IFOM ETS, The AIRC Institute of Molecular Oncology, Milan, Italy.
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, Segrate, Italy.
Cell Rep. 2023 Aug 29;42(8):113001. doi: 10.1016/j.celrep.2023.113001. Epub 2023 Aug 16.
Tissue fluidification and collective motility are pivotal in regulating embryonic morphogenesis, wound healing, and tumor metastasis. These processes frequently require that each cell constituent of a tissue coordinates its migration activity and directed motion through the oriented extension of lamellipodium cell protrusions, promoted by RAC1 activity. While the upstream RAC1 regulators in individual migratory cells or leader cells during invasion or wound healing are well characterized, how RAC1 is controlled in follower cells remains unknown. Here, we identify a MYO6-DOCK7 axis essential for spatially restricting RAC1 activity in a planar polarized fashion in model tissue monolayers. The MYO6-DOCK7 axis specifically controls the extension of cryptic lamellipodia required to drive tissue fluidification and cooperative-mode motion in otherwise solid and static carcinoma cell collectives.
组织液流和集体运动在调节胚胎形态发生、伤口愈合和肿瘤转移中起着关键作用。这些过程通常需要组织中的每个细胞成分通过 RAC1 活性促进片状伪足细胞突起的定向延伸来协调其迁移活动和定向运动。虽然在侵袭或伤口愈合过程中单个迁移细胞或先导细胞中的上游 RAC1 调节剂已得到很好的描述,但在跟随细胞中 RAC1 如何被控制尚不清楚。在这里,我们确定了一个 MYO6-DOCK7 轴,该轴对于在模型组织单层中以平面极化的方式空间限制 RAC1 活性是必不可少的。MYO6-DOCK7 轴专门控制需要驱动组织液流和合作模式运动的隐蔽片状伪足的延伸,否则固着静止的癌细胞集体将无法进行这些运动。