Nissen Silas Boye, Weiner Alexis T, Suyama Kaye, Bosch Pablo Sanchez, Yu Maiya, Song Song, Gu Yuan, Dunn Alexander R, Axelrod Jeffrey D
Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
The Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, Copenhagen, Denmark.
bioRxiv. 2025 Jan 31:2024.10.21.619498. doi: 10.1101/2024.10.21.619498.
In planar cell polarity (PCP) signaling, distinct molecular subcomplexes segregate to opposite sides of each cell, where they interact across intercellular junctions to form asymmetric clusters. Although proximal-distal asymmetry within PCP clusters is the defining feature of PCP signaling, the mechanism by which this asymmetry develops remains unclear. Here, we developed a method to count the number of monomers of core PCP proteins within individual clusters in live animals and used it to infer the underlying molecular dynamics of cluster assembly and polarization. Measurements over time and space in wild type and in strategically chosen mutants demonstrate that cluster assembly is required for polarization, and together with mathematical modeling provide evidence that clusters become increasingly asymmetric and correctly oriented as they increase in size. We propose that cluster assembly dynamics amplify weak and noisy inputs into a robust cellular output, in this case cell and tissue-level polarization.
在平面细胞极性(PCP)信号传导中,不同的分子亚复合物分隔到每个细胞的相对两侧,在那里它们通过细胞间连接相互作用形成不对称簇。尽管PCP簇内的近端 - 远端不对称是PCP信号传导的决定性特征,但这种不对称形成的机制仍不清楚。在这里,我们开发了一种方法来计算活体动物单个簇内核心PCP蛋白的单体数量,并利用它来推断簇组装和极化的潜在分子动力学。在野生型和经过精心选择的突变体中进行的时空测量表明,簇组装是极化所必需的,并且与数学建模一起提供了证据,表明簇随着尺寸的增加而变得越来越不对称且方向正确。我们提出,簇组装动力学将微弱且有噪声的输入放大为强大的细胞输出,在这种情况下是细胞和组织水平的极化。