Guidance Molecules in Vascular Smooth Muscle

Several highly conserved families of guidance molecules, including ephrins, Semaphorins, Netrins, and Slits, play conserved and distinct roles in tissue remodeling during tissue patterning and disease pathogenesis. Primarily, these guidance molecules function as either secreted or surface-bound liga...

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Main Authors: Alexandra Christine Finney, Anthony Wayne Orr
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-09-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphys.2018.01311/full
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spelling doaj-d249cb594da74f65b849fd2336470b992020-11-25T00:44:16ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2018-09-01910.3389/fphys.2018.01311411316Guidance Molecules in Vascular Smooth MuscleAlexandra Christine Finney0Anthony Wayne Orr1Anthony Wayne Orr2Anthony Wayne Orr3Department of Cellular Biology and Anatomy, Louisiana State University Health Sciences Center Shreveport, Shreveport, LA, United StatesDepartment of Cellular Biology and Anatomy, Louisiana State University Health Sciences Center Shreveport, Shreveport, LA, United StatesDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center Shreveport, Shreveport, LA, United StatesDepartment of Pathology and Translational Medicine, Louisiana State University Health Sciences Center Shreveport, Shreveport, LA, United StatesSeveral highly conserved families of guidance molecules, including ephrins, Semaphorins, Netrins, and Slits, play conserved and distinct roles in tissue remodeling during tissue patterning and disease pathogenesis. Primarily, these guidance molecules function as either secreted or surface-bound ligands that interact with their receptors to activate a variety of downstream effects, including cell contractility, migration, adhesion, proliferation, and inflammation. Vascular smooth muscle cells, contractile cells comprising the medial layer of the vessel wall and deriving from the mural population, regulate vascular tone and blood pressure. While capillaries lack a medial layer of vascular smooth muscle, mural-derived pericytes contribute similarly to capillary tone to regulate blood flow in various tissues. Furthermore, pericyte coverage is critical in vascular development, as perturbations disrupt vascular permeability and viability. During cardiovascular disease, smooth muscle cells play a more dynamic role in which suppression of contractile markers, enhanced proliferation, and migration lead to the progression of aberrant vascular remodeling. Since many types of guidance molecules are expressed in vascular smooth muscle and pericytes, these may contribute to blood vessel formation and aberrant remodeling during vascular disease. While vascular development is a large focus of the existing literature, studies emerged to address post-developmental roles for guidance molecules in pathology and are of interest as novel therapeutic targets. In this review, we will discuss the roles of guidance molecules in vascular smooth muscle and pericyte function in development and disease.https://www.frontiersin.org/article/10.3389/fphys.2018.01311/fullguidance moleculesvascular smooth muscle cellspericytesvascular remodelingcardiovascular disease
collection DOAJ
language English
format Article
sources DOAJ
author Alexandra Christine Finney
Anthony Wayne Orr
Anthony Wayne Orr
Anthony Wayne Orr
spellingShingle Alexandra Christine Finney
Anthony Wayne Orr
Anthony Wayne Orr
Anthony Wayne Orr
Guidance Molecules in Vascular Smooth Muscle
Frontiers in Physiology
guidance molecules
vascular smooth muscle cells
pericytes
vascular remodeling
cardiovascular disease
author_facet Alexandra Christine Finney
Anthony Wayne Orr
Anthony Wayne Orr
Anthony Wayne Orr
author_sort Alexandra Christine Finney
title Guidance Molecules in Vascular Smooth Muscle
title_short Guidance Molecules in Vascular Smooth Muscle
title_full Guidance Molecules in Vascular Smooth Muscle
title_fullStr Guidance Molecules in Vascular Smooth Muscle
title_full_unstemmed Guidance Molecules in Vascular Smooth Muscle
title_sort guidance molecules in vascular smooth muscle
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2018-09-01
description Several highly conserved families of guidance molecules, including ephrins, Semaphorins, Netrins, and Slits, play conserved and distinct roles in tissue remodeling during tissue patterning and disease pathogenesis. Primarily, these guidance molecules function as either secreted or surface-bound ligands that interact with their receptors to activate a variety of downstream effects, including cell contractility, migration, adhesion, proliferation, and inflammation. Vascular smooth muscle cells, contractile cells comprising the medial layer of the vessel wall and deriving from the mural population, regulate vascular tone and blood pressure. While capillaries lack a medial layer of vascular smooth muscle, mural-derived pericytes contribute similarly to capillary tone to regulate blood flow in various tissues. Furthermore, pericyte coverage is critical in vascular development, as perturbations disrupt vascular permeability and viability. During cardiovascular disease, smooth muscle cells play a more dynamic role in which suppression of contractile markers, enhanced proliferation, and migration lead to the progression of aberrant vascular remodeling. Since many types of guidance molecules are expressed in vascular smooth muscle and pericytes, these may contribute to blood vessel formation and aberrant remodeling during vascular disease. While vascular development is a large focus of the existing literature, studies emerged to address post-developmental roles for guidance molecules in pathology and are of interest as novel therapeutic targets. In this review, we will discuss the roles of guidance molecules in vascular smooth muscle and pericyte function in development and disease.
topic guidance molecules
vascular smooth muscle cells
pericytes
vascular remodeling
cardiovascular disease
url https://www.frontiersin.org/article/10.3389/fphys.2018.01311/full
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