Laboratory of Neural Circuit Assembly, Brain Research Institute, University of Zurich, Zurich 8057, Switzerland; Neuroscience Center Zurich (ZNZ), Zurich 8057, Switzerland.
Department of Neurobiology, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA; Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.
Cell Rep. 2022 Aug 16;40(7):111209. doi: 10.1016/j.celrep.2022.111209.
Microglia play a key role in shaping the formation and refinement of the excitatory network of the brain. However, less is known about whether and how they organize the development of distinct inhibitory networks. We find that microglia are essential for the proper development of somatostatin-positive (SST) cell synapses during the second postnatal week. We further identify a pair of molecules that act antagonistically to one another in the organization of SST cell axonal elaboration. Whereas CX3CL1 acts to suppress axonal growth and complexity, CXCL12 promotes it. Assessing the functional importance of microglia in the development of cortical activity, we find that a whisker stimulation paradigm that drives SST cell activation leads to reduced cortical spiking in brains depleted of microglia. Collectively, our data demonstrate an important role of microglia in regulating the development of SST cell output early in life.
小胶质细胞在塑造大脑兴奋性网络的形成和精细化方面发挥着关键作用。然而,关于它们是否以及如何组织不同抑制性网络的发展,我们知之甚少。我们发现小胶质细胞对于在出生后第二周期间,生长抑素阳性(SST)细胞突触的正常发育是必需的。我们进一步鉴定出一对分子,它们在 SST 细胞轴突延伸的组织中相互拮抗。CX3CL1 作用于抑制轴突生长和复杂性,而 CXCL12 则促进其生长。评估小胶质细胞在皮质活动发育中的功能重要性,我们发现一种刺激胡须的范式可以驱动 SST 细胞的激活,从而导致小胶质细胞耗竭的大脑中皮质尖峰活动减少。总的来说,我们的数据表明小胶质细胞在调节生命早期 SST 细胞输出的发育中起着重要作用。