CSF1 Overexpression has Pleiotropic Effects on Microglia In Vivo

被引:52
作者
De, Ishani [1 ,2 ]
Nikodemova, Maria [3 ]
Steffen, Megan D. [1 ,2 ]
Sokn, Emily [1 ,2 ]
Maklakova, Vilena I. [1 ,2 ]
Watters, Jyoti J. [3 ]
Collier, Lara S. [1 ,2 ]
机构
[1] Univ Wisconsin, Carbone Comprehens Canc Ctr, Sch Pharm, Div Pharmaceut Sci, Madison, WI 53705 USA
[2] Univ Wisconsin, Mol & Cellular Pharmacol Grad Program, Madison, WI 53705 USA
[3] Univ Wisconsin, Dept Comparat Biosci, Madison, WI 53705 USA
关键词
Csf1 (Mcsf); microglia; PLX3397; M1; M2; polarization; COLONY-STIMULATING FACTOR; STEM-CELL FACTOR; OSTEOPETROTIC OP/OP MICE; C-KIT RECEPTOR; ALZHEIMERS-DISEASE; LANGERHANS CELLS; GENE-EXPRESSION; ADULT MICROGLIA; TRANSGENIC MICE; MOUSE-BRAIN;
D O I
10.1002/glia.22717
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Macrophage colony stimulating factor (CSF1) is a cytokine that is upregulated in several diseases of the central nervous system (CNS). To examine the effects of CSF1 overexpression on microglia, transgenic mice that overexpress CSF1 in the glial fibrillary acidic protein (GFAP) compartment were generated. CSF1 overexpressing mice have increased microglial proliferation and increased microglial numbers compared with controls. Treatment with PLX3397, a small molecule inhibitor of the CSF1 receptor CSF1R and related kinases, decreases microglial numbers by promoting microglial apoptosis in both CSF1 overexpressing and control mice. Microglia in CSF1 overexpressing mice exhibit gene expression profiles indicating that they are not basally M1 or M2 polarized, but they do have defects in inducing expression of certain genes in response to the inflammatory stimulus lipopolysaccharide. These results indicate that the CSF1 overexpression observed in CNS pathologies likely has pleiotropic influences on microglia. Furthermore, small molecule inhibition of CSF1R has the potential to reverse CSF1-driven microglial accumulation that is frequently observed in CNS pathologies, but can also promote apoptosis of normal microglia. GLIA 2014;62:1955-1967
引用
收藏
页码:1955 / 1967
页数:13
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