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PDX1+ 细胞在干细胞衍生胰岛球体系统中的芽生形态发生。

PDX1+ cell budding morphogenesis in a stem cell-derived islet spheroid system.

机构信息

Life Sciences Institute, Departments of Cellular & Physiological Sciences and Surgery, University of British Columbia, Vancouver, BC, Canada.

Institute of Molecular Medicine, School of Future Technology, National Biomedical Imaging Center, Peking University, Beijing, China.

出版信息

Nat Commun. 2024 Jul 13;15(1):5894. doi: 10.1038/s41467-024-50109-2.

Abstract

Remarkable advances in protocol development have been achieved to manufacture insulin-secreting islets from human pluripotent stem cells (hPSCs). Distinct from current approaches, we devised a tunable strategy to generate islet spheroids enriched for major islet cell types by incorporating PDX1+ cell budding morphogenesis into staged differentiation. In this process that appears to mimic normal islet morphogenesis, the differentiating islet spheroids organize with endocrine cells that are intermingled or arranged in a core-mantle architecture, accompanied with functional heterogeneity. Through in vitro modelling of human pancreas development, we illustrate the importance of PDX1 and the requirement for EphB3/4 signaling in eliciting cell budding morphogenesis. Using this new approach, we model Mitchell-Riley syndrome with RFX6 knockout hPSCs illustrating unexpected morphogenesis defects in the differentiation towards islet cells. The tunable differentiation system and stem cell-derived islet models described in this work may facilitate addressing fundamental questions in islet biology and probing human pancreas diseases.

摘要

在从人类多能干细胞(hPSC)制造分泌胰岛素的胰岛方面已经取得了显著的进展。与当前的方法不同,我们设计了一种可调策略,通过将 PDX1+细胞芽生形态发生纳入阶段性分化,来生成富含主要胰岛细胞类型的胰岛球体。在这个过程中,似乎模拟了正常的胰岛形态发生,分化的胰岛球体与内分泌细胞组织在一起,或排列在核心-外壳结构中,伴随着功能异质性。通过对人类胰腺发育的体外建模,我们说明了 PDX1 的重要性以及 EphB3/4 信号在引发细胞芽生形态发生中的必要性。使用这种新方法,我们对 RFX6 敲除 hPSC 的 Mitchell-Riley 综合征进行建模,说明了在向胰岛细胞分化过程中出乎意料的形态发生缺陷。本文所述的可调分化系统和干细胞衍生的胰岛模型可能有助于解决胰岛生物学中的基本问题,并探究人类胰腺疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a89b/11246529/004da9431d12/41467_2024_50109_Fig1_HTML.jpg

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