Hang Yan, Miranda Mario Alex, Yan Ziqiao, Zhao Weichen, Kim Seung K
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.
Mol Metab. 2025 Aug;98:102188. doi: 10.1016/j.molmet.2025.102188. Epub 2025 Jun 11.
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.
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。