학술논문

Distinct populations of inflammatory fibroblasts and myofibroblasts in pancreatic cancer
Document Type
article
Source
Journal of Experimental Medicine. 214(3)
Subject
Rare Diseases
Pancreatic Cancer
Cancer
Digestive Diseases
Aetiology
2.1 Biological and endogenous factors
Actins
Animals
Carcinoma
Pancreatic Ductal
Cells
Cultured
Cytokines
Fibroblasts
Humans
Mice
Mice
Inbred C57BL
Myofibroblasts
Pancreatic Neoplasms
STAT3 Transcription Factor
Medical and Health Sciences
Immunology
Language
Abstract
Pancreatic stellate cells (PSCs) differentiate into cancer-associated fibroblasts (CAFs) that produce desmoplastic stroma, thereby modulating disease progression and therapeutic response in pancreatic ductal adenocarcinoma (PDA). However, it is unknown whether CAFs uniformly carry out these tasks or if subtypes of CAFs with distinct phenotypes in PDA exist. We identified a CAF subpopulation with elevated expression of α-smooth muscle actin (αSMA) located immediately adjacent to neoplastic cells in mouse and human PDA tissue. We recapitulated this finding in co-cultures of murine PSCs and PDA organoids, and demonstrated that organoid-activated CAFs produced desmoplastic stroma. The co-cultures showed cooperative interactions and revealed another distinct subpopulation of CAFs, located more distantly from neoplastic cells, which lacked elevated αSMA expression and instead secreted IL6 and additional inflammatory mediators. These findings were corroborated in mouse and human PDA tissue, providing direct evidence for CAF heterogeneity in PDA tumor biology with implications for disease etiology and therapeutic development.