Volume 15, Issue 5 pp. 362-367

Expression of vanilloid receptor 1 in cultured fibroblast

Seong-Jin Kim

Corresponding Author

Seong-Jin Kim

Department of Dermatology, Chonnam National University, Gwangju, South Korea;

Seong-Jin Kim MD
Department of Dermatology
Chonnam National University Medical School
8 Hak-Dong
Dong-Gu
Gwangju 501-757
South Korea
Tel.: +82 62 220 6683
Fax: +82 62 222 4058
e-mail: [email protected]Search for more papers by this author
Su-A Lee

Su-A Lee

Department of Biology, Chonnam National University, Gwangju, South Korea;

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Sook Jung Yun

Sook Jung Yun

Department of Dermatology, Chonnam National University, Gwangju, South Korea;

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Jong-Keun Kim

Jong-Keun Kim

Department of Pharmacology, Chonnam National University, Gwangju, South Korea;

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Jong-Seong Park

Jong-Seong Park

Department of Physiology, Chonnam National University, Gwangju, South Korea;

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Han-Seong Jeong

Han-Seong Jeong

Department of Physiology, Chonnam National University, Gwangju, South Korea;

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Jeung-Hoon Lee

Jeung-Hoon Lee

Department of Dermatology, Chungnam National University, Daejeon;

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Seong-Joon Moon

Seong-Joon Moon

Skin Research Institute, Amore Pacific R&D Center, Yongin-si, South Korea

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Young-Ho Won

Young-Ho Won

Department of Dermatology, Chonnam National University, Gwangju, South Korea;

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First published: 30 March 2006
Citations: 27

Abstract

Abstract: Although the vanilloid receptor 1 (VR1) was originally discovered on primary sensory neurons, its broad tissue expression in non-neuronal cells has been reported on. Recently, VR1 expression was clearly demonstrated in a variety of cutaneous components, such as keratinocytes, glandular epithelium, mast cells and sebocytes, except for melanocytes and fibroblasts. However, we demonstrated the VR1 expression in the cultured human skin fibroblasts as follows. Previously cloned human VR1 primers that corresponded to the expected size of 680 bp by reverse transcriptase polymerase chain reaction were identified on the fibroblasts, the same as was noted for the positive control, the HaCaT cells. A positive immunoreactivity of the VR1 was observed both on fibroblasts and on HaCaT cells by Western blotting analysis. Fibroblasts treated with capsaicin, an agonist to the VR1, induced significant changes of the membrane current and the intracellular calcium level, and these changes were antagonized by capsazepin. Capsaicin treatment also showed a positive immunocytochemistry result. Our results suggest the existence of VR1 on fibroblasts; this receptor is likely to be influenced by ligand-dependent activation.

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