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两步法诱导诱导多能干细胞分化为小梁网细胞用于青光眼。

Two-step induction of trabecular meshwork cells from induced pluripotent stem cells for glaucoma.

机构信息

Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, USA.

Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, USA; Department of Ophthalmology, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

Biochem Biophys Res Commun. 2020 Aug 20;529(2):411-417. doi: 10.1016/j.bbrc.2020.05.225. Epub 2020 Jul 1.

Abstract

Glaucoma is a leading cause of irreversible blindness worldwide. Reducing intraocular pressure is currently the only effective treatment. Elevated intraocular pressure is associated with increased resistance of the outflow pathway, mainly the trabecular meshwork (TM). Despite great progress in the field, the development of novel and effective treatment for glaucoma is still challenging. In this study, we reported that human induced pluripotent stem cells (iPSCs) can be cultured as colonies and monolayer cells expressing OCT4, alkaline phosphatase, SSEA4 and SSEA1. After induction to neural crest cells (NCCs) positive to NGFR and HNK1, the iPSCs can differentiate into TM cells. The induced iPSC-TM cells expressed TM cell marker CHI3L1, were responsive to dexamethasone treatment with increased expression of myocilin, ANGPTL7, and formed CLANs, comparable to primary TM cells. To the best of our knowledge, this is the first study that induces iPSCs to TM cells through a middle neural crest stage, which ensures a stable NCC pool and ensures the high output of the same TM cells. This system can be used to develop personalized treatments using patient-derived iPSCs, explore high throughput screening of new drugs focusing on TM response for controlling intraocular pressure, and investigate stem cell-based therapy for TM regeneration.

摘要

青光眼是全球导致不可逆性失明的主要原因。降低眼内压是目前唯一有效的治疗方法。眼内压升高与流出道阻力增加有关,主要是小梁网(TM)。尽管该领域取得了巨大进展,但开发新型有效的青光眼治疗方法仍然具有挑战性。在这项研究中,我们报告说,人诱导多能干细胞(iPSCs)可以培养成表达 OCT4、碱性磷酸酶、SSEA4 和 SSEA1 的集落和单层细胞。在诱导为对 NGFR 和 HNK1 呈阳性的神经嵴细胞(NCC)后,iPSCs 可以分化为 TM 细胞。诱导的 iPSC-TM 细胞表达 TM 细胞标志物 CHI3L1,对地塞米松治疗有反应,肌球蛋白、ANGPTL7 的表达增加,并形成与原代 TM 细胞相当的 CLANs。据我们所知,这是第一项通过中间神经嵴阶段诱导 iPSCs 成为 TM 细胞的研究,它确保了稳定的 NCC 池,并确保了相同 TM 细胞的高产量。该系统可用于使用患者来源的 iPSCs 开发个性化治疗方法,探索针对 TM 反应的高通量新药筛选以控制眼内压,并研究基于干细胞的 TM 再生治疗。

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Regenerating Eye Tissues to Preserve and Restore Vision.再生眼部组织以保存和恢复视力。
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