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HypoxamiR-210 accelerates wound healing in diabetic mice by improving cellular metabolism

Medicine and Health

HypoxamiR-210 accelerates wound healing in diabetic mice by improving cellular metabolism

S. Narayanan, S. E. Angelstig, et al.

This groundbreaking study by Sampath Narayanan and colleagues explores how miR-210 influences diabetic wound healing. By restoring metabolic balance and enhancing crucial processes such as cellular proliferation and angiogenesis, local miR-210 administration has shown promising results in accelerating wound recovery in diabetic mice.... show more
Abstract
Wound healing is a high energy demanding process that needs a good coordination of the mitochondria with glycolysis in the characteristic highly hypoxic environment. In diabetes, hyperglycemia impairs the adaptive responses to hypoxia with profound negative effects on different cellular compartments of wound healing. miR-210 is a hypoxia-induced microRNA that regulates cellular metabolism and processes important for wound healing. Here, we show that hyperglycemia blunted the hypoxia-dependent induction of miR-210 both in vitro and in human and mouse diabetic wounds. The impaired regulation of miR-210 in diabetic wounds is pathogenic, since local miR-210 administration accelerated wound healing specifically in diabetic but not in non-diabetic mice. miR-210 reconstitution restores the metabolic balance in diabetic wounds by reducing oxygen consumption rate and ROS production and by activating glycolysis with positive consequences on cellular migration. In conclusion, miR-210 accelerates wound healing specifically in diabetes through improvement of the cellular metabolism.
Publisher
Communications Biology
Published On
Dec 14, 2020
Authors
Sampath Narayanan, Sofie Eliasson Angelstig, Cheng Xu, Jacob Grünler, Allan Zhao, Wan Zhu, Ning Xu Landén, Mona Ståhle, Jingping Zhang, Mircea Ivan, Raluca Georgiana Maltesen, Ileana Ruxandra Botusan, Neda Rajamand Ekberg, Xiaowei Zheng, Sergiu-Bogdan Catrina
Tags
miR-210
diabetic wound healing
hyperglycemia
angiogenesis
metabolic balance
glycolysis
ROS production
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