CD34 is a specific marker of mature murine mast cells

被引:67
作者
Drew, E [1 ]
Merkens, H [1 ]
Chelliah, S [1 ]
Doyonnas, R [1 ]
McNagny, KM [1 ]
机构
[1] Univ British Columbia, Biomed Res Ctr, Vancouver, BC V6T 1Z3, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1016/S0301-472X(02)00890-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. CD34 is a 90- to 120-kDa cell surface sialomucin that is widely used for the enrichment of human hematopoietic stem cells (HSCs) because of its selective expression on progenitor cells and absence on mature hematopoietic cells. Recently we found that CD34 is the prototypic member of a family of three proteins with similar structure and gene organization. In light of this observation, we further examined the distribution of CD34 family members in the mouse. Materials and Methods. Hematopoietic cell lines and primary tissues were evaluated for CD34 mRNA expression by Northern blot and protein expression by cell surface immunofluorescence. To confirm specific reactivity of the CD34 antibody, cells from CD34-deficient mice were used as controls. Results. Although CD34 mRNA was undetectable in all murine progenitor cell lines tested, high level expression was detected for bone marrow-derived mast cells (BMMCs). Likewise, cell surface immunofluorescence confirmed that CD34 is expressed by BMMCs and by in vivo peritoneal mast cells. No protein expression was observed for CD34-deficient mast cells. In addition, our data show that mast cells highly express the stem cell antigen Sca-1 and the well-known stem cell and mast cell antigen c-kit. Conclusions. Our results demonstrate that, contrary to current dogma, CD34 is expressed by one mature hematopoietic lineage: mast cells. Our data also demonstrate that antigenically, murine mast cells and their precursors closely resemble HSCs and suggest caution should be used in the phenotypic characterization of HSCs to prevent mast cell contamination of stem cell preparations. (C) 2002 International Society for Experimental Hematology. Published by Elsevier Science Inc.
引用
收藏
页码:1211 / 1218
页数:8
相关论文
共 62 条
[1]   AN ATTEMPT TO PRODUCE PRE-T CELL HYBRIDOMAS AND TO IDENTIFY THEIR ANTIGENS [J].
AIHARA, Y ;
BUHRING, HJ ;
AIHARA, M ;
KLEIN, J .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1986, 16 (11) :1391-1399
[2]   BINDING OF L-SELECTIN TO THE VASCULAR SIALOMUCIN CD34 [J].
BAUMHUETER, S ;
SINGER, MS ;
HENZEL, W ;
HEMMERICH, S ;
RENZ, M ;
ROSEN, SD ;
LASKY, LA .
SCIENCE, 1993, 262 (5132) :436-438
[3]  
Bensinger WI, 1996, BLOOD, V88, P4132
[4]   ANTIGEN CD34+ MARROW-CELLS ENGRAFT LETHALLY IRRADIATED BABOONS [J].
BERENSON, RJ ;
ANDREWS, RG ;
BENSINGER, WI ;
KALAMASZ, D ;
KNITTER, G ;
BUCKNER, CD ;
BERNSTEIN, ID .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (03) :951-955
[5]   A newly discovered class of human hematopoietic cells with SCID-repopulating activity [J].
Bhatia, M ;
Bonnet, D ;
Murdoch, B ;
Gan, OI ;
Dick, JE .
NATURE MEDICINE, 1998, 4 (09) :1038-1045
[6]   THE GENE ENCODING THE STEM-CELL ANTIGEN, CD34, IS CONSERVED IN MOUSE AND EXPRESSED IN HEMATOPOIETIC PROGENITOR-CELL LINES, BRAIN, AND EMBRYONIC FIBROBLASTS [J].
BROWN, J ;
GREAVES, MF ;
MOLGAARD, HV .
INTERNATIONAL IMMUNOLOGY, 1991, 3 (02) :175-184
[7]   Differential distribution of lumican and fibromodulin in tooth cementum [J].
Cheng, H ;
Caterson, B ;
Neame, PJ ;
Lester, GE ;
Yamauchi, M .
CONNECTIVE TISSUE RESEARCH, 1996, 34 (02) :87-+
[8]   Flk-2 is a marker in hematopoietic stem cell differentiation: A simple method to isolate long-term stem cells [J].
Christensen, JL ;
Weissman, IL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14541-14546
[9]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[10]  
DELIMA AA, 1993, ENVIRON TOXIC WATER, V8, P1, DOI 10.1002/tox.2530080102