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Uninephrectomy and class II PI3K‐C2β inactivation synergistically protect against obesity, insulin resistance and liver steatosis in mice
Author(s) -
Alliouachene Samira,
Kieswich Julius E.,
Bilanges Benoit,
McCafferty Kieran,
Thiemermann Christoph,
Vanhaesebroeck Bart,
Yaqoob Muhammad M.
Publication year - 2021
Publication title -
american journal of transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.89
H-Index - 188
eISSN - 1600-6143
pISSN - 1600-6135
DOI - 10.1111/ajt.16470
Subject(s) - insulin resistance , steatosis , medicine , endocrinology , insulin , kidney , fatty liver , pi3k/akt/mtor pathway , insulin receptor , kidney disease , type 2 diabetes , protein kinase b , diabetes mellitus , biology , signal transduction , disease , biochemistry
Uninephrectomy (UNx) in living kidney donors for transplantation is now routine clinical practice. While chronic kidney disease, due to bilateral kidney dysfunction, is associated with insulin resistance, liver steatosis, and type 2 diabetes, the metabolic impact of UNx remains unclear. To better understand the crosstalk between the kidney and insulin target tissues, we studied the metabolic consequences of UNx and the potential involvement of class II PI3K‐C2β, the inactivation of which has been reported to result in insulin sensitization. Mice underwent UNx or sham operation followed by either normal chow or high‐fat diet (HFD). Seventeen weeks post‐UNx, mice showed improved glucose tolerance, insulin sensitivity, and decreased HFD‐induced liver steatosis. This was associated with an enhanced serum FGF21 and insulin‐stimulated Akt signaling in the liver and muscle of both lean and obese mice. Remarkably, the combination of UNx and PI3K‐C2β inactivation protected against HFD‐induced obesity and further potentiated the metabolic improvement observed in WT UNx mice correlating with a synergistic increase in metabolic tissues of (1) insulin‐stimulated Akt signaling (2) FGFR1 and βKlotho expression. We demonstrated a potential beneficial effect of kidney donation and more effectively with PI3K‐C2β inactivation to protect against metabolic disorders through a mutual insulin/FGF21 sensitization