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      Pericytes and vascular smooth muscle cells in central nervous system arteriovenous malformations

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          Abstract

          Previously considered passive support cells, mural cells—pericytes and vascular smooth muscle cells—have started to garner more attention in disease research, as more subclassifications, based on morphology, gene expression, and function, have been discovered. Central nervous system (CNS) arteriovenous malformations (AVMs) represent a neurovascular disorder in which mural cells have been shown to be affected, both in animal models and in human patients. To study consequences to mural cells in the context of AVMs, various animal models have been developed to mimic and predict human AVM pathologies. A key takeaway from recently published work is that AVMs and mural cells are heterogeneous in their molecular, cellular, and functional characteristics. In this review, we summarize the observed perturbations to mural cells in human CNS AVM samples and CNS AVM animal models, and we discuss various potential mechanisms relating mural cell pathologies to AVMs.

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          Most cited references150

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          A molecular atlas of cell types and zonation in the brain vasculature

          Cerebrovascular disease is the third most common cause of death in developed countries, but our understanding of the cells that compose the cerebral vasculature is limited. Here, using vascular single-cell transcriptomics, we provide molecular definitions for the principal types of blood vascular and vessel-associated cells in the adult mouse brain. We uncover the transcriptional basis of the gradual phenotypic change (zonation) along the arteriovenous axis and reveal unexpected cell type differences: a seamless continuum for endothelial cells versus a punctuated continuum for mural cells. We also provide insight into pericyte organotypicity and define a population of perivascular fibroblast-like cells that are present on all vessel types except capillaries. Our work illustrates the power of single-cell transcriptomics to decode the higher organizational principles of a tissue and may provide the initial chapter in a molecular encyclopaedia of the mammalian vasculature.
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            Pericytes: developmental, physiological, and pathological perspectives, problems, and promises.

            Pericytes, the mural cells of blood microvessels, have recently come into focus as regulators of vascular morphogenesis and function during development, cardiovascular homeostasis, and disease. Pericytes are implicated in the development of diabetic retinopathy and tissue fibrosis, and they are potential stromal targets for cancer therapy. Some pericytes are probably mesenchymal stem or progenitor cells, which give rise to adipocytes, cartilage, bone, and muscle. However, there is still confusion about the identity, ontogeny, and progeny of pericytes. Here, we review the history of these investigations, indicate emerging concepts, and point out problems and promise in the field of pericyte biology. Copyright © 2011 Elsevier Inc. All rights reserved.
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              Pericyte loss and microaneurysm formation in PDGF-B-deficient mice.

              Platelet-derived growth factor (PDGF)-B-deficient mouse embryos were found to lack microvascular pericytes, which normally form part of the capillary wall, and they developed numerous capillary microaneurysms that ruptured at late gestation. Endothelial cells of the sprouting capillaries in the mutant mice appeared to be unable to attract PDGF-Rbeta-positive pericyte progenitor cells. Pericytes may contribute to the mechanical stability of the capillary wall. Comparisons made between PDGF null mouse phenotypes suggest a general role for PDGFs in the development of myofibroblasts.
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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                04 August 2023
                2023
                : 14
                : 1210563
                Affiliations
                [1] 1 Department of Biological Sciences , Ohio University , Athens, OH, United States
                [2] 2 Neuroscience Program , Ohio University , Athens, OH, United States
                [3] 3 Department of Neurosurgery , University Hospital 12 de Octubre , Madrid, Spain
                [4] 4 Department of Surgery , Universidad Complutense de Madrid , Madrid, Spain
                [5] 5 Instituto de Investigación Imas12 , Madrid, Spain
                [6] 6 Molecular and Cellular Biology Program , Ohio University , Athens, OH, United States
                [7] 7 Centro Nacional de Investigaciones Cardiovasculares Carlos III (F.S.P) , Madrid, Spain
                Author notes

                Edited by: Shaun L. Sandow, University of the Sunshine Coast, Australia

                Reviewed by: Walter Lee Murfee, University of Florida, United States

                Ethan Winkler, University of California, San Francisco, United States

                *Correspondence: Henar Cuervo, hcuervo@ 123456cnic.es ; Corinne M. Nielsen, nielsenc@ 123456ohio.edu
                Article
                1210563
                10.3389/fphys.2023.1210563
                10437819
                37601628
                e1a7e26f-4f5b-4708-b7af-330f58f6ba6d
                Copyright © 2023 Nakisli, Lagares, Nielsen and Cuervo.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 April 2023
                : 29 June 2023
                Funding
                Funded by: Instituto de Salud Carlos III , doi 10.13039/501100004587;
                Award ID: FIS PI21/01844
                Funded by: National Institutes of Health , doi 10.13039/100000002;
                Award ID: R15 NS111376
                Funded by: Comunidad de Madrid , doi 10.13039/100012818;
                Award ID: 2020-T1/BMD-19985 mod.1 grant
                Funded by: Ministerio de Ciencia e Innovación , doi 10.13039/501100004837;
                Award ID: MICIN/AEI/10.13039/501100011033
                This work was supported by the Ohio University Neuroscience Program Confocal Graduate Assistantship and College of Arts and Sciences Graduate Student Research Fund grant to SN; ISCIII and FEDER European institutions through Fondo de Investigación en Salud (FIS) project PI21/01844 to AL; NIH R15 NS111376 to CN; and 2020-T1/BMD-19985 mod.1 grant funded by “Atracción de Talento Investigador” call from Comunidad de Madrid to HC The CNIC is supported by the Instituto de Salud Carlos III (ISCIII), the Ministerio de Ciencia e Innovación (MCIN) and the Pro CNIC Foundation, and is a Severo Ochoa Center of Excellence (grant CEX 2020-001041-S funded by MICIN/AEI/10.13039/501100011033).
                Categories
                Physiology
                Review
                Custom metadata
                Cell Physiology

                Anatomy & Physiology
                arteriovenous malformation,central nervous system,mural cell,pericyte,smooth muscle cell,vascular malformations,brain vessels

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