THE EXTRACELLULAR-MATRIX OF THE HEMATOPOIETIC MICROENVIRONMENT

被引:122
作者
KLEIN, G
机构
[1] Department of Internal Medicine II, Section, for Transplantation Immunology and Immunohematology, University Medical Clinic, Tübingen, D-72076
来源
EXPERIENTIA | 1995年 / 51卷 / 9-10期
关键词
CELL-MATRIX INTERACTIONS; ADHESION; CYTOKINES; COLLAGENS; PROTEOGLYCANS; TENASCIN; LAMININ; FIBRONECTIN; CELLULAR RECEPTORS;
D O I
10.1007/BF01921741
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The bone marrow microenvironment plays an important role in promoting hematopoietic progenitor cell proliferation and differentiation and the controlled egress of these developing hematopoietic cells. The establishment of long-term bone marrow cultures, which are thought to mimic hematopoiesis in vitro, and various stromal cell lines has greatly facilitated the analysis of the functions of this microenvironment. Extracellular matrix (ECM) molecules of all three categories (collagens, proteoglycans and glycoproteins) have been identified as part of this microenvironment and have been shown to be involved in different biological functions such as cell adhesion and anti-adhesion. binding and presentation of various cytokines and regulation of cell growth. It is suggested that these matrix molecules in combination with cytokines are crucial for compartmentalization of the bone marrow. Although many cell adhesion molecules have been characterized on the surface of hematopoietic progenitor cells, the nature of cellular receptors for the ECM components is less well defined. During leukemia, many immature blood cells are released from bone marrow, but it is not yet known whether these abnormalities in hematopoiesis are also caused by an altered microenvironment or altered composition of its extracellular matrix. The elucidation of the involvement of specific ECM-isoforms and as yet not characterized ECM components and their receptors in the bone marrow will certainly help towards a better understanding of these phenomena.
引用
收藏
页码:914 / 926
页数:13
相关论文
共 126 条
[101]  
SICZKOWSKI M, 1992, EXP HEMATOL, V20, P1285
[102]  
SINGER JW, 1985, RECENT ADV HAEMATOLO, P1
[103]   TENASCIN IMMUNOREACTIVITY IN NORMAL AND PATHOLOGICAL BONE-MARROW [J].
SOINI, Y ;
KAMEL, D ;
APAJASARKKINEN, M ;
VIRTANEN, I ;
LEHTO, VP .
JOURNAL OF CLINICAL PATHOLOGY, 1993, 46 (03) :218-221
[104]   EXPRESSION OF INTEGRINS IN HUMAN BONE-MARROW [J].
SOLIGO, D ;
SCHIRO, R ;
LUKSCH, R ;
MANARA, G ;
QUIRICI, N ;
PARRAVICINI, C ;
DELILIERS, GL .
BRITISH JOURNAL OF HAEMATOLOGY, 1990, 76 (03) :323-332
[105]   REGULATION OF HEMATOPOIESIS IN LONG-TERM BONE-MARROW CULTURES .4. GLYCOSAMINOGLYCAN SYNTHESIS AND THE STIMULATION OF HEMATOPOIESIS BY BETA-D-XYLOSIDES [J].
SPOONCER, E ;
GALLAGHER, JT ;
KRIZSA, F ;
DEXTER, TM .
JOURNAL OF CELL BIOLOGY, 1983, 96 (02) :510-514
[106]   2 CONTRARY FUNCTIONS OF TENASCIN - DISSECTION OF THE ACTIVE-SITES BY RECOMBINANT TENASCIN FRAGMENTS [J].
SPRING, J ;
BECK, K ;
CHIQUETEHRISMANN, R .
CELL, 1989, 59 (02) :325-334
[107]   ADHESION RECEPTORS OF THE IMMUNE-SYSTEM [J].
SPRINGER, TA .
NATURE, 1990, 346 (6283) :425-434
[108]  
SRIRAMARAO P, 1993, J CELL SCI, V105, P1001
[109]  
SUCHARD SJ, 1994, J IMMUNOL, V152, P877
[110]   INDUCTION OF PROGRAMMED CELL-DEATH IN HUMAN HEMATOPOIETIC-CELL LINES BY FIBRONECTIN VIA ITS INTERACTION WITH VERY LATE ANTIGEN-5 [J].
SUGAHARA, H ;
KANAKURA, Y ;
FURITSU, T ;
ISHIHARA, K ;
ORITANI, K ;
IKEDA, H ;
KITAYAMA, H ;
ISHIKAWA, J ;
HASHIMOTO, K ;
KANAYAMA, Y ;
MATSUZAWA, Y .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (06) :1757-1766