Zarb Yvette, Sridhar Sucheta, Nassiri Sina, Utz Sebastian Guido, Schaffenrath Johanna, Maheshwari Upasana, Rushing Elisabeth J, Nilsson K Peter R, Delorenzi Mauro, Colonna Marco, Greter Melanie, Keller Annika
Department of Neurosurgery, Clinical Neurocentre, Zurich University Hospital, Zurich University, Zürich, Switzerland.
Neuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland.
Sci Adv. 2021 Feb 26;7(9). doi: 10.1126/sciadv.abc4898. Print 2021 Feb.
Microglia participate in central nervous system (CNS) development and homeostasis and are often implicated in modulating disease processes. However, less is known about the role of microglia in the biology of the neurovascular unit (NVU). In particular, data are scant on whether microglia are involved in CNS vascular pathology. In this study, we use a mouse model of primary familial brain calcification, , to investigate the role of microglia in calcification of the NVU. We report that microglia enclosing vessel calcifications, coined calcification-associated microglia, display a distinct activation phenotype. Pharmacological ablation of microglia with the CSF1R inhibitor PLX5622 leads to aggravated vessel calcification. Mechanistically, we show that microglia require functional TREM2 for controlling vascular calcification. Our results demonstrate that microglial activity in the setting of pathological vascular calcification is beneficial. In addition, we identify a previously unrecognized function of microglia in halting the expansion of vascular calcification.
小胶质细胞参与中枢神经系统(CNS)的发育和稳态,并且常常与调节疾病进程有关。然而,关于小胶质细胞在神经血管单元(NVU)生物学中的作用,我们了解得较少。特别是,关于小胶质细胞是否参与中枢神经系统血管病理的相关数据很少。在本研究中,我们使用原发性家族性脑钙化的小鼠模型来研究小胶质细胞在NVU钙化中的作用。我们报告称,包围血管钙化的小胶质细胞(称为钙化相关小胶质细胞)表现出独特的激活表型。使用CSF1R抑制剂PLX5622对小胶质细胞进行药理学消融会导致血管钙化加重。从机制上讲,我们表明小胶质细胞需要功能性的TREM2来控制血管钙化。我们的结果表明,在病理性血管钙化情况下,小胶质细胞的活性是有益的。此外,我们确定了小胶质细胞在阻止血管钙化扩展方面以前未被认识到的功能。