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10.1007/s00109-014-1209-3

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suck abstract from ncbi


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pmid25249008      J+Mol+Med+(Berl) 2014 ; 92 (12): 1245-56
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  • Urinary semaphorin 3A correlates with diabetic proteinuria and mediates diabetic nephropathy and associated inflammation in mice #MMPMID25249008
  • Mohamed R; Ranganathan P; Jayakumar C; Nauta FL; Gansevoort RT; Weintraub NL; Brands M; Ramesh G
  • J Mol Med (Berl) 2014[Dec]; 92 (12): 1245-56 PMID25249008show ga
  • Semaphorin3A (sema3A) was recently identified as an early diagnostic biomarker of acute kidney injury. However, its role as a biomarker and/or mediator of chronic kidney disease (CKD) related to diabetic nephropathy is unknown. We examined the expression of sema3A in diabetic animal models and in humans and tested whether sema3A plays a pathogenic role in the development of diabetic nephropathy. The expression of sema3A was localized to podocytes and epithelial cells in distal tubules and collecting ducts in control animals, and its expression was increased following induction of diabetes. Quantification of sema3A urinary excretion in three different diabetic mouse models showed that excretion was increased as early as 2 weeks after induction of diabetes and increased over time, in conjunction with the development of nephropathy. Consistent with the mouse data, increased sema3A urinary excretion was detected in diabetic patients with albuminuria, particularly in those with macroalbuminuria. Genetic ablation of sema3A, or pharmacological inhibition with a novel sema3A inhibitory peptide, protected against diabetes-induced albuminuria, kidney fibrosis, inflammation, oxidative stress and renal dysfunction. We conclude that sema3A is both a biomarker and a mediator of diabetic kidney disease and could be a promising therapeutic target in diabetic nephropathy.
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