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Axl tyrosine kinase protects against tubulo-interstitial apoptosis and progression of renal failure in a murine model of chronic kidney disease and hyperphosphataemia

Hyde, Gareth D.; Taylor, Rebecca F.; Ashton, Nick; Borland, Samantha J.; Sing Geoffrey Wu, Hon; Gilmore, Andrew P.; Canfield, Ann E.

Axl tyrosine kinase protects against tubulo-interstitial apoptosis and progression of renal failure in a murine model of chronic kidney disease and hyperphosphataemia Thumbnail


Authors

Gareth D. Hyde

Rebecca F. Taylor

Nick Ashton

Hon Sing Geoffrey Wu

Andrew P. Gilmore

Ann E. Canfield



Abstract

Chronic kidney disease (CKD) is defined as the progressive loss of renal function often involving glomerular, tubulo- interstitial and vascular pathology. CKD is associated with vascular calcification; the extent of which predicts morbidity and mortality. However, the molecular regulation of these events and the progression of chronic kidney disease are not fully elucidated. To investigate the function of Axl receptor tyrosine kinase in CKD we performed a sub-total nephrectomy and fed high phosphate (1%) diet to Axl+/+ and Axl2/2 mice. Plasma Gas6 (Axl’ ligand), renal Axl expression and downstream Akt signalling were all significantly up-regulated in Axl+/+ mice following renal mass reduction and high phosphate diet, compared to age-matched controls. Axl2/2 mice had significantly enhanced uraemia, reduced bodyweight and significantly reduced survival following sub-total nephrectomy and high phosphate diet compared to Axl+/+ mice; only 45% of Axl2/2 mice survived to 14 weeks post-surgery compared to 87% of Axl+/+ mice. Histological analysis of kidney remnants revealed no effect of loss of Axl on glomerular hypertrophy, calcification or renal sclerosis but identified significantly increased tubulo-interstitial apoptosis in Axl2/2 mice. Vascular calcification was not induced in Axl+/+ or Axl2/2 mice in the time frame we were able to examine. In conclusion, we identify the up-regulation of Gas6/Axl signalling as a protective mechanism which reduces tubulo-interstitial apoptosis and slows progression to end-stage renal failure in the murine nephrectomy and high phosphate diet model of CKD.

Citation

Hyde, G. D., Taylor, R. F., Ashton, N., Borland, S. J., Sing Geoffrey Wu, H., Gilmore, A. P., & Canfield, A. E. (2014). Axl tyrosine kinase protects against tubulo-interstitial apoptosis and progression of renal failure in a murine model of chronic kidney disease and hyperphosphataemia. PloS one, 9(7), Article e102096. https://doi.org/10.1371/journal.pone.0102096

Journal Article Type Article
Acceptance Date Jun 13, 2013
Publication Date Jul 14, 2014
Deposit Date Dec 19, 2024
Publicly Available Date Dec 20, 2024
Journal PLoS ONE
Print ISSN 1932-6203
Publisher Public Library of Science
Peer Reviewed Peer Reviewed
Volume 9
Issue 7
Article Number e102096
DOI https://doi.org/10.1371/journal.pone.0102096

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