Acidic deoxycholic acid and chenodeoxycholic acid induce interleukin‐8 production through p38 mitogen‐activated protein kinase and protein kinase A in a squamous epithelial model. Issue 5 (25th April 2013)
- Record Type:
- Journal Article
- Title:
- Acidic deoxycholic acid and chenodeoxycholic acid induce interleukin‐8 production through p38 mitogen‐activated protein kinase and protein kinase A in a squamous epithelial model. Issue 5 (25th April 2013)
- Main Title:
- Acidic deoxycholic acid and chenodeoxycholic acid induce interleukin‐8 production through p38 mitogen‐activated protein kinase and protein kinase A in a squamous epithelial model
- Authors:
- Shan, Jing
Oshima, Tadayuki
Fukui, Hirokazu
Watari, Jiro
Miwa, Hiroto - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12139-sec-0001" sec-type="section"> <title>Background and Aim</title> <p>Immune‐mediated mucosal inflammation characterized by the production of interleukin (IL)‐8 is associated with the development of gastroesophageal reflux disease. The effects of bile acids, which are major components of reflux fluid, on the production of IL‐8 and related mechanisms remain unclear. This study aimed to address these questions using an esophageal stratified squamous epithelial model.</p> </sec> <sec id="jgh12139-sec-0002" sec-type="section"> <title>Methods</title> <p>Normal human esophageal epithelial cells were seeded on the Transwell inserts and cultured with the air‐liquid interface system to establish the model. Bile acids under different pH conditions were added to the apical compartment to examine their effects on IL‐8 production and the underlying cellular signaling.</p> </sec> <sec id="jgh12139-sec-0003" sec-type="section"> <title>Results</title> <p>Conjugated bile acids under a neutral or acidic condition did not induce IL‐8 production, and unconjugated bile acids, deoxycholic acid (DCA), and chenodeoxycholic acid (CDCA) all significantly induced IL‐8 production, dose‐ and time‐dependently, only under weakly acid conditions. Inhibition of p38 mitogen‐activated protein kinase (p38 MAPK) and protein kinase A (PKA) attenuated the production of IL‐8 induced by acidic DCA and CDCA. Inhibition of PKA did not block the<abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12139-sec-0001" sec-type="section"> <title>Background and Aim</title> <p>Immune‐mediated mucosal inflammation characterized by the production of interleukin (IL)‐8 is associated with the development of gastroesophageal reflux disease. The effects of bile acids, which are major components of reflux fluid, on the production of IL‐8 and related mechanisms remain unclear. This study aimed to address these questions using an esophageal stratified squamous epithelial model.</p> </sec> <sec id="jgh12139-sec-0002" sec-type="section"> <title>Methods</title> <p>Normal human esophageal epithelial cells were seeded on the Transwell inserts and cultured with the air‐liquid interface system to establish the model. Bile acids under different pH conditions were added to the apical compartment to examine their effects on IL‐8 production and the underlying cellular signaling.</p> </sec> <sec id="jgh12139-sec-0003" sec-type="section"> <title>Results</title> <p>Conjugated bile acids under a neutral or acidic condition did not induce IL‐8 production, and unconjugated bile acids, deoxycholic acid (DCA), and chenodeoxycholic acid (CDCA) all significantly induced IL‐8 production, dose‐ and time‐dependently, only under weakly acid conditions. Inhibition of p38 mitogen‐activated protein kinase (p38 MAPK) and protein kinase A (PKA) attenuated the production of IL‐8 induced by acidic DCA and CDCA. Inhibition of PKA did not block the bile acid‐induced p38 MAPK activation.</p> </sec> <sec id="jgh12139-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Compared with conjugated bile acids, the unconjugated bile acids DCA and CDCA are more likely to induce IL‐8 production <italic>in vivo</italic>, especially under weakly acid conditions. This process involves two independent signaling pathways, p38 MAPK and PKA.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of gastroenterology and hepatology. Volume 28:Issue 5(2013:May)
- Journal:
- Journal of gastroenterology and hepatology
- Issue:
- Volume 28:Issue 5(2013:May)
- Issue Display:
- Volume 28, Issue 5 (2013)
- Year:
- 2013
- Volume:
- 28
- Issue:
- 5
- Issue Sort Value:
- 2013-0028-0005-0000
- Page Start:
- 823
- Page End:
- 828
- Publication Date:
- 2013-04-25
- Subjects:
- Gastroenterology -- Periodicals
Digestive organs -- Diseases -- Periodicals
Liver -- Diseases -- Periodicals
Gastroenterology -- Periodicals
Liver Diseases -- Periodicals
616.33 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1440-1746 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/jgh ↗ - DOI:
- 10.1111/jgh.12139 ↗
- Languages:
- English
- ISSNs:
- 0815-9319
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4987.615000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4386.xml