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LL-37对映体激活TRPV2和BKCa通道可刺激癌细胞的钙内流和迁移。

Activation of TRPV2 and BKCa channels by the LL-37 enantiomers stimulates calcium entry and migration of cancer cells.

作者信息

Gambade Audrey, Zreika Sami, Guéguinou Maxime, Chourpa Igor, Fromont Gaëlle, Bouchet Ana Maria, Burlaud-Gaillard Julien, Potier-Cartereau Marie, Roger Sébastien, Aucagne Vincent, Chevalier Stéphan, Vandier Christophe, Goupille Caroline, Weber Günther

机构信息

Inserm, UMR1069, Nutrition, Croissance et Cancer, Tours, France.

Department of Medical Lab Technology, Jinan University, Tripoli, Lebanon.

出版信息

Oncotarget. 2016 Apr 26;7(17):23785-800. doi: 10.18632/oncotarget.8122.

Abstract

Expression of the antimicrobial peptide hCAP18/LL-37 is associated to malignancy in various cancer forms, stimulating cell migration and metastasis. We report that LL-37 induces migration of three cancer cell lines by activating the TRPV2 calcium-permeable channel and recruiting it to pseudopodia through activation of the PI3K/AKT pathway. Ca2+ entry through TRPV2 cooperated with a K+ efflux through the BKCa channel. In a panel of human breast tumors, the expression of TRPV2 and LL-37 was found to be positively correlated. The D-enantiomer of LL-37 showed identical effects as the L-peptide, suggesting that no binding to a specific receptor was involved. LL-37 attached to caveolae and pseudopodia membranes and decreased membrane fluidity, suggesting that a modification of the physical properties of the lipid membrane bilayer was the underlying mechanism of its effects.

摘要

抗菌肽hCAP18/LL-37的表达与多种癌症形式的恶性肿瘤相关,可刺激细胞迁移和转移。我们报告称,LL-37通过激活TRPV2钙通透通道并通过PI3K/AKT途径的激活将其募集到伪足,从而诱导三种癌细胞系的迁移。通过TRPV2的Ca2+内流与通过BKCa通道的K+外流协同作用。在一组人类乳腺肿瘤中,发现TRPV2和LL-37的表达呈正相关。LL-37的D-对映体显示出与L-肽相同的作用,表明不涉及与特定受体的结合。LL-37附着于小窝和伪足膜并降低膜流动性,表明脂质膜双层物理性质的改变是其作用的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b6/5029663/70149e41eeb2/oncotarget-07-23785-g001.jpg

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