Abstract A066: A novel approach for exocrine pancreas transcriptomics reveals the cellular landscape of the pancreas

胰腺 腺泡细胞 转录组 胰腺炎 生物 胰腺癌 外分泌胰腺 免疫系统 电池类型 细胞 癌症研究 病理 癌症 内科学 基因 基因表达 医学 内分泌学 免疫学 生物化学 遗传学
作者
Katherine J. Aney,Woo‐Jeong Jeong,Andrés F. Vallejo,Ethan Chen,Austin Wang,Stephanie K. Dougan,Kellie Wise,Kirk B. Jensen,Luciano G. Martelotto,Sahar Nissim
出处
期刊:Cancer Research [American Association for Cancer Research]
卷期号:84 (2_Supplement): A066-A066
标识
DOI:10.1158/1538-7445.panca2023-a066
摘要

Abstract Pancreatic acinar cells are responsible for producing large amounts of digestive enzymes, which are essential for nutrient breakdown but make it difficult to capture the transcriptome of individual cells. To address this challenge, we use a reversible fixative that is compatible with 10X Genomics, thereby preserving the acinar transcriptome and capturing cell composition more faithful to histology. Using this method, we transcriptionally characterize all cell types in the healthy mouse pancreas, and track how these populations change during acute pancreatitis and subsequent recovery. We identify immune cells in the healthy and inflamed pancreas at a level of detail previously unappreciated, characterizing T cell subsets including Th2, γδT, and regulatory T cells. Pancreatitis elicits an influx of neutrophils along with activation and proliferation of macrophages and dendritic cells. Observing significant transcriptional changes in acinar cells after pancreatitis, we define an Acinar to Ductal Metaplasia Index (ADMI), a gene signature that can be used to measure deviation from normal acinar identity in bulk or single cell RNA datasets. We corroborate ADMI using orthogonal GeoMx data, and validate its utility in independent published datasets. We are now expanding our study to perform transcriptomics using our fixation method on pancreatic cancer precursor lesions. Together, we aim to characterize cell types in the mouse pancreas under healthy, inflamed, and precursor conditions to establish a reference atlas for future research on the exocrine pancreas in healthy and diseased states. Citation Format: Katherine J. Aney, Woo-Jeong Jeong, Andres F. Vallejo, Ethan Chen, Austin Wang, Stephanie K. Dougan, Kellie Wise, Kirk Jensen, Luciano Martelotto, Sahar Nissim. A novel approach for exocrine pancreas transcriptomics reveals the cellular landscape of the pancreas [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Pancreatic Cancer; 2023 Sep 27-30; Boston, Massachusetts. Philadelphia (PA): AACR; Cancer Res 2024;84(2 Suppl):Abstract nr A066.

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