Anti-Inflammatory Effect of Licochalcone A via Regulation of ORAI1 and K+ Channels in T-Lymphocytesopen access
- Authors
- Phan, Hong T. L.; Kim, Hyun J.; Jo, Sungwoo; Kim, Woo K.; Namkung, Wan; Nam, Joo H.
- Issue Date
- Oct-2021
- Publisher
- MDPI
- Keywords
- licochalcone A; store-operated calcium entry; calcium-release-activated calcium channel protein 1; calcium-activated potassium channel; voltage-gated potassium channel; anti-inflammatory effect
- Citation
- INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.22, no.19
- Indexed
- SCIE
SCOPUS
- Journal Title
- INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Volume
- 22
- Number
- 19
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/4412
- DOI
- 10.3390/ijms221910847
- ISSN
- 1661-6596
1422-0067
- Abstract
- Calcium signaling plays a vital role in the regulation of various cellular processes, including activation, proliferation, and differentiation of T-lymphocytes, which is mediated by ORAI1 and potassium (K+) channels. These channels have also been identified as highly attractive therapeutic targets for immune-related diseases. Licochalcone A is a licorice-derived chalconoid known for its multifaceted beneficial effects in pharmacological treatments, including its anti-inflammatory, anti-asthmatic, antioxidant, antimicrobial, and antitumorigenic properties. However, its anti-inflammatory effects involving ion channels in lymphocytes remain unclear. Thus, the present study aimed to investigate whether licochalcone A inhibits ORAI1 and K+ channels in T-lymphocytes. Our results indicated that licochalcone A suppressed all three channels (ORAI1, Kv1.3, and KCa3.1) in a concentration-dependent matter, with IC50 values of 2.97 & PLUSMN; 1.217 mu M, 0.83 & PLUSMN; 1.222 mu M, and 11.21 & PLUSMN; 1.07 mu M, respectively. Of note, licochalcone A exerted its suppressive effects on the IL-2 secretion and proliferation in CD3 and CD28 antibody-induced T-cells. These results indicate that the use of licochalcone A may provide an effective treatment strategy for inflammation-related immune diseases.
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Collections - Graduate School > Department of Medicine > 1. Journal Articles

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