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人胚胎干细胞向中胚层亚型的分化:血管、造血和间充质谱系细胞。

Differentiation of hESCs into Mesodermal Subtypes: Vascular-, Hematopoietic- and Mesenchymal-lineage Cells.

作者信息

Moon Sung-Hwan, Kim Jung Mo, Hong Ki-Sung, Shin Jeong Min, Kim Jumi, Chung Hyung-Min

机构信息

CHA Bio & Diostech Co. Ltd.

出版信息

Int J Stem Cells. 2011 Jun;4(1):24-34. doi: 10.15283/ijsc.2011.4.1.24.

Abstract

To date, studies on the application of mesodermally derived mesenchymal-, hematopoietic- and vascular-lineage cells for cell therapy have provided either poor or insufficient data. The results are equivocal with regard to therapeutic efficiency and yield. Since the establishment of human embryonic stem cells (hESCs) in 1998, the capacity of hESCs to differentiate into various mesodermal lineages has sparked considerable interest in the regenerative medicine community, a group interested in generating specialized cells to treat patients suffering from degenerative diseases. Even though hESCs are sensitive, effective methods for guiding the differentiation of hESCs into specific mesodermal cell types are still being developed. In addition, to understand the functional properties of hESC derivatives, numerous animal model studies have been performed by many research groups over the last decade. In this review, we describe and summarize the protocols currently used for differentiation of hESCs into multiple mesodermal lineages and their therapeutic efficiency in different animal models. Furthermore, we discuss the technical hurdles associated with each protocol and the safety of hESC derivatives for therapeutic applications. Technical improvement of the methods used to produce hESC derivatives for therapeutic use in patients with degenerative diseases should remain an objective of future studies, as should the development of effective and stable induction systems.

摘要

迄今为止,关于中胚层来源的间充质、造血和血管谱系细胞用于细胞治疗的应用研究,所提供的数据要么不佳,要么不充分。在治疗效果和产量方面,结果并不明确。自1998年人类胚胎干细胞(hESCs)建立以来,hESCs分化为各种中胚层谱系的能力在再生医学领域引发了相当大的兴趣,该领域致力于生成专门的细胞来治疗患有退行性疾病的患者。尽管hESCs很敏感,但引导hESCs分化为特定中胚层细胞类型的有效方法仍在不断开发中。此外,为了了解hESC衍生物的功能特性,在过去十年中,许多研究小组进行了大量动物模型研究。在这篇综述中,我们描述并总结了目前用于将hESCs分化为多种中胚层谱系的方案及其在不同动物模型中的治疗效果。此外,我们还讨论了与每个方案相关的技术障碍以及hESC衍生物用于治疗应用的安全性。改进用于为退行性疾病患者生产hESC衍生物以供治疗使用的方法的技术,以及开发有效且稳定的诱导系统,都应成为未来研究的目标。

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