天生的免疫和促炎信号通过Tak1-STRIPAK-Tao轴激活河马路径
Yinan Yang1, Huijing Zhou1, Xiawei Huang1
1State Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen, Fujian, 361102, China.
Nature communications
|January 3, 2024
概括
天生的免疫信号通过Tak1激酶激活Hippo路径,导致Cka降解和STRIPAK复合体抑制. 这将天生的免疫与疾病中的组织生长调节联系在一起.
科学领域:
- 细胞生物学 细胞生物学
- 免疫学 免疫学 免疫学
- 发育生物学 发展生物学
背景情况:
- 河马通路调节组织生长,并与各种疾病有关.
- 天生的免疫和炎症刺激可以激活Hippo路径,但机制尚不清楚.
研究的目的:
- 阐明将天生的免疫信号与Hippo路径激活连接的分子机制.
- 为了确定关键的信号分子和参与这种交叉通话的途径.
主要方法:
- 研究了Tak1激酶在Hippo通路激活中的作用.
- 分析了Tak1对Cka的影响,这是STRIPAK复合物的子单元.
- 研究了下游的信号事件,包括陶霍波信号.
- 研究了Tak1介导的Hippo信号在细胞过程中的参与.
主要成果:
- 确定了一个保存的信号级联,其中Tak1激活了Hippo路径.
- Tak1诱导了Cka的溶酶体降解,这是Hippo信号的抑制剂.
- 压制STRIPAK复合体导致Hippo通路通过Tao-Hpo信号激活.
- Tak1介导的Hippo信号影响细胞死亡,细胞和先天免疫记忆.
结论:
- 揭示了天生的免疫/炎症信号与河马通路之间的分子联系.
- 这种交叉通话对于理解传染性,炎症性和恶性疾病至关重要.
- 这些发现有助于理解组织生长调节对免疫刺激的反应.
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