Yu Peijie, Liu Bin, Dong Cheng, Chang Yun
Department of Biomedical Engineering, The Hong Kong Polytechnic University, Hunghom, Hong Kong 999077, China.
The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen 518057, China.
Cells. 2025 Apr 21;14(8):619. doi: 10.3390/cells14080619.
A significant increase in life expectancy worldwide has resulted in a growing aging population, accompanied by a rise in aging-related diseases that pose substantial societal, economic, and medical challenges. This trend has prompted extensive efforts within many scientific and medical communities to develop and enhance therapies aimed at delaying aging processes, mitigating aging-related functional decline, and addressing aging-associated diseases to extend health span. Research in aging biology has focused on unraveling various biochemical and genetic pathways contributing to aging-related changes, including genomic instability, telomere shortening, and cellular senescence. The advent of induced pluripotent stem cells (iPSCs), derived through reprogramming human somatic cells, has revolutionized disease modeling and understanding in humans by addressing the limitations of conventional animal models and primary human cells. iPSCs offer significant advantages over other pluripotent stem cells, such as embryonic stem cells, as they can be obtained without the need for embryo destruction and are not restricted by the availability of healthy donors or patients. These attributes position iPSC technology as a promising avenue for modeling and deciphering mechanisms that underlie aging and associated diseases, as well as for studying drug effects. Moreover, iPSCs exhibit remarkable versatility in differentiating into diverse cell types, making them a promising tool for personalized regenerative therapies aimed at replacing aged or damaged cells with healthy, functional equivalents. This review explores the breadth of research in iPSC-based regenerative therapies and their potential applications in addressing a spectrum of aging-related conditions.
全球预期寿命的显著增加导致了老龄人口的不断增长,同时与衰老相关的疾病也在增加,这给社会、经济和医疗带来了重大挑战。这一趋势促使许多科学和医学领域做出广泛努力,以开发和改进旨在延缓衰老过程、减轻与衰老相关的功能衰退以及应对与衰老相关疾病以延长健康寿命的疗法。衰老生物学的研究集中在揭示导致衰老相关变化的各种生化和遗传途径,包括基因组不稳定、端粒缩短和细胞衰老。通过对人类体细胞进行重编程获得的诱导多能干细胞(iPSC)的出现,通过克服传统动物模型和原代人类细胞的局限性,彻底改变了人类疾病建模和理解方式。与其他多能干细胞(如胚胎干细胞)相比,iPSC具有显著优势,因为它们的获取无需破坏胚胎,且不受健康供体或患者可用性的限制。这些特性使iPSC技术成为一种有前景的途径,可用于建模和解读衰老及相关疾病的潜在机制,以及研究药物效果。此外,iPSC在分化为多种细胞类型方面表现出显著的通用性,使其成为个性化再生疗法的有前景工具,旨在用健康、功能等同的细胞替代老化或受损细胞。本综述探讨了基于iPSC的再生疗法的研究广度及其在应对一系列与衰老相关病症方面的潜在应用。