Abstract

Arginase (ARG) represents an important evolutionarily conserved enzyme that is expressed by multiple cell types in the skin. Arg acts as the mediator of the last step of the urea cycle, thus providing protection against excessive ammonia under homeostatic conditions through the production of L-ornithine and urea. L-ornithine represents the intersection point between the ARG-dependent pathways and the urea cycle, therefore contributing to cell detoxification, proliferation and collagen production. The ARG pathways help balance pro- and anti-inflammatory responses in the context of wound healing. However, local and systemic dysfunctionalities of the ARG pathways have been shown to contribute to the hindrance of the healing process and the occurrence of chronic wounds. This review discusses the functions of ARG in macrophages and fibroblasts while detailing the deleterious implications of a malfunctioning ARG enzyme in chronic skin conditions such as leg ulcers. The review also highlights how ARG links with the microbiota and how this impacts on infected chronic wounds. Lastly, the review depicts chronic wound treatments targeting the ARG pathway, alongside future diagnosis and treatment perspectives.

Highlights

  • The skin represents a multifaceted organ with a complex architecture and biology

  • Due to the vast array of skin components and functions, it follows that cutaneous wound healing has to be a wellcoordinated cascade of intricate events to ensure a re-establishment of protection against environmental hazards and infections

  • This review aims to give an overview of ARG activity and the current understanding of how it relates to wound healing

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Summary

Introduction

Due to the vast array of skin components and functions, it follows that cutaneous wound healing has to be a wellcoordinated cascade of intricate events to ensure a re-establishment of protection against environmental hazards and infections. There has been an increasing interest in the Arginase (ARG) pathways and their link to the proper progression through the wound healing cascade. ARG has been shown to have ample physiological implications, due to being the nexus of upstream signalling events as well as downstream metabolism of polyamines and proline (Caldwell et al, 2018). More and more studies are highlighting a link between this enzyme and impaired wound healing (Jude et al, 1999; Abd-El-Aleem et al, 2000; Campbell et al, 2013; Abd El-Aleem et al, 2019). The implications of a malfunctioning ARG enzyme in wound chronicity are not well-understood

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