Lee Hyun Jik, Chae Chang Woo, Han Ho Jae
Laboratory of Veterinary Physiology, College of Veterinary Medicine and Veterinary Medicine Center, Chungbuk National University, Cheongju 28644, Republic of South Korea; Institute for Stem Cell & Regenerative Medicine (ISCRM), Chungbuk National University, Cheongju 28644, Republic of South Korea.
Department of Veterinary Physiology, College of Veterinary Medicine, Research Institute for Veterinary Science, and BK21 Four Future Veterinary Medicine Leading Education & Research Center, Seoul National University, Seoul 08826, Republic of Korea.
Biomed Pharmacother. 2023 Dec;168:115759. doi: 10.1016/j.biopha.2023.115759. Epub 2023 Oct 20.
Mesenchymal stem cell (MSC) transplantation offers significant potential for the treatment of diabetes mellitus (DM) and its complications. However, hyperglycemic conditions can induce senescence and dysfunction in both transplanted and resident MSCs, thereby limiting their therapeutic potential. Mitochondrial dysfunction and oxidative stress are key contributors to this process in MSCs exposed to hyperglycemia. As such, strategies aimed at mitigating mitochondrial dysfunction could enhance the therapeutic efficacy of MSC transplantation in DM. In this review, we provide an updated overview of how mitochondrial dysfunction mediates MSC senescence. We present experimental evidence for the molecular mechanisms behind high glucose-induced mitochondrial dysfunction in MSCs, which include impairment of mitochondrial biogenesis, mitochondrial calcium regulation, the mitochondrial antioxidant system, mitochondrial fusion-fission dynamics, mitophagy, and intercellular mitochondrial transfer. Furthermore, we propose potential pharmacological candidates that could improve the efficacy of MSC transplantation by enhancing mitochondrial function in patients with DM and related complications.
间充质干细胞(MSC)移植为糖尿病(DM)及其并发症的治疗提供了巨大潜力。然而,高血糖状况可诱导移植的和内源性间充质干细胞衰老及功能障碍,从而限制其治疗潜力。线粒体功能障碍和氧化应激是暴露于高血糖环境中间充质干细胞这一过程的关键促成因素。因此,旨在减轻线粒体功能障碍的策略可提高间充质干细胞移植治疗糖尿病的疗效。在本综述中,我们提供了线粒体功能障碍如何介导间充质干细胞衰老的最新概述。我们展示了间充质干细胞中高糖诱导的线粒体功能障碍背后分子机制的实验证据,这些机制包括线粒体生物发生受损、线粒体钙调节、线粒体抗氧化系统、线粒体融合-分裂动态、线粒体自噬和细胞间线粒体转移。此外,我们提出了潜在的药理学候选药物,通过增强糖尿病患者及其相关并发症患者的线粒体功能,可提高间充质干细胞移植的疗效。