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GHK-Cu-liposomes accelerate scald wound healing in mice by promoting cell proliferation and angiogenesis

Study · human · Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society · 2017 · DOI 10.1111/wrr.12520 · PMID 28370978

Plain-language summary

Paraphrased from the published abstract below — not a verdict on whether anything works.

In this mouse and human cell (HUVEC) study, researchers prepared liposomes encapsulating GHK-Cu (glycyl-l-histidyl-l-lysine-Cu) and examined effects on human umbilical vein endothelial cell (HUVEC) proliferation and scald wound healing in mice. GHK-Cu-liposomes were associated with a 33.1% increase in HUVEC proliferation rate, increased cell number at G1 stage and decreased cell number at G2 stage, and increased expression of vascular endothelial growth factor, fibroblast growth factor-2, CDK4, and CyclinD1. In a mouse scald model, GHK-Cu-liposomes were associated with greater angiogenesis in burned skin compared with free GHK-Cu, increased CD31 and Ki67 signal, and wound healing time shortened to 14 days post injury.

Abstract

Glycyl-l-histidyl-l-lysine (GHK)-Cu is considered to be an activator of tissue remodeling, and has been used in cosmetic products. In this study, we prepared liposomes encapsulating GHK-Cu and analyzed their effect on human umbilical vein endothelial cells (HUVECs) proliferation and scald wound healing in mice. The nanoscaled GHK-Cu-liposomes promoted HUVECs proliferation, with a 33.1% increased rate. Flow cytometry analysis showed increased cell number at G1 stage and decreased cell number at G2 stage after GHK-Cu-liposomes treatment. Western blotting indicated that the expression of vascular endothelial growth factor and fibroblast grow factors-2 were both enhanced, as well as cell cycle-related proteins CDK4 and CyclinD1. In a mice scald model, angiogenesis in burned skin treated with GHK-Cu-liposomes was better compared with free GHK-Cu, and immunofluorescence analysis showed enhanced signal of CD31 and Ki67 in GHK-Cu-liposomes treated mice. Moreover, the wound healing time was shortened to 14 days post injury. Our results provide the evidence that GHK-Cu-liposomes could be utilized as a treatment for skin wounds.

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