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Enhancing Human Cutaneous Wound Healing through Targeted Suppression of Large Conductance Ca2+-Activated K+ Channelsopen access

Authors
Choi, Chang-RokKim, Eun-JinChoi, Tae HyunHan, JaeheeKang, Dawon
Issue Date
Jan-2024
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
cutaneous wound healing; human neonatal dermal fibroblast; large conductance Ca<sup>2+</sup>-activated K<sup>+</sup> channel; normal human epidermal keratinocyte
Citation
International Journal of Molecular Sciences, v.25, no.2
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Molecular Sciences
Volume
25
Number
2
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/69639
DOI
10.3390/ijms25020803
ISSN
1661-6596
1422-0067
Abstract
The modulation of K+ channels plays a crucial role in cell migration and proliferation, but the effect of K+ channels on human cutaneous wound healing (CWH) remains underexplored. This study aimed to determine the necessity of modulating K+ channel activity and expression for human CWH. The use of 25 mM KCl as a K+ channel blocker markedly improved wound healing in vitro (in keratinocytes and fibroblasts) and in vivo (in rat and porcine models). K+ channel blockers, such as quinine and tetraethylammonium, aided in vitro wound healing, while Ba2+ was the exception and did not show similar effects. Single-channel recordings revealed that the Ba2+-insensitive large conductance Ca2+-activated K+ (BKCa) channel was predominantly present in human keratinocytes. NS1619, an opener of the BKCa channel, hindered wound healing processes like proliferation, migration, and filopodia formation. Conversely, charybdotoxin and iberiotoxin, which are BKCa channel blockers, dramatically enhanced these processes. The downregulation of BKCa also improved CWH, whereas its overexpression impeded these healing processes. These findings underscore the facilitative effect of BKCa channel suppression on CWH, proposing BKCa channels as potential molecular targets for enhancing human cutaneous wound healing. © 2024 by the authors.
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