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招募内源性干细胞:一种治疗勃起功能障碍的新方法。

Recruiting endogenous stem cells: a novel therapeutic approach for erectile dysfunction.

作者信息

Xin Zhong-Cheng, Xu Yong-De, Lin Guiting, Lue Tom F, Guo Ying-Lu

机构信息

Andrology Center, Peking University First Hospital, Peking University, Beijing 100034, USA.

出版信息

Asian J Androl. 2016 Jan-Feb;18(1):10-5. doi: 10.4103/1008-682X.150040.

Abstract

Transplanted stem cells (SCs), owing to their regenerative capacity, represent one of the most promising methods to restore erectile dysfunction (ED). However, insufficient source, invasive procedures, ethical and regulatory issues hamper their use in clinical applications. The endogenous SCs/progenitor cells resident in organ and tissues play critical roles for organogenesis during development and for tissue homeostasis in adulthood. Even without any therapeutic intervention, human body has a robust self-healing capability to repair the damaged tissues or organs. Therefore, SCs-for-ED therapy should not be limited to a supply-side approach. The resident endogenous SCs existing in patients could also be a potential target for ED therapy. The aim of this review was to summarize contemporary evidence regarding: (1) SC niche and SC biological features in vitro; (2) localization and mobilization of endogenous SCs; (3) existing evidence of penile endogenous SCs and their possible mode of mobilization. We performed a search on PubMed for articles related to these aspects in a wide range of basic studies. Together, numerous evidences hold the promise that endogenous SCs would be a novel therapeutic approach for the therapy of ED.

摘要

移植的干细胞(SCs)因其再生能力,是恢复勃起功能障碍(ED)最有前景的方法之一。然而,来源不足、侵入性操作、伦理和监管问题阻碍了它们在临床应用中的使用。存在于器官和组织中的内源性SCs/祖细胞在发育过程中的器官形成以及成年期的组织稳态中起着关键作用。即使没有任何治疗干预,人体也具有强大的自我修复能力来修复受损组织或器官。因此,用于治疗ED的SCs不应局限于供应方方法。患者体内存在的内源性SCs也可能是ED治疗的潜在靶点。本综述的目的是总结关于以下方面的当代证据:(1)SCs微环境和SCs的体外生物学特性;(2)内源性SCs的定位和动员;(3)阴茎内源性SCs的现有证据及其可能的动员方式。我们在PubMed上搜索了广泛基础研究中与这些方面相关的文章。总之,大量证据表明内源性SCs有望成为治疗ED的一种新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3bc/4736335/a631641251b3/AJA-18-10-g001.jpg

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