The Hippo kinase LATS2 impairs pancreatic β-cell survival in diabetes through the mTORC1-autophagy axis

Diabetes is characterized by dysfunction and loss of beta-cells, and promoting beta-cell survival is of therapeutic interest. Here the authors show that Large-tumor suppressor 2 (LATS2), a core component of the Hippo signaling pathway, induces beta-cell failure through mTORC1 hyperactivation and aut...

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Main Authors: Ting Yuan, Karthika Annamalai, Shruti Naik, Blaz Lupse, Shirin Geravandi, Anasua Pal, Aleksandra Dobrowolski, Jaee Ghawali, Marina Ruhlandt, Kanaka Durga Devi Gorrepati, Zahra Azizi, Dae-Sik Lim, Kathrin Maedler, Amin Ardestani
Format: Article
Language:English
Published: Nature Publishing Group 2021-08-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-021-25145-x
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spelling doaj-fff43c630ec94cdfb9d466891db5de812021-08-15T11:40:42ZengNature Publishing GroupNature Communications2041-17232021-08-0112111810.1038/s41467-021-25145-xThe Hippo kinase LATS2 impairs pancreatic β-cell survival in diabetes through the mTORC1-autophagy axisTing Yuan0Karthika Annamalai1Shruti Naik2Blaz Lupse3Shirin Geravandi4Anasua Pal5Aleksandra Dobrowolski6Jaee Ghawali7Marina Ruhlandt8Kanaka Durga Devi Gorrepati9Zahra Azizi10Dae-Sik Lim11Kathrin Maedler12Amin Ardestani13Centre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenDepartment of Biological Sciences, KAIST 291 Daehak-ro, Yuseong-guCentre for Biomolecular Interactions Bremen, University of BremenCentre for Biomolecular Interactions Bremen, University of BremenDiabetes is characterized by dysfunction and loss of beta-cells, and promoting beta-cell survival is of therapeutic interest. Here the authors show that Large-tumor suppressor 2 (LATS2), a core component of the Hippo signaling pathway, induces beta-cell failure through mTORC1 hyperactivation and autophagic flux suppression.https://doi.org/10.1038/s41467-021-25145-x
collection DOAJ
language English
format Article
sources DOAJ
author Ting Yuan
Karthika Annamalai
Shruti Naik
Blaz Lupse
Shirin Geravandi
Anasua Pal
Aleksandra Dobrowolski
Jaee Ghawali
Marina Ruhlandt
Kanaka Durga Devi Gorrepati
Zahra Azizi
Dae-Sik Lim
Kathrin Maedler
Amin Ardestani
spellingShingle Ting Yuan
Karthika Annamalai
Shruti Naik
Blaz Lupse
Shirin Geravandi
Anasua Pal
Aleksandra Dobrowolski
Jaee Ghawali
Marina Ruhlandt
Kanaka Durga Devi Gorrepati
Zahra Azizi
Dae-Sik Lim
Kathrin Maedler
Amin Ardestani
The Hippo kinase LATS2 impairs pancreatic β-cell survival in diabetes through the mTORC1-autophagy axis
Nature Communications
author_facet Ting Yuan
Karthika Annamalai
Shruti Naik
Blaz Lupse
Shirin Geravandi
Anasua Pal
Aleksandra Dobrowolski
Jaee Ghawali
Marina Ruhlandt
Kanaka Durga Devi Gorrepati
Zahra Azizi
Dae-Sik Lim
Kathrin Maedler
Amin Ardestani
author_sort Ting Yuan
title The Hippo kinase LATS2 impairs pancreatic β-cell survival in diabetes through the mTORC1-autophagy axis
title_short The Hippo kinase LATS2 impairs pancreatic β-cell survival in diabetes through the mTORC1-autophagy axis
title_full The Hippo kinase LATS2 impairs pancreatic β-cell survival in diabetes through the mTORC1-autophagy axis
title_fullStr The Hippo kinase LATS2 impairs pancreatic β-cell survival in diabetes through the mTORC1-autophagy axis
title_full_unstemmed The Hippo kinase LATS2 impairs pancreatic β-cell survival in diabetes through the mTORC1-autophagy axis
title_sort hippo kinase lats2 impairs pancreatic β-cell survival in diabetes through the mtorc1-autophagy axis
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2021-08-01
description Diabetes is characterized by dysfunction and loss of beta-cells, and promoting beta-cell survival is of therapeutic interest. Here the authors show that Large-tumor suppressor 2 (LATS2), a core component of the Hippo signaling pathway, induces beta-cell failure through mTORC1 hyperactivation and autophagic flux suppression.
url https://doi.org/10.1038/s41467-021-25145-x
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