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干细胞在先天性巨结肠症治疗中作用的最新进展

Update on the Role of Stem Cells in the Treatment of Hirschsprung Disease.

作者信息

Lui Kathy Nga-Chu, Tam Paul Kwong Hang, Ngan Elly Sau-Wai

机构信息

Department of Surgery, The University of Hong Kong, Hong Kong, Hong Kong.

出版信息

Eur J Pediatr Surg. 2018 Jun;28(3):215-221. doi: 10.1055/s-0038-1646925. Epub 2018 Apr 24.

Abstract

Stem cells possess the ability of self-renewal and the potency to differentiate into multiple cell lineages. Somatic stem cells are present in adult tissues, but they usually exhibit limited differentiation capacity and life span. On the other hand, somatic cells from adult tissues can be reprogrammed into induced pluripotent stem cells (iPSCs) that retain a full differentiation capacity with unlimited self-renewal ability. Autologous origin of iPSCs makes them an ideal source of cells for regenerative medicine to replenish the missing or damaged cells in the patients. iPSCs nowadays have also been widely used to build human disease models to study pathological mechanisms of the diseases. Hirschsprung disease (HSCR) is a congenital disorder caused by defects in the development of enteric neural crest stem cells. The failures of the ENCCs to proliferate, differentiate, and/or migrate lead to the absence of enteric neurons in the distal colon, resulting in colonic motility dysfunction. The lack of effective treatment for HSCR urges continuous efforts to develop new therapies for this congenital disorder. In this review, we will discuss the potential applications of somatic stem cells and iPSCs for the cell-based therapy of HSCR. We will also highlight the recent advances in stem cell research for the establishment of human HSCR models for the development of novel therapies.

摘要

干细胞具有自我更新能力以及分化为多种细胞谱系的潜能。成体干细胞存在于成体组织中,但它们通常表现出有限的分化能力和寿命。另一方面,来自成体组织的体细胞可以被重编程为诱导多能干细胞(iPSC),这些细胞保留了完全的分化能力以及无限的自我更新能力。iPSC的自体来源使其成为再生医学中用于补充患者体内缺失或受损细胞的理想细胞来源。如今,iPSC也已被广泛用于构建人类疾病模型,以研究疾病的病理机制。先天性巨结肠(HSCR)是一种由肠神经嵴干细胞发育缺陷引起的先天性疾病。肠神经嵴细胞(ENCC)增殖、分化和/或迁移失败会导致远端结肠中缺乏肠神经元,从而导致结肠运动功能障碍。由于缺乏针对HSCR的有效治疗方法,因此需要不断努力开发针对这种先天性疾病的新疗法。在这篇综述中,我们将讨论成体干细胞和iPSC在HSCR细胞治疗中的潜在应用。我们还将重点介绍干细胞研究在建立人类HSCR模型以开发新疗法方面的最新进展。

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