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ABSTRACT: Significance
Vascular mural cells, defined as smooth muscle cells (SMCs) and pericytes, influence brain microcirculation, but how they contribute is not fully understood. Most approaches used to investigate pericyte and capillary interactions include ex vivo retinal/slice preparations or in vivo two-photon microscopy. However, neither method adequately captures mural cell behavior without interfering neuronal tissue. Thus, there is a need to isolate vessels with their respective mural cells to study functional and pathological changes.Aim
The aim of our work was to implement an ex vivo method that recapitulates vessel dynamics in the brain.Approach
Expanding upon our established ex vivo capillary-parenchymal arteriole (CaPA) preparation,
SUBMITTER: Jeffrey DA
PROVIDER: S-EPMC9225307 | biostudies-literature | 2022 Jul
REPOSITORIES: biostudies-literature