Cell Reports (Aug 2023)

A planar polarized MYO6-DOCK7-RAC1 axis promotes tissue fluidification in mammary epithelia

  • Luca Menin,
  • Janine Weber,
  • Stefano Villa,
  • Emanuele Martini,
  • Elena Maspero,
  • Carlos A. Niño,
  • Valeria Cancila,
  • Alessandro Poli,
  • Paolo Maiuri,
  • Andrea Palamidessi,
  • Emanuela Frittoli,
  • Fabrizio Bianchi,
  • Claudio Tripodo,
  • Kylie J. Walters,
  • Fabio Giavazzi,
  • Giorgio Scita,
  • Simona Polo

Journal volume & issue
Vol. 42, no. 8
p. 113001

Abstract

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Summary: 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.

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