Linvill Katie, Russell Liam J, Vanderleest Timothy E, Miao Hui, Xie Yi, Blankenship J Todd, Loerke Dinah
Department of Physics and Astronomy, University of Denver, Denver, CO, USA.
Department of Biological Sciences, University of Denver, Denver, CO, USA.
J Cell Biol. 2025 Apr 3;224(4). doi: 10.1083/jcb.202309069. Epub 2025 Jan 23.
In the early Drosophila embryo, germband elongation is driven by oriented cell intercalation through t1 transitions, where vertical (dorsal-ventral aligned) interfaces contract and then resolve into new horizontal (anterior-posterior aligned) interfaces. Here, we show that contractile events produce a continuous "rectification" of cell interfaces, in which interfaces systematically rotate toward more vertical orientations. As interfaces rotate, their behavior transitions from elongating to contractile regimes, indicating that the planar polarized identities of cell-cell interfaces are continuously re-interpreted in time depending on their orientation angle. Rotating interfaces acquire higher levels of Myosin II motor proteins as they become more vertical, while disruptions to the contractile molecular machinery reduce the rates of rotation. Through this angle rectification, the available pool of contractile interfaces is continuously replenished, as new interfaces acquire a contractile identity through rotation. Thus, individual cells acquire additional interfaces that are capable of undergoing t1 transitions, allowing cells to participate in multiple staggered rounds of intercalation events.
在早期果蝇胚胎中,胚带延长是由通过t1转变的定向细胞插入驱动的,其中垂直(背腹对齐)界面收缩,然后分解为新的水平(前后对齐)界面。在这里,我们表明收缩事件会对细胞界面产生连续的“整流”,其中界面会系统地朝着更垂直的方向旋转。随着界面旋转,它们的行为从伸长状态转变为收缩状态,这表明细胞 - 细胞界面的平面极化特性会根据其取向角随时间不断重新解释。旋转的界面在变得更加垂直时会获得更高水平的肌球蛋白II运动蛋白,而对收缩分子机制的破坏会降低旋转速率。通过这种角度整流,收缩界面的可用库会不断得到补充,因为新的界面通过旋转获得收缩特性。因此,单个细胞会获得能够经历t1转变的额外界面,从而使细胞能够参与多轮交错的插入事件。