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Microglial SIRPa regulates the emergence of CD11c+ microglia and demyelination damage in white matter

مؤلف البحث
Miho Sato-Hashimoto1, Tomomi Nozu1, Riho Toriba1, Ayano Horikoshi1, Miho Akaike1, Kyoko Kawamoto1, Ayaka Hirose1, Yuriko Hayashi1, Hiromi Nagai1, Wakana Shimizu1, Ayaka Saiki1, Tatsuya Ishikawa2,3,4, Ruwaida Elhanbly2,3,4,5, Takenori Kotani6, Yoji Murata6
ملخص البحث

A characteristic subset of microglia expressing CD11c appears in response to brain
damage. However, the functional role of CD11c+ microglia, as well as the mechanism of its
induction, are poorly understood. Here we report that the genetic ablation of signal regulatory
protein a (SIRPa), a membrane protein, induced the emergence of CD11c+ microglia in the brain
white matter. Mice lacking CD47, a physiological ligand of SIRPa, and microglia-specific SIRPa-
knockout mice exhibited the same phenotype, suggesting that an interaction between microglial
SIRPa and CD47 on neighbouring cells suppressed the emergence of CD11c+ microglia. A lack of
SIRPa did not cause detectable damage to the white matter, but resulted in the increased
expression of genes whose expression is characteristic of the repair phase after demyelination. In
addition, cuprizone-induced demyelination was alleviated by the microglia-specific ablation of
SIRPa. Thus, microglial SIRPa suppresses the induction of CD11c+ microglia that have the potential
to accelerate the repair of damaged white matter.

تاريخ البحث
مجلة البحث
e Life
المشارك في البحث
الناشر
eLife Sciences Publications
تصنيف البحث
5.879
عدد البحث
8
موقع البحث
https://doi.org/10.7554/eLife.42025
سنة البحث
2019
صفحات البحث
1-29