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端锚聚合酶抑制促进人多能干细胞来源的胰腺祖细胞的内分泌分化。

Tankyrase inhibition promotes endocrine commitment of hPSC-derived pancreatic progenitors.

机构信息

McEwen Stem Cell Institute, University Health Network, Toronto, ON, M5G 1L7, Canada.

Department of Physiology, University of Toronto, Toronto, ON, M5S 1A8, Canada.

出版信息

Nat Commun. 2024 Oct 9;15(1):8754. doi: 10.1038/s41467-024-53068-w.

Abstract

Human pluripotent stem cells (hPSCs) have the potential to differentiate into various cell types, including pancreatic insulin-producing β cells, which are crucial for developing therapies for diabetes. However, current methods for directing hPSC differentiation towards pancreatic β-like cells are often inefficient and produce cells that do not fully resemble the native counterparts. Here, we report that highly selective tankyrase inhibitors, such as WIKI4, significantly enhances pancreatic differentiation from hPSCs. Our results show that WIKI4 promotes the formation of pancreatic progenitors that give rise to islet-like cells with improved β-like cell frequencies and glucose responsiveness compared to our standard cultures. These findings not only advance our understanding of pancreatic development, but also provide a promising new tool for generating pancreatic cells for research and potential therapeutic applications.

摘要

人多能干细胞(hPSCs)具有分化为多种细胞类型的潜力,包括产生胰岛素的胰腺β细胞,这对于开发糖尿病治疗方法至关重要。然而,目前将 hPSC 分化为胰腺β样细胞的方法通常效率不高,并且产生的细胞不能完全类似于天然的对应物。在这里,我们报告说,高度选择性的 Tankyrase 抑制剂,如 WIKI4,可显著增强 hPSC 的胰腺分化。我们的结果表明,WIKI4 促进了胰腺祖细胞的形成,这些祖细胞产生的胰岛样细胞具有更高的β样细胞频率和对葡萄糖的反应性,与我们的标准培养相比。这些发现不仅推进了我们对胰腺发育的理解,而且为生成用于研究和潜在治疗应用的胰腺细胞提供了一种有前途的新工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bb3/11464881/bed64923c350/41467_2024_53068_Fig1_HTML.jpg

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