Zeltzer Assaf, Keren Aviad, Paus Ralf, Gilhar Amos
Plastic & Reconstructive Surgery Department, Rambam Health Care Campus, Haifa 3525408, Israel.
Skin Research Laboratory, Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 3200003, Israel.
Int J Mol Sci. 2025 Jun 17;26(12):5787. doi: 10.3390/ijms26125787.
Novel senotherapeutics are needed to reverse aging-related skin decline. The research question addressed was whether mesoglycan, a clinically approved glycosaminoglycan formulation known to enhance perfusion, angiogenesis, and VEGF-A signaling, possesses therapeutic potential for rejuvenating photo aged human skin. To test this, we treated full-thickness photoaged facial human skin samples (mean age: 72 ± 5 years) from seven women ex vivo. The samples were treated with topical or medium-delivered mesoglycan (100, 200, and 300 µM) for 6 days under serum-free conditions that accelerate skin aging. Biomarkers associated with aging were assessed using quantitative immunohistomorphometry. Mesoglycan treatment improved key skin aging biomarkers at all doses. Compared to vehicle-treated skin, mesoglycan broadly enhanced epidermal structure and function, improved pigmentation-related markers, reduced cellular senescence, boosted mitochondrial performance and antioxidant defenses, and improved dermal matrix structure and microvasculature density. Notably, mesoglycan also upregulated VEGF-A and VEGFR2, promoting skin rejuvenation. Medium-delivered mesoglycan produced stronger overall effects, while rete ridge reappearance was observed exclusively after topical application. Mesoglycan demonstrates senotherapeutic potential in photoaged human skin, acting via complementary pathways, including VEGF-A upregulation. Although medium-delivered mesoglycan yielded the greatest biomarker improvements topical application restored rete ridges, a sign of epidermal reorganization and also significantly enhanced basement membrane structure, pigmentation, mitochondrial function and antioxidant defenses, while avoiding systemic exposure, making it the safer and more feasible route for localized skin anti-aging.
需要新型衰老疗法来逆转与衰老相关的皮肤衰退。本研究探讨的问题是,硫酸乙酰肝素(一种临床批准的糖胺聚糖制剂,已知可增强灌注、血管生成和VEGF-A信号传导)是否具有使光老化人类皮肤恢复活力的治疗潜力。为了验证这一点,我们对来自7名女性的全层光老化面部人类皮肤样本(平均年龄:72±5岁)进行了体外处理。在加速皮肤衰老的无血清条件下,将样本用局部或培养基递送的硫酸乙酰肝素(100、200和300µM)处理6天。使用定量免疫组织形态计量学评估与衰老相关的生物标志物。硫酸乙酰肝素处理在所有剂量下均改善了关键的皮肤衰老生物标志物。与赋形剂处理的皮肤相比,硫酸乙酰肝素广泛增强了表皮结构和功能,改善了色素沉着相关标志物,减少了细胞衰老,增强了线粒体性能和抗氧化防御,并改善了真皮基质结构和微血管密度。值得注意的是,硫酸乙酰肝素还上调了VEGF-A和VEGFR2,促进皮肤年轻化。培养基递送的硫酸乙酰肝素产生了更强的总体效果,而仅在局部应用后观察到 rete嵴再现。硫酸乙酰肝素在光老化人类皮肤中显示出衰老治疗潜力,通过包括VEGF-A上调在内的互补途径发挥作用。尽管培养基递送的硫酸乙酰肝素在生物标志物改善方面效果最佳,但局部应用恢复了rete嵴,这是表皮重组的迹象,还显著增强了基底膜结构、色素沉着、线粒体功能和抗氧化防御,同时避免了全身暴露,使其成为局部皮肤抗衰老更安全、更可行的途径。