Expression of leptin receptor in renal tubules is sparse but implicated in leptin-dependent kidney gene expression and function

Leptin regulates energy balance via leptin receptors expressed in central and peripheral tissues, but little is known about leptinsensitive kidney genes and the role of the tubular leptin receptor (Lepr) in response to a high-fat diet (HFD). Quantitative RT-PCR analysis of Lepr splice variants A, B, and C revealed a ratio of 100:10:1 in the mouse kidney cortex and medulla, with medullary levels being -10 times higher. Leptin replacement in ob/ob mice for 6 days reduced hyperphagia, hyperglycemia, and albuminuria, associated with normalization of kidney mRNA expression of molecular markers of glycolysis, gluconeogenesis, amino acid synthesis, and megalin. Normalization of leptin for 7 h in ob/ob mice did not normalize hyperglycemia or albuminuria. Tubular knockdown of Lepr [Pax8-Lepr knockout (KO)] and in situ hybridization revealed a minor fraction of Lepr mRNA in tubular cells compared with endothelial cells. Nevertheless, Pax8-Lepr KO mice had lower kidney weight. Moreover, while HFD-induced hyperleptinemia, increases in kidney weight and glomerular filtration rate, and a modest blood pressure lowering effect were similar compared with controls, they showed a blunted rise in albuminuria. Use of Pax8-Lepr KO and leptin replacement in ob/ob mice identified acetoacetyl-CoA synthetase and gremlin 1 as tubular Lepr-sensitive genes that are increased and reduced by leptin, respectively. In conclusion, leptin deficiency may increase albuminuria via systemic metabolic effects that impinge on kidney megalin expression, whereas hyperleptinemia may induce albuminuria by direct tubular Lepr effects. Implications of Lepr variants and the novel tubular Lepr/acetoacetyl-CoA synthetase/gremlin 1 axis remain to be determined.NEW & NOTEWORTHY This study provides new insights into kidney gene expression of leptin receptor splice variants, leptinsensitive kidney gene expression, and the role of the leptin receptor in renal tubular cells for the response to diet-induced hyperleptinemia and obesity including albuminuria.

Automated summary

This study reveals the expression of leptin receptor splice variants in the kidney, and the role of the tubular leptin receptor in response to a high-fat diet. Leptin replacement in mice reduces hyperphagia, hyperglycemia, and albuminuria, and normalizes kidney mRNA expression of key metabolic markers. Additionally, the study identifies tubular Lepr-sensitive genes, including acetoacetyl-CoA synthetase and gremlin 1. These findings provide valuable insights into the role of the leptin receptor in renal function and metabolism.