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人多能干细胞来源的长期 3D 视网膜中的光感受器外节样结构。

Photoreceptor Outer Segment-like Structures in Long-Term 3D Retinas from Human Pluripotent Stem Cells.

机构信息

Wilmer Eye Institute, The Johns Hopkins Wilmer Eye Institute 600 N. Wolfe Street, Baltimore, MD, 21287, USA.

Shiley Eye Institute, University of California San Diego, La Jolla, California, USA.

出版信息

Sci Rep. 2017 Apr 10;7(1):766. doi: 10.1038/s41598-017-00774-9.

Abstract

The retinal degenerative diseases, which together constitute a leading cause of hereditary blindness worldwide, are largely untreatable. Development of reliable methods to culture complex retinal tissues from human pluripotent stem cells (hPSCs) could offer a means to study human retinal development, provide a platform to investigate the mechanisms of retinal degeneration and screen for neuroprotective compounds, and provide the basis for cell-based therapeutic strategies. In this study, we describe an in vitro method by which hPSCs can be differentiated into 3D retinas with at least some important features reminiscent of a mature retina, including exuberant outgrowth of outer segment-like structures and synaptic ribbons, photoreceptor neurotransmitter expression, and membrane conductances and synaptic vesicle release properties consistent with possible photoreceptor synaptic function. The advanced outer segment-like structures reported here support the notion that 3D retina cups could serve as a model for studying mature photoreceptor development and allow for more robust modeling of retinal degenerative disease in vitro.

摘要

视网膜退行性疾病是全球范围内导致遗传性失明的主要原因之一,目前尚无有效治疗方法。开发可靠的方法,从人类多能干细胞(hPSC)中培养复杂的视网膜组织,可能为研究人类视网膜发育提供一种手段,为研究视网膜退行性疾病的机制和筛选神经保护化合物提供平台,并为基于细胞的治疗策略提供基础。在这项研究中,我们描述了一种体外方法,通过该方法,hPSC 可以分化为具有至少一些类似于成熟视网膜特征的 3D 视网膜,包括外节样结构和突触带的大量生长、光感受器神经递质表达以及与光感受器突触功能一致的膜电导和突触小泡释放特性。这里报道的先进的外节样结构支持这样一种观点,即 3D 视网膜杯可以作为研究成熟光感受器发育的模型,并允许更有效地在体外模拟视网膜退行性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa3b/5429674/64b0d207a449/41598_2017_774_Fig1_HTML.jpg

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