光生物调节PI3K/AKT/mTOR在伤口愈合中的研究进展

IF 3.261
Patricia Kasowanjete, Sathish Sundar Dhilip Kumar, Nicolette N. Houreld
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引用次数: 0

摘要

伤口愈合包括一系列细胞和分子的过程来愈合受伤的组织。生长因子如血管内皮生长因子(VEGF)和信号通路如磷脂酰肌醇3-激酶、蛋白激酶B和哺乳动物雷帕霉素靶蛋白(PI3K/AKT/mTOR)在伤口愈合中至关重要。VEGF与细胞内信号通路相关,包括PI3K/AKT/mTOR,其控制细胞生长、代谢、增殖、凋亡和蛋白质合成。在光生物调节(PBM)过程中,使用可见红色和近红外(NIR)光谱中的低水平光来促进愈合,减轻疼痛,炎症和水肿。几项研究表明,PBM可提高体外细胞存活、增殖、迁移和活力,然而,这些益处的确切细胞和分子机制尚未确定。本文旨在探讨PBM对伤口愈合过程中PI3K/AKT/mTOR信号通路的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A review of photobiomodulation on PI3K/AKT/mTOR in wound healing

A review of photobiomodulation on PI3K/AKT/mTOR in wound healing

Wound healing involves a series of cellular and molecular processes to heal injured tissue. Growth factors such as vascular endothelial growth factor (VEGF), and signalling pathways such as phosphatidylinositol 3-kinase, protein kinase B, and mammalian target of rapamycin (PI3K/AKT/mTOR) are essential in wound healing. VEGF is linked to intracellular signalling pathways including PI3K/AKT/mTOR, which controls cell growth, metabolism, proliferation, apoptosis, and protein synthesis. During photobiomodulation (PBM), low-level light in the visible red and near-infrared (NIR) spectrum is employed to promote healing, and reduce pain, inflammation, and oedema. Several studies demonstrate that PBM enhances cellular survival, proliferation, migration, and viability in vitro, however, the exact cellular and molecular mechanisms responsible for these benefits have not yet been identified. The aim of this review is to explore the effects of PBM on the PI3K/AKT/mTOR signalling pathway in wound healing.

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