Oh J, Kim N, Seo S, Kim I-H
Laboratory of Cellular Oncology, Korea University Ansan Hospital, Gojan 1-dong, Danwon gu, Ansan, Gyeonggi do 425-707, Korea.
Br J Dermatol. 2007 Aug;157(2):306-10. doi: 10.1111/j.1365-2133.2007.08061.x.
Nonablative laser therapy is widely practised for skin rejuvenation, which stimulates collagen production and dermal matrix remodelling. Matrix remodelling is primarily modulated by a coordinated action of matrix metalloproteinases (MMPs) and their inhibitors, but the effects of nonablative lasers on these matrix modulators are not fully investigated.
To evaluate the changes in matrix modulators, such as MMP-1, MMP-2, MMP-3, MMP-9 and MT1-MMP, and their inhibitors (TIMP-1, TIMP-2 and RECK in particular), after nonablative laser treatments of human facial skin.
Twenty-four adult volunteers received a series of four nonablative laser treatments separated by 3-week intervals on facial skin. Two-millimetre skin punch biopsies were obtained at baseline and 3 weeks after the last treatment.
Nonablative laser treatments led to a robust increase in two major dermal matrix components, type I collagen and tropoelastin. Among MMPs tested, levels of MMP-2 mRNA were statistically significantly increased, but the amount of active MMP-2 was rather reduced. More importantly, the expression level of RECK was significantly enhanced by laser treatments.
Clinical outcomes following nonablative laser treatments may result not only from increased biosynthesis but also from decreased degradation, via an induction of RECK expression, of matrix proteins.
非剥脱性激光疗法广泛应用于皮肤年轻化,可刺激胶原蛋白生成和真皮基质重塑。基质重塑主要由基质金属蛋白酶(MMPs)及其抑制剂的协同作用调节,但非剥脱性激光对这些基质调节剂的影响尚未得到充分研究。
评估非剥脱性激光治疗人面部皮肤后基质调节剂(如MMP-1、MMP-2、MMP-3、MMP-9和MT1-MMP)及其抑制剂(尤其是TIMP-1、TIMP-2和RECK)的变化。
24名成年志愿者在面部皮肤接受了一系列4次非剥脱性激光治疗,每次治疗间隔3周。在基线和最后一次治疗后3周获取2毫米皮肤穿刺活检样本。
非剥脱性激光治疗导致两种主要真皮基质成分(I型胶原蛋白和原弹性蛋白)显著增加。在所检测的MMPs中,MMP-2 mRNA水平有统计学意义的显著升高,但活性MMP-2的量反而减少。更重要的是,激光治疗显著增强了RECK的表达水平。
非剥脱性激光治疗后的临床效果可能不仅源于生物合成增加,还源于通过诱导RECK表达减少基质蛋白降解。