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Bidirectional regulation of i-type lysozyme on cutaneous wound healing. | LitMetric

Bidirectional regulation of i-type lysozyme on cutaneous wound healing.

Biomed Pharmacother

School of Chinese Material Medica, Beijing University of Chinese Medicine, Yangguang South Road, Fangshan District, Beijing, China. Electronic address:

Published: November 2020

AI Article Synopsis

  • The study investigated the impact of i-type lysozyme on wound healing in both animal models and cell cultures, focusing on its regenerative effects.
  • Daily application of i-type lysozyme on wound sites showed improved skin regeneration, as it sped up the healing process and reduced excessive scarring.
  • Results indicated that i-type lysozyme promotes cell proliferation and migration in various skin cell types, suggesting its potential as an effective treatment for enhancing wound repair while minimizing scar formation.

Article Abstract

Objective: This study aimed to assess the effect and mechanism of i-type lysozyme on cutaneous wound healing animal model and Multiple cell models both in vivo and in vitro.

Methods: Therefore, to evaluate its regenerative efficacy on wound healing process, we daily applied i-type lysozyme on murine full-thickness excisional wounds. After sacrifice on indicated days, skin tissues around surgical defects were harvested and assessed for re-epithelialization, granulation tissue formation, neovascularization and remodeling. To elucidate the underlying mechanisms, i-type lysozyme was analyzed for its tissue regenerative potency on the proliferation, invasion, migration and tube formation against keratinocytes, fibroblasts and endothelial cells. Antioxidant and antimicrobial experiments were also conducted to elucidate protective ability of i-type lysozyme to wound bed.

Results: It displayed excellent bi-directional regulation in wound repair, with significant acceleration of epidermal and dermal regeneration as well as the efficient attenuation of excessive collagen deposition and fibrosis in the surgical lesion. I-type lysozyme treatment augmented the proliferation and migration of HaCaT, NIH 3T3 and HUVECs, enhanced the invasion of HaCaT and HUVECs as well as accelerated tube formation of HUVECs. Additionally, it significantly recovered the proliferation of HO-damaged cells, whereas represented no microbicidal effect under effective concentration of wound healing.

Conclusion: Our findings demonstrate the bi-directional regulation of i-type lysozyme in wound healing process through promoting tissue regeneration while hampering scar formation, implying that it is a promising therapeutic agent for wound repair.

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Source
http://dx.doi.org/10.1016/j.biopha.2020.110700DOI Listing

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