Potassium channels as potential drug targets for limb wound repair and regeneration

Abstract Background Ion channels are a large family of transmembrane proteins, accessible by soluble membrane-impermeable molecules, and thus are targets for development of therapeutic drugs. Ion channels are the second most common target for existing drugs, after G protein-coupled receptors, and ar...

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Published in:Precision clinical medicine Vol. 3; no. 1; pp. 22 - 33
Main Authors: Zhang, Wengeng, Das, Pragnya, Kelangi, Sarah, Bei, Marianna
Format: Journal Article
Language:English
Published: England Oxford University Press 01-03-2020
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Summary:Abstract Background Ion channels are a large family of transmembrane proteins, accessible by soluble membrane-impermeable molecules, and thus are targets for development of therapeutic drugs. Ion channels are the second most common target for existing drugs, after G protein-coupled receptors, and are expected to make a big impact on precision medicine in many different diseases including wound repair and regeneration. Research has shown that endogenous bioelectric signaling mediated by ion channels is critical in non-mammalian limb regeneration. However, the role of ion channels in regeneration of limbs in mammalian systems is not yet defined. Methods To explore the role of potassium channels in limb wound repair and regeneration, the hindlimbs of mouse embryos were amputated at E12.5 when the wound is expected to regenerate and E15.5 when the wound is not expected to regenerate, and gene expression of potassium channels was studied. Results Most of the potassium channels were downregulated, except for the potassium channel kcnj8 (Kir6.1) which was upregulated in E12.5 embryos after amputation. Conclusion This study provides a new mouse limb regeneration model and demonstrates that potassium channels are potential drug targets for limb wound healing and regeneration.
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Present address: Department of Pediatrics, Division of Neonatology, Drexel University College of Medicine, Philadelphia, PA 19102, USA
ISSN:2096-5303
2516-1571
DOI:10.1093/pcmedi/pbz029