TY - JOUR
T1 - mTORC1 hampers Hedgehog signaling in Tsc2 deficient cells
AU - Larsen, Lasse Jonsgaard
AU - Østergaard, Elsebet
AU - Møller, Lisbeth Birk
N1 - © 2024 Larsen et al.
PY - 2024/11
Y1 - 2024/11
N2 - 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 Tsc2 -/- 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, Gli1 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.
AB - 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 Tsc2 -/- 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, Gli1 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.
KW - Animals
KW - Mechanistic Target of Rapamycin Complex 1/metabolism
KW - Signal Transduction
KW - Mice
KW - Cilia/metabolism
KW - Hedgehog Proteins/metabolism
KW - Tuberous Sclerosis Complex 2 Protein/metabolism
KW - Zinc Finger Protein Gli2/metabolism
KW - Smoothened Receptor/metabolism
KW - Tumor Suppressor Proteins/metabolism
KW - Zinc Finger Protein GLI1/metabolism
KW - Fibroblasts/metabolism
KW - Kruppel-Like Transcription Factors/metabolism
KW - Cell Membrane/metabolism
KW - Mice, Knockout
UR - https://www.scopus.com/pages/publications/85202542868
U2 - 10.26508/lsa.202302419
DO - 10.26508/lsa.202302419
M3 - Journal article
C2 - 39187374
SN - 2575-1077
VL - 7
JO - Life Science Alliance
JF - Life Science Alliance
IS - 11
M1 - e202302419
ER -