Transcriptional Control of Acinar Development and Homeostasis
Overview
Affiliations
Pancreatic acinar cells are highly specialized exocrine factories that produce copious amounts of digestive enzymes for intestinal digestion. Acinar cells arise from a population of multipotent progenitor cells (MPCs) that also produce ductal cells, which channel the acinar secretions to the intestine, and endocrine cells, which populate the islets of Langerhans. During a final stage of differentiation, acinar cells acquire powerful systems for maintaining cellular homeostasis in the face of great demands for protein synthesis and energy production. We summarize the pancreatic transcription factors that guide pancreatic development through the formation of the MPC population, the resolution of acinar, ductal, and islet lineages, the initiation of the acinar developmental program, and the completion of acinar cell differentiation. We discuss the evidence for the specific roles of these factors at each developmental transition and review the plasticity of mature acinar cells.
Specific Temporal Requirement of Prox1 Activity During Pancreatic Acinar Cell Development.
Martinez-Ramirez A, Borders T, Paul L, Schipma M, Wang X, Korobova F Gastro Hep Adv. 2023; 1(5):807-823.
PMID: 37829188 PMC: 10569262. DOI: 10.1016/j.gastha.2022.05.013.
Xu H, Li Y, Jiang Y, Wang J, Sun H, Wu W Front Genet. 2022; 13:827840.
PMID: 35774514 PMC: 9237400. DOI: 10.3389/fgene.2022.827840.
Li X, He J, Xie K Cell Oncol (Dordr). 2022; 45(2):201-225.
PMID: 35290607 DOI: 10.1007/s13402-022-00664-x.
Genome-wide association study of pancreatic fat: The Multiethnic Cohort Adiposity Phenotype Study.
Streicher S, Lim U, Park S, Li Y, Sheng X, Hom V PLoS One. 2021; 16(7):e0249615.
PMID: 34329319 PMC: 8323875. DOI: 10.1371/journal.pone.0249615.
MECOM permits pancreatic acinar cell dedifferentiation avoiding cell death under stress conditions.
Backx E, Wauters E, Baldan J, Van Bulck M, Michiels E, Heremans Y Cell Death Differ. 2021; 28(9):2601-2615.
PMID: 33762742 PMC: 8408219. DOI: 10.1038/s41418-021-00771-6.