Are "resting" microglia more "m2"?
作者信息
Cherry Jonathan D, Olschowka John A, O'Banion M Kerry
机构信息
Department of Pathology and Laboratory Medicine, University of Rochester School of Medicine and Dentistry , Rochester, NY , USA.
Department of Neurobiology and Anatomy, University of Rochester School of Medicine and Dentistry , Rochester, NY , USA.
出版信息
Front Immunol. 2014 Nov 18;5:594. doi: 10.3389/fimmu.2014.00594. eCollection 2014.
Abstract
摘要
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J Innate Immun. 2014;6(6):716-26. doi: 10.1159/000364945. Epub 2014 Aug 13.
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CNS myelin induces regulatory functions of DC-SIGN-expressing, antigen-presenting cells via cognate interaction with MOG.中枢神经系统髓磷脂通过与髓鞘少突胶质细胞糖蛋白（MOG）的同源相互作用诱导表达树突状细胞特异性细胞间黏附分子-3抓取非整合素（DC-SIGN）的抗原呈递细胞的调节功能。
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Neuroinflammation and M2 microglia: the good, the bad, and the inflamed.神经炎症与M2小胶质细胞：有益、有害与炎症状态
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Phagosome maturation in polarized macrophages.极化巨噬细胞中的吞噬体成熟
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Colony-stimulating factor 1 receptor signaling is necessary for microglia viability, unmasking a microglia progenitor cell in the adult brain.集落刺激因子 1 受体信号对于小胶质细胞的存活是必要的，揭示了成年大脑中的小胶质细胞祖细胞。
Neuron. 2014 Apr 16;82(2):380-97. doi: 10.1016/j.neuron.2014.02.040.
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