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用于基因和功能分析的活的人δ细胞的分离。

Isolation of live human δ cells for genetic and functional analysis.

作者信息

Hang Yan, Miranda Mario Alex, Yan Ziqiao, Zhao Weichen, Kim Seung K

机构信息

Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA, 94305, USA; Stanford Diabetes Research Center, Stanford University School of Medicine, Stanford, CA, 94305, USA.

Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA, 94305, USA.

出版信息

Mol Metab. 2025 Aug;98:102188. doi: 10.1016/j.molmet.2025.102188. Epub 2025 Jun 11.

Abstract

Investigations of human pancreatic islets have been empowered by strategies to isolate and study live islet cell subsets, like β cells and α cells. To advance experimentation with human islet δ cells, which remain relatively understudied, we generated combinatorial cell sorting approaches to separate human δ cells from β cells, yielding highly-enriched human δ cells. We used molecular analysis, immunohistology, and electroporation-based targeting to demonstrate the quality of δ cell purification. We also demonstrated the feasibility of prospectively studying human δ cell function in pseudoislet organoids. Innovations detailed here should promote discovery of genetic, signaling and physiological mechanisms governing δ cell function and roles in human islets.

摘要

对人类胰岛的研究因分离和研究活的胰岛细胞亚群(如β细胞和α细胞)的策略而得到加强。为了推进对研究相对较少的人类胰岛δ细胞的实验,我们开发了组合细胞分选方法,以将人类δ细胞与β细胞分离,从而获得高度富集的人类δ细胞。我们使用分子分析、免疫组织学和基于电穿孔的靶向技术来证明δ细胞纯化的质量。我们还证明了在前体胰岛类器官中前瞻性研究人类δ细胞功能的可行性。这里详细介绍的创新应能促进对控制人类胰岛中δ细胞功能和作用的遗传、信号传导和生理机制的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3989/12256296/f0a1e8f6855b/gr1.jpg

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