Cargando…
An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress
Cells communicate with their environment via surface proteins and secreted factors. Unconventional protein secretion (UPS) is an evolutionarily conserved process, via which distinct cargo proteins are secreted upon stress. Most UPS types depend upon the Golgi-associated GRASP55 protein. However, its...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382303/ https://www.ncbi.nlm.nih.gov/pubmed/34245671 http://dx.doi.org/10.1016/j.molcel.2021.06.017 |
_version_ | 1783741522374557696 |
---|---|
author | Nüchel, Julian Tauber, Marina Nolte, Janica L. Mörgelin, Matthias Türk, Clara Eckes, Beate Demetriades, Constantinos Plomann, Markus |
author_facet | Nüchel, Julian Tauber, Marina Nolte, Janica L. Mörgelin, Matthias Türk, Clara Eckes, Beate Demetriades, Constantinos Plomann, Markus |
author_sort | Nüchel, Julian |
collection | PubMed |
description | Cells communicate with their environment via surface proteins and secreted factors. Unconventional protein secretion (UPS) is an evolutionarily conserved process, via which distinct cargo proteins are secreted upon stress. Most UPS types depend upon the Golgi-associated GRASP55 protein. However, its regulation and biological role remain poorly understood. Here, we show that the mechanistic target of rapamycin complex 1 (mTORC1) directly phosphorylates GRASP55 to maintain its Golgi localization, thus revealing a physiological role for mTORC1 at this organelle. Stimuli that inhibit mTORC1 cause GRASP55 dephosphorylation and relocalization to UPS compartments. Through multiple, unbiased, proteomic analyses, we identify numerous cargoes that follow this unconventional secretory route to reshape the cellular secretome and surfactome. Using MMP2 secretion as a proxy for UPS, we provide important insights on its regulation and physiological role. Collectively, our findings reveal the mTORC1-GRASP55 signaling hub as the integration point in stress signaling upstream of UPS and as a key coordinator of the cellular adaptation to stress. |
format | Online Article Text |
id | pubmed-8382303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83823032021-08-30 An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress Nüchel, Julian Tauber, Marina Nolte, Janica L. Mörgelin, Matthias Türk, Clara Eckes, Beate Demetriades, Constantinos Plomann, Markus Mol Cell Article Cells communicate with their environment via surface proteins and secreted factors. Unconventional protein secretion (UPS) is an evolutionarily conserved process, via which distinct cargo proteins are secreted upon stress. Most UPS types depend upon the Golgi-associated GRASP55 protein. However, its regulation and biological role remain poorly understood. Here, we show that the mechanistic target of rapamycin complex 1 (mTORC1) directly phosphorylates GRASP55 to maintain its Golgi localization, thus revealing a physiological role for mTORC1 at this organelle. Stimuli that inhibit mTORC1 cause GRASP55 dephosphorylation and relocalization to UPS compartments. Through multiple, unbiased, proteomic analyses, we identify numerous cargoes that follow this unconventional secretory route to reshape the cellular secretome and surfactome. Using MMP2 secretion as a proxy for UPS, we provide important insights on its regulation and physiological role. Collectively, our findings reveal the mTORC1-GRASP55 signaling hub as the integration point in stress signaling upstream of UPS and as a key coordinator of the cellular adaptation to stress. Cell Press 2021-08-19 /pmc/articles/PMC8382303/ /pubmed/34245671 http://dx.doi.org/10.1016/j.molcel.2021.06.017 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Nüchel, Julian Tauber, Marina Nolte, Janica L. Mörgelin, Matthias Türk, Clara Eckes, Beate Demetriades, Constantinos Plomann, Markus An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress |
title | An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress |
title_full | An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress |
title_fullStr | An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress |
title_full_unstemmed | An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress |
title_short | An mTORC1-GRASP55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress |
title_sort | mtorc1-grasp55 signaling axis controls unconventional secretion to reshape the extracellular proteome upon stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382303/ https://www.ncbi.nlm.nih.gov/pubmed/34245671 http://dx.doi.org/10.1016/j.molcel.2021.06.017 |
work_keys_str_mv | AT nucheljulian anmtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT taubermarina anmtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT noltejanical anmtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT morgelinmatthias anmtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT turkclara anmtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT eckesbeate anmtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT demetriadesconstantinos anmtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT plomannmarkus anmtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT nucheljulian mtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT taubermarina mtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT noltejanical mtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT morgelinmatthias mtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT turkclara mtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT eckesbeate mtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT demetriadesconstantinos mtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress AT plomannmarkus mtorc1grasp55signalingaxiscontrolsunconventionalsecretiontoreshapetheextracellularproteomeuponstress |