CLONING OF A THYMIC STROMAL CELL CAPABLE OF PROTECTING THYMOCYTES FROM APOPTOSIS

被引:20
作者
AMARANTEMENDES, JGP
CHAMMAS, R
ABRAHAMSOHN, P
PATEL, PC
POTWOROWSKI, EF
MACEDO, MS
机构
[1] UNIV SAO PAULO, INST BIOMED SCI, DEPT IMMUNOL, BR-05508900 SAO PAULO, BRAZIL
[2] UNIV SAO PAULO, INST BIOMED SCI, DEPT HISTOL & EMBRYOL, BR-05508900 SAO PAULO, BRAZIL
[3] LUDWIG INST CANC RES, SAO PAULO BRANCH, SAO PAULO, BRAZIL
关键词
D O I
10.1006/cimm.1995.1024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A clone of thymic stromal cells, namely 2BH4, was established by primary culture, cellular transfection and limiting dilution, Morphological analysis by transmission electron microscopy revealed that these cells grow as multilayers, producing a well-defined basement membrane to which they attach and frequently form structures similar to hemidesmosomes, The adjoining cells are connected by intercellular junctions, as tight junctions, intermediate junctions, and desmosome-like junctions, as well as interdigitations. Their cytoplasm contains microtubules, strands of actin filaments, and scarce intermediate filaments, Fluorescence microscopy revealed that 2BH4 cells stain with anti-cytokeratin antibodies, the majority of them giving a faint reaction, In addition, they express Thy-1.1, LFA-1, ICAM-1, and the gp23 epithelial antigen, and synthesize laminin, They have a doubling time of 16 hr and are able to bind thymocytes, Thymocytes cultured in the presence of 2BH4 cells are partially protected from both spontaneous and PMA- or dexamethasone-induced apoptosis, This protection is conferred neither by soluble factors normally produced by the 2BH4, cells nor by the sole contact with fixed 2BH4 cells, Rather, thymocytes must interact with metabolically active 2BH4 cells in order to receive the protective signal(s). (C) 1995 Academic Press, Inc.
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页码:173 / 180
页数:8
相关论文
共 35 条
  • [1] AMARANTEMENDES JGP, 1994, BRAZ J MED BIOL RES, V27, P1321
  • [2] AMARANTEMENDES JGP, 1993, THESIS U SAO PAULO B
  • [3] POSITIVE SELECTION OF THE T-CELL REPERTOIRE - WHERE AND WHEN DOES IT OCCUR
    BENOIST, C
    MATHIS, D
    [J]. CELL, 1989, 58 (06) : 1027 - 1033
  • [4] COHEN JJ, 1991, ADV IMMUNOL, V50, P55
  • [5] COHEN JJ, 1984, J IMMUNOL, V132, P38
  • [6] REGULATION OF THE CYTOSKELETON IN MESOTHELIAL CELLS - REVERSIBLE LOSS OF KERATIN AND INCREASE IN VIMENTIN DURING RAPID GROWTH IN CULTURE
    CONNELL, ND
    RHEINWALD, JG
    [J]. CELL, 1983, 34 (01) : 245 - 253
  • [7] TYROSINE KINASE ACTIVATION IN THYMIC EPITHELIAL-CELLS - NECESSITY OF THYMOCYTE CONTACT THROUGH THE GP23/45/90 ADHESION COMPLEX
    COUTURE, C
    AMARANTEMENDES, G
    POTWOROWSKI, EF
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (10) : 2579 - 2585
  • [8] A NOVEL THYMIC EPITHELIAL ADHESION MOLECULE
    COUTURE, C
    PATEL, PC
    POTWOROWSKI, EF
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (12) : 2769 - 2773
  • [9] GORMAN C, 1985, DNA CLONING, V2, P152
  • [10] HARLOW E, 1988, ANTIBODIES LABORATOR