https://ror.org/03mchdq19 Department of Genetics, Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Glostrup, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Life Sci Alliance. 2024 Aug 26;7(11). doi: 10.26508/lsa.202302419. Print 2024 Nov.
The mTORC1-complex is negatively regulated by TSC1 and TSC2. Activation of Hedgehog signaling is strictly dependent on communication between Smoothened and the Hedgehog-signaling effector and transcription factor, GLI2, in the primary cilium. Details about this communication are not known, and we wanted to explore this further. Here we report that in MEFs constitutively activated mTORC1 led to mis-localization of Smoothened to the plasma membrane, combined with increased concentration of GLI2 in the cilia and reduced Hedgehog signaling, measured by reduced expression of the Hedgehog target gene, Inhibition of mTORC1 rescued the cellular localization of Smoothened to the cilia, reduced the cilia concentration of GLI2, and restored Hedgehog signaling. Our results reveal evidence for a two-step activation process of GLI2. The first step includes GLI2 stabilization and cilium localization, whereas the second step includes communication with cilia-localized Smoothened. We found that mTORC1 inhibits the second step. This is the first demonstration that mTORC1 is involved in the regulation of Hedgehog signaling.
mTORC1 复合物受 TSC1 和 TSC2 的负调控。Hedgehog 信号的激活严格依赖于 Smoothened 和 Hedgehog 信号效应物和转录因子 GLI2 在初级纤毛之间的通讯。关于这种通讯的细节尚不清楚,我们希望进一步探讨。在这里,我们报告说在 MEFs 中持续激活的 mTORC1 导致 Smoothened 错误定位到质膜,同时导致 GLI2 在纤毛中的浓度增加,Hedgehog 信号减少,这可以通过 Hedgehog 靶基因的表达减少来衡量。抑制 mTORC1 可挽救 Smoothened 向纤毛的细胞定位,减少纤毛中 GLI2 的浓度,并恢复 Hedgehog 信号。我们的结果揭示了 GLI2 的两步激活过程的证据。第一步包括 GLI2 的稳定和纤毛定位,而第二步包括与纤毛定位的 Smoothened 进行通讯。我们发现 mTORC1 抑制第二步。这是第一个证明 mTORC1 参与 Hedgehog 信号调节的例子。