S. D. Spencer, S. Baumhueter,
K. J. Carroll, J. Hooley, K. Bauer, and W. Matthews. 1994. Cellular and molecular characterization of the role of the Flk-2/Flt-3 receptor tyrosine kinase in
hematopoietic stem cells. Blood 84:2422.
54. Kosugi, A., S. Saitoh, S. Narumiya, K. Miyake, and T. Hamaoka. 1994. Activation-induced expression of thymic shared antigen-1 on T lymphocytes and its
inhibitory role for TCR-mediated IL-2 production. Int. Immunol. 6:1967.
55. Ziegler, S. F., S. D. Levin, L. Johnson, N. G. Copeland, D. J. Gilbert,
N. A. Jenkins, E. Baker, G. R. Sutherland, A. L. Feldhaus, and F. Ramsdell. 1994.
The mouse CD69 gene: structure, expression, and mapping to the NK gene complex. J. Immunol. 152:1228.
56. Borriello, F., G. J. Freeman, S. Edelhoff, C. M. Disteche, L. M. Nadler, and
A. H. Sharpe. 1994. Characterization of the murine B7-1 genomic locus reveals
an additional exon encoding an alternative cytoplasmic domain and a chromosomal location of chromosome 16, band B5. J. Immunol. 153:5038.
57. Chen, C., A. Gault, L. Shen, and N. Nabavi. 1994. Molecular cloning and expression of early T cell costimulatory molecule-1 and its characterization as B7-2
molecule. J. Immunol. 152:4929.
Downloaded from http://www.jimmunol.org/ by guest on November 23, 2015
3. Schlossman, S. F., L. Bloumsell, W. Gilks, J. M. Harlan, T. Kishimoto,
C. Morimoto, J. Ritz, S. Shaw, R. L. Silverstein, T. A. Springer, T. F. Tedder, and
R. F. Todd, eds. 1995. Leucocyte Typing V: White Cell Differentiation Antigens.
Oxford University Press, New York.
4. Lai, L., N. Alaverdi, Z. Chen, F. G. M. Kroese, N. A. Bos, and E. C.-M. Huang.
1996. Monoclonal antibodies to human, mouse, and rat cluster of differentiation
(CD) antigens. In Weir’s Handbook of Experimental Immunology, 5th Ed. Blackwell Science, New York, p. 61.1.
5. Ballas, Z. K., and W. Rasmussen. 1993. Lymphokine-activated killer cells. VII.
IL-4 induces an NK1.11CD8a1b2 TCR-ab B2201 lymphokine-activated killer
subset. J. Immunol. 150:17.
6. Rolink, A., E. ten Boekel, F. Melchers, D. Fearon, I. Krop, and J. Andersson.
1996. A subpopulation of B2201 cells in murine bone marrow does not express
CD19 and contains natural killer cell progenitors. J. Exp. Med. 183:187.
7. Tedder, T. F., G. Klejman, C. M. Disteche, D. A. Adler, S. F. Schlossman, and
H. Saito. 1988. Cloning of a complementary DNA encoding a new mouse B
lymphocyte differentiation antigen homologous to the human B1 (CD20) antigen,
and localization of the gene to chromosome 19. J. Immunol. 141:4388.
8. Waldschmidt, T. J., K. Snapp, T. Foy, L. Tygrett, and C. Carpenter. 1992. B-cell
subsets defined by the FceR. Ann. NY Acad. Sci. 651:84.
9. Stall, A. M., and S. M. Wells. 1996. FACS analysis of murine B cell populations.
In Weir’s Handbook of Experimental Immunology, 5th Ed. Blackwell Science,
New York, p. 63.1.
10. Sanderson, R. D., P. Lalor, and M. Bernfield. 1989. B lymphocytes express and
lose syndecan at specific stages of differentiation. Cell Regul. 1:27.
11. McNagny, K. M., P. A. Cazenave, and M. D. Cooper. 1988. BP-3 alloantigen: a
cell surface glycoprotein that marks early B lineage cells and mature myeloid
lineage cells in mice. J. Immunol. 141:2551.
12. Dong, C., J. Wang, P. Neame, and M. D. Cooper. 1994. The murine BP-3 gene
encodes a relative of the CD38/NAD glycohydrolase family. Int. Immunol.
6:1353.
13. Kinoshita, T., J. Takeda, K. Hong, H. Kozono, H. Sakai, and K. Inoue. 1988.
Monoclonal antibodies to mouse complement receptor type 1 (CR1): their use in
a distribution study showing that mouse erythrocytes and platelets are CR1-negative. J. Immunol. 140:3066.
14. Hasbold, J., C. Johnson-Ledger, C. J. Atkins, E. A. Clark, and G. G. B. Klaus.
1994. Properties of mouse CD40: cellular distribution of CD40 and B cell activation by monoclonal anti-mouse CD40 antibodies. Eur. J. Immunol. 24:1835.
15. Subbarao, B., and D. E. Mosier. 1983. Induction of B lymphocyte proliferation by
monoclonal anti-Lyb 2 antibody. J. Immunol. 130:2033.
16. Torres, R. M., C. L. Law, L. Santos-Argumendo, P. A. Kirkham, K. Grabstein,
R. M. E. Parkhouse, and E. A. Clark. 1992. Identification and characterization of
the murine homologue of CD22, a B lymphocyte-restricted adhesion molecule.
J. Immunol. 149:2641.
17. McKearn, J. P., C. Baum, and J. M. Davie. 1984. Cell surface antigens expressed
by subsets of pre-B cells and B cells. J. Immunol. 132:332.
18. Miyake, K., Y. Yamashita, M. Ogata, T. Sudo, and M. Kimoto. 1995. RP105, a
novel B cell surface molecule implicated in B cell activation, is a member of the
leucine-rich repeat protein family. J. Immunol. 154:3333.
19. Yamashita, Y., K. Miyake, Y. Miura, Y., Kaneko, H. Yagita, T. Suda, S. Nagata,
J. Nomura, N. Sagaguchi, and M. Kimoto. 1996. Activation mediated by RP105
but not CD40 makes normal B cells susceptible to anti-IgM-induced apoptosis: a
role for Fc receptor coligation. J. Exp. Med. 184:113.
20. Gravestein, L. A., J. D. Nieland, A. M. Kruisbeek, and J. Borst. 1995. Novel
mAbs reveal potent co-stimulatory activity of murine CD27. Int. Immunol. 7:551.
21. Gross, J. A., T. St. John, and J. P. Allison. 1990. The murine homologue of the
T lymphocyte antigen CD28: molecular cloning and cell surface expression.
J. Immunol. 144:3201.
22. Yoshikawa, K., M. Seto, R. Ueda, Y. Obata, H. Fukatsu, A. Segawa, and
T. Takahashi. 1993. Isolation and characterization of mouse CD7 cDNA. Immunogenetics 37:114.
23. Vicari, P. A., and A. Zlotnik. 1996. Mouse NK1.11 T cells: a new family of T
cells. Immunol. Today 17:71.
24. Budd, R. C., J. C. Cerottini, and H. R. MacDonald. 1987. Selectively increased
production of interferon-g by subsets of Lyt-21 and L3T41 T cells identified by
expression of Pgp-1. J. Immunol. 138:3583.
25. Lee, W. T., and E. S. Vitetta. 1991. The differential expression of homing and
adhesion molecules on virgin and memory T cells in the mouse. Cell. Immunol.
132:215.
26. Lee, W. T., and E. S. Vitetta. 1990. Limiting dilution analysis of CD45Rhi and
CD45Rlo T cells: further evidence that CD45Rlo cells are memory cells. Cell.
Immunol. 130:459.
27. Weller, A., S. Isenmann, and D. Vestweber. 1992. Cloning of the mouse endothelial selectins: expression of both E- and P-selectin is inducible by tumor necrosis factor a. J. Biol. Chem. 267:15176.
28. Lanier, L. 1997. Natural killer cells: from no receptors to too many. Immunity
6:371.
29. Rojo, S., D. N. Burshtyn, E. O. Long, and N. Wagtmann. 1997. Type I transmembrane receptor with inhibitory function in mouse mast cells and NK cells.
Immunology 158:9.
30. McKnight, A. J., A. J. MacFarlane, P. Dri, L. Turley, A. C. Willis, and S. Gordon.
1996. Molecular cloning of F4/80, a murine macrophage-restricted cell surface
glycoprotein with homology to the G-protein-linked transmembrane 7 hormone
receptor family. J. Biol. Chem. 271:486.
MOUSE CELL SURFACE Ags