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Innate immune and proinflammatory signals activate the Hippo pathway via a Tak1-STRIPAK-Tao axis.

Yinan YangHuijing ZhouXiawei HuangChengfang WuKewei ZhengJingrong DengYonggang ZhengJiahui WangXiaofeng ChiXianjue MaHuimin PanRui ShenDuojia PanBo Liu
Published in: Nature communications (2024)
The Hippo pathway controls developmental, homeostatic and regenerative tissue growth, and is frequently dysregulated in various diseases. Although this pathway can be activated by innate immune/inflammatory stimuli, the underlying mechanism is not fully understood. Here, we identify a conserved signaling cascade that leads to Hippo pathway activation by innate immune/inflammatory signals. We show that Tak1, a key kinase in innate immune/inflammatory signaling, activates the Hippo pathway by inducing the lysosomal degradation of Cka, an essential subunit of the STRIPAK PP2A complex that suppresses Hippo signaling. Suppression of STRIPAK results in the activation of Hippo pathway through Tao-Hpo signaling. We further show that Tak1-mediated Hippo signaling is involved in processes ranging from cell death to phagocytosis and innate immune memory. Our findings thus reveal a molecular connection between innate immune/inflammatory signaling and the evolutionally conserved Hippo pathway, thus contributing to our understanding of infectious, inflammatory and malignant diseases.
Keyphrases
  • innate immune
  • cell death
  • oxidative stress
  • stem cells
  • signaling pathway
  • mesenchymal stem cells
  • cell proliferation
  • gene expression
  • bone marrow
  • dna methylation
  • cell therapy
  • protein kinase