Murine Bone Marrow Niches from Hematopoietic Stem Cells to B Cells

被引:40
作者
Aurrand-Lions, Michel [1 ]
Mancini, Stephane J. C. [1 ]
机构
[1] Aix Marseille Univ, CNRS, INSERM, Inst Paoli Calmettes,CRCM, F-13009 Marseille, France
关键词
early hematopoiesis; B lymphopoiesis; bone marrow niches; stromal cells; COMMON LYMPHOID PROGENITORS; CHEMOKINE RECEPTOR CXCR4; PRE-B; STROMAL CELLS; PLASMA-CELLS; IN-VIVO; LINEAGE COMMITMENT; DEFICIENT MICE; C-KIT; MULTIPOTENT PROGENITORS;
D O I
10.3390/ijms19082353
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
After birth, the development of hematopoietic cells occurs in the bone marrow. Hematopoietic differentiation is finely tuned by cell-intrinsic mechanisms and lineage-specific transcription factors. However, it is now clear that the bone marrow microenvironment plays an essential role in the maintenance of hematopoietic stem cells (HSC) and their differentiation into more mature lineages. Mesenchymal and endothelial cells contribute to a protective microenvironment called hematopoietic niches that secrete specific factors and establish a direct contact with developing hematopoietic cells. A number of recent studies have addressed in mouse models the specific molecular events that are involved in the cellular crosstalk between hematopoietic subsets and their niches. This has led to the concept that hematopoietic differentiation and commitment towards a given hematopoietic pathway is a dynamic process controlled at least partially by the bone marrow microenvironment. In this review, we discuss the evolving view of murine hematopoietic-stromal cell crosstalk that is involved in HSC maintenance and commitment towards B cell differentiation.
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页数:18
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