Boston and Cambridge, Mass.; Padua, Italy; and Tokyo, Japan From the Tissue Engineering and Wound Healing Laboratory, Division of Plastic Surgery, Brigham and Women's Hospital, Harvard Medical School; Tufts University School of Medicine; the University of Padua; the Department of Electronics and Mechanical, Wentworth Institute of Technology; simulation group, CIMIT, Massachusetts Institute of Technology; and the Department of Plastic, Reconstructive, and Aesthetic Surgery, Nippon Medical School.
Plast Reconstr Surg. 2009 Jul;124(1):102-113. doi: 10.1097/PRS.0b013e3181a81542.
Mechanical forces modulate wound healing and scar formation through mechanotransduction. In response to mechanical stimulation, neuropeptides are released from peripheral terminals of primary afferent sensory neurons, influencing skin and immune cell functions and increasing vascular permeability, causing neurogenic inflammation.
A computer-controlled device was used to stretch murine skin. C57Bl6 mice (n = 26) were assigned to a cyclical square-wave tensile stimulation for 4 hours or continuous stimulation for 4 hours. Stretched skin was analyzed for expression of the neuropeptides, substance P and calcitonin gene-related peptide, their receptors (NK1R and calcitonin gene-related peptide receptor component protein), and growth factors (nerve growth factor, transforming growth factor beta1, vascular endothelial growth factor, and epidermal growth factor) using immunohistochemistry and real-time reverse-transcriptase polymerase chain reaction.
Cyclical stimulation resulted in a significant increase in expression of neuropeptides and growth factors, whereas the corresponding peptide receptors were down-regulated. Transcription of neuropeptide mRNA was elevated in stretched skin, which proves that neuropeptides are released from not only peripheral terminals of nerve fibers but also resident skin cells.
The authors' results suggest that skin stretching may alter cell physiology by stimulating neuropeptide expression, and that cyclical mechanical force may be more effectively stimulating mechanosensitive nociceptors or mechanoreceptors (mechanosensors) on cells.
机械力通过力学转导调节伤口愈合和瘢痕形成。在外周初级感觉神经元的末梢受到机械刺激时,神经肽被释放出来,影响皮肤和免疫细胞的功能,增加血管通透性,引起神经源性炎症。
使用计算机控制的装置拉伸鼠皮。将 C57Bl6 小鼠(n = 26)分为周期性方波拉伸刺激 4 小时或连续刺激 4 小时组。使用免疫组织化学和实时逆转录聚合酶链反应分析拉伸皮肤中神经肽、P 物质和降钙素基因相关肽及其受体(NK1R 和降钙素基因相关肽受体成分蛋白)和生长因子(神经生长因子、转化生长因子β1、血管内皮生长因子和表皮生长因子)的表达。
周期性刺激导致神经肽和生长因子的表达显著增加,而相应的肽受体下调。拉伸皮肤中神经肽 mRNA 的转录水平升高,证明神经肽不仅从神经纤维的外周末端释放,也从驻留的皮肤细胞中释放。
作者的研究结果表明,皮肤拉伸可能通过刺激神经肽表达来改变细胞生理学,而周期性机械力可能更有效地刺激细胞上的机械敏感伤害感受器或机械感受器(机械感受器)。