生理状态下,C1q与海马小胶质细胞吞噬有关

Irune Díaz-Aparicio, A. Sierra
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引用次数: 5

摘要

补体蛋白C1q最近成为清除凋亡细胞的重要分子。然而,在生理条件下,它在大脑中的作用却很少被探索。以新生细胞经历凋亡并被小胶质细胞吞噬的成人神经源性级联为模型,在本研究中,我们利用facs分类的fms-EGFP小鼠小胶质细胞的免疫荧光和RTqPCR发现了三个主要发现。首先,我们发现生理条件下C1q主要由海马小胶质细胞产生。其次,我们观察到吞噬小胶质细胞和C1q之间的关系,正如C1q在大多数小胶质吞噬囊内的存在所表明的那样。最后,我们发现C1q在小胶质细胞中的功能可能不仅仅是吞噬作用,因为在非吞噬性小胶质细胞中也发现了C1q。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C1q is related to microglial phagocytosis in the hippocampus in physiological conditions
The complement protein C1q has lately emerged as an important molecule in the clearance of apoptotic cells. However, its role in the brain in physiological conditions is less explored. Using as a model the adult neurogenic cascade, where newborn cells undergo apoptosis and are phagocytosed by microglia, in the present study we have discovered three major findings using immunofluorescence and RTqPCR from FACSsorted microglia in fms-EGFP mice. First, we found that C1q is mainly produced by microglia in the hippocampus in physiological conditions. Second, we observed a relationship between phagocytic microglia and C1q, as suggested by the presence of C1q within the majority of the microglial phagocytic pouches. Finally, we discovered that the functions of C1q in microglia may go beyond phagocytosis, as C1q was also found in non-phagocytic microglia.
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