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Transcription factor Twist1 drives fibroblast activation to promote kidney fibrosis via signaling proteins Prrx1/TNC.

Publication ,  Journal Article
Sun, L; Liu, L; Jiang, J; Liu, K; Zhu, J; Wu, L; Lu, X; Huang, Z; Yuan, Y; Crowley, SD; Mao, H; Xing, C; Ren, J
Published in: Kidney Int
November 2024

The transcription factor Twist1 plays a vital role in normal development in many tissue systems and continues to be important throughout life. However, inappropriate Twist1 activity has been associated with kidney injury and fibrosis, though the underlying mechanisms involved remain incomplete. Here, we explored the role of Twist1 in regulating fibroblast behaviors and the development kidney fibrosis. Initially Twist1 protein and activity was found to be markedly increased within interstitial myofibroblasts in fibrotic kidneys in both humans and rodents. Treatment of rat kidney interstitial fibroblasts with transforming growth factor-β1 (a profibrotic factor) also induced Twist1 expression in vitro. Gain- and loss-of-function experiments supported that Twist1 signaling was responsible for transforming growth factor-β1-induced fibroblast activation and fetal bovine serum-induced fibroblast proliferation. Mechanistically, Twist1 protein promoted kidney fibroblast activation by driving the expression of downstream signaling proteins, Prrx1 and Tnc. Twist1 directly enhanced binding to the promoter of Prrx1 but not TNC, whereas the promoter of TNC was directly bound by Prrx1. Finally, mice with fibroblast-specific deletion of Twist1 exhibited less Prrx1 and TNC protein abundance, interstitial extracellular matrix deposition and kidney inflammation in both the unilateral ureteral obstruction and ischemic-reperfusion injury-induced-kidney fibrotic models. Inhibition of Twist1 signaling with Harmine, a β-carboline alkaloid, improved extracellular matrix deposition in both injury models. Thus, our results suggest that Twist1 signaling promotes the activation and proliferation of kidney fibroblasts, contributing to the development of interstitial fibrosis, offering a potential therapeutic target for chronic kidney disease.

Duke Scholars

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Published In

Kidney Int

DOI

EISSN

1523-1755

Publication Date

November 2024

Volume

106

Issue

5

Start / End Page

840 / 855

Location

United States

Related Subject Headings

  • Urology & Nephrology
  • Ureteral Obstruction
  • Twist-Related Protein 1
  • Transforming Growth Factor beta1
  • Signal Transduction
  • Reperfusion Injury
  • Rats
  • Nuclear Proteins
  • Myofibroblasts
  • Mice, Knockout
 

Citation

APA
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Sun, L., Liu, L., Jiang, J., Liu, K., Zhu, J., Wu, L., … Ren, J. (2024). Transcription factor Twist1 drives fibroblast activation to promote kidney fibrosis via signaling proteins Prrx1/TNC. Kidney Int, 106(5), 840–855. https://doi.org/10.1016/j.kint.2024.07.028
Sun, Lianqin, Lishan Liu, Juanjuan Jiang, Kang Liu, Jingfeng Zhu, Lin Wu, Xiaohan Lu, et al. “Transcription factor Twist1 drives fibroblast activation to promote kidney fibrosis via signaling proteins Prrx1/TNC.Kidney Int 106, no. 5 (November 2024): 840–55. https://doi.org/10.1016/j.kint.2024.07.028.
Sun L, Liu L, Jiang J, Liu K, Zhu J, Wu L, et al. Transcription factor Twist1 drives fibroblast activation to promote kidney fibrosis via signaling proteins Prrx1/TNC. Kidney Int. 2024 Nov;106(5):840–55.
Sun, Lianqin, et al. “Transcription factor Twist1 drives fibroblast activation to promote kidney fibrosis via signaling proteins Prrx1/TNC.Kidney Int, vol. 106, no. 5, Nov. 2024, pp. 840–55. Pubmed, doi:10.1016/j.kint.2024.07.028.
Sun L, Liu L, Jiang J, Liu K, Zhu J, Wu L, Lu X, Huang Z, Yuan Y, Crowley SD, Mao H, Xing C, Ren J. Transcription factor Twist1 drives fibroblast activation to promote kidney fibrosis via signaling proteins Prrx1/TNC. Kidney Int. 2024 Nov;106(5):840–855.
Journal cover image

Published In

Kidney Int

DOI

EISSN

1523-1755

Publication Date

November 2024

Volume

106

Issue

5

Start / End Page

840 / 855

Location

United States

Related Subject Headings

  • Urology & Nephrology
  • Ureteral Obstruction
  • Twist-Related Protein 1
  • Transforming Growth Factor beta1
  • Signal Transduction
  • Reperfusion Injury
  • Rats
  • Nuclear Proteins
  • Myofibroblasts
  • Mice, Knockout