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实验性脑卒中后早期瘢痕形成中 AQP4 的解体和定位错误。

Disassembly and Mislocalization of AQP4 in Incipient Scar Formation after Experimental Stroke.

机构信息

Division of Anatomy, Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, 0372 Oslo, Norway.

Cardiovascular Research Group IMB, Department of Medical Biology, Faculty of Health Sciences, UiT-The Arctic University of Norway, 9019 Tromsø, Norway.

出版信息

Int J Mol Sci. 2022 Jan 20;23(3):1117. doi: 10.3390/ijms23031117.

Abstract

There is an urgent need to better understand the mechanisms involved in scar formation in the brain. It is well known that astrocytes are critically engaged in this process. Here, we analyze incipient scar formation one week after a discrete ischemic insult to the cerebral cortex. We show that the infarct border zone is characterized by pronounced changes in the organization and subcellular localization of the major astrocytic protein AQP4. Specifically, there is a loss of AQP4 from astrocytic endfoot membranes that anchor astrocytes to pericapillary basal laminae and a disassembly of the supramolecular AQP4 complexes that normally abound in these membranes. This disassembly may be mechanistically coupled to a downregulation of the newly discovered AQP4 isoform AQP4ex. AQP4 has adhesive properties and is assumed to facilitate astrocyte mobility by permitting rapid volume changes at the leading edges of migrating astrocytes. Thus, the present findings provide new insight in the molecular basis of incipient scar formation.

摘要

目前迫切需要更好地理解大脑中瘢痕形成的机制。众所周知,星形胶质细胞在这个过程中起着至关重要的作用。在这里,我们分析了大脑皮质局灶性缺血损伤后一周时初始瘢痕形成的情况。我们发现,梗死边界区的主要星形胶质细胞蛋白 AQP4 的组织和亚细胞定位发生了明显变化。具体来说,AQP4 从锚定星形胶质细胞到毛细血管基底膜的星形胶质细胞足突膜上丢失,以及正常存在于这些膜中的 AQP4 超分子复合物解体。这种解体可能与新发现的 AQP4 亚型 AQP4ex 的下调在机制上相关。AQP4 具有粘附特性,并通过允许迁移星形胶质细胞前缘的快速体积变化,从而假定促进星形胶质细胞的迁移。因此,目前的发现为初始瘢痕形成的分子基础提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ae/8835637/8bb84be2f774/ijms-23-01117-g001.jpg

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