The differential regulation of Smad7 in kidney tubule cells by connective tissue growth factor and transforming growth factor-beta1

Authors

  • WEIER QI,

    1. Kolling Institute, Department of Medicine, Royal North Shore Hospital and University of Sydney,
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    • *

      Dr Weier Qi and Dr Xinming Chen equally contributed to this work.

  • XINMING CHEN,

    1. Kolling Institute, Department of Medicine, Royal North Shore Hospital and University of Sydney,
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    • *

      Dr Weier Qi and Dr Xinming Chen equally contributed to this work.

  • STEPHEN TWIGG,

    1. Department of Medicine, University of Sydney, and
    2. Royal Prince Alfred Hospital, Sydney, New South Wales,
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  • YUAN ZHANG,

    1. Department of Medicine, University of Melbourne, St Vincent's Hospital, Melbourne, Victoria, Australia; and
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  • RICHARD E GILBERT,

    1. Department of Medicine, University of Melbourne, St Vincent's Hospital, Melbourne, Victoria, Australia; and
    2. Department Medicine, University of Toronto, St. Michael's Hospital, Toronto, Ontario, Canada
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  • DARREN J KELLY,

    1. Department of Medicine, University of Melbourne, St Vincent's Hospital, Melbourne, Victoria, Australia; and
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  • CAROL A POLLOCK

    Corresponding author
    1. Kolling Institute, Department of Medicine, Royal North Shore Hospital and University of Sydney,
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Professor Carol A Pollock, Department of Medicine, Level 3, Wallace Freeborn Professorial Block, Royal North Shore Hospital, St Leonards, NSW 2065, Australia. Email: carpol@med.usyd.edu.au

Summary:

Aims:  Smad7 is an inhibitory Smad that regulates transforming growth factor-β (TGF-β) signaling. Connective tissue growth factor (CTGF) is recognized as a potent downstream mediator of the fibrogenic effects of TGF-β1. SMAD binding sites have been identified in both TGF-β and CTGF promoters. The effect of CTGF on Smad7 expression and its role in the regulation of Smad7 induced by TGF-β1 in renal tubular cells is unknown.

Methods:  Human model of proximal tubular cells (HK-2 cells) was used and confirmed using a diabetic rat model. RT-PCR was performed to measure Smad7, TGF-β1 and Smad2 and ELISA was performed to measure active TGF-β1. CTGF or TGF-β1 was silenced in HK-2 cells using siRNA methodology.

Results:  TGF-β1 induced Smad7 in a time-dependent manner, peaking at 30 min (P < 0.0005) but sustained up to 24 hrs (p < 0.005). Conversely, CTGF reduced Smad7, which was maximal at 24 hrs (p < 0.05). This was supported by our in vivo data demonstrating that CTGF protein significantly increased while Smad7 mRNA level was reduced in a diabetic rat model. The basal expression level of Smad7 decreased in TGF-β1 silenced cells compared to cells transfected with non-specific siRNA (p < 0.0005). The basal expression level of Smad7 increased in CTGF silenced cells (p < 0.05), which was increased by TGF-β1 (p < 0.005). Both mRNA and protein levels of TGF-β1 decreased in CTGF silenced cells (p < 0.05 and p < 0.005 respectively) accompanied by reduction in Smad2 mRNA level in CTGF silenced cells.

Conclusions:  Smad7 is induced rapidly by TGF-β1 limiting the response to TGF-β1. CTGF likely plays a key role in promoting TGF-β1 activity by decreasing the availability of Smad7 and increasing Smad2.

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