Basic Research
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Mar 15, 2003; 9(3): 590-594
Published online Mar 15, 2003. doi: 10.3748/wjg.v9.i3.590
In situ detection of TGF betas, TGF beta receptor II mRNA and telomerase activity in rat cholangiocarcinogenesis
Jian-Ping Lu, Jian-Qun Mao, Ming-Sheng Li, Shi-Lun Lu, Xi-Qi Hu, Shi-Neng Zhu, Shintaro Nomura
Jian-Ping Lu, Department of Pathology, Medical Center of Fudan University (Former Shanghai Medical University), Shanghai 200032, China. Max-Planck-Institute for Cell Biology, Ladenburg 68526, Germany
Jian-Qun Mao, Ming-Sheng Li, Shi-Lun Lu, Xi-Qi Hu, Shi-Neng Zhu, Department of Pathology, Medical Center of Fudan University, (Former Shanghai Medical University), Shanghai 200032, China
Shintaro Nomura, Department of Pathology, Osaka University, School of Medicine, Fukita 565, Japan
Author contributions: All authors contributed equally to the work.
Supported by China National Natural Science Foundation, No. 30070846/C03031904
Correspondence to: Jian-Ping Lu, Ph.D. Max-Planck-Institute for Cell Biology, Ladenburg 68526, Germany. lu_jp@hotmail.com
Telephone: +49-6203-106-208 Fax: +49-6203-106-122
Received: October 9, 2002
Revised: October 28, 2002
Accepted: November 4, 2002
Published online: March 15, 2003
Abstract

AIM: Initial report on the in situ examination of the mRNA expression of transforming growth factor betas (TGFβs), TGFβ type II receptor (TβRII) and telomerase activity in the experimental rat liver tissue during cholangiocarcinogenesis.

METHODS: Rat liver cholangiocarcinogenesis was induced by 3’-methyl 4-dimethylazobenzene (3’Me-DAB). In situ hybridization was used to examine the TGFβs) and TGFβ type II receptor (TβRII) mRNA, in situ TRAP was used to check the telomerase activity in the tissue samples.

RESULTS: There was no TGFβs, TβRII mRNA expression or telomerase activity in the control rat cholangiocytes. The expression of TGFβ1, TβRII was increased in regenerative, hyperplastic, dysplastic cholangiocytes and cholangiocarcinoma (CC) cells. The expression of TGFβ2 mRNA was observed in only a part of hyperplastic, dysplastic cholangiocytes. TGFβ3 expression was very weak, only in hyperplastic lesion. There was positive telomerase activity in the regenerative, hyperplastic, dysplastic cholangiocytes, and CC cells. Stroma fibroblasts of these lesions also showed positive TGFβs, TβRII mRNA expression and telomerase activity.

CONCLUSION: There were TGFβs, TβRII expression and telomerase activity in hyperplastic, dysplastic cholangiocytes, cholangiocarcinoma cells as well as in stroma fibroblasts during cholangiocarcinogenesis. Their expression or activity is important in cholangiocarcinogenesis andstroma formation.

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