Microglial diversity arises from the interplay between inherent genetic programs and external environmental signals. However, the mechanisms by which these processes develop and interact within the growing brain are not yet fully understood. Here, we show that radial glia-expressed integrin beta 8 (ITGB8) activates microglia-expressed TGFβ1 to drive microglial development. Domain-restricted deletion of Itgb8 in these progenitors results in regionally restricted and developmentally arrested microglia that persist into adulthood. In the absence of autocrine TGFβ1 signaling, microglia adopt a similar phenotype, leading to neuromotor symptoms almost identical to Itgb8 mutant mice. In contrast, microglia lacking the canonical TGFβ signal transducers Smad2 and Smad3 have a less polarized dysmature phenotype and correspondingly less severe neuromotor dysfunction. Our study describes the spatio-temporal regulation of TGFβ activation and signaling in the brain necessary to promote microglial development, and provides evidence for the adoption of microglial developmental signaling pathways in brain injury or disease.
Radial glia integrin avb8 regulates cell autonomous microglial TGFβ1 signaling that is necessary for microglial identity.
放射状胶质细胞整合素avb8调节细胞自主的小胶质细胞TGFβ1信号传导,这是小胶质细胞特性所必需的
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作者:McKinsey Gabriel L, Santander Nicolas, Zhang Xiaoming, Kleemann Kilian L, Tran Lauren, Katewa Aditya, Conant Kaylynn, Barraza Matthew, Waddell Kian, Lizama Carlos O, La Russa Marie, Koo Ji Hyun, Lee Hyunji, Mukherjee Dibyanti, Paidassi Helena, Anton E S, Atabai Kamran, Sheppard Dean, Butovsky Oleg, Arnold Thomas D
| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2025 | 起止号: | 2025 Mar 22; 16(1):2840 |
| doi: | 10.1038/s41467-025-57684-y | 研究方向: | 细胞生物学 |
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