HUMAN HEMATOPOIETIC STEM-CELL ADHERENCE TO CYTOKINES AND MATRIX MOLECULES

被引:136
作者
LONG, MW [1 ]
BRIDDELL, R [1 ]
WALTER, AW [1 ]
BRUNO, E [1 ]
HOFFMAN, R [1 ]
机构
[1] INDIANA UNIV,SCH MED,DEPT MED,DIV HEMATOL ONCOL,INDIANAPOLIS,IN 46202
关键词
THROMBOSPONDIN; PROGENITOR CELLS; C-KIT LIGAND; EXTRACELLULAR MATRIX;
D O I
10.1172/JCI115844
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The hematopoietic microenvironment is a complex structure in which stem cells, progenitor cells, stromal cells, growth factors, and extracellular matrix (ECM) molecules each interact to direct the coordinate regulation of blood cell development. While much is known concerning the individual components of this microenvironment, little is understood of the interactions among these various components or, in particular, the nature of those interactions responsible for the regional localization of specific developmental signals. We hypothesized that cytokines act together with ECM molecules to anchor stem cells within the microenvironment, thus modulating their function. In order to analyze matrix-cytokine-stem cell interactions, we developed an ECM model system in which purified stem cell populations and plastic-immobilized individual proteins are used to assess the role of various matrix molecules and/or cytokines in human hematopoietic cell development. Analysis of these interactions revealed that a single ECM protein, thrombospondin, in conjunction with a single cytokine (e.g., c-kit ligand), constitutes a developmental signal that synergistically modulates hematopoietic stem cell function.
引用
收藏
页码:251 / 255
页数:5
相关论文
共 25 条
[1]   MOLECULAR-CLONING OF MAST-CELL GROWTH-FACTOR, A HEMATOPOIETIN THAT IS ACTIVE IN BOTH MEMBRANE-BOUND AND SOLUBLE FORMS [J].
ANDERSON, DM ;
LYMAN, SD ;
BAIRD, A ;
WIGNALL, JM ;
EISENMAN, J ;
RAUCH, C ;
MARCH, CJ ;
BOSWELL, HS ;
GIMPEL, SD ;
COSMAN, D ;
WILLIAMS, DE .
CELL, 1990, 63 (01) :235-243
[2]  
BERNSTEIN ID, 1991, BLOOD, V77, P2316
[3]   CHARACTERIZATION OF A HUMAN HEMATOPOIETIC PROGENITOR-CELL CAPABLE OF FORMING BLAST CELL CONTAINING COLONIES INVITRO [J].
BRANDT, J ;
BAIRD, N ;
LU, L ;
SROUR, E ;
HOFFMAN, R .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (03) :1017-1027
[4]   CYTOKINE-DEPENDENT LONG-TERM CULTURE OF HIGHLY ENRICHED PRECURSORS OF HEMATOPOIETIC PROGENITOR CELLS FROM HUMAN BONE-MARROW [J].
BRANDT, J ;
SROUR, EF ;
VANBESIEN, K ;
BRIDDELL, RA ;
HOFFMAN, R .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (03) :932-941
[5]  
BRIDDELL RA, 1989, BLOOD, V74, P145
[6]   MAST-CELL GROWTH-FACTOR MAPS NEAR THE STEEL LOCUS ON MOUSE CHROMOSOME-10 AND IS DELETED IN A NUMBER OF STEEL ALLELES [J].
COPELAND, NG ;
GILBERT, DJ ;
CHO, BC ;
DONOVAN, PJ ;
JENKINS, NA ;
COSMAN, D ;
ANDERSON, D ;
LYMAN, SD ;
WILLIAMS, DE .
CELL, 1990, 63 (01) :175-183
[7]  
COULOMBEL L, 1988, BLOOD, V71, P329
[8]   TRANSMEMBRANE FORM OF THE KIT LIGAND GROWTH-FACTOR IS DETERMINED BY ALTERNATIVE SPLICING AND IS MISSING IN THE SI(D) MUTANT [J].
FLANAGAN, JG ;
CHAN, DC ;
LEDER, P .
CELL, 1991, 64 (05) :1025-1035
[9]  
GALLAGHER JT, 1983, J CELL SCI, V63, P155
[10]   COMPARTMENTALIZATION OF A HEMATOPOIETIC GROWTH-FACTOR (GM-CSF) BY GLYCOSAMINOGLYCANS IN THE BONE-MARROW MICROENVIRONMENT [J].
GORDON, MY ;
RILEY, GP ;
WATT, SM ;
GREAVES, MF .
NATURE, 1987, 326 (6111) :403-405