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Expression of vanilloid receptor subtype 1 in cutaneous sensory nerve fibers, mast cells, and epithelial cells of appendage structures

辣椒素 P物质 神经源性炎症 TRPV1型 结节性痒疹 感觉神经 内分泌学 受体 化学 降钙素基因相关肽 汗腺 伤害 内科学 人体皮肤 神经肽 皮神经 生物 医学 解剖 感觉系统 免疫学 汗水 瞬时受体电位通道 遗传学 神经科学
作者
Sonja Ständer,Corinna Moormann,Mark Schumacher,Joerg Buddenkotte,Metin Artuc,Victoria Shpacovitch,Thomas Brzoska,Undine Lippert,Beate M. Henz,Thomas A. Luger,Dieter Metze,Martin Steinhoff
出处
期刊:Experimental Dermatology [Wiley]
卷期号:13 (3): 129-139 被引量:401
标识
DOI:10.1111/j.0906-6705.2004.0178.x
摘要

The vanilloid receptor subtype 1 (VR1)/(TRPV1), binding capsaicin, is a non-selective cation channel that recently has been shown in human keratinocytes in vitro and in vivo. However, a description of VR1 localization in other cutaneous compartments in particular cutaneous nerve fibers is still lacking. We therefore investigated VR1 immunoreactivity as well as mRNA and protein expression in a series (n = 26) of normal (n = 7), diseased (n = 13) [prurigo nodularis (PN) (n = 10), generalized pruritus (n = 1), and mastocytosis (n = 2)], and capsaicin-treated human skin (n = 6). VR1 immunoreactivity could be observed in cutaneous sensory nerve fibers, mast cells, epidermal keratinocytes, dermal blood vessels, the inner root sheet and the infundibulum of hair follicles, differentiated sebocytes, sweat gland ducts, and the secretory portion of eccrine sweat glands. Upon reverse transcriptase-polymerase chain reaction and Western blot analysis, VR1 was detected in mast cells and keratinocytes from human skin. In pruritic skin of PN, VR1 expression was highly increased in epidermal keratinocytes and nerve fibers, which was normalized after capsaicin application. During capsaicin therapy, a reduction of neuropeptides (substance P, calcitonin gene-related peptide) was observed. After cessation of capsaicin therapy, neuropeptides re-accumulated in skin nerves. In conclusion, VR1 is widely distributed in the skin, suggesting a major role for this receptor, e.g. in nociception and neurogenic inflammation.
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