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在. 的视网膜晶状体发育过程中,细胞类型特异性的机械反应和肌球蛋白动力学。

Cell-type-specific mechanical response and myosin dynamics during retinal lens development in .

机构信息

MRC Laboratory for Molecular Cell Biology.

Department of Physics and Astronomy, and.

出版信息

Mol Biol Cell. 2020 Jun 15;31(13):1355-1369. doi: 10.1091/mbc.E19-09-0523. Epub 2020 Apr 22.

Abstract

During organogenesis, different cell types need to work together to generate functional multicellular structures. To study this process, we made use of the genetically tractable fly retina, with a focus on the mechanisms that coordinate morphogenesis between the different epithelial cell types that make up the optical lens. Our work shows that these epithelial cells present contractile apical-medial MyosinII meshworks, which control the apical area and junctional geometry of these cells during lens development. Our study also suggests that these MyosinII meshworks drive cell shape changes in response to external forces, and thus they mediate part of the biomechanical coupling that takes place between these cells. Importantly, our work, including mathematical modeling of forces and material stiffness during lens development, raises the possibility that increased cell stiffness acts as a mechanism for limiting this mechanical coupling. We propose this might be required in complex tissues, where different cell types undergo concurrent morphogenesis and where averaging out of forces across cells could compromise individual cell apical geometry and thereby organ function.

摘要

在器官发生过程中,不同的细胞类型需要协同工作,以产生具有功能的多细胞结构。为了研究这个过程,我们利用遗传上易于操作的果蝇视网膜作为模型,重点研究协调构成光学晶状体的不同上皮细胞类型之间形态发生的机制。我们的工作表明,这些上皮细胞具有收缩性的顶端-中部肌球蛋白 II 网格,它在晶状体发育过程中控制这些细胞的顶端区域和连接几何形状。我们的研究还表明,这些肌球蛋白 II 网格可以响应外力驱动细胞形状变化,因此介导了这些细胞之间发生的部分生物力学耦合。重要的是,我们的工作包括在晶状体发育过程中对力和材料硬度进行数学建模,提出了增加细胞硬度作为限制这种机械耦合的机制的可能性。我们认为,在不同细胞类型同时发生形态发生的复杂组织中,这种机制是必需的,因为在细胞之间平均分配力可能会损害单个细胞的顶端几何形状,从而影响器官功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a31/7353141/d18f583b1575/mbc-31-1355-g001.jpg

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