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Updated: Apr 20, 2026

Human Ex vivo Wound Model and Whole-Mount Staining Approach to Accurately Evaluate Skin Repair
Published on: February 17, 2021
Stem cells and aberrant signaling of molecular systems in skin aging
Yan Peng1, Min Xuan2, Victor Y L Leung3
1Department of Orthopaedics & Traumatology, LKS Faculty of Medicine, The University of Hong Kong, L9-12, Lab block, Hong Kong, SAR, China; Department of Plastic Surgery, Guangzhou General Hospital of Guangzhou command, The Key Laboratory of Trauma Treatment & Tissue Repair of Tropical Area, PLA, GuangDong, 510010, PR China.
Abstract:
The skin is the body's largest organ and it is able to self-repair throughout an individual's life. With advanced age, skin is prone to degenerate in response to damage. Although cosmetic surgery has been widely adopted to rejuvinate skin, we are far from a clear understanding of the mechanisms responsible for skin aging. Recently, adult skin-resident stem/progenitor cells, growth arrest, senescence or apoptotic death and dysfunction caused by alterations in key signaling genes, such as Ras/Raf/MEK/ERK, PI3K/Akt-kinases, Wnt, p21 and p53, have been shown to play a vital role in skin regeneration. Simultaneously, enhanced telomere attrition, hormone exhaustion, oxidative stress, genetic events and ultraviolet radiation exposure that result in severe DNA damage, genomic instability and epigenetic mutations also contribute to skin aging. Therefore, cell replacement and targeting of the molecular systems found in skin hold great promise for controlling or even curing skin aging.
Insights
Skin aging involves stem cell dysfunction and molecular pathway alterations. Targeting these mechanisms offers potential for skin regeneration and controlling aging effects.
Area of Science:
- Dermatology and regenerative medicine, focusing on skin aging mechanisms.
Background:
- The skin, the body's largest organ, possesses self-repair capabilities that decline with age.
- Skin aging is characterized by degeneration due to damage, with underlying molecular mechanisms not fully understood.
- Current rejuvenation methods like cosmetic surgery lack a deep mechanistic basis.
Purpose of the Study:
- To elucidate the key molecular and cellular factors contributing to skin aging.
- To explore the role of stem/progenitor cells and signaling pathways in skin regeneration and aging.
- To identify potential therapeutic targets for controlling or reversing skin aging.
Main Methods:
- Review of recent findings on cellular processes like senescence and apoptosis in aging skin.
- Analysis of critical signaling pathways (Ras/Raf/MEK/ERK, PI3K/Akt, Wnt, p21, p53) involved in skin regeneration.
- Examination of contributing factors such as telomere attrition, oxidative stress, and DNA damage.
Main Results:
- Adult skin stem/progenitor cells, senescence, apoptosis, and signaling pathway dysfunction are crucial in skin aging.
- Factors like telomere attrition, hormone changes, oxidative stress, and UV exposure accelerate skin aging.
- These factors lead to DNA damage, genomic instability, and epigenetic mutations.
Conclusions:
- Cellular dysfunction and molecular alterations are central to skin aging.
- Cell replacement strategies and targeted molecular interventions show promise for managing skin aging.
- Understanding these mechanisms could lead to treatments for skin aging and age-related skin conditions.
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