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Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process

Within eukaryotic cells, translation is regulated independent of transcription, enabling nuanced, localized, and rapid responses to stimuli. Neurons respond transcriptionally and translationally to synaptic activity. Although transcriptional responses are documented in astrocytes, here we test wheth...

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Autores principales: Sapkota, Darshan, Kater, Mandy S.J., Sakers, Kristina, Nygaard, Kayla R., Liu, Yating, Koester, Sarah K., Fass, Stuart B., Lake, Allison M., Khazanchi, Rohan, Khankan, Rana R., Krawczyk, Mitchell C., Smit, August B., Maloney, Susan E., Verheijen, Mark H.G., Zhang, Ye, Dougherty, Joseph D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624251/
https://www.ncbi.nlm.nih.gov/pubmed/36261025
http://dx.doi.org/10.1016/j.celrep.2022.111474
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author Sapkota, Darshan
Kater, Mandy S.J.
Sakers, Kristina
Nygaard, Kayla R.
Liu, Yating
Koester, Sarah K.
Fass, Stuart B.
Lake, Allison M.
Khazanchi, Rohan
Khankan, Rana R.
Krawczyk, Mitchell C.
Smit, August B.
Maloney, Susan E.
Verheijen, Mark H.G.
Zhang, Ye
Dougherty, Joseph D.
author_facet Sapkota, Darshan
Kater, Mandy S.J.
Sakers, Kristina
Nygaard, Kayla R.
Liu, Yating
Koester, Sarah K.
Fass, Stuart B.
Lake, Allison M.
Khazanchi, Rohan
Khankan, Rana R.
Krawczyk, Mitchell C.
Smit, August B.
Maloney, Susan E.
Verheijen, Mark H.G.
Zhang, Ye
Dougherty, Joseph D.
author_sort Sapkota, Darshan
collection PubMed
description Within eukaryotic cells, translation is regulated independent of transcription, enabling nuanced, localized, and rapid responses to stimuli. Neurons respond transcriptionally and translationally to synaptic activity. Although transcriptional responses are documented in astrocytes, here we test whether astrocytes have programmed translational responses. We show that seizure activity rapidly changes the transcripts on astrocyte ribosomes, some predicted to be downstream of BDNF signaling. In acute slices, we quantify the extent to which cues of neuronal activity activate translation in astrocytes and show that this translational response requires the presence of neurons, indicating that the response is non-cell autonomous. We also show that this induction of new translation extends into the periphery of astrocytes. Finally, synaptic proteomics show that new translation is required for changes that occur in perisynaptic astrocyte protein composition after fear conditioning. Regulation of translation in astrocytes by neuronal activity suggests an additional mechanism by which astrocytes may dynamically modulate nervous system functioning.
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spelling pubmed-96242512022-11-01 Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process Sapkota, Darshan Kater, Mandy S.J. Sakers, Kristina Nygaard, Kayla R. Liu, Yating Koester, Sarah K. Fass, Stuart B. Lake, Allison M. Khazanchi, Rohan Khankan, Rana R. Krawczyk, Mitchell C. Smit, August B. Maloney, Susan E. Verheijen, Mark H.G. Zhang, Ye Dougherty, Joseph D. Cell Rep Article Within eukaryotic cells, translation is regulated independent of transcription, enabling nuanced, localized, and rapid responses to stimuli. Neurons respond transcriptionally and translationally to synaptic activity. Although transcriptional responses are documented in astrocytes, here we test whether astrocytes have programmed translational responses. We show that seizure activity rapidly changes the transcripts on astrocyte ribosomes, some predicted to be downstream of BDNF signaling. In acute slices, we quantify the extent to which cues of neuronal activity activate translation in astrocytes and show that this translational response requires the presence of neurons, indicating that the response is non-cell autonomous. We also show that this induction of new translation extends into the periphery of astrocytes. Finally, synaptic proteomics show that new translation is required for changes that occur in perisynaptic astrocyte protein composition after fear conditioning. Regulation of translation in astrocytes by neuronal activity suggests an additional mechanism by which astrocytes may dynamically modulate nervous system functioning. 2022-10-18 /pmc/articles/PMC9624251/ /pubmed/36261025 http://dx.doi.org/10.1016/j.celrep.2022.111474 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Sapkota, Darshan
Kater, Mandy S.J.
Sakers, Kristina
Nygaard, Kayla R.
Liu, Yating
Koester, Sarah K.
Fass, Stuart B.
Lake, Allison M.
Khazanchi, Rohan
Khankan, Rana R.
Krawczyk, Mitchell C.
Smit, August B.
Maloney, Susan E.
Verheijen, Mark H.G.
Zhang, Ye
Dougherty, Joseph D.
Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process
title Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process
title_full Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process
title_fullStr Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process
title_full_unstemmed Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process
title_short Activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process
title_sort activity-dependent translation dynamically alters the proteome of the perisynaptic astrocyte process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624251/
https://www.ncbi.nlm.nih.gov/pubmed/36261025
http://dx.doi.org/10.1016/j.celrep.2022.111474
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