CD82 (KAI1), a member of the tetraspan family, is expressed on early haemopoietic progenitor cells and up-regulated in distinct human leukaemias

被引:18
作者
Burchert, A
Notter, M
Menssen, HD
Schwartz, S
Knauf, W
Neubauer, A
Thiel, E
机构
[1] Free Univ Berlin, Klinikum Benjamin Franklin, Med Klin 3, D-12200 Berlin, Germany
[2] Univ Marburg, Abt Hamatol Onkol & Immunol, Marburg, Germany
关键词
CD82; expression; haemopoiesis; leukaemia; CD34(+) progenitor cells; differentiation;
D O I
10.1046/j.1365-2141.1999.01741.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CD82 (KAI1) is a member of the tetraspan transmembrane protein family which has been cloned from lpmphoblastoid variant cell lines. However, a role for CD82 in early normal and malignant haemopoiesis has not yet been characterized. We studied the CD82 expression in 33 normal donor samples and 98 leukaemias by fluorescence activated cell sorting (FACS) and reverse transcriptase polymerase chain reaction (RT-PCR). We demonstrated that CD82 was moderately expressed in the vast majority of normal granulocytes and monocytes. Ln contrast, only about one third of the peripheral blood lymphocytes were weakly CD82 positive (CD82(+)). Interestingly judgement of the CD82 transcription and expression in various leukaemias revealed that CD82 was overexpressed in chronic myeloid leukaemia (CML) patients in accelerated or blastic phase (CML-AP/BP) as well as in acute myeloid leukaemia (AML) and chronic lymphocytic leukaemia (CLL) patients. Analysis of AML patients with CD34(+)/CD82(+) blasts prompted us to expand our studies on haemopoietic CD34(+) progenitor cells. Intriguingly, 84-95% of the CD34(+) cells isolated from healthy bone marrow cord blood or peripheral blood were highly CD82(+), CD82 was abundantly expressed on primitive as well as on committed haemopoietic progenitor cells. After in vitro induction of myeloid differentiation in CD34(+) peripheral blood progenitor cells (PBPC), the expression of CD82 decreased to levels similar to those found on peripheral blood granulocytes. These observations suggest for the first time a role for CD82 in normal and malignant haemopoiesis.
引用
收藏
页码:494 / 504
页数:11
相关论文
共 31 条
  • [1] Novel staging protocol for non-small-cell lung cancers according to MRP-1/CD9 and KAI1/CD82 gene expression
    Adachi, M
    Taki, T
    Konishi, T
    Huang, CI
    Higashiyama, M
    Miyake, M
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) : 1397 - 1406
  • [2] ANGELISOVA P, 1994, IMMUNOGENETICS, V39, P249
  • [3] Differential requirements for alpha 4 integrins during fetal and adult hematopoiesis
    Arroyo, AG
    Yang, JT
    Rayburn, H
    Hynes, RO
    [J]. CELL, 1996, 85 (07) : 997 - 1008
  • [4] Expression of the neural cell adhesion molecule CD56 is associated with short remission duration and survival in acute myeloid leukemia with t(8;21)(q22;q22)
    Baer, MR
    Stewart, CC
    Lawrence, D
    Arthur, DC
    Byrd, JC
    Davey, FR
    Schiffer, CA
    Bloomfield, CD
    [J]. BLOOD, 1997, 90 (04) : 1643 - 1648
  • [5] KAI1, A METASTASIS SUPPRESSOR GENE FOR PROSTATE-CANCER ON HUMAN-CHROMOSOME 11P11.2
    DONG, JT
    LAMB, PW
    RINKERSCHAEFFER, CW
    VUKANOVIC, J
    ICHIKAWA, T
    ISAACS, JT
    BARRETT, JC
    [J]. SCIENCE, 1995, 268 (5212) : 884 - 886
  • [6] Dong JT, 1996, CANCER RES, V56, P4387
  • [7] Selective enrichment of tetraspan proteins on the internal vesicles of multivesicular endosomes and on exosomes secreted by human B-lymphocytes
    Escola, JM
    Kleijmeer, MJ
    Stoorvogel, W
    Griffith, JM
    Yoshie, O
    Geuze, HJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (32) : 20121 - 20127
  • [8] FORSYTH KD, 1991, IMMUNOLOGY, V72, P292
  • [9] IDENTIFICATION OF MEMBRANE ANTIGEN C33 RECOGNIZED BY MONOCLONAL-ANTIBODIES INHIBITORY TO HUMAN T-CELL LEUKEMIA-VIRUS TYPE-1 (HTLV-1)-INDUCED SYNCYTIUM FORMATION - ALTERED GLYCOSYLATION OF C33 ANTIGEN IN HTLV-1-POSITIVE T-CELLS
    FUKUDOME, K
    FURUSE, M
    IMAI, T
    NISHIMURA, M
    TAKAGI, S
    HINUMA, Y
    YOSHIE, O
    [J]. JOURNAL OF VIROLOGY, 1992, 66 (03) : 1394 - 1401
  • [10] GIL ML, 1992, J IMMUNOL, V148, P2826