Innate Immunity Derived Factors as External Modulators of the CXCL12-CXCR4 Axis and Their Role in Stem Cell Homing and Mobilization

被引:29
作者
Ratajczak, Mariusz Z. [1 ,2 ]
Serwin, Karol
Schneider, Gabriela [2 ]
机构
[1] Univ Louisville, James Graham Brown Canc Ctr, Stem Cell Inst, Stem Cell Biol Program, Louisville, KY 40202 USA
[2] Pomeranian Med Univ, Dept Physiol, Szczecin, Poland
来源
THERANOSTICS | 2013年 / 3卷 / 01期
关键词
CXCR4; CXCL12; SDF-1; C3a; LL-37; stem cell mobilization; stem cell homing; HEMATOPOIETIC STEM/PROGENITOR CELLS; CHEMOKINE RECEPTOR CXCR4; BONE-MARROW; PROGENITOR CELLS; FUNCTIONAL CXCR4; CD34(+) CELLS; PERIPHERAL-BLOOD; BIOACTIVE LIPIDS; SDF-1; GRADIENT; T-LYMPHOCYTES;
D O I
10.7150/thno.4621
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 alpha-chemokine CXCL12 (stromal derived factor-1; SDF-1) and its corresponding G(alpha 1) protein-coupled CXCR4 receptor axis play an important role in retention of hematopoietic stem progenitor cells (HSPCs) in bone marrow (BM) stem cell niches. CXCL12 has also been identified as a strong chemoattractant for HSPCs and implicated both in homing of HSPCs to BM after transplantation and in egress of these cells from BM into peripheral blood (PB). However, since CXCL12, as a peptide, is highly susceptible to degradation by proteolytic enzymes, its real biological availability in biological fluids may be somewhat limited. In this review, we will present data demonstrating that the CXCL12-CXCR4 axis is positively modulated by innate immunity-derived several external factors, ensuring that even low (near threshold) doses of CXCL12 still exert a robust chemotactic influence on HSPCs.
引用
收藏
页码:3 / 10
页数:8
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