Engineering mesenchymal stem cells for premature ovarian failure: overcoming challenges and innovating therapeutic strategies

被引:1
作者
Yuan, Zijun [1 ]
Zhang, Yinping [1 ]
He, Xinyu [1 ]
Wang, Xiang [1 ]
Wang, Xingyue [1 ]
Ren, Siqi [1 ]
Su, Jiahong [1 ]
Shen, Jing [1 ,3 ]
Li, Xiang [2 ]
Xiao, Zhangang [1 ,4 ,5 ]
机构
[1] Southwest Med Univ, Sch Pharm, Dept Pharmacol, Lab Mol Pharmacol, Luzhou, Peoples R China
[2] Sichuan Coll Tradit Chinese Med, Mianyang 621000, Sichuan, Peoples R China
[3] Cell Therapy & Cell Drugs Luzhou Key Lab, Luzhou, Sichuan, Peoples R China
[4] Sichuan Coll Tradit Chinese Med, Sch Pharm, Dept Pharmacol, Mianyang 621000, Sichuan, Peoples R China
[5] Luzhou Peoples Hosp, Luzhou, Sichuan, Peoples R China
来源
THERANOSTICS | 2024年 / 14卷 / 17期
基金
中国国家自然科学基金;
关键词
mesenchymal stem cells; premature ovarian failure; heterogeneity; genetic engineering; tissue engineering; STROMAL CELLS; OSTEOGENIC DIFFERENTIATION; RAT MODEL; IMMUNOSUPPRESSIVE PROPERTIES; ARTICULAR-CARTILAGE; GROWTH-FACTOR; TGF-BETA; IN-VITRO; PROMOTES; SURVIVAL;
D O I
10.7150/thno.102641
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Premature ovarian failure (POF) is a leading cause of infertility in women, causing significant psychological and physical distress. Current therapeutic options are limited, necessitating the exploration of new treatments. Mesenchymal stem cells (MSCs), known for their remarkable homing and regenerative properties, have emerged as a promising intervention for POF. However, their clinical efficacy has been inconsistent. This paper aims to address these challenges by examining the cellular heterogeneity within MSC populations, which is crucial for identifying and selecting specific functional subpopulations for clinical applications. Understanding this heterogeneity can enhance therapeutic efficacy and ensure treatment stability. Additionally, this review comprehensively examines the literature on the effectiveness, safety, and ethical considerations of MSCs for ovarian regeneration, with a focus on preclinical and clinical trials. We also discuss potential strategies involving genetically and tissue-engineered MSCs. By integrating insights from these studies, we propose new directions for the design of targeted MSC treatments for POF and related disorders, potentially improving outcomes, addressing safety concerns, and expanding therapeutic options while ensuring ethical compliance.
引用
收藏
页码:6487 / 6515
页数:29
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