RESUMO
Tight junctions (TJs) are essential components of epithelial tissues connecting neighboring cells to provide protective barriers. While their general function to seal compartments is well understood, their role in collective cell migration is largely unexplored. Here, the importance of the TJ zonula occludens (ZO) proteins ZO1 and ZO2 for epithelial migration is investigated employing video microscopy in conjunction with velocimetry, segmentation, cell tracking, and atomic force microscopy/spectroscopy. The results indicate that ZO proteins are necessary for fast and coherent migration. In particular, ZO1 and 2 loss (dKD) induces actomyosin remodeling away from the central cortex towards the periphery of individual cells, resulting in altered viscoelastic properties. A tug-of-war emerges between two subpopulations of cells with distinct morphological and mechanical properties: 1) smaller and highly contractile cells with an outward bulging apical membrane, and 2) larger, flattened cells, which, due to tensile stress, display a higher proliferation rate. In response, the cell density increases, leading to crowding-induced jamming and more small cells over time. Co-cultures comprising wildtype and dKD cells migrate inefficiently due to phase separation based on differences in contractility rather than differential adhesion. This study shows that ZO proteins are necessary for efficient collective cell migration by maintaining tissue fluidity and controlling proliferation.
Assuntos
Movimento Celular/fisiologia , Junções Íntimas/química , Junções Íntimas/metabolismo , Proteínas da Zônula de Oclusão/química , Proteínas da Zônula de Oclusão/metabolismo , Animais , Linhagem Celular , Cães , Células Epiteliais/química , Células Epiteliais/metabolismo , Epitélio/química , Epitélio/metabolismoRESUMO
Tight junctions are cell-adhesion complexes that seal tissues and are involved in cell polarity and signaling. Supra-molecular assembly and positioning of tight junctions as continuous networks of adhesion strands are dependent on the membrane-associated scaffolding proteins ZO1 and ZO2. To understand how zona occludens (ZO) proteins organize junction assembly, we performed quantitative cell biology and in vitro reconstitution experiments. We discovered that ZO proteins self-organize membrane-attached compartments via phase separation. We identified the multivalent interactions of the conserved PDZ-SH3-GuK supra-domain as the driver of phase separation. These interactions are regulated by phosphorylation and intra-molecular binding. Formation of condensed ZO protein compartments is sufficient to specifically enrich and localize tight-junction proteins, including adhesion receptors, cytoskeletal adapters, and transcription factors. Our results suggest that an active-phase transition of ZO proteins into a condensed membrane-bound compartment drives claudin polymerization and coalescence of a continuous tight-junction belt.
Assuntos
Junções Íntimas/genética , Proteínas da Zônula de Oclusão/genética , Proteína da Zônula de Oclusão-1/genética , Proteína da Zônula de Oclusão-2/genética , Animais , Sítios de Ligação/genética , Adesão Celular/genética , Polaridade Celular/genética , Cães , Células HEK293 , Humanos , Células Madin Darby de Rim Canino , Proteínas de Membrana/genética , Domínios PDZ/genética , Fosfoproteínas/genética , Fosforilação/genética , Ligação Proteica/genética , Transdução de Sinais/genética , Junções Íntimas/metabolismo , Proteínas da Zônula de Oclusão/química , Proteínas da Zônula de Oclusão/ultraestrutura , Proteína da Zônula de Oclusão-1/química , Proteína da Zônula de Oclusão-1/ultraestrutura , Proteína da Zônula de Oclusão-2/química , Proteína da Zônula de Oclusão-2/ultraestrutura , Domínios de Homologia de src/genéticaRESUMO
O-GlcNAcylation of proteins regulates important cellular processes. A few reports noted that O-GlcNAcylation exhibits cross-talk with tyrosine phosphorylation. With an activity-based microarray analysis of 256 tyrosine kinase peptide substrates, we found that phosphorylation of six peptides by Jak2 inhibits their subsequent O-GlcNAcylation. However, O-GlcNAcylation has no detectable effect on their subsequent phosphorylation. A specific peptide (ZO3_357_371), derived from the ZO-3 protein, was studied in detail. Kinetic results show that the presence of a phosphate at Tyr364 of ZO3_357_371 slows the O-GlcNAcylation of nearby Ser369, while the presence of a GlcNAc at Ser369 has no significant effect on the phosphorylation of this peptide at Tyr364. These findings provide a glimpse into the new paradigm for cellular signaling control by cross-talk.
