The Role of Twist1 in Chronic Pancreatitis-Associated Pancreatic Stellate Cells.
MMP-9
NADPH oxidase 1
Twist1
collagen I/III
pancreatic stellate cells
Journal
The American journal of pathology
ISSN: 1525-2191
Titre abrégé: Am J Pathol
Pays: United States
ID NLM: 0370502
Informations de publication
Date de publication:
18 Jul 2024
18 Jul 2024
Historique:
received:
23
12
2023
revised:
18
06
2024
accepted:
28
06
2024
medline:
21
7
2024
pubmed:
21
7
2024
entrez:
20
7
2024
Statut:
aheadofprint
Résumé
In a healthy pancreas, pancreatic stellate cells (PaSCs) synthesize the basement membrane, which is mainly composed of collagen IV and laminin. In chronic pancreatitis (CP), PaSCs are responsible for the production of a rigid extracellular matrix (ECM), which is mainly composed of fibronectin and collagen I/III. Reactive oxygen species (ROS) evoke the formation of the rigid ECM by PaSCs. One of the sources of ROS is NADPH oxidase (Nox) enzymes. Nox1 up-regulates the expression of Twist1 and matrix metalloproteinase (MMP) 9 in PaSCs from mice with CP. Here 1) the functional relationship between Twist1 and MMP-9, and other PaSC-produced proteins, and 2) the extent to which Twist1 regulates the digestion of ECM proteins in CP were determined. Twist1 induced the expression of MMP-9 in mPaSCs. The action of Twist1 was not selective to MMP-9 because Twist1 induced the expression of collagen I, collagen IV, fibronectin, TGF-β, and αSMA. Using luciferase assay, Twist1 in hPaSCs increased the expression of MMP-9 at the transcriptional level in a NF-ĸB dependent manner. The digestion of collagen I/III by MMP-9 secreted by PaSCs from mice with CP was dependent on Twist1. Thus, Twist1 in PaSCs from mice with CP induces the production of a rigid ECM and the transcription of MMP-9 in a NF-ĸB dependent mechanism that selectively displays a proteolytic activity toward collagen I/III.
Identifiants
pubmed: 39032603
pii: S0002-9440(24)00234-7
doi: 10.1016/j.ajpath.2024.06.003
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024. Published by Elsevier Inc.