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提取物及其成分京尼平可抑制CD3/CD28共刺激的CD4 T细胞ORAI1通道的激活。

extract and its constituent, genipin, inhibit activation of CD3/CD28 co-stimulated CD4 T cells ORAI1 channel.

作者信息

Kim Hyun Jong, Nam Yu Ran, Woo JooHan, Kim Woo Kyung, Nam Joo Hyun

机构信息

Channelopathy Research Center (CRC), Dongguk University College of Medicine, Korea.

Department of Internal Medicine, Graduate School of Medicine, Dongguk University, Goyang 10326, Korea.

出版信息

Korean J Physiol Pharmacol. 2020 Jul 1;24(4):363-372. doi: 10.4196/kjpp.2020.24.4.363.

Abstract

() is a widely used herbal medicine with antiinflammatory properties, but its effects on the ORAI1 channel, which is important in generating intracellular calcium signaling for T cell activation, remain unknown. In this study, we investigated whether 70% ethanolic extract () and its subsequent fractions inhibit ORAI1 and determined which constituents contributed to this effect. Whole-cell patch clamp analysis revealed that (64.7% ± 3.83% inhibition at 0.1 mg/ml) and all its fractions showed inhibitory effects on the ORAI1 channel. Among the fractions, the hexane fraction (, 66.8% ± 9.95% at 0.1 mg/ml) had the most potent inhibitory effects in hORAI1-hSTIM1 co-transfected HEK293T cells. Chemical constituent analysis revealed that the strong ORAI1 inhibitory effect of was due to linoleic acid, and in other fractions, we found that genipin inhibited ORAI1. Genipin significantly inhibited I and interleukin-2 production in CD3/ CD28-stimulated Jurkat T lymphocytes by 35.9% ± 3.02% and 54.7% ± 1.32% at 30 μM, respectively. Furthermore, the same genipin concentration inhibited the proliferation of human primary CD4+ T lymphocytes stimulated with CD3/CD28 antibodies by 54.9% ± 8.22%, as evaluated by carboxyfluorescein succinimidyl ester assay. Our findings suggest that genipin may be one of the active components of responsible for T cell suppression, which is partially mediated by activation of the ORAI1 channel. This study helps us understand the mechanisms of in the treatment of inflammatory diseases.

摘要

()是一种具有抗炎特性的广泛使用的草药,但它对在T细胞激活中产生细胞内钙信号传导起重要作用的ORAI1通道的影响尚不清楚。在本研究中,我们研究了70%乙醇提取物()及其后续馏分是否抑制ORAI1,并确定了哪些成分促成了这种作用。全细胞膜片钳分析显示,(0.1mg/ml时抑制率为64.7%±3.83%)及其所有馏分对ORAI1通道均有抑制作用。在这些馏分中,己烷馏分(0.1mg/ml时为66.8%±9.95%)在hORAI1-hSTIM1共转染的HEK293T细胞中具有最有效的抑制作用。化学成分分析表明,的强烈ORAI1抑制作用归因于亚油酸,在其他馏分中,我们发现京尼平抑制ORAI1。在30μM时,京尼平分别显著抑制CD3/CD28刺激的Jurkat T淋巴细胞中I和白细胞介素-2的产生,抑制率分别为35.9%±3.02%和54.7%±1.32%。此外,通过羧基荧光素琥珀酰亚胺酯测定评估,相同浓度的京尼平抑制用CD3/CD28抗体刺激的人原代CD4+T淋巴细胞的增殖,抑制率为54.9%±8.22%。我们的研究结果表明,京尼平可能是中负责T细胞抑制的活性成分之一,这部分是由ORAI1通道的激活介导的。这项研究有助于我们理解在治疗炎症性疾病中的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92a3/7317176/936792173ad4/KJPP-24-363-f1.jpg

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