Vitamin A inhibits pancreatic stellate cell activation: implications for treatment of pancreatic fibrosis.

Abstract

BACKGROUND AND AIMS:

Activated pancreatic stellate cells (PSCs) are implicated in the production of alcohol induced pancreatic fibrosis. PSC activation is invariably associated with loss of cytoplasmic vitamin A (retinol) stores. Furthermore, retinol and ethanol are known to be metabolised by similar pathways. Our group and others have demonstrated that ethanol induced PSC activation is mediated by the mitogen activated protein kinase (MAPK) pathway but the specific role of retinol and its metabolites all-trans retinoic acid (ATRA) and 9-cis retinoic acid (9-RA) in PSC quiescence/activation, or its influence on ethanol induced PSC activation is not known. Therefore, the aims of this study were to (i) examine the effects of retinol, ATRA, and 9-RA on PSC activation; (ii) determine whether retinol, ATRA, and 9-RA influence MAPK signalling in PSCs; and (iii) assess the effect of retinol supplementation on PSCs activated by ethanol.

METHODS:

Cultured rat PSCs were incubated with retinol, ATRA, or 9-RA for varying time periods and assessed for: (i) proliferation; (ii) expression of alpha smooth muscle actin (alpha-SMA), collagen I, fibronectin, and laminin; and (iii) activation of MAPKs (extracellular regulated kinases 1 and 2, p38 kinase, and c-Jun N terminal kinase). The effect of retinol on PSCs treated with ethanol was also examined by incubating cells with ethanol in the presence or absence of retinol for five days, followed by assessment of alpha-SMA, collagen I, fibronectin, and laminin expression.

RESULTS:

Retinol, ATRA, and 9-RA significantly inhibited: (i) cell proliferation, (ii) expression of alpha-SMA, collagen I, fibronectin, and laminin, and (iii) activation of all three classes of MAPKs. Furthermore, retinol prevented ethanol induced PSC activation, as indicated by inhibition of the ethanol induced increase in alpha-SMA, collagen I, fibronectin, and laminin expression.

CONCLUSIONS:

Retinol and its metabolites ATRA and 9-RA induce quiescence in culture activated PSCs associated with a significant decrease in the activation of all three classes of MAPKs in PSCs. Ethanol induced PSC activation is prevented by retinol supplementation.

• Authors: J A McCarroll, P A Phillips, N Santucci, R C Pirola, J S Wilson, M V Apte
• Journal: Gut (Gut) Vol. 55 Issue 1 Pg. 79-89 (Jan 2006) ISSN: 0017-5749 [Print] England
• PMID: 16043492 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• Cell Cycle Proteins
• Enzyme Inhibitors
• Extracellular Matrix Proteins
• Immediate-Early Proteins
• Receptors, Retinoic Acid
• Retinoid X Receptors
• Vitamin A
• Alitretinoin
• Ethanol
• Vanadates
• Tretinoin
• Mitogen-Activated Protein Kinases
• Phosphoprotein Phosphatases
• Protein Phosphatase 1
• Dual Specificity Phosphatase 1
• Dusp1 protein, rat
• Protein Tyrosine Phosphatases

Topics

• Alitretinoin
• Animals
• Cell Cycle Proteins (metabolism)
• Cell Proliferation (drug effects)
• Cells, Cultured
• Dual Specificity Phosphatase 1
• Enzyme Activation (drug effects)
• Enzyme Inhibitors (pharmacology)
• Ethanol (antagonists & inhibitors, pharmacology)
• Extracellular Matrix Proteins (metabolism)
• Fibrosis
• Immediate-Early Proteins (metabolism)
• Mitogen-Activated Protein Kinases (metabolism)
• Pancreas (cytology, drug effects, metabolism, pathology)
• Phosphoprotein Phosphatases (metabolism)
• Protein Phosphatase 1
• Protein Tyrosine Phosphatases (metabolism)
• Rats
• Receptors, Retinoic Acid (metabolism)
• Retinoid X Receptors (metabolism)
• Reverse Transcriptase Polymerase Chain Reaction (methods)
• Tretinoin (pharmacology)
• Vanadates (pharmacology)
• Vitamin A (pharmacology)