α-Parvin regulation of cell re-arrangement is critical for ureteric bud branching morphogenesis
Dong, X.; Bock, F. M.; Hashmi, A.; Bulus, N.; Mernaugh, G.; Gonzalez-Lliberos, G. B.; Li, S.; Zhu, W.; Melzer, M.; Brown, K. L.; Miler, C.; Viquez, O. M.; Montanez, E.; Pozzi, A.; Wickstrom, S.; Zent, R.
Show abstract
All branched tubular structures, including the kidney collecting system, are formed by branching morphogenesis, a process that includes tip branching and trunk narrowing. Tight control of cell movement and rearrangements is a prerequisite for branching morphogenesis. The role of integrin-associated adhesion proteins in coordinating actin dynamics and cell rearrangements during branching morphogenesis is poorly understood. Here we used 3D live imaging of mouse ureteric bud branching to show that -parvin, a component of the integrin binding ILK-PINCH-Parvin (IPP) complex, regulates tip branching and tubule thinning by inhibiting excessive cell adhesion and actin polymerization. Mechanistically, -parvin promotes actin turnover by inhibiting activation of the small GTPases RhoA and Cdc42, which in turn enhances the severing function of the actin regulatory protein, cofilin. These results underscore the importance of adhesion protein-regulated actin dynamics in the critical process of cell rearrangement, which is required for branching morphogenesis. TeaserScaffold protein -parvin limits cell adhesion and actin polymerization, enabling cell rearrangements that drive kidney branching
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Kidney single-cell atlas reveals myeloid heterogeneity in progression and regression of kidney disease. 96%
- Hyperactivation of YAP/TAZ drives alterations in mesangial cells through stabilization of N-MYC in diabetic nephropathy 96%
- Nephron progenitor maintenance is controlled through FGFs and Sprouty1 Interaction 95%
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
- PKD1 and PKD2 mRNA cis-inhibition drives polycystic kidney disease progression 96%
- HIFalpha isoform specific activities drive cell-type specificity of VHL-associated oncogenesis 95%
- Age-Dependent Changes in the Progenitor Translatome Coordinated in part by Tsc1 Increase Perception of Signaling Inputs to End Nephrogenesis 95%
Similar papers in this journal
- A weak link with actin organizes tight junctions to control epithelial permeability 94%
- A p53-dependent translational program directs tissue-selective phenotypes in a model of ribosomopathies 93%
- Limiting Self-Renewal of the Basal Compartment Induces Differentiation and Alters Evolution of Mammary Tumors 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.