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靶向血管平滑肌细胞衰老:血管疾病的新策略。

Targeting Vascular Smooth Muscle Cell Senescence: A Novel Strategy for Vascular Diseases.

机构信息

Department of Physiology, Institute of Neuroscience Research, Hengyang Medical School, University of South China, Hengyang, 421001, Hunan, China.

Department of Rheumatology, Shaoyang Central Hospital, Shaoyang, 422000, China.

出版信息

J Cardiovasc Transl Res. 2023 Oct;16(5):1010-1020. doi: 10.1007/s12265-023-10377-7. Epub 2023 Mar 27.


DOI:10.1007/s12265-023-10377-7
PMID:36973566
Abstract

Vascular diseases are a major threat to human health, characterized by high rates of morbidity, mortality, and disability. VSMC senescence contributes to dramatic changes in vascular morphology, structure, and function. A growing number of studies suggest that VSMC senescence is an important pathophysiological mechanism for the development of vascular diseases, including pulmonary hypertension, atherosclerosis, aneurysm, and hypertension. This review summarizes the important role of VSMC senescence and senescence-associated secretory phenotype (SASP) secreted by senescent VSMCs in the pathophysiological process of vascular diseases. Meanwhile, it concludes the progress of antisenescence therapy targeting VSMC senescence or SASP, which provides new strategies for the prevention and treatment of vascular diseases.

摘要

血管疾病是人类健康的主要威胁,其特点是发病率、死亡率和残疾率高。血管平滑肌细胞衰老导致血管形态、结构和功能的显著变化。越来越多的研究表明,血管平滑肌细胞衰老是血管疾病发展的重要病理生理机制,包括肺动脉高压、动脉粥样硬化、动脉瘤和高血压。本综述总结了血管平滑肌细胞衰老及其分泌的衰老相关分泌表型(SASP)在血管疾病病理生理过程中的重要作用。同时,总结了针对血管平滑肌细胞衰老或 SASP 的抗衰老治疗的进展,为血管疾病的预防和治疗提供了新策略。

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Targeting Vascular Smooth Muscle Cell Senescence: A Novel Strategy for Vascular Diseases.

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[2]
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[8]
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[9]
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引用本文的文献

[1]
Arterial stiffness and vascular aging: mechanisms, prevention, and therapy.

Signal Transduct Target Ther. 2025-9-1

[2]
Nicotinamide Mononucleotide (NMN) Improves the Senescence of Mouse Vascular Smooth Muscle Cells Induced by Ang II Through Activating p-AMPK/KLF4 Pathway.

Pharmaceuticals (Basel). 2025-4-9

[3]
Vascular smooth muscle cell-derived SO sulphenylated interferon regulatory factor 1 to inhibit VSMC senescence.

Front Pharmacol. 2025-3-28

[4]
MG-132 activates sodium palmitate-induced autophagy in human vascular smooth muscle cells and inhibits senescence via the PI3K/AKT/mTOR axis.

Lipids Health Dis. 2024-9-4

[5]
Elucidating VSMC phenotypic transition mechanisms to bridge insights into cardiovascular disease implications.

Front Cardiovasc Med. 2024-5-13

[6]
Dipeptidyl peptidase-4 inhibition targeting vascular senescence as a novel treatment for atherosclerosis.

J Diabetes Investig. 2024-2

本文引用的文献

[1]
Short-term rapamycin treatment increases life span and attenuates aortic aneurysm in a murine model of Marfan-Syndrome.

Biochem Pharmacol. 2022-11

[2]
EZH2 Regulates ANXA6 Expression via H3K27me3 and Is Involved in Angiotensin II-Induced Vascular Smooth Muscle Cell Senescence.

Oxid Med Cell Longev. 2022

[3]
Cellular senescence and senolytics: the path to the clinic.

Nat Med. 2022-8

[4]
Targeting p53-MDM2 interaction by small-molecule inhibitors: learning from MDM2 inhibitors in clinical trials.

J Hematol Oncol. 2022-7-13

[5]
Both high glucose and phosphate overload promote senescence-associated calcification of vascular muscle cells.

Int Urol Nephrol. 2022-10

[6]
PGF2-FP Receptor Ameliorates Senescence of VSMCs in Vascular Remodeling by Src/PAI-1 Signal Pathway.

Oxid Med Cell Longev. 2022

[7]
Cellular autophagy, an unbidden effect of caspase inhibition by zVAD-fmk.

FEBS J. 2022-6

[8]
The role and biology of senescent cells in ageing-related tissue damage and repair.

Mech Ageing Dev. 2022-3

[9]
Mulberry polyphenol extracts attenuated senescence through inhibition of Ras/ERK via promoting Ras degradation in VSMC.

Int J Med Sci. 2022

[10]
PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Triggers Vascular Smooth Muscle Cell Senescence and Apoptosis: Implication of Its Direct Role in Degenerative Vascular Disease.

Arterioscler Thromb Vasc Biol. 2022-1

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