Structural identification of the hematopoietic progenitor antigen ER-MP12 as the vascular endothelial adhesion molecule PECAM-1 (CD31)

被引:39
作者
Ling, V [1 ]
Luxenberg, D [1 ]
Wang, J [1 ]
Nickbarg, E [1 ]
Leenen, PJM [1 ]
Neben, S [1 ]
Kobayashi, M [1 ]
机构
[1] ERASMUS UNIV ROTTERDAM,DEPT IMMUNOL,NL-3000 DR ROTTERDAM,NETHERLANDS
关键词
hematopoiesis; stem cell; embryo; angiogenesis; adhesion;
D O I
10.1002/eji.1830270223
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The monoclonal antibody ER-MP12 was recently described to recognize an antigen present on cell subpopulations of adult mouse bone marrow including pluripotent hematopoietic stem cells. In an effort to understand the function of ER-MP12 antigen in hematopoiesis, we used biochemical and physical methods to determine its identity. ER-MP12 antigen was isolated by immunoprecipitation from FDCP-1 cell membrane proteins, yielding a glycosylated 113-kDa band upon analysis by polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate. Thirteen peptides derived from trypsinized ER-MP12 antigen were analyzed by electrospray ionization mass spectrometry and compared to a protein sequence database. The search revealed the identity of the ER-MP12 antigen as platelet endothelial cell adhesion molecule-1, CD31 (PECAM-1). This result was subsequently confirmed by Edman sequencing of a single ER-MP12 peptide fragment followed by comparison with PECAM-1 sequence. In addition, flow cytometric analysis of bone marrow and embryonic stem cells revealed highly similar profiles between ER-MP12 and CD31 (MEC 13.3 antibody)-stained cells. The presence of PECAM-1 on primitive hematopoietic stem cells supports the theory for the interaction of hematopoietic progenitor and stem cells with bone marrow stroma and transendothelial migration.
引用
收藏
页码:509 / 514
页数:6
相关论文
共 21 条
  • [1] Hematopoietic stem cells in the mouse embryonic yolk sac
    Auerbach, R
    Huang, H
    Lu, LS
    [J]. STEM CELLS, 1996, 14 (03) : 269 - 280
  • [2] BALDWIN HS, 1994, DEVELOPMENT, V120, P2539
  • [3] CONSTRUCTION OF VALIDATED, NONREDUNDANT COMPOSITE PROTEIN-SEQUENCE DATABASES
    BLEASBY, AJ
    WOOTTON, JC
    [J]. PROTEIN ENGINEERING, 1990, 3 (03): : 153 - 159
  • [4] BOGEN SA, 1992, AM J PATHOL, V141, P843
  • [5] DISTINCT MOUSE BONE-MARROW MACROPHAGE PRECURSORS IDENTIFIED BY DIFFERENTIAL EXPRESSION OF ER-MP12 AND ER-MP20 ANTIGENS
    DEBRUIJN, MFTR
    SLIEKER, WAT
    VANDERLOO, JCM
    VOERMAN, JSA
    VANEWIJK, W
    LEENEN, PJM
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (10) : 2279 - 2284
  • [6] AN APPROACH TO CORRELATE TANDEM MASS-SPECTRAL DATA OF PEPTIDES WITH AMINO-ACID-SEQUENCES IN A PROTEIN DATABASE
    ENG, JK
    MCCORMACK, AL
    YATES, JR
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (11) : 976 - 989
  • [7] HUNT DF, 1991, CURRENT RES PROTEIN, P441
  • [8] MURINE MACROPHAGE PRECURSOR CHARACTERIZATION .2. MONOCLONAL-ANTIBODIES AGAINST MACROPHAGE PRECURSOR ANTIGENS
    LEENEN, PJM
    MELIS, M
    SLIEKER, WAT
    VANEWIJK, W
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (01) : 27 - 34
  • [9] MARKERS OF MOUSE MACROPHAGE DEVELOPMENT DETECTED BY MONOCLONAL-ANTIBODIES
    LEENEN, PJM
    DEBRUIJN, MFTR
    VOERMAN, JSA
    CAMPBELL, PA
    VANEWIJK, W
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1994, 174 (1-2) : 5 - 19
  • [10] LING V, 1997, IN PRESS J CELL PHYS