CSF-1, IGF-1, and the control of postnatal growth and development

被引：78
作者：
Gow, Deborah J.
Sester, David P.
Hume, David A. [1 ]
机构：
[1] Univ Edinburgh, Roslin Inst, Roslin EH25 9PS, Midlothian, Scotland
来源：
JOURNAL OF LEUKOCYTE BIOLOGY | 2010年 / 88卷 / 03期
基金：
英国医学研究理事会;
关键词：
macrophage; hormone; extrahepatic; somatomedin hypothesis; COLONY-STIMULATING FACTOR; MONONUCLEAR PHAGOCYTE SYSTEM; OSTEOPETROTIC OP/OP MICE; FACTOR-I EXPRESSION; ACTIVATOR GENE-TRANSCRIPTION; OP OP MOUSE; BONE-GROWTH; OSTEOCLAST DIFFERENTIATION; GRANULOCYTE-MACROPHAGE; MURINE MACROPHAGES;
D O I：
10.1189/jlb.0310158
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
Growth hormone controls somatic growth in mammals by regulating the production of IGF-1, which is predominantly made by the liver. The development of cells within the MPS is controlled by the lineage-specific growth factor M-CSF (CSF-1). In this review, we summarize the role of CSF-1-dependent macrophages in somatic growth and organogenesis. We propose that macrophages are the major extrahepatic source of IGF-1 and that a surge of CSF-1 production contributes to the control of postnatal growth and organ maturation. Accordingly, CSF-1 may be considered a part of the GH/IGF-1 axis. J. Leukoc. Biol. 88: 475-481; 2010.
引用
收藏
页码：475 / 481
页数：7
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