基质金属蛋白酶Nas15调控脊索动物脊索膜的形成和扩张

IF 2.4 3区 环境科学与生态学 Q2 ECOLOGY
Jianqing Bi, Yonghang Ge, Zhuqing Wang, Hongzhe Peng, Bo Dong
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引用次数: 0

摘要

管腔的形成是生物管道构建的关键过程,在营养和废物运输、气体交换和结构支撑等各种生理过程中至关重要。然而,人们对肾小管管腔发育的机制仍不完全清楚。在本研究中,我们发现了一种基质金属蛋白酶--Nas15,它富集于洋葱胚胎脊索顶端结构域。在脊索内腔形成和扩张过程中,Nas15基因的表达水平显著增加。Nas15功能缺失会导致脊索软骨发育异常。此外,酵母双杂交筛选和CO-IP结果表明,磷酸酶2催化亚基α(PPP2CA)与Nas15存在物理相互作用。PPP2CA还通过定位Nas15参与了脊索管腔的形成。此外,我们还研究了层粘连蛋白在 Nas15 干扰胚胎中的分布。总之,我们的研究结果揭示了脊索细胞如何通过金属蛋白酶介导的 ECM 定位来调节管腔扩张的机制。这些发现有助于深入了解小管器官管腔形成的机制,并为人类异常管腔形成疾病的研究提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Matrix metalloproteinase Nas15 regulates the lumen formation and expansion in Ciona notochord
Lumen formation, as a key process of biological tube construction, is essential in various physiological processes such as nutrient and waste transporting, gas exchanging, and structural supporting. However, the mechanisms underlying tubular lumen development are still not fully understood. In the present study, we identified a matrix metalloproteinase, Nas15, which is enriched in the apical domain of the Ciona embryonic notochord. The expression level of the Nas15 gene significantly increased during notochord lumen formation and expansion. Nas15 loss-of-function resulted in abnormal notochord lumen expansion in Ciona embryos. Besides, yeast two-hybrid screening and CO-IP results indicated a Phosphatase 2 Catalytic Subunit Alpha (PPP2CA) physically interacted with Nas15. PPP2CA also involved in notochord lumen formation via localizing Nas15. Furthermore, we investigated the distribution of laminin in Nas15 disrupted embryos. In conclusion, our results revealed a mechanisms of how notochord cells regulating lumen expansion via metalloproteinase-mediated ECM localization. This findings provide insight into the mechanisms of tubular organ lumen formation and serve as a reference for research on human abnormal lumenogenesis diseases.
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来源期刊
Frontiers in Ecology and Evolution
Frontiers in Ecology and Evolution Environmental Science-Ecology
CiteScore
4.00
自引率
6.70%
发文量
1143
审稿时长
12 weeks
期刊介绍: Frontiers in Ecology and Evolution publishes rigorously peer-reviewed research across fundamental and applied sciences, to provide ecological and evolutionary insights into our natural and anthropogenic world, and how it should best be managed. Field Chief Editor Mark A. Elgar at the University of Melbourne is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Eminent biologist and theist Theodosius Dobzhansky’s astute observation that “Nothing in biology makes sense except in the light of evolution” has arguably even broader relevance now than when it was first penned in The American Biology Teacher in 1973. One could similarly argue that not much in evolution makes sense without recourse to ecological concepts: understanding diversity — from microbial adaptations to species assemblages — requires insights from both ecological and evolutionary disciplines. Nowadays, technological developments from other fields allow us to address unprecedented ecological and evolutionary questions of astonishing detail, impressive breadth and compelling inference. The specialty sections of Frontiers in Ecology and Evolution will publish, under a single platform, contemporary, rigorous research, reviews, opinions, and commentaries that cover the spectrum of ecological and evolutionary inquiry, both fundamental and applied. Articles are peer-reviewed according to the Frontiers review guidelines, which evaluate manuscripts on objective editorial criteria. Through this unique, Frontiers platform for open-access publishing and research networking, Frontiers in Ecology and Evolution aims to provide colleagues and the broader community with ecological and evolutionary insights into our natural and anthropogenic world, and how it might best be managed.
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