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Form and function of F-actin during biomineralization revealed from live experiments on foraminifera

机译:从有孔虫的活体实验中揭示了生物矿化过程中F-肌动蛋白的形式和功能

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摘要

Although the emergence of complex biomineralized forms has been investigated for over a century, still little is known on how single cells control morphology of skeletal structures, such as frustules, shells, spicules, or scales. We have run experiments on the shell formation in foraminifera, unicellular, mainly marine organisms that can build shells by successive additions of chambers. We used live imaging to discover that all stages of chamber/shell formation are controlled by dedicated actin-driven pseudopodial structures. Successive reorganization of an F-actin meshwork, associated with microtubular structures, is actively involved in formation of protective envelope, followed by dynamic scaffolding of chamber morphology. Then lamellar dynamic templates create a confined space and control mineralization separated from seawater. These observations exclude extracellular calcification assumed in selected foraminiferal clades, and instead suggest a semiintracellular biomineralization pattern known from other unicellular calcifying and silicifying organisms. These results give a challenging prospect to decipher the vital effect on geochemical proxies applied to paleoceanographic reconstructions. They have further implications for understanding multiscale complexity of biomineralization and show a prospect for material science applications.
机译:尽管已经研究了复杂的生物矿化形式的出现了一个多世纪,但对于单个细胞如何控制骨骼结构(例如,rust壳,壳,针状体或鳞片)的形态知之甚少。我们对有孔虫的壳形成进行了实验,有孔虫是单细胞的主要是海洋生物,可以通过相继添加小室来构建壳。我们使用实时成像发现腔室/壳形成的所有阶段均受专用的肌动蛋白驱动的假足结构控制。与微管结构相关的F-肌动蛋白网的连续重组积极参与保护性包膜的形成,随后动态形成腔室形态。然后,层状动态模板创建一个密闭空间并控制与海水分离的矿化作用。这些观察结果排除了在选定的有孔虫进化枝中假定的细胞外钙化,而是暗示了其他单细胞钙化和硅化生物体中已知的半细胞内生物矿化模式。这些结果为破译对应用于古海洋重建的地球化学代理的重要影响提供了具有挑战性的前景。它们对于理解生物矿化的多尺度复杂性具有进一步的意义,并显示了材料科学应用的前景。

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