| First Author | Zhao F | Year | 2022 |
| Journal | Nat Commun | Volume | 13 |
| Issue | 1 | Pages | 6117 |
| PubMed ID | 36253375 | Mgi Jnum | J:330192 |
| Mgi Id | MGI:7366492 | Doi | 10.1038/s41467-022-33836-2 |
| Citation | Zhao F, et al. (2022) Brain milieu induces early microglial maturation through the BAX-Notch axis. Nat Commun 13(1):6117 |
| abstractText | Microglia are derived from primitive myeloid cells and gain their early identity in the embryonic brains. However, the mechanism by which the brain milieu confers microglial maturation signature remains elusive. Here, we demonstrate that the bax(cq55) zebrafish and Bax(tm1Sjk) mouse embryos exhibit similarly defective early microglial maturation. BAX, a typical pro-apoptotic factor, is highly enriched in neuronal cells and regulates microglial maturation through both pro-apoptotic and non-apoptotic mechanisms. BAX regulates dlb via the CaMKII-CREB axis calcium-dependently in living neurons while ensuring the efficient Notch activation in the immigrated pre-microglia by apoptotic neurons. Notch signaling is conserved in supporting embryonic microglia maturation. Compromised microglial development occurred in the Cx3cr1(Cre/+)Rbpj(fl/fl) embryonic mice; however, microglia acquire their appropriate signature when incubated with DLL3 in vitro. Thus, our findings elucidate a BAX-CaMKII-CREB-Notch network triggered by the neuronal milieu in microglial development, which may provide innovative insights for targeting microglia in neuronal disorder treatment. |
