医学
间质细胞
干细胞
间充质干细胞
睾酮(贴片)
诱导多能干细胞
促黄体激素
生物信息学
干细胞疗法
不育
移植
肿瘤科
成体干细胞
内分泌学
内科学
激素
胚胎干细胞
病理
体外
生物
细胞生物学
内皮干细胞
遗传学
怀孕
基因
作者
Lü Li,Vassilios Papadopoulos
标识
DOI:10.1038/s41585-021-00480-2
摘要
In Leydig cell dysfunction, cells respond weakly to stimulation by pituitary luteinizing hormone, and, therefore, produce less testosterone, leading to primary hypogonadism. The most widely used treatment for primary hypogonadism is testosterone replacement therapy (TRT). However, TRT causes infertility and has been associated with other adverse effects, such as causing erythrocytosis and gynaecomastia, worsening obstructive sleep apnoea and increasing cardiovascular morbidity and mortality risks. Stem-cell-based therapy that re-establishes testosterone-producing cell lineages in the body has, therefore, become a promising prospect for treating primary hypogonadism. Over the past two decades, substantial advances have been made in the identification of Leydig cell sources for use in transplantation surgery, including the artificial induction of Leydig-like cells from different types of stem cells, for example, stem Leydig cells, mesenchymal stem cells, and pluripotent stem cells (PSCs). PSC-derived Leydig-like cells have already provided a powerful in vitro model to study the molecular mechanisms underlying Leydig cell differentiation and could be used to treat men with primary hypogonadism in a more specific and personalized approach.
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