Transcriptional regulation and therapeutic targeting of P2X7 receptors in diabetic nephropathy

Robert Menzies, John W.r. Booth, John Mullins, Matthew Bailey, Frederick W K Tam, Jill T. Norman, Robert J Unwin

Research output: Contribution to conferenceAbstract

Abstract / Description of output

Purine P2X7 receptors are essential components of pro-inflammatory signalling, functionally expressed on multiple immune and non-immune cells. Renal biopsies from patients with diabetic nephropathy show widespread, glomerular mesangial expansion, immune cell infiltration and fibrosis. Here we show that in diabetic patients, renal P2X7 expression is associated with severe mesangial expansion, impaired glomerular filtration (≥40ml/min), and increased fibrosis (50%+) compared with non-diabetic controls. P2rx7-deficient mice developed STZ-induced hyperglycaemia similar to controls but had reduced glomerular macrophage attraction and collagen IV deposition. Activation of P2X7 was investigated in a rat model of diabetic nephropathy. Wister rats underwent uninephrectomy and STZ-induction. Whole kidney P2rx7 mRNA expression was increased (2.2-fold; P<0.05) compared with sham controls by 8 weeks of induction. Glomerular and interstitial macrophage accrual increased, reflecting the pathology seen in patient biopsies. Rats were then randomly selected to receive drug vehicle or selective P2X7R antagonist (AZ11657312; 50mg/kg IP) twice daily for the following 4-weeks. P2X7R antagonism supressed transcription of pro-inflammatory signalling molecules compared with the vehicle group, and reduced interstitial macrophage accrual. These data suggest that P2rx7 contributes to renal inflammation in diabetics and P2X7R antagonists may have therapeutic potential.
Original languageEnglish
Publication statusPublished - 2017


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