Aging phenotype(s) in kidneys of diabetic mice are p66ShcA dependent

• Published in: American journal of physiology. Renal physiology Vol. 315; no. 6; p. F1833
• Main Authors: Vashistha, H, Marrero, L, Reiss, K, Cohen, A J, Malhotra, A, Javed, T, Bradley, A, Abbruscato, F, Giusti, S, Jimenez, A, Mehra, S, Kaushal, D, Giorgio, M, Pelicci, P G, Kakoki, M, Singhal, P C, Bunnell, B, Meggs, L G
• Format: Journal Article
• Language: English
• Published: United States 01-12-2018
• Subjects: Age Factors; Aging - genetics; Aging - metabolism; Aging - pathology; Animals; Apoptosis; Cell Differentiation; Cell Proliferation; Cells, Cultured; Cellular Senescence; Diabetic Nephropathies - genetics; Diabetic Nephropathies - metabolism; Diabetic Nephropathies - pathology; Disease Models, Animal; Glucose - metabolism; Kidney - metabolism; Kidney - pathology; Mesenchymal Stem Cells - metabolism; Mesenchymal Stem Cells - pathology; Mice, Knockout; Phenotype; Reactive Oxygen Species - metabolism; Src Homology 2 Domain-Containing, Transforming Protein 1 - deficiency; Src Homology 2 Domain-Containing, Transforming Protein 1 - genetics; Src Homology 2 Domain-Containing, Transforming Protein 1 - metabolism; Stem Cell Niche; Wnt Signaling Pathway; diabetes; aging
• ISSN: 1522-1466
• DOI: 10.1152/ajprenal.00608.2017

The p66ShcA protein controls cellular responses to oxidative stress, senescence, and apoptosis. Here, we test the hypothesis that aging phenotype(s) commonly associated with the broad category of chronic kidney disease are accelerated in diabetic kidneys and linked to the p66ShcA locus. At the organ level, tissue stem cells antagonize senescent phenotypes by replacing old dysfunctional cells. Using established methods, we isolated a highly purified population of stem cell antigen-1-positive mesenchymal stem cells (Sca-1
MSCs) from kidneys of wild-type (WT) and p66 knockout (p66 KO) mice. Cells were plated in culture medium containing normal glucose (NG) or high glucose (HG). Reactive oxygen species (ROS) metabolism was substantially increased in WT MSCs in HG medium in association with increased cell death by apoptosis and acquisition of the senescent phenotype. DNA microarray analysis detected striking differences in the expression profiles of WT and p66 KO-MSCs in HG medium. Unexpectedly, the analysis for p66 KO-MSCs revealed upregulation of Wnt genes implicated in self-renewal and differentiation. To test the in vivo consequences of constitutive p66 expression in diabetic kidneys, we crossed the Akita diabetic mouse with the p66KO mouse. Homozygous mutation at the p66 locus delays or prevents aging phenotype(s) in the kidney that may be precursors to diabetic nephropathy.