The role of novel and known extracellular matrix and adhesion molecules in the homeostatic and regenerative bone marrow microenvironment

被引:69
作者
Klamer, Sofieke [1 ]
Voermans, Carlijn [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Hematopoiesis, Sanquin Res,Landsteiner Lab, NL-1105 AZ Amsterdam, Netherlands
关键词
haematopoietic stem cells; extracellular matrix; bone marrow niche; BIGH3; integrins; periostin; bone marrow regeneration; adhesion molecules; matrix proteins; differentiation; HEMATOPOIETIC STEM-CELL; GROWTH-FACTOR-BETA; IMMUNODEFICIENCY-REPOPULATING CELLS; WNT GENE FAMILY; HERG K+ CHANNEL; PROGENITOR CELLS; SELF-RENEWAL; L-SELECTIN; IN-VITRO; STIMULATING FACTOR;
D O I
10.4161/19336918.2014.968501
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Maintenance of haematopoietic stem cells and differentiation of committed progenitors occurs in highly specialized niches. The interactions of haematopoietic stem and progenitor cells (HSPCs) with cells, growth factors and extracellular matrix (ECM) components of the bone marrow (BM) microenvironment control homeostasis of HSPCs. We only start to understand the complexity of the haematopoietic niche(s) that comprises endosteal, arterial, sinusoidal, mesenchymal and neuronal components. These distinct niches produce a broad range of soluble factors and adhesion molecules that modulate HSPC fate during normal hematopoiesis and BM regeneration. Adhesive interactions between HSPCs and the microenvironment will influence their localization and differentiation potential. In this review we highlight the current understanding of the functional role of ECM- and adhesion (regulating) molecules in the haematopoietic niche during homeostatic and regenerative hematopoiesis. This knowledge may lead to the improvement of current cellular therapies and more efficient development of future cellular products.
引用
收藏
页码:563 / 577
页数:15
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