RRC ID 35995
Author Kai T, Tsukamoto Y, Hijiya N, Tokunaga A, Nakada C, Uchida T, Daa T, Iha H, Takahashi M, Nomura T, Sato F, Mimata H, Ikawa M, Seto M, Matsuura K, Moriyama M.
Title Kidney-specific knockout of Sav1 in the mouse promotes hyperproliferation of renal tubular epithelium through suppression of the Hippo pathway.
Journal J. Pathol.
Abstract We have previously reported that Salvador homologue 1 (SAV1), a component of the Hippo pathway, is significantly down-regulated in high-grade clear cell renal cell carcinoma (ccRCC) due to 14q copy number loss, and that this down-regulation contributes to the proliferation and survival of renal tubular epithelial cells through activation of Yes-associated protein 1 (YAP1), a downstream target of the Hippo pathway. However, the impact of SAV1 loss on the proliferation and survival of kidney cells in vivo remained to be determined. To address this issue, we generated kidney-specific Sav1-knockout (Cdh16-Cre;Sav1(fl/fl) ) mice. Sav1 deficiency enhanced the proliferation of renal tubular epithelial cells in Cdh16-Cre;Sav1(fl/fl) mice, accompanied by nuclear localization of Yap1, suggesting suppression of the Hippo pathway. Sav1 deficiency in renal tubules also caused structural and cellular abnormalities of the epithelial cells, including significant enlargement of their nuclei. Furthermore, Cdh16-Cre;Sav1(fl/fl) mice developed both glomerular and tubular cysts. Although lining cells of the glomerular cysts showed no atypia, those of the tubular cysts showed variations in cell size and nuclear shape, which became more severe as the mice aged. In aged Cdh16-Cre;Sav1(fl/fl) mice, we observed focal disruption of proximal tubules and perivascular lymphocytic infiltration. In conclusion, Sav1 is required for the maintenance of growth, nuclear size and structure of renal tubules under physiological conditions, and its deficiency leads to the acquisition of enhanced proliferation of renal epithelial cells through suppression of Hippo signalling.
Volume 239(1)
Pages 97-108
Published 2016-5
DOI 10.1002/path.4706
PMID 26913567
MeSH Adaptor Proteins, Signal Transducing / metabolism Adenocarcinoma, Clear Cell / etiology Animals Cadherins / metabolism Cell Cycle Proteins / deficiency* Cell Proliferation / physiology* Embryonic Stem Cells / metabolism Epithelial Cells / metabolism Kidney Neoplasms / etiology Kidney Tubules / metabolism* Mice, Transgenic Nephritis / etiology Phosphoproteins / metabolism Protein-Serine-Threonine Kinases / metabolism* Signal Transduction / physiology
IF 6.253
Times Cited 1
Mice C57BL/6-Tg(CAG-flpe)36Ito/ItoRbrc(RBRC01834)