Lazimi Charles S, Stis Austin E, Panzer Julia K, Hiller Helmut, Beery Maria L, Linnemann Amelia K, Stabler Cherie L, Mathews Clayton E, Phelps Edward A
J. Crayton Pruitt Family Department of Biomedical Engineering, Herbert Wertheim College of Engineering, University of Florida, Gainesville, FL, United States.
Department of Diabetes Immunology, Arthur Riggs Diabetes and Metabolism Research Institute, City of Hope, Duarte, CA.
bioRxiv. 2025 Mar 25:2025.03.21.644659. doi: 10.1101/2025.03.21.644659.
This study combines live pancreas tissue slices with adenoviral transduction of the Calcium Modulated Photoactivatable Ratiometric Integrator 2 (CaMPARI2) biosensor for high-throughput analysis of islet calcium responses. Pancreas slices preserve islets within their native microenvironment, adding tissue context to the study of islet function and pathology. A key challenge of the pancreas slice model has been efficient transgene delivery while maintaining viability and function. Here, we demonstrate a robust adenoviral gene delivery approach using targeted and universal promoters. By transducing slices with CaMPARI2 and applying 405 nm photoconverting light, we permanently marked glucose-induced calcium activity across entire islet populations while preserving the in situ tissue context. Applied to nPOD donor tissues, including from individuals with type 1 diabetes, type 2 diabetes, and non-diabetic controls, this approach demonstrated glucose responsive CaMPARI2 labeling that correlated with insulin secretion. Integrating CaMPARI2 with pancreas slices enables multiplexed analyses, linking a functional readout with spatial context through immunostaining or gene expression to advance understanding of human islet behavior.
本研究将活的胰腺组织切片与钙调制光激活比率积分器2(CaMPARI2)生物传感器的腺病毒转导相结合,用于胰岛钙反应的高通量分析。胰腺切片在其天然微环境中保留胰岛,为胰岛功能和病理学研究增添了组织背景。胰腺切片模型的一个关键挑战是在维持活力和功能的同时实现有效的转基因递送。在这里,我们展示了一种使用靶向和通用启动子的强大腺病毒基因递送方法。通过用CaMPARI2转导切片并施加405nm光转换光,我们在保留原位组织背景的同时,永久标记了整个胰岛群体中葡萄糖诱导的钙活性。应用于nPOD供体组织,包括1型糖尿病、2型糖尿病个体和非糖尿病对照,该方法证明了与胰岛素分泌相关的葡萄糖反应性CaMPARI2标记。将CaMPARI2与胰腺切片整合能够进行多重分析,通过免疫染色或基因表达将功能读数与空间背景联系起来,以促进对人类胰岛行为的理解。