Tian Lipeng, Eldridge Lindsey, Chaudhari Pooja, Zhang Linyi, Anders Robert A, Schwarz Kathleen B, Ye Zhaohui, Jang Yoon-Young
Department of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, USA.
Division of Cellular and Gene Therapies, Center for Biologics Evaluation and Research, US Food and Drug Administration, USA.
Stem Cell Res. 2017 Oct;24:25-28. doi: 10.1016/j.scr.2017.08.001. Epub 2017 Aug 8.
Biliary atresia (BA) is a common cause of pediatric end-stage liver disease. While its etiology is not yet clear, evidence has suggested that BA results from interactions between genetic susceptibility and environmental factors. Disease relevant human cellular models of BA will facilitate identification of both genetic and environmental factors that are important for disease prevention and treatment. Here we report the generation of a human induced pluripotent stem cell line from a BA patient using episomal vectors. Patient-specific BA iPSC lines provide valuable tools for disease mechanism study and drug development.
胆道闭锁(BA)是小儿终末期肝病的常见病因。虽然其病因尚不清楚,但有证据表明,BA是由遗传易感性和环境因素相互作用所致。与疾病相关的BA人类细胞模型将有助于识别对疾病预防和治疗至关重要的遗传和环境因素。在此,我们报告了使用附加型载体从一名BA患者中生成人诱导多能干细胞系。患者特异性BA诱导多能干细胞系为疾病机制研究和药物开发提供了有价值的工具。