Dionne Olivier, Sabatié Salomé, Fortin Fléchère, Corbin François, Laurent Benoit
Department of Biochemistry and Functional Genomics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada.
Medical Genetics division, Centre Hospitalier Universitaire de Sherbrooke (CHUS), Sherbrooke, QC, Canada.
Front Cell Dev Biol. 2024 Nov 22;12:1489190. doi: 10.3389/fcell.2024.1489190. eCollection 2024.
Human induced pluripotent stem cells (iPSCs) are a valuable tool for studying human development and diseases. iPSCs can be generated by reprogramming from any somatic cells, however establishing primary cell cultures can involve invasive procedures (e.g., skin biopsy) and be labor-intensive. In this paper, we describe an efficient, reliable, and non-invasive method for cultivating primary urine-derived cells (UDCs) and efficiently reprogram them into iPSCs using a feeder-free and non-integrative system. This approach has several advantages: (i) UDCs collection and culture are non-invasive, straightforward, and do not require medical personnel; (ii) reprogramming UDCs using commercially available Sendai viruses is highly efficient and reliable; and (iii) iPSCs generated from UDCs demonstrate strong differentiation potential. To showcase the effectiveness of this method, we generated iPSC lines from UDCs of three control individuals and three patients with Fragile X syndrome.
人诱导多能干细胞(iPSC)是研究人类发育和疾病的宝贵工具。iPSC可以通过对任何体细胞进行重编程来产生,然而建立原代细胞培养可能涉及侵入性程序(例如皮肤活检)且劳动强度大。在本文中,我们描述了一种高效、可靠且非侵入性的方法,用于培养原代尿液衍生细胞(UDC),并使用无饲养层和非整合系统将其高效重编程为iPSC。这种方法有几个优点:(i)UDC的收集和培养是非侵入性的、直接的,并且不需要医务人员;(ii)使用市售仙台病毒对UDC进行重编程是高效且可靠的;(iii)由UDC产生的iPSC表现出强大的分化潜力。为了展示这种方法的有效性,我们从三名对照个体和三名脆性X综合征患者的UDC中生成了iPSC系。