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模拟微重力诱导的 PI3K-nos2b 信号对斑马鱼心血管丛网络形成的影响。

Effect of simulated microgravity induced PI3K-nos2b signalling on zebrafish cardiovascular plexus network formation.

机构信息

Key Laboratory of Biorheological and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing 400030, China; The School of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan Province 646000, China.

Key Laboratory of Biorheological and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, Bioengineering College of Chongqing University, Chongqing 400030, China.

出版信息

J Biomech. 2019 Apr 18;87:83-92. doi: 10.1016/j.jbiomech.2019.02.019. Epub 2019 Feb 28.

Abstract

Local abnormal angiogenesis and cardiovascular system reorganization have been observed in embryos exposed to a simulated microgravity (SM) environment. In this study, changes in key molecular signals and pathways in cardiovascular development have been investigated under microgravity conditions. In particular, the caudal vein plexus (CVP) network, formed by sprouting angiogenesis has been chosen. Zebrafish embryos were exposed to SM using a ground-based microgravity bioreactor for 24 and 36 h. The SM was observed to have no effect on the zebrafish length, tail width and incubation time whereas it was observed to significantly reduce the heart rate frequency and to promote abnormal development of the CVP network in the embryos. Nitric oxide (NO) content demonstrated that the total proteins in zebrafish embryos were significantly higher in SM than in the control group grown under normal conditions. It was then preliminarily determined how NO signals were involved in SM regulated zebrafish CVP network formation. nos2b MO was injected and CVP network evolution was observed in 36 h post fertilization (hpf) under SM condition. The results showed that the CVP network formation was considerably decreased in the nos2b MO treated group. However, this inhibition of the CVP network development was not observed in control MO group, indicating that nos2b is involved in the SM-regulated vascular development process in zebrafish. Moreover, specific phosphoinositide 3-kinase (PI3K) inhibitors such as LY294002 were also tested on zebrafish embryos under SM condition. This treatment significantly inhibited the formation of zebrafish CVP network. Furthermore, overexpression of nos2b partly rescued the LY294002-caused CVP network failure. Therefore, it can be concluded that SM affects zebrafish CVP network remodeling by enhancing angiogenesis. Additionally, the PI3K-nos2b signaling pathway is involved in this process.

摘要

胚胎在模拟微重力(SM)环境下会出现局部异常血管生成和心血管系统重组。本研究探讨了在微重力条件下心血管发育关键分子信号和途径的变化。特别是选择了由发芽血管生成形成的尾静脉丛(CVP)网络。使用地面微重力生物反应器将斑马鱼胚胎暴露于 SM 中 24 和 36 小时。SM 对斑马鱼的长度、尾巴宽度和孵化时间没有影响,但观察到它显著降低了心率频率,并促进了胚胎中 CVP 网络的异常发育。一氧化氮(NO)含量表明,SM 中的斑马鱼胚胎总蛋白明显高于在正常条件下生长的对照组。然后初步确定了 NO 信号如何参与 SM 调节的斑马鱼 CVP 网络形成。在 SM 条件下,在受精后 36 小时(hpf)注射 nos2b MO 并观察 CVP 网络的演变。结果表明,nos2b MO 处理组的 CVP 网络形成明显减少。然而,在对照 MO 组中未观察到这种 CVP 网络发育的抑制,表明 nos2b 参与了 SM 调节的斑马鱼血管发育过程。此外,还在 SM 条件下对斑马鱼胚胎进行了特定的磷酸肌醇 3-激酶(PI3K)抑制剂如 LY294002 的测试。这种处理显著抑制了斑马鱼 CVP 网络的形成。此外,nos2b 的过表达部分挽救了 LY294002 引起的 CVP 网络故障。因此,可以得出结论,SM 通过增强血管生成来影响斑马鱼 CVP 网络重塑。此外,PI3K-nos2b 信号通路参与了这一过程。

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