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Flos Magnoliae and Its Constituent Linoleic Acid suppress T Lymphocyte Activation via Store‐Operated Calcium Entry.
Author(s) -
KIM HYUN JONG,
Nam Joo Hyun
Publication year - 2020
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2020.34.s1.03177
Subject(s) - orai1 , jurkat cells , chemistry , calcium in biology , calcium , t cell , intracellular , cytokine , microbiology and biotechnology , voltage dependent calcium channel , pharmacology , biochemistry , immunology , biology , immune system , organic chemistry
Intracellular calcium signaling is crucial for type 2 helper T cell and mast cell activation, which is essential for allergic inflammation. It is initiated by antigen‐mediated receptor stimulation that triggers store‐operated calcium entry (SOCE) via ORAI1 calcium channel. Flos Magnoliae (FM) is widely used to treat allergic diseases such as allergic rhinitis and asthma. Although many studies have reported that FM regulates intracellular calcium signaling, research on the exact type of calcium channel modulated by FM is scarce. Therefore, we hypothesized that the anti‐allergic effects of FM might result from ORAI1 inhibition in T cells. We investigated whether a 70% ethanolic extract of FM (FM EtOH ) and its constituents inhibit ORAI1 channel activity and subsequent T cell activation. We performed conventional whole‐cell patch clamp studies in STIM1 and ORAI1‐overexpressing HEK293T cells (HEK ORAI1 ). Intracellular calcium concentration was determined using Fura‐2 dye and cytokine production measurement in Jurkat T lymphocytes. FM EtOH (0.03 mg/mL) and its fractions, especially hexane fraction (FM Hex , 0.01 mg/mL), significantly inhibited SOCE and IL‐2 cytokine production in Jurkat T lymphocytes. GC/MS analysis showed linoleic acid (LA) as the major component of FM Hex . FM Hex at 0.01 mg/mL (equivalent to 10 μM LA) inhibited not only SOCE but also IL‐2 production, as well as CD3/CD28 receptor co‐stimulation induced calcium signaling in Jurkat T lymphocytes. FM EtOH and LA suppressed CD4+ T lymphocyte activation, at least in part, by inhibiting I SOCE . Thus, I SOCE inhibition may be a potential strategy to inhibit immune responses in inflammation.Linoleic acid (LA) inhibits I SOCE and IL‐2 production to similar levels.FM EtOH and its fractions inhibit store‐operated Ca2+ entry mediated current (I SOCE ) in ORAI1 and STIM1 co‐overexpressing HEK293T cells (HEK ORAI1 ).