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谱系重编程:胰腺β细胞再生的一条充满希望的途径。

Lineage Reprogramming: A Promising Road for Pancreatic β Cell Regeneration.

作者信息

Wei Rui, Hong Tianpei

机构信息

Department of Endocrinology and Metabolism, Peking University Third Hospital, Beijing 100191, China.

Department of Endocrinology and Metabolism, Peking University Third Hospital, Beijing 100191, China.

出版信息

Trends Endocrinol Metab. 2016 Mar;27(3):163-176. doi: 10.1016/j.tem.2016.01.002. Epub 2016 Jan 23.

Abstract

Cell replacement therapy is a promising method to restore pancreatic β cell function and cure diabetes. Distantly related cells (fibroblasts, keratinocytes, and muscle cells) and developmentally related cells (hepatocytes, gastrointestinal, and pancreatic exocrine cells) have been successfully reprogrammed into β cells in vitro and in vivo. However, while some reprogrammed β cells bear similarities to bona fide β cells, others do not develop into fully functional β cells. Here we review various strategies currently used for β cell reprogramming, including ectopic expression of specific transcription factors associated with islet development, repression of maintenance factors of host cells, regulation of epigenetic modifications, and microenvironmental changes. Development of simple and efficient reprogramming methods is a key priority for developing fully functional β cells suitable for cell replacement therapy.

摘要

细胞替代疗法是恢复胰腺β细胞功能并治愈糖尿病的一种有前景的方法。远亲细胞(成纤维细胞、角质形成细胞和肌肉细胞)以及发育相关细胞(肝细胞、胃肠道细胞和胰腺外分泌细胞)已在体外和体内成功重编程为β细胞。然而,虽然一些重编程的β细胞与真正的β细胞有相似之处,但其他细胞并未发育成功能完全的β细胞。在这里,我们综述了目前用于β细胞重编程的各种策略,包括与胰岛发育相关的特定转录因子的异位表达、宿主细胞维持因子的抑制、表观遗传修饰的调控以及微环境变化。开发简单有效的重编程方法是开发适用于细胞替代疗法的功能完全的β细胞的关键优先事项。

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