Volume 9, Issue 5 (September 2007) 9, 634–640; 10.1111/j.1745-7262.2007.00291.x
Distribution profiles of transient receptor potential melastatin-related and vanilloid-related channels in prostatic tissue in rat
Huai-Peng Wang, Xiao-Yong Pu and Xing-Huan Wang
Department of Urology, Guangdong Provnicial People's Hospital, Guangzhou 510080, China
Correspondence: Dr Xing-Huan Wang, Department of Urology, Guangdong Provincial People Hospital, Guangzhou 510080, China. Fax: +86-20-8382-7712. E-mail: urologist@126.com
Received 19 November 2006; Accepted 4 April 2007.
Abstract |
Aim: To investigate the expression and distribution of the members of the transient receptor potential (TRP) channel members of TRP melastatin (TRPM) and TRP vanilloid (TRPV) subfamilies in rat prostatic tissue.
Methods: Prostate tissue was obtained from male Sprague-Dawley rats. Reverse transcription polymerase chain reaction (RT-PCR) and quantitative real-time polymerase chain reaction (PCR) were used to check the expression of all TRPM and TRPV channel members with specific primers. Immunohistochemistry staining for TRPM8 and TRPV1 were also performed in rat tissues.
Results: TRPM2, TRPM3, TRPM4, TRPM6, TRPM7, TRPM8, TRPV2 and TRPV4 mRNA were detected in all rat prostatic tissues. Very weak signals for TRPM1, TRPV1 and TRPV3 were also detected. The mRNA of TRPM5, TRPV5 and TRPV6 were not detected in all RT-PCR experiments. Quantitative real-time RT-PCR showed that TRPM2, TRPM3, TRPM4, TRPM8, TRPV2 and TRPV4 were the most abundantly expressed TRPM and TRPV subtypes, respectively. Fluorescence immunohistochemistry indicated that TRPM8 and TRPV1 are highly expressed in both epithelial and smooth muscle cells.
Conclusion: Our results demonstrate that mRNA or protein for TRPM1, TRPM2, TRPM3, TRPM4, TRPM6, TRPM7, TRPM8, TRPV1, TRPV2, TRPV3 and TRPV4 exist in rat prostatic tissue. The data presented here assists in elucidating the physiological function of TRPM and TRPV channels.
Keywords: transient receptor potential channels, prostate, cation channels
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