Characteristic pancreatic and splenic immune cell infiltration patterns in mouse acute pancreatitis

• Published in: Cell & bioscience Vol. 11; no. 1; pp. 28 - 13
• Main Authors: Yang, Baibing, Davis, Joy M, Gomez, Thomas H, Younes, Mamoun, Zhao, Xiurong, Shen, Qiang, Wang, Run, Ko, Tien C, Cao, Yanna
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 02.02.2021; BioMed Central; BMC
• Subjects: Alcohol; Amylases; Analysis; Animal models; B cells; Beta cells; Dendritic cells; Diabetes; Embedding; Ethanol; Flow cytometry; Gating; Immune profiling; Immune response; Infiltration; Injection; Lymphocytes; Mice; Monounsaturated fatty acids; Mouse acute pancreatitis; Neutrophils; Palmitoleic acid; Pancreas; Pancreatic cancer; Pancreatitis; Pathogenesis; PhenoGraph; Spleen; Splenocytes; Stochasticity; t-distributed stochastic neighbor embedding (t-SNE); Visualization; Alcohol; t-distributed stochastic neighbor embedding (t-SNE); Immune profiling; PhenoGraph; Mouse acute pancreatitis
• ISSN: 2045-3701; 2045-3701
• DOI: 10.1186/s13578-021-00544-1

A systemic evaluation of immune cell infiltration patterns in experimental acute pancreatitis (AP) is lacking. Using multi-dimensional flow cytometry, this study profiled infiltrating immune cell types in multiple AP mouse models. Three AP models were generated in C57BL/6 mice via cerulein (CAE) injection, alcohol and palmitoleic acid (EtOH + POA) injection, and alcohol diet feeding and cerulein (EtOH + CAE) injection. Primary pancreatic cells and splenocytes were prepared, and multi-dimensional flow cytometry was performed and analyzed by manual gating and computerized PhenoGraph, followed by visualization with t-distributed stochastic neighbor embedding (t-SNE). CAE treatment induced a time-dependent increase of major innate immune cells and a decrease of follicular B cells, and T cells and the subtypes in the pancreas, whereas elicited a reversed pattern in the spleen. EtOH + POA treatment resulted in weaker effects than CAE treatment. EtOH feeding enhanced CAE-induced amylase secretion, but unexpectedly attenuated CAE-induced immune cell regulation. In comparison with manual gating analysis, computerized analysis demonstrated a remarkable time efficiency and reproducibility on the innate immune cells and B cells. The reverse pattern of increased innate and decreased adaptive immune cells was consistent in the pancreas in CAE and EtOH + POA treatments. Alcohol feeding opposed the CAE effect on immune cell regulation. Together, the immune profiling approach utilized in this study provides a better understanding of overall immune responses in AP, which may facilitate the identification of intervention windows and new therapeutic strategies. Computerized analysis is superior to manual gating by dramatically reducing analysis time.