Dallos Attila, Kiss Mária, Polyánka Hilda, Dobozy Attila, Kemény Lajos, Husz Sándor
Department of Dermatology and Allergology, University of Szeged, Korányi fasor 6, H-6720 Szeged, Hungary.
Neuropeptides. 2006 Aug;40(4):251-63. doi: 10.1016/j.npep.2006.06.002. Epub 2006 Aug 10.
Neuropeptides released from the cutaneous sensory nerve endings have neurotransmitter and immunoregulatory roles; they exert mitogenic actions and can influence the functions of different cell types in the skin. The aims of this study were a systematic investigation of the effects of the neuropeptides substance P (SP), calcitonin gene-related peptide (CGRP), vasoactive intestinal polypeptide (VIP) and galanin (GAL) on the inflammatory cytokine production (IL-1alpha, IL-8 and TNF-alpha) of the keratinocytes, and a study of their role in the production and secretion of nerve growth factor (NGF) and its precursor molecule (proNGF). Cultures of normal human keratinocytes were treated with 10(-8)M SP, CGRP, VIP or GAL for 30 min. After different time intervals, cells were harvested for total RNA isolation; in addition, cell lysates and supernatants were collected. The effects of the neuropeptides on the mRNA expressions of the different cytokines and NGF were investigated by Q-RT-PCR and the protein levels were studied by means of ELISA assays and Western blotting. Each of the four neuropeptides induced increases in the expressions of IL-1alpha, IL-8 and TNF-alpha mRNA. Increases appeared in the amount of the IL-1alpha protein in the supernatants of neuropeptide-treated cells, and the IL-8 secretion was mildly elevated, while secretion of TNF-alpha remained undetectable. The four neuropeptides increased the NGF mRNA expression to different extents. In the cell lysates of the keratinocytes, only proNGF could be detected, its concentration in the neuropeptide-treated cells being approximately twice that in the time-matched controls. Both control cultures and neuropeptide-treated cultures were found to secrete proNGF and mature NGF, but neuropeptide-treated cell cultures produced markedly higher (3-7-fold) amounts of NGF-like immunoreactive materials. The results demonstrated that neuropeptides released from cutaneous nerves after an injurious stimulus are able to induce an upregulation of IL-1alpha and IL-8 production; they are additionally able to influence the expressions of proNGF/NGF and their secretion from the keratinocytes. These findings may contribute toward an understanding of the neural influence on skin health and disease.
从皮肤感觉神经末梢释放的神经肽具有神经递质和免疫调节作用;它们具有促有丝分裂作用,并能影响皮肤中不同细胞类型的功能。本研究的目的是系统研究神经肽P物质(SP)、降钙素基因相关肽(CGRP)、血管活性肠肽(VIP)和甘丙肽(GAL)对角质形成细胞炎性细胞因子产生(IL-1α、IL-8和TNF-α)的影响,以及它们在神经生长因子(NGF)及其前体分子(proNGF)产生和分泌中的作用。将正常人角质形成细胞培养物用10⁻⁸M的SP、CGRP、VIP或GAL处理30分钟。在不同的时间间隔后,收集细胞用于总RNA提取;此外,收集细胞裂解物和上清液。通过Q-RT-PCR研究神经肽对不同细胞因子和NGF mRNA表达的影响,并通过ELISA分析和蛋白质印迹法研究蛋白质水平。四种神经肽中的每一种都诱导IL-1α、IL-8和TNF-α mRNA表达增加。在神经肽处理细胞的上清液中,IL-1α蛋白量增加,IL-8分泌轻度升高,而TNF-α分泌仍未检测到。四种神经肽不同程度地增加了NGF mRNA表达。在角质形成细胞的细胞裂解物中,只能检测到proNGF,其在神经肽处理细胞中的浓度约为时间匹配对照的两倍。发现对照培养物和神经肽处理培养物均分泌proNGF和成熟NGF,但神经肽处理的细胞培养物产生的NGF样免疫反应性物质明显更高(3至7倍)。结果表明,损伤刺激后从皮肤神经释放的神经肽能够诱导IL-1α和IL-8产生的上调;它们还能够影响proNGF/NGF的表达及其从角质形成细胞中的分泌。这些发现可能有助于理解神经对皮肤健康和疾病的影响。