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中国临床药理学与治疗学 ›› 2024, Vol. 29 ›› Issue (1): 114-120.doi: 10.12092/j.issn.1009-2501.2024.01.013

• 综述与讲座 • 上一篇    

间充质干细胞对OSAHS病理生理调节机制的研究进展

许金回1,岳红梅1,2,李雅亭1,刘苗苗1,武兴东1,朱浩斌1   

  1. 1兰州大学第一临床医学院,兰州  730000,甘肃;2兰州大学第一医院呼吸与危重症医学科,兰州  730000,甘肃

  • 收稿日期:2023-07-17 修回日期:2023-08-30 出版日期:2024-01-26 发布日期:2024-01-15
  • 通讯作者: 岳红梅,女,硕士,主任医师,博士生导师,研究方向:呼吸系统疾病。 E-mail: yuehongmei@sina.com
  • 作者简介:许金回,女,在读硕士,研究方向:阻塞性睡眠呼吸暂停。 E-mail: xujinhui0829@163.com
  • 基金资助:
    甘肃省科技计划(科技重大专项计划)(22ZD1FA001)

Advances in the study of mesenchymal stem cells in obstructive sleep apnea hypoventilation syndrome

XU Jinhui1, YUE Hongmei1,2, LI Yating1, LIU Miaomiao1, WU Xingdong1, ZHU Haobin1   

  1. 1 The First Clinical College of Medicine, Lanzhou University, Lanzhou 730000, Gansu, China; 2 Department of Respiratory and Critical Care Medicine, The First Hospital of Lanzhou University, Lanzhou 730000, Gansu, China
  • Received:2023-07-17 Revised:2023-08-30 Online:2024-01-26 Published:2024-01-15

摘要:

间充质干细胞(MSCs)是一种自我再生、快速增殖的多能干细胞,主要依赖其衍生的促血管生成、炎症调节和营养因子发挥有益作用。这些因子能减弱有害的炎症反应,减少血管损伤,促进组织修复和再生。阻塞性睡眠呼吸暂停低通气综合征(OSAHS)是一种慢性疾病,其标志是睡眠过程中口咽塌陷,导致短暂的气流减少,胸内压力大幅波动,以及间歇性缺氧和高碳酸血症。OSAHS存在细胞因子介导的炎症级联反应、氧化应激和缺血,从炎症和损伤组织中招募MSCs,通过MSCs衍生的抗炎和促进血管生成因子的活性,在OSAHS损伤组织中降低缺氧、抑制炎症、促进再生、防治纤维化。本文将从OSAHS角度阐述炎症、氧化应激、纤维化和缺血的发病机制,着重介绍目前关于MSCs依赖调节OSAHS相关病理的研究进展。

关键词: 阻塞性睡眠呼吸暂停低通气综合征, 间充质干细胞, 作用机制, 研究进展

Abstract:

Mesenchymal stem cells (MSCs) are self-regenerating, rapidly proliferating pluripotent stem cells that depend primarily on their derived pro-angiogenic, inflammatory regulatory, and trophic factors to exert beneficial effects that attenuate deleterious inflammatory responses, reduce vascular damage, and promote tissue repair and regeneration. Obstructive sleep apnea hypoventilation syndrome (OSAHS) is a chronic disorder marked by oropharyngeal collapse during sleep, resulting in transient reduced airflow, large fluctuations in intrathoracic pressure, and intermittent hypoxia and hypercapnia. OSAHS subsequently cytokine-mediated inflammatory cascades, oxidative stress, and ischemia, recruit MSCs from inflamed and damaged tissues through MSCs-derived of anti-inflammatory and pro-angiogenic factor activity, reduce hypoxia, suppress inflammation, promote regeneration, and prevent fibrosis in OSAHS-injured tissues. In this paper, we will describe the pathogenesis of inflammation, oxidative stress, fibrosis and ischemia from the perspective of OSAHS, highlighting the current research progress on MSCs-dependent regulation of OSAHS-related pathology.

Key words: obstructive sleep apnea hypoventilation syndrome, mesenchymal stem cells, mechanism of action, research progress

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