CD84 expression on human hematopoietic progenitor cells

被引:29
作者
Zaiss, M
Hirtreiter, C
Rehli, M
Rehm, A
Kunz-Schughart, LA
Andreesen, R
Hennemann, B
机构
[1] Univ Regensburg, Abt Hamatol & Internist Onkol, D-93042 Regensburg, Germany
[2] Univ Regensburg, Inst Pathol, D-93042 Regensburg, Germany
关键词
D O I
10.1016/S0301-472X(03)00187-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. CD84 is a member of the CD2 subgroup of the immunoglobulin receptor superfamily. Members of this family have been implicated in the activation of T cells and NK cells. Expression of CD84 was originally described on most mononuclear blood cells as well as platelets. To elucidate its presence on other blood cell types, we analyzed the expression pattern of CD84 on human immature CD34(+) and mature hematopoietic cells. Methods. Expression analysis was carried out by flow cytometry. The differentiation potential of CD84(+) progenitor cells was assessed by colony-forming assays and long-term cultures. RTPCR was used to analyze CD84 mRNA isoforms. Results. In addition to monocytes, macrophages, B cells, and some T cells, CD84 is expressed on the cell surface of the majority of granulocytes. In addition, 64% +/- 5% of CD34(+) progenitor cells isolated from peripheral blood and 30.5% +/- 5% from bone marrow of healthy volunteers also express CD84. The majority of CD34(+) cells coexpressing lineage antigens were CD84(+). In methylcellulose CD34(+)CD84(+) cells formed primarily erythroid colonies, whereas myeloid or mixed colonies were scarce. The frequency of long-term culture-initiating cells in peripheral blood was approximately fivefold higher in CD34(+)CD84(-) vs CD34(+)CD84(+) cells. In short-term cultures, 95% of the initially CD34(+)CD84(-) cells became CD84(+) after 72 hours. Conclusions. CD84 is expressed on cells from almost all hematopoietic lineages and on CD34(+) hematopoietic progenitor cells. The proliferative potential of CD34(+) cells decreases with increasing CD84 expression, suggesting that CD84 serves as a marker for committed hematopoietic progenitor cells. (C) 2003 International Society for Experimental Hematology. Published by Elsevier Inc.
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页码:798 / 805
页数:8
相关论文
共 39 条
  • [1] ANDREESEN R, 1986, BLOOD, V67, P1257
  • [2] MICROCULTURE ASSAY FOR HUMAN MACROPHAGE MATURATION INVITRO - CELL-ELISA ANALYSIS OF DIFFERENTIATION ANTIGEN EXPRESSION
    ANDREESEN, R
    MACKENSEN, A
    OSTERHOLZ, J
    BRUGGER, W
    LOHR, GW
    [J]. INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1988, 86 (03): : 281 - 287
  • [3] Expression of CD41 and c-mpl does not indicate commitment to the megakaryocyte lineage during haemopoietic development
    Basch, RS
    Zhang, XM
    Dolzhanskiy, A
    Karpatkin, S
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 105 (04) : 1044 - 1054
  • [4] Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice
    Bhatia, M
    Wang, JCY
    Kapp, U
    Bonnet, D
    Dick, JE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) : 5320 - 5325
  • [5] Studies of cell adhesion and flow cytometric analyses of degranulation, surface phenotype, and viability using human eosinophils, basophils, and mast cells
    Bochner, BS
    Sterbinsky, SA
    Saini, SA
    Columbo, M
    MacGlashan, DW
    [J]. METHODS, 1997, 13 (01) : 61 - 68
  • [6] BRUGGER W, 1991, CANCER DETECT PREV, V15, P407
  • [7] Bruno E, 1998, SEMIN HEMATOL, V35, P183
  • [8] Peripheral blood progenitor cell mobilization in healthy donors receiving recombinant human granulocyte colony-stimulating factor
    Carlo-Stella, C
    Cesana, C
    Regazzi, E
    Falzetti, F
    Aversa, F
    Rizzoli, V
    Martelli, M
    Tabilio, A
    [J]. EXPERIMENTAL HEMATOLOGY, 2000, 28 (02) : 216 - 224
  • [9] Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene
    Coffey, AJ
    Brooksbank, RA
    Brandau, O
    Oohashi, T
    Howell, GR
    Bye, JM
    Cahn, AP
    Durham, J
    Heath, P
    Wray, P
    Pavitt, R
    Wilkinson, J
    Leversha, M
    Huckle, E
    Shaw-Smith, CJ
    Dunham, A
    Rhodes, S
    Schuster, V
    Porta, G
    Yin, L
    Serafini, P
    Sylla, B
    Zollo, M
    Franco, B
    Bolino, A
    Seri, M
    Lanyi, A
    Davis, JR
    Webster, D
    Harris, A
    Lenoir, G
    St Basile, GD
    Jones, A
    Behloradsky, BH
    Achatz, H
    Murken, J
    Fassler, R
    Sumegi, J
    Romeo, G
    Vaudin, M
    Ross, MT
    Meindl, A
    Bentley, DR
    [J]. NATURE GENETICS, 1998, 20 (02) : 129 - 135
  • [10] Expansion in vitro of transplantable human cord blood stem cells demonstrated using a quantitative assay of their lympho-myeloid repopulating activity in nonobese diabetic-scid/scid mice
    Conneally, E
    Cashman, J
    Petzer, A
    Eaves, C
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (18) : 9836 - 9841