Chinese Journal of Nephrology, Dialysis & Transplantation ›› 2017, Vol. 26 ›› Issue (2): 142-147.DOI: 10.3969/cndt.j.issn.1006-298X.2017.02.008
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Objective:To study the expression of transient receptor potential melastatin 3 (TRPM3) in the internationally recognized db/db mouse model of type 2 diabetic nephropathy, in human tubular epithelial cells (HK2) and conditionally immortalized mouse podocytes (MPC) under high glucose. Methodology:Twenty male fiveweek db/db mice were randomly divided into two groups (each n=10), and we used db/m mice of littermate as the normal control group (n=20). At the age of 10 weeks and 18 weeks, the samples of blood, urine and renal tissues were collected. The biochemical indexes were measured. The expression of TRPM3 in renal tissues was assessed by Western blot、qRTPCR and immunohistochemistry respectively. HK2 and MPC were cultured in vitro and divided into the following groups: (1) Normal control group (Dglucose 56 mmol/L); (2) Mannitol group (Dglucose 56 mmol/L+Dmannitol 244 mmol/L); (3) High glucose group (Dglucose 30 mmol/L).The corresponding indexes were measured at 24th,48th and 72th hour. Western blot and qRTPCR were used to examine the expression of TRPM3 in protein and mRNA. Results:Compared with the 10w db/m mice, the expression of TRPM3 in the 10w db/db and 18w db/db mice was increased significantly (P<005). In cultured HK2 and MPC, the protein and mRNA expression of TRPM3 was increased in High glucose group, compared with the normal control group (P<005). Conclusion:TRPM3 can be expressed in the renal tubules and glomerulus of mouse, and high glucose can induce the higher expression of TRPM3 in HK2 and MPC. TRPM3 may be involved in the development of diabetic nephropathy.
YU Haixia,,GUO Jia,LIU Dongwei,et al. Expression of transient receptor potential melastatin 3 in diabetic nephropathy mice[J]. Chinese Journal of Nephrology, Dialysis & Transplantation, 2017, 26(2): 142-147.
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URL: http://www.njcndt.com/EN/10.3969/cndt.j.issn.1006-298X.2017.02.008
http://www.njcndt.com/EN/Y2017/V26/I2/142