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Sterol carrier protein 2: A promising target in the pathogenesis of atherosclerosis

Atherosclerosis, the underlying pathophysiological basis of cardiovascular disease, has been recognized as a lipid-driven chronic inflammatory disease. Sterol carrier protein 2 (SCP-2) is a 13-kDa non-specific lipid-transfer protein expressed by various tissues and cells, such as liver, heart, vascu...

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Detalles Bibliográficos
Autores principales: Xu, Can, Li, Heng, Tang, Chao-Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201558/
https://www.ncbi.nlm.nih.gov/pubmed/37223526
http://dx.doi.org/10.1016/j.gendis.2021.12.007
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author Xu, Can
Li, Heng
Tang, Chao-Ke
author_facet Xu, Can
Li, Heng
Tang, Chao-Ke
author_sort Xu, Can
collection PubMed
description Atherosclerosis, the underlying pathophysiological basis of cardiovascular disease, has been recognized as a lipid-driven chronic inflammatory disease. Sterol carrier protein 2 (SCP-2) is a 13-kDa non-specific lipid-transfer protein expressed by various tissues and cells, such as liver, heart, vascular smooth muscle cells (VSMCs), and macrophages. SCP-2 has an extensive role in cardiovascular and metabolic diseases. Recently, SCP-2 was reported to promote the development of atherosclerosis by regulating lipid metabolism and peroxidation, endocannabinoid metabolism, vascular inflammation, and fatty acid metabolism. In this review, we summarized the recent advances regarding the role of SCP-2 in the pathogenesis of atherosclerosis and tried to provide a rationale for future investigation and a better understanding of the biological functions of SCP-2 in atherosclerotic cardiovascular disease.
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spelling pubmed-102015582023-05-23 Sterol carrier protein 2: A promising target in the pathogenesis of atherosclerosis Xu, Can Li, Heng Tang, Chao-Ke Genes Dis Review Article Atherosclerosis, the underlying pathophysiological basis of cardiovascular disease, has been recognized as a lipid-driven chronic inflammatory disease. Sterol carrier protein 2 (SCP-2) is a 13-kDa non-specific lipid-transfer protein expressed by various tissues and cells, such as liver, heart, vascular smooth muscle cells (VSMCs), and macrophages. SCP-2 has an extensive role in cardiovascular and metabolic diseases. Recently, SCP-2 was reported to promote the development of atherosclerosis by regulating lipid metabolism and peroxidation, endocannabinoid metabolism, vascular inflammation, and fatty acid metabolism. In this review, we summarized the recent advances regarding the role of SCP-2 in the pathogenesis of atherosclerosis and tried to provide a rationale for future investigation and a better understanding of the biological functions of SCP-2 in atherosclerotic cardiovascular disease. Chongqing Medical University 2022-01-10 /pmc/articles/PMC10201558/ /pubmed/37223526 http://dx.doi.org/10.1016/j.gendis.2021.12.007 Text en © 2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Xu, Can
Li, Heng
Tang, Chao-Ke
Sterol carrier protein 2: A promising target in the pathogenesis of atherosclerosis
title Sterol carrier protein 2: A promising target in the pathogenesis of atherosclerosis
title_full Sterol carrier protein 2: A promising target in the pathogenesis of atherosclerosis
title_fullStr Sterol carrier protein 2: A promising target in the pathogenesis of atherosclerosis
title_full_unstemmed Sterol carrier protein 2: A promising target in the pathogenesis of atherosclerosis
title_short Sterol carrier protein 2: A promising target in the pathogenesis of atherosclerosis
title_sort sterol carrier protein 2: a promising target in the pathogenesis of atherosclerosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201558/
https://www.ncbi.nlm.nih.gov/pubmed/37223526
http://dx.doi.org/10.1016/j.gendis.2021.12.007
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