Diabetes Research Institute, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
Department of Cell Biology and Anatomy, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
Nat Commun. 2020 Jun 29;11(1):3265. doi: 10.1038/s41467-020-17040-8.
The culture of live pancreatic tissue slices is a powerful tool for the interrogation of physiology and pathology in an in vitro setting that retains near-intact cytoarchitecture. However, current culture conditions for human pancreatic slices (HPSs) have only been tested for short-term applications, which are not permissive for the long-term, longitudinal study of pancreatic endocrine regeneration. Using a culture system designed to mimic the physiological oxygenation of the pancreas, we demonstrate high viability and preserved endocrine and exocrine function in HPS for at least 10 days after sectioning. This extended lifespan allowed us to dynamically lineage trace and quantify the formation of insulin-producing cells in HPS from both non-diabetic and type 2 diabetic donors. This technology is expected to be of great impact for the conduct of real-time regeneration/developmental studies in the human pancreas.
胰腺组织活体切片培养是一种强大的工具,可在体外环境中研究生理学和病理学,同时保留近乎完整的细胞结构。然而,目前用于人类胰腺切片(HPS)的培养条件仅经过短期应用测试,并不允许对胰腺内分泌再生进行长期的纵向研究。我们使用一种旨在模拟胰腺生理氧合的培养系统,证明了 HPS 在切片后至少 10 天内具有高活力和保留的内分泌和外分泌功能。这种延长的寿命使我们能够动态地对非糖尿病和 2 型糖尿病供体的 HPS 中胰岛素产生细胞的形成进行谱系追踪和定量。这项技术有望对人类胰腺进行实时再生/发育研究产生重大影响。