Basic Research
Copyright ©2005 Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Nov 7, 2005; 11(41): 6466-6471
Published online Nov 7, 2005. doi: 10.3748/wjg.v11.i41.6466
Bile salts inhibit growth and induce apoptosis of culture human normal esophageal mucosal epithelial cells
Ru Zhang, Jun Gong, Hui Wang, Li Wang
Ru Zhang, Jun Gong, Li Wang, the Second Hospital of Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China
Hui Wang, Department of Anesthesia, Shaanxi Provincial People’s Hospital, Xi’an 710068, Shaanxi Province, China
Author contributions: All authors contributed equally to the work.
Supported by the Clinical Key Programs of Ministry of Public Health, China, No. 20012130
Correspondence to: Dr. Jun Gong, Digestive Department of the Second Hospital, Xi’an Jiaotong University, Xi’an 710004, Shaanxi Province, China. zhzhru@sohu.com
Telephone: +86-29-88083495 Fax: +86-29-87678758
Received: January 7, 2005
Revised: April 8, 2005
Accepted: April 11, 2005
Published online: November 7, 2005
Abstract

AIM: To investigate the effect of six bile salts: glycocholate (GC), glycochenodeoxycholate (GCDC), glycodeoxycholate (GDC), taurocholate (TC), taurochenodeoxycholate (TCDC), taurodeoxycholate (TDC), and their mixture on cultured human normal esophageal mucosal epithelial cells.

METHODS: Human normal esophageal mucosal epithelial cells were cultured with serum-free keratinocyte medium. 3-[4,5-Dimethylthiaolyl]-2,5-diphenyl-tetrazolium bromide assay was applied to the detection of cell proliferation. Apoptotic morphology was observed by phase-contrast video microscopy and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay. Sub-G1 DNA fragmentations and early apoptotic cells were assayed by flow cytometry (FCM) with propidium iodide (PI) staining and annexin V-FITC conjugated with PI staining. Apoptotic DNA ladders on agarose gel electrophoresis were observed.

RESULTS: Except for GC, GCDC, GDC, TC, TCDC, TDC and their mixture could initiate growth inhibition of esophageal mucosal epithelial cells in a dose- and time-dependent manner. TUNEL and FCM assays demonstrated that the bile salts at 500 μmol/L and their mixture at 1 500 μmol/L induced apoptosis except for GC. The percentage of sub-G1 detected by FCM with PI staining was 83.5% in cells treated with 500 μmol/L TC for 2 h, and 19.8%, 20.4%, 25.6%, 13.5%, and 75.8% in cells treated with 500 μmol/L GCDC, TCDC, GDC, TDC, and 1 500 μmol/L mixture for 24 h, respectively, which were higher than that of the control (1.5%). The percentage was 1.4% in cells with 500 μmol/L GC for 24 h. DNA ladders on agarose gel electrophoresis were seen in cells treated with 500 μmol/L TC for 2 h and 1 500 μmol/L mixture for 24 h.

CONCLUSION: All GCDC, GDC, TC, TCDC, TDC and their mixture can inhibit growth and induce apoptosis of cultured human normal esophageal mucosal epithelial cells, but GC is well tolerated by the cells.

Keywords: Bile salts; Duodenogastroesophageal reflux; Esophageal mucosal epithelial cells; Apoptosis