Emerging Roles of Pericytes in the Regulation of the Neurovascular Unit in Health and Disease

被引:0
作者
Jeremy Hill
Slava Rom
Servio H. Ramirez
Yuri Persidsky
机构
[1] Temple University School of Medicine,Department of Pathology and Laboratory Medicine
[2] Temple University School of Medicine,Center for Substance Abuse Research
来源
Journal of Neuroimmune Pharmacology | 2014年 / 9卷
关键词
Blood brain barrier; Pericyte; Brain endothelial cells; Neuroinflammation; Neurovascular unit;
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学科分类号
摘要
Pericytes of the central nervous system (CNS) are uniquely positioned within a multicellular structure termed the neurovascular unit (NVU) to provide crucial support to blood brain barrier (BBB) formation, maintenance, and stability. Numerous CNS diseases are associated with some aspect of BBB dysfunction. A dysfunction can manifest as one or multiple disruptions to any of the following barriers: physical, metabolic, immunological and transport barrier. A breach in the BBB can notably result in BBB hyper-permeability, endothelial activation and enhanced immune-endothelial interaction. How the BBB is regulated within this integrated unit remains largely unknown, especially as it relates to pericyte-endothelial interaction. We summarize the latest findings on pericyte origin, possible marker expression, and availability within different organ systems. We highlight pericyte-endothelial cell interactions, concentrating on extra- and intra- cellular signaling mechanisms linked to platelet derived growth factor-B, transforming growth factor -β, angiopoietins, Notch, and gap junctions. We discuss the role of pericytes in the NVU under inflammatory insult, focusing on how pericytes may indirectly affect leukocyte CNS infiltration, the direct role of pericyte-mediated basement membrane modifications, and immune responses. We review new findings of pericyte actions in CNS pathologies including Alzheimer’s disease, stroke, multiple sclerosis, diabetic retinopathy, and HIV-1 infection. The uncovering of the regulatory role of pericytes on the BBB will provide key insight into how barrier integrity can be re-established during neuroinflammation.
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页码:591 / 605
页数:14
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  • [1] Abramsson A(2007)Defective N-sulfation of heparan sulfate proteoglycans limits PDGF-BB binding and pericyte recruitment in vascular development Genes Dev 21 316-331
  • [2] Kurup S(2002)Sphingosine-1-phosphate receptors and the development of the vascular system Biochimica Et Biophysica Acta 1582 222-227
  • [3] Busse M(2011)Disruption of central nervous system barriers in multiple sclerosis Biochimica Et Biophysica Acta 1812 252-264
  • [4] Yamada S(2005)Endothelial/pericyte interactions Circ Res 97 512-523
  • [5] Lindblom P(2011)Pericytes and the blood–brain barrier: recent advances and implications for the delivery of CNS therapy Ther Deliv 2 419-422
  • [6] Schallmeiner E(2011)Pericytes: developmental, physiological, and pathological perspectives, problems, and promises Dev Cell 21 193-215
  • [7] Stenzel D(2010)Pericytes regulate the blood–brain barrier Nature 468 557-561
  • [8] Sauvaget D(2013)Transendothelial migration enables subsequent transmigration of neutrophils through underlying pericytes PLoS One 8 e60025-213
  • [9] Ledin J(2007)Characterization of an indoleamine 2,3-dioxygenase-like protein found in humans and mice Gene 396 203-44
  • [10] Ringvall M(2001)Contractile proteins in pericytes at the blood–brain and blood-retinal barriers J Neurocytol 30 35-427