bioRxivCell Biology
Pericyte Heterogeneity Identified by 3D Ultrastructural Analysis of the Microvessel Wall
H. Abdelazim, L. B. Payne, K. Nolan, K. Paralkar, V. Bradley, R. Kanodia, R. Gude, R. Ward, A. Monavarfeshani, M. Fox, J. C. Chappell
Abstract
ABSTRACT/SUMMARYUnequivocal pericyte identification remains a limitation in the field of vascular biology given the lack of unique molecular marker. Compounding this challenge are the recently described heterogeneities in pericyte morphology across microvascular networks. Here, we found further support on the ultrastructural level for classifying pericytes into sub-types - "thin-strand" (TSPs), mesh (MP), and ensheathing (EP) pericytes - based on their architecture in the mouse brain microcirculation. We also observed several instances of an additional cell type in the medial layer between endothelial cells and pericytes, specifically associated with EPs. A conserved characteristic across PC subtypes was extracellular matrix (ECM) encompassing the vascular unit and dispersed among neighboring cells. ECM thicknesses fell within a specific range depending on vessel location, and only thinned where cells were in closer proximity. Pericytes and endothelial cells formed "peg-and-socket" structures at these locations, providing another distinguishing feature across PC subtypes. Unique contact locations seemed to be present between medial and endothelial cells, as well as between vascular cells and the brain parenchyma. The ECM surrounding EPs exhibited another notable configuration in that thin extensions radiated out from the vessel wall into the surrounding parenchyma, suggesting mechanical and/or biochemical roles. Considering these data together, ultrastructural observations may provide an orthogonal perspective on pericyte heterogeneity and the presence of medial cells in cerebrovascular walls as well as assessing ECM coverage as a criterion for PC identification and exploring PC-associated ECM extensions that may have unique relevance in health and disease.
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