2026/01/26 by Shensen Li, Fabian Bock, Olga M. Viquez +12 · 1 voice
Biochemistry, Genetics and Molecular Biology · Medicine · #Cell Adhesion Molecules Research #Nuclear Structure and Function #Renal and related cancers
paper · pdf · doi:10.1242/dev.205044
openalex publication_date 2026/01/26 · openalex created_date 2026/01/27 · openalex updated_date 2026/07/02
The kidney collecting system develops from the ureteric bud (UB), which undergoes multiple rounds of iterative branching. This process is controlled by growth factors and requires the interaction between the extracellular matrix and β1-containing integrin receptors. Integrin affinity for its ligands is regulated by integrin-binding proteins including kindlins, which bind well-defined motifs within the β subunit cytoplasmic tail. We show that mice expressing β1 integrins with mutations that abrogate kindlin binding in the developing UB have mild medullary hypoplasia and a moderate branching defect. Collecting duct (CD) cells expressing the same mutations in the β1 subunit have moderate tubulogenesis, spreading and adhesion defects, but show intact growth factor-dependent signaling. In contrast, mice lacking kindlins in the UB are anephric due to a complete absence of UB budding. Kindlin-knockout CD cells are unable to spread, adhere or respond to growth factors, irrespective of whether the integrins are bound to a ligand. Thus, in addition to regulating integrin function, kindlins mediate crucial growth factor signaling required for initial UB formation.