TY - JOUR
T1 - Vinculin is required to maintain glomerular barrier integrity
AU - Lausecker, Franziska
AU - Tian, Xuefei
AU - Inoue, Kazunori
AU - Wang, Zhen
AU - Pedigo, Christopher E.
AU - Hassan, Hossam
AU - Liu, Chang
AU - Zimmer, Margaret
AU - Jinno, Stephanie
AU - Huckle, Abby L
AU - Hamidi, Hellyeh
AU - Ross, Robert S.
AU - Zent, Roy
AU - Ballestrem, Christoph
AU - Lennon, Rachel
AU - Ishibe, Shuta
PY - 2017
Y1 - 2017
N2 - Cell-matrix interactions and podocyte intercellular junctions are key for maintaining the glomerular filtration barrier. Vinculin, a cytoplasmic protein, couples actin filaments to integrin-mediated cell-matrix adhesions and to cadherin-based intercellular junctions. Here, we examined the role of vinculin in podocytes by the generation of a podocyte-specific knockout mouse. Mice lacking podocyte vinculin had increased albuminuria and foot process effacement following injury in vivo. Analysis of primary podocytes isolated from the mutant mice revealed defects in cell protrusions, altered focal adhesion size and signaling, as well as impaired cell migration. Furthermore, we found a marked mislocalization of the intercellular junction protein zonula occludens-1. In kidney sections from patients with focal segmental glomerulosclerosis, minimal change disease and membranous nephropathy, we observed dramatic differences in the expression levels and localization of vinculin. Thus, our results suggest that vinculin is necessary to maintain the integrity of the glomerular filtration barrier by modulating podocyte foot processes and stabilizing intercellular junctions.
AB - Cell-matrix interactions and podocyte intercellular junctions are key for maintaining the glomerular filtration barrier. Vinculin, a cytoplasmic protein, couples actin filaments to integrin-mediated cell-matrix adhesions and to cadherin-based intercellular junctions. Here, we examined the role of vinculin in podocytes by the generation of a podocyte-specific knockout mouse. Mice lacking podocyte vinculin had increased albuminuria and foot process effacement following injury in vivo. Analysis of primary podocytes isolated from the mutant mice revealed defects in cell protrusions, altered focal adhesion size and signaling, as well as impaired cell migration. Furthermore, we found a marked mislocalization of the intercellular junction protein zonula occludens-1. In kidney sections from patients with focal segmental glomerulosclerosis, minimal change disease and membranous nephropathy, we observed dramatic differences in the expression levels and localization of vinculin. Thus, our results suggest that vinculin is necessary to maintain the integrity of the glomerular filtration barrier by modulating podocyte foot processes and stabilizing intercellular junctions.
KW - glomerular disease
KW - podocyte
KW - cell adhesion
KW - vinculin
KW - glomerular filtration barrier
U2 - 10.1016/j.kint.2017.09.021
DO - 10.1016/j.kint.2017.09.021
M3 - Article
SN - 0085-2538
JO - Kidney International
JF - Kidney International
ER -