Regulatory Effect of 1,25(OH)2D3 on TGF-β1 and miR-130b Expression in Streptozotocin-Induced Diabetic Nephropathy in Rats

Author:

Liu Yuetong1ORCID,Yang Ye2ORCID,Wang Qin2ORCID,Kahaer Apaer2ORCID,Zhang Jiyun3ORCID,Liao Jing2ORCID,Abudureyimu Mairemugu2ORCID,Yahefu Reyila2ORCID,Qi Jing4ORCID,Zhao Lei4ORCID,Zhu Jun5ORCID

Affiliation:

1. Department of Endocrinology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, Xinjiang, China

2. Department of No. 1 Cadres, The Second Affiliated Hospital of Xinjiang Medical University, Urumqi 830063, Xinjiang, China

3. Department of Rheumatology and Immunology, The Second Affiliated Hospital of Xinjiang Medical University, Urumqi 830063, Xinjiang, China

4. Department of Chu Medical, The Second Affiliated Hospital of Xinjiang Medical University, Urumqi 830063, Xinjiang, China

5. Department of Endocrinology, People’s Hospital of Shenzhen Baoan District, The Second School of Clinical Medicine, Southern Medical University, Shenzhen, Guangdong 518101, China

Abstract

Objective. To investigate the role of microRNA-130b in 1,25(OH)2D3 mediated improvement of renal fibrosis via transforming growth factor-beta 1 in a rat model of diabetic nephropathy (DN). Methods. DN was induced in 30 rats by intraperitoneal injection of streptozotocin. These rats were randomly allocated to the DN group, TGF-β1 overexpression group (in situ injection of TGF-β1 lentivirus to kidney tissues), and TGF-β1 siRNA group (in situ injection of TGF-β1 siRNA lentivirus to kidney tissues). Rats with different expression levels of TGF-β1 were administered 1,25(OH)2D3 (0.03 μg/kg/d) or peanut oil as control. DN rats were treated only with peanut oil. All rats were randomly divided into five groups (n = 6 per group): TGF-β1 overexpression + oil, TGF-β1 overexpression + 1,25(OH)2D3, TGF-β1 siRNA + oil, TGF-β1 siRNA + 1,25(OH)2D3, and DN + oil groups. After 37 days, kidney samples were collected and the expression of TGF-β1 and miR-130b was determined by real-time PCR, western blotting, and immunohistochemistry. Hematoxylin and eosin staining and Masson staining were used to evaluate kidney morphological and fibrogenic changes. Differences were determined using ANOVA and Student’s t-test. Results. RT-PCR, western blotting, and immunohistochemistry revealed that interference of TGF-β1 significantly decreased mRNA and protein levels of TGF-β1 in renal tissues of DN rats compared to those in renal tissues of rats overexpressing TGF-β1 (p<0.05). Histological analysis showed that upregulated TGF-β1 led to disorganized kidney structure and severe kidney fibrosis. The expression of miR-130b was significantly lowered upon lentivirus-mediated overexpression of TGF-β1 than upon downregulation of TGF-β1 (p<0.05). Treatment with 1,25(OH)2D3 led to a significant reduction of TGF-β1 at the mRNA and protein levels (both p<0.05), improvement of renal structure and fibrosis, and an increase in miR-130b expression (p<0.05). Conclusion. TGF-β1 can decrease the expression of miR-130b in kidney tissues of DN rats. Moreover, miR-130b may be involved in the protective effect of 1,25(OH)2D3 on renal fibrosis via TGF-β1.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Endocrine and Autonomic Systems,Endocrinology,Endocrinology, Diabetes and Metabolism

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