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<p>Transforming growth factor-β (TGF-β) can promote myocardial fibrosis (MF). However, it was reported that regulatory T cells (Tregs) can reverse MF via secretion of anti-inflammatory cytokine IL-10. At present, the pathway of pro-myocardial fibrosis factors secreted by Tregs cells is not clear. Kv1.3 channel is closely related to the activation of Treg cells, which is a potential target for immuno-regulation. Here, we investigated whether the communication between co-cultured cells of Tregs and cardiac fibroblasts (CFs) was affected by the reduction of TGF-β secreted from Tregs by Kv1.3 knockdown, as well as whether exosome pathway mediates the pro-myocardial fibrosis process of Tregs. After co-culturing of Tregs transfected by RNA interference Kv1.3 potassium channel with CFs, we measured CFs proliferation, Tregs-derived exosomes level, TGF-β levels and expression of fibrosis-associated factors. In addition, after co-culturing of exosome extracted from Tregs with CFs, we also measured the CFs proliferation and TGF-β levels. Co-culture of CFs with Tregs-exosomes elevated TGF-β level, and promoted CFs proliferation. Importantly, Tregs transfected by RNA interference Kv1.3 channel reduced the accumulation of TGF-β, inhibited CFs proliferation and exocome releasing. The proliferation of CFs was activated with the co-cultured Tregs-exosome by secretion of TGF-β, which could be inhibited by blocking the Kv1.3 channel. Tregs could promote the viability of CFs by increasing the level of TGF-β primarily in the co-culture system, which was mediated by exosomes secreted from Tregs; and the promotion procedure could be inhibited by knocking-down of Kv1.3 potassium channels directly. </p>

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Activation/inactivation of Tregs mediated by Kv1.3 potassium channels synergistically with exosome secretion to regulate myocardial fibrosis

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年12月1日

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  • Mengjia Li,
  • Yang Wu,
  • Yongzheng Zhang,
  • Zihang Wang,
  • Lufeng Cheng,
  • Xiang Xie

摘要

Transforming growth factor-β (TGF-β) can promote myocardial fibrosis (MF). However, it was reported that regulatory T cells (Tregs) can reverse MF via secretion of anti-inflammatory cytokine IL-10. At present, the pathway of pro-myocardial fibrosis factors secreted by Tregs cells is not clear. Kv1.3 channel is closely related to the activation of Treg cells, which is a potential target for immuno-regulation. Here, we investigated whether the communication between co-cultured cells of Tregs and cardiac fibroblasts (CFs) was affected by the reduction of TGF-β secreted from Tregs by Kv1.3 knockdown, as well as whether exosome pathway mediates the pro-myocardial fibrosis process of Tregs. After co-culturing of Tregs transfected by RNA interference Kv1.3 potassium channel with CFs, we measured CFs proliferation, Tregs-derived exosomes level, TGF-β levels and expression of fibrosis-associated factors. In addition, after co-culturing of exosome extracted from Tregs with CFs, we also measured the CFs proliferation and TGF-β levels. Co-culture of CFs with Tregs-exosomes elevated TGF-β level, and promoted CFs proliferation. Importantly, Tregs transfected by RNA interference Kv1.3 channel reduced the accumulation of TGF-β, inhibited CFs proliferation and exocome releasing. The proliferation of CFs was activated with the co-cultured Tregs-exosome by secretion of TGF-β, which could be inhibited by blocking the Kv1.3 channel. Tregs could promote the viability of CFs by increasing the level of TGF-β primarily in the co-culture system, which was mediated by exosomes secreted from Tregs; and the promotion procedure could be inhibited by knocking-down of Kv1.3 potassium channels directly.