Marine cyclotripeptide X-13 promotes angiogenesis in zebrafish and human endothelial cells via PI3K/Akt/eNOS signaling pathways.

Marine cyclotripeptide X-13 promotes angiogenesis in zebrafish and human endothelial cells via PI3K/Akt/eNOS signaling pathways.
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海洋环三肽 X-13 通过 PI3K/Akt/eNOS 信号通路促进斑马鱼和人内皮细胞的血管生成

DOI:
10.3390/md10061307
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发表时间:
2012-06
期刊:
影响因子:
5.4
通讯作者:
Pei Z
Pei Z
中科院分区:
医学2区
文献类型:
--
作者:
Lu XL;Xu ZL;Yao XL;Su FJ;Ye CH;Li J;Lin YC;Wang GL;Zeng JS;Huang RX;Ou JS;Sun HS;Wang LP;Pang JY;Pei Z

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环三肽X-13是从红树林真菌Xylaria sp. (no. 13)中分离得到的新型海洋化合物xyloallenoide a的核心。2508)。我们发现X-13剂量依赖性诱导斑马鱼胚胎和人内皮细胞血管生成,并伴有eNOS、Akt磷酸化和NO释放增加。LY294002或L-NAME抑制PI3K/Akt/eNOS抑制x -13诱导的血管生成。目前的研究表明,X-13通过PI3K/Akt/eNOS通路促进血管生成。
Cyclotripeptide X-13 is a core of novel marine compound xyloallenoide A isolated from mangrove fungus Xylaria sp. (no. 2508). We found that X-13 dose-dependently induced angiogenesis in zebrafish embryos and in human endothelial cells, which was accompanied by increased phosphorylation of eNOS and Akt and NO release. Inhibition of PI3K/Akt/eNOS by LY294002 or L-NAME suppressed X-13-induced angiogenesis. The present work demonstrates that X-13 promotes angiogenesis via PI3K/Akt/eNOS pathways.
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