mTORC1 hampers Hedgehog signaling in<i>Tsc2</i>deficient cells

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 <i>Tsc2</i> <sup><i>-/-</i></sup> 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, <i>Gli1</i> 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.

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Publication Details

Journal
Life Science Alliance
Published
2024-08-26
DOI
https://doi.org/10.26508/lsa.202302419
Citations
1
Primary Topic
Hedgehog Signaling Pathway Studies
Type
article
Field-Weighted Citation Impact
0.23

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article

mTORC1 hampers Hedgehog signaling inTsc2deficient cells

Lisbeth Birk Møller, Lasse Jonsgaard Larsen, Elsebet Østergaard
1 citations
Life Science Alliance
Hedgehog Signaling Pathway Studies
0.23
article

mTORC1 hampers Hedgehog signaling inTsc2deficient cells

Lisbeth Birk Møller, Lasse Jonsgaard Larsen, Elsebet Østergaard
article en
1 citations

Abstract

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 <i>Tsc2</i> <sup><i>-/-</i></sup> 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, <i>Gli1</i> 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.

Life Science AllianceVol. 7(11)
University of Copenhagen (DK), Glostrup Hospital (DK), Copenhagen University Hospital (DK), Rigshospitalet (DK), Kennedy Center (DK)
Harvard University
Openalex Percentile: Top 43%
Hedgehog Signaling Pathway Studies
0.23
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mTORC1 hampers Hedgehog signaling in<i>Tsc2</i>deficient cells — Lisbeth Birk Møller, Lasse Jonsgaard Larsen, et al. · Life Science Alliance (2024) | TGRS Research Map | TGRS