Bolideei Mansoor, Barzigar Rambod, Gahrouei Razieh Bahrami, Mohebbi Elham, Haider Khawaja Husnain, Paul Sayan, Paul Manash K, Mehran Mohammad Javad
Department of Respiratory and Critical Care Medicine, the Center for Biomedical Research, NHC Key Laboratory of Respiratory Diseases, Tongji Hospital, Tongji Medical College, Huazhong University of Sciences and Technology, Wuhan, China.
Department of Biotechnology, SJCE Technical Campus, JSS Research Foundation, University of Mysore, Mysore, 570006, Karnataka, India.
Stem Cell Rev Rep. 2025 Feb 27. doi: 10.1007/s12015-025-10857-0.
Stem cell research is a dynamic and fast-advancing discipline with great promise for the treatment of diverse human disorders. The incorporation of gene editing technologies, including ZFNs, TALENs, and the CRISPR/Cas system, in conjunction with progress in nanotechnology, is fundamentally transforming stem cell therapy and research. These innovations not only provide a glimmer of optimism for patients and healthcare practitioners but also possess the capacity to radically reshape medical treatment paradigms. Gene editing and nanotechnology synergistically enhance stem cell-based therapies' precision, efficiency, and applicability, offering transformative potential for treating complex diseases and advancing regenerative medicine. Nevertheless, it is important to acknowledge that these technologies also give rise to ethical considerations and possible hazards, such as inadvertent genetic modifications and the development of genetically modified organisms, therefore creating a new age of designer infants. This review emphasizes the crucial significance of gene editing technologies and nanotechnology in the progress of stem cell treatments, particularly for degenerative pathologies and injuries. It emphasizes their capacity to restructure and comprehensively revolutionize medical treatment paradigms, providing fresh hope and optimism for patients and healthcare practitioners.
干细胞研究是一个充满活力且快速发展的学科,在治疗各种人类疾病方面具有巨大潜力。基因编辑技术,包括锌指核酸酶(ZFNs)、转录激活样效应因子核酸酶(TALENs)和CRISPR/Cas系统,与纳米技术的进展相结合,正在从根本上改变干细胞治疗和研究。这些创新不仅为患者和医疗从业者带来了一线希望,还具有从根本上重塑医疗治疗模式的能力。基因编辑和纳米技术协同提高了基于干细胞疗法的精准性、效率和适用性,为治疗复杂疾病和推进再生医学提供了变革潜力。然而,必须认识到这些技术也引发了伦理考量和潜在风险,如意外的基因修饰和转基因生物的出现,从而催生了设计婴儿的新时代。本综述强调了基因编辑技术和纳米技术在干细胞治疗进展中的关键意义,特别是对于退行性疾病和损伤。它强调了它们重构和全面革新医疗治疗模式的能力,为患者和医疗从业者带来新希望和乐观前景。