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ω-3脂肪酸在内源性表达FFA4的人结肠上皮细胞系中诱导Ca(2+)动员反应。

Omega-3 fatty acids induce Ca(2+) mobilization responses in human colon epithelial cell lines endogenously expressing FFA4.

作者信息

Kim Jung-min, Lee Kyoung-pil, Park Soo-jin, Kang Saeromi, Huang Jin, Lee Jung-min, Sato Koichi, Chung Hae-young, Okajima Fumikazu, Im Dong-soon

机构信息

Molecular Inflammation Research Center for Aging Intervention (MRCA) and College of Pharmacy, Pusan National University, Busan 609-735, Republic of Korea.

Laboratory of Signal Transduction, Institute for Molecular and Cellular Regulation, Gunma University, 3-39-15 Showa-machi, Maebashi 371-8512, Japan.

出版信息

Acta Pharmacol Sin. 2015 Jul;36(7):813-20. doi: 10.1038/aps.2015.29. Epub 2015 May 25.

Abstract

AIM

Free fatty acid receptor 4 (FFA4; formerly known as GPR120) is the G protein-coupled receptor (GPCR) for omega-3 polyunsaturated fatty acids. FFA4 has been found to express in the small intestines and colons of mice and humans. In this study we investigate the effects of omega-3 polyunsaturated fatty acids on FFA4 in human colon epithelial cells in vitro.

METHODS

HCT116 and HT-29 human colon epithelial cell lines endogenously expressing FFA4 were used. Intracellular Ca(2+) concentration ([Ca(2+)]i) was measured in fura 2-AM-loaded cells with fluorescence spectrophotometry. RT-PCR and immunohistochemistry were used to detect FFA4.

RESULTS

Ten to 100 μmol/L of omega-3 polyunsaturated fatty acids α-linolenic acid (αLA) or eicosapentaenoic acid (EPA) induced dose-dependent [Ca(2+)]i increase in HCT116 and HT-29 cells, whereas docosahexaenoic acid (DHA) had no effect. In addition, the omega-6 fatty acids linoleic acid and γ-linoleic acid also dose-dependently increase [Ca(2+)]i, but the mono-unsaturated fatty acid oleic acid and saturated fatty acids such as stearic acid and palmitic acid had no effect. In HCT116 and HT-29 cells, the αLA-induced [Ca(2+)]i increase was partially inhibited by pretreatment with EGTA, phospholipase C inhibitor edelfosine, cADPR inhibitors 8-bro-cADPR or DAB, and abolished by pretreatment with Ca(2+)ATPase inhibitor thapsigargin, but was not affected by Gi/o protein inhibitor PTX or IP3R inhibitor 2-APB.

CONCLUSION

Omega-3 and omega-6 long-chain polyunsaturated fatty acids (C18-20) induce Ca(2+) mobilization responses in human colonic epithelial cells in vitro through activation of FFA4 and PTX-insensitive Gi/o protein, followed by Ca(2+) release from thapsigargin-sensitive Ca(2+) stores and Ca(2+) influx across the plasma membrane.

摘要

目的

游离脂肪酸受体4(FFA4;以前称为GPR120)是ω-3多不饱和脂肪酸的G蛋白偶联受体(GPCR)。已发现FFA4在小鼠和人类的小肠及结肠中表达。在本研究中,我们在体外研究ω-3多不饱和脂肪酸对人结肠上皮细胞中FFA4的影响。

方法

使用内源性表达FFA4的HCT116和HT-29人结肠上皮细胞系。用荧光分光光度法在负载fura 2-AM的细胞中测量细胞内Ca(2+)浓度([Ca(2+)]i)。采用RT-PCR和免疫组织化学检测FFA4。

结果

10至100μmol/L的ω-3多不饱和脂肪酸α-亚麻酸(αLA)或二十碳五烯酸(EPA)在HCT116和HT-29细胞中诱导剂量依赖性的[Ca(2+)]i增加,而二十二碳六烯酸(DHA)无作用。此外,ω-6脂肪酸亚油酸和γ-亚麻酸也剂量依赖性地增加[Ca(2+)]i,但单不饱和脂肪酸油酸以及饱和脂肪酸如硬脂酸和棕榈酸无作用。在HCT116和HT-29细胞中,αLA诱导的[Ca(2+)]i增加被EGTA预处理、磷脂酶C抑制剂依地福新、环ADP核糖(cADPR)抑制剂8-溴-cADPR或DAB部分抑制,并被Ca(2+)ATP酶抑制剂毒胡萝卜素预处理消除,但不受Gi/o蛋白抑制剂PTX或肌醇三磷酸受体(IP3R)抑制剂2-APB影响。

结论

ω-3和ω-6长链多不饱和脂肪酸(C18 - 20)在体外通过激活FFA4和对PTX不敏感的Gi/o蛋白,继而从对毒胡萝卜素敏感的Ca(2+)储存库释放Ca(2+)并使Ca(2+)跨质膜内流,诱导人结肠上皮细胞中的Ca(2+)动员反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aef/4648116/28a19b7d6e00/aps201529f1.jpg

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