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Article

Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells

  • Authors:
    • Gangyi Chen
    • Xingju Zhang
    • Chao Li
    • Yingying Lin
    • Yu Meng
    • Shuifu Tang
  • View Affiliations / Copyright

    Affiliations: Division of Nephrology, The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine, Guangzhou, Guangdong 510405, P.R. China, BGI‑Shenzhen, Shenzhen, Guangdong 518083, P.R. China , Shenzhen Engineering Laboratory for Genomics‑Assisted Animal Breeding, BGI‑Shenzhen, Shenzhen, Guangdong 518083, P.R. China , Department of Internal Medicine, Guangdong Second Provincial Traditional Chinese Medicine Hospital, Guangzhou, Guangdong 510095, P.R. China, Division of Nephrology, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong 510630, P.R. China
  • Pages: 2471-2476
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    Published online on: August 18, 2014
       https://doi.org/10.3892/mmr.2014.2497
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Abstract

Tanshinone ⅡA (TⅡA) is widely used for the treatment of a number human diseases, including diabetic nephropathy (DN) (1). The present study was performed to examine the role of the transforming growth factor β (TGFβ)/p65 pathway under TⅡA treatment in a glomerular mesangial cell model of DN. Firstly, it was identified that TⅡA inhibited the proliferation of HBZY‑1 cells, while simultaneously suppressing the expression of TGFβ and p65. In addition, glucose-induced HBZY‑1 cells were treated with TⅡA, si‑TGFβ and si‑p65. The results revealed that si‑TGFβ or si‑p65 were able to inhibit the proliferation of HBZY‑1 cells as well. Finally, the expression of TGFβ and p65 in a rat model of DN treated with TⅡA was detected. The results demonstrated that renal hypertrophy and 24 h urinary protein excretion were ameliorated in TⅡA-treated rats with DN. Furthermore, it was revealed that the protein levels of TGFβ and p65 were decreased in the DN rats following TⅡA treatment. In conclusion, the present study demonstrated that TGFβ and p65 were activated by TⅡA in HBZY‑1 cells. In addition, the expression of TGFβ and of p65 was downregulated in rats with DN treated with TⅡA.
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Copy and paste a formatted citation
Spandidos Publications style
Chen G, Zhang X, Li C, Lin Y, Meng Y and Tang S: Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells. Mol Med Rep 10: 2471-2476, 2014.
APA
Chen, G., Zhang, X., Li, C., Lin, Y., Meng, Y., & Tang, S. (2014). Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells. Molecular Medicine Reports, 10, 2471-2476. https://doi.org/10.3892/mmr.2014.2497
MLA
Chen, G., Zhang, X., Li, C., Lin, Y., Meng, Y., Tang, S."Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells". Molecular Medicine Reports 10.5 (2014): 2471-2476.
Chicago
Chen, G., Zhang, X., Li, C., Lin, Y., Meng, Y., Tang, S."Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells". Molecular Medicine Reports 10, no. 5 (2014): 2471-2476. https://doi.org/10.3892/mmr.2014.2497
Copy and paste a formatted citation
x
Spandidos Publications style
Chen G, Zhang X, Li C, Lin Y, Meng Y and Tang S: Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells. Mol Med Rep 10: 2471-2476, 2014.
APA
Chen, G., Zhang, X., Li, C., Lin, Y., Meng, Y., & Tang, S. (2014). Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells. Molecular Medicine Reports, 10, 2471-2476. https://doi.org/10.3892/mmr.2014.2497
MLA
Chen, G., Zhang, X., Li, C., Lin, Y., Meng, Y., Tang, S."Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells". Molecular Medicine Reports 10.5 (2014): 2471-2476.
Chicago
Chen, G., Zhang, X., Li, C., Lin, Y., Meng, Y., Tang, S."Role of the TGFβ/p65 pathway in tanshinone ⅡA-treated HBZY‑1 cells". Molecular Medicine Reports 10, no. 5 (2014): 2471-2476. https://doi.org/10.3892/mmr.2014.2497
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