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交联透明质酸诱导的累积和持续临床改善的意义:人体的体内生化/显微镜研究。

Implications for cumulative and prolonged clinical improvement induced by cross-linked hyaluronic acid: An in vivo biochemical/microscopic study in humans.

机构信息

Department of Dermatology, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

Exp Dermatol. 2024 Jan;33(1):e14998. doi: 10.1111/exd.14998.

Abstract

In photoaged human skin, type I collagen fragmentation impairs dermal extracellular matrix (ECM) integrity, resulting in collapsed/contracted fibroblasts with reduced type I procollagen synthesis. Injections of cross-linked hyaluronic acid (CL-HA) reverse these deleterious changes. To investigate the time course and effects of biochemical changes induced by injected CL-HA, particularly whether fibroblast activation leads to accumulation/deposition of dermal collagen, we injected CL-HA into photoaged skin of human participants over 60 years-old and performed biochemical/microscopic analyses of skin samples. Beginning 1 week post-injection and lasting 6-9 months, fibroblasts exhibited activation, including increased immunostaining and gene expression of markers of type I collagen synthesis, such as heat shock protein 47 and components of the transforming growth factor-β pathway. At 1 week post-injection, multiphoton microscopy revealed elongation/stretching of fibroblasts, indicating enhanced dermal mechanical support. At 4 weeks, second-harmonic generation microscopy revealed thick collagen bundles densely packed around pools of injected CL-HA. At 12 months, accumulation of thick collagen bundles was observed and injected CL-HA remained present in substantial amounts. Thus, by occupying space in the dermal ECM, injected CL-HA rapidly and durably enhances mechanical support, stimulating fibroblast elongation and activation, which results in thick, densely packed type I collagen bundles accumulating as early as 4 weeks post-injection and continuing for at least a year. These observations indicate that early and prolonged clinical improvement following CL-HA injection results from space-filling and collagen deposition. As type I collagen has an estimated half-life of 15 years, our data provide the foundations for optimizing the timing/frequency of repeat CL-HA injections.

摘要

在光老化的人类皮肤中,I 型胶原的碎片化会损害真皮细胞外基质(ECM)的完整性,导致成纤维细胞塌陷/收缩,I 型原胶原合成减少。交联透明质酸(CL-HA)的注射可逆转这些有害变化。为了研究注射 CL-HA 诱导的生化变化的时程和影响,特别是成纤维细胞的激活是否会导致真皮胶原的积累/沉积,我们对 60 岁以上的光老化皮肤的人类参与者进行了 CL-HA 注射,并对皮肤样本进行了生化/显微镜分析。从注射后 1 周开始,持续 6-9 个月,成纤维细胞表现出激活,包括增加 I 型胶原合成标志物如热休克蛋白 47 和转化生长因子-β通路成分的免疫染色和基因表达。在注射后 1 周,多光子显微镜显示成纤维细胞伸长/拉伸,表明真皮机械支撑增强。在 4 周时,二次谐波产生显微镜显示密集堆积在注射 CL-HA 周围的厚胶原束。在 12 个月时,观察到厚胶原束的积累,并且仍然存在大量注射的 CL-HA。因此,通过占据真皮 ECM 的空间,注射的 CL-HA 迅速而持久地增强机械支撑,刺激成纤维细胞伸长和激活,导致厚而密集的 I 型胶原束在注射后 4 周就开始积累,并持续至少 1 年。这些观察结果表明,CL-HA 注射后早期和长期的临床改善是由于空间填充和胶原沉积。由于 I 型胶原的半衰期估计为 15 年,我们的数据为优化重复 CL-HA 注射的时间/频率提供了基础。

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