Institute of Ophthalmology, University College London, London, EC1V 9EL, UK.
Institute of Epigenetics and Stem Cells, Helmholtz Zentrum München, D-81377, Munich, Germany.
Sci Rep. 2018 Jan 19;8(1):1204. doi: 10.1038/s41598-018-19579-5.
Tight junctions are required for the formation of tissue barriers and function as suppressors of signalling mechanisms that control gene expression and cell behaviour; however, little is known about the physiological and developmental importance of such signalling functions. Here, we demonstrate that depletion of MarvelD3, a transmembrane protein of tight junctions, disrupts neural crest formation and, consequently, development of neural crest-derived tissues during Xenopus embryogenesis. Using embryos and explant cultures combined with a small molecule inhibitor or mutant mRNAs, we show that MarvelD3 is required to attenuate JNK signalling during neural crest induction and that inhibition of JNK pathway activation is sufficient to rescue the phenotype induced by MarvelD3 depletion. Direct JNK stimulation disrupts neural crest development, supporting the importance of negative regulation of JNK. Our data identify the junctional protein MarvelD3 as an essential regulator of early vertebrate development and neural crest induction and, thereby, link tight junctions to the control and timing of JNK signalling during early development.
紧密连接对于组织屏障的形成是必需的,并作为控制基因表达和细胞行为的信号机制的抑制剂发挥作用;然而,对于这种信号功能的生理和发育重要性知之甚少。在这里,我们证明了跨膜紧密连接蛋白 MarvelD3 的耗竭会破坏神经嵴的形成,从而破坏神经嵴衍生组织在非洲爪蟾胚胎发生过程中的发育。我们使用胚胎和外植体培养物结合小分子抑制剂或突变的 mRNA,表明 MarvelD3 在神经嵴诱导过程中需要减弱 JNK 信号,并且抑制 JNK 途径的激活足以挽救 MarvelD3 耗竭引起的表型。直接 JNK 刺激会破坏神经嵴的发育,这支持了 JNK 的负调控的重要性。我们的数据将连接蛋白 MarvelD3 确定为早期脊椎动物发育和神经嵴诱导的必需调节剂,从而将紧密连接与早期发育过程中 JNK 信号的控制和定时联系起来。