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The Role of Twist1 in Chronic Pancreatitis-Associated Pancreatic Stellate Cells.
Geister, Emma; Ard, Dalton; Patel, Heer; Findley, Alyssa; DeSouza, Godfrey; Martin, Lyndsay; Knox, Henry; Gavara, Natasha; Lugea, Aurelia; Sabbatini, Maria Eugenia.
Afiliação
  • Geister E; Department of Biological Sciences, Augusta University, Augusta, Georgia.
  • Ard D; Department of Biological Sciences, Augusta University, Augusta, Georgia.
  • Patel H; Department of Biological Sciences, Augusta University, Augusta, Georgia.
  • Findley A; Department of Biological Sciences, Augusta University, Augusta, Georgia.
  • DeSouza G; Department of Biological Sciences, Augusta University, Augusta, Georgia.
  • Martin L; Department of Biological Sciences, Augusta University, Augusta, Georgia.
  • Knox H; Department of Biological Sciences, Augusta University, Augusta, Georgia.
  • Gavara N; Department of Biological Sciences, Augusta University, Augusta, Georgia.
  • Lugea A; Cedars-Sinai Medical Center, Los Angeles, California.
  • Sabbatini ME; Department of Biological Sciences, Augusta University, Augusta, Georgia. Electronic address: msabbatini@augusta.edu.
Am J Pathol ; 2024 Jul 18.
Article em En | MEDLINE | ID: mdl-39032603
ABSTRACT
In a healthy pancreas, pancreatic stellate cells (PaSCs) synthesize the basement membrane, which is mainly composed of type IV collagen and laminin. In chronic pancreatitis (CP), PaSCs are responsible for the production of a rigid extracellular matrix (ECM) that is mainly composed of fibronectin and type I/III collagen. Reactive oxygen species evoke the formation of the rigid ECM by PaSCs. One source of reactive oxygen species is NADPH oxidase (Nox) enzymes. Nox1 up-regulates the expression of Twist1 and matrix metalloproteinase-9 (MMP-9) in PaSCs from mice with CP. This study determined the functional relationship between Twist1 and MMP-9, and other PaSC-produced proteins, and the extent to which Twist1 regulates digestion of ECM proteins in CP. Twist1 induced the expression of MMP-9 in mouse PaSCs. The action of Twist1 was not selective to MMP-9 because Twist1 induced the expression of types I and IV collagen, fibronectin, transforming growth factor, and α-smooth muscle actin. Using luciferase assay, Twist1 in human primary PaSCs increased the expression of MMP-9 at the transcriptional level in an NF-κB dependent manner. The digestion of type I/III collagen by MMP-9 secreted by PaSCs from mice with CP depended on Twist1. Thus, Twist1 in PaSCs from mice with CP induces rigid ECM production and MMP-9 transcription in an NF-κB-dependent mechanism that selectively displays proteolytic activity toward type I/III collagen.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article