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Astrocytic phagocytosis is a compensatory mechanism for microglial dysfunction
Author(s) -
Konishi Hiroyuki,
Okamoto Takayuki,
Hara Yuichiro,
Komine Okiru,
Tamada Hiromi,
Maeda Mitsuyo,
Osako Fumika,
Kobayashi Masaaki,
Nishiyama Akira,
Kataoka Yosky,
Takai Toshiyuki,
Udagawa Nobuyuki,
Jung Steffen,
Ozato Keiko,
Tamura Tomohiko,
Tsuda Makoto,
Yamanaka Koji,
Ogi Tomoo,
Sato Katsuaki,
Kiyama Hiroshi
Publication year - 2020
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.15252/embj.2020104464
Subject(s) - neuroscience , library science , biology , computer science
Microglia are the principal phagocytes that clear cell debris in the central nervous system ( CNS ). This raises the question, which cells remove cell debris when microglial phagocytic activity is impaired. We addressed this question using Siglech dtr mice, which enable highly specific ablation of microglia. Non‐microglial mononuclear phagocytes, such as CNS ‐associated macrophages and circulating inflammatory monocytes, did not clear microglial debris. Instead, astrocytes were activated, exhibited a pro‐inflammatory gene expression profile, and extended their processes to engulf microglial debris. This astrocytic phagocytosis was also observed in Irf8 ‐deficient mice, in which microglia were present but dysfunctional. RNA ‐seq demonstrated that even in a healthy CNS , astrocytes express TAM phagocytic receptors, which were the main astrocytic phagocytic receptors for cell debris in the above experiments, indicating that astrocytes stand by in case of microglial impairment. This compensatory mechanism may be important for the maintenance or prolongation of a healthy CNS .

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