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Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila

Protein homeostasis (proteostasis) is crucial for the maintenance of cellular homeostasis. Impairment of proteostasis activates proteotoxic and unfolded protein response pathways to resolve cellular stress or induce apoptosis in damaged cells. However, the responses of individual tissues to proteoto...

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Autores principales: Yamada, Takayuki, Yoshinari, Yuto, Tobo, Masayuki, Habara, Okiko, Nishimura, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474126/
https://www.ncbi.nlm.nih.gov/pubmed/37658058
http://dx.doi.org/10.1038/s41467-023-41103-1
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author Yamada, Takayuki
Yoshinari, Yuto
Tobo, Masayuki
Habara, Okiko
Nishimura, Takashi
author_facet Yamada, Takayuki
Yoshinari, Yuto
Tobo, Masayuki
Habara, Okiko
Nishimura, Takashi
author_sort Yamada, Takayuki
collection PubMed
description Protein homeostasis (proteostasis) is crucial for the maintenance of cellular homeostasis. Impairment of proteostasis activates proteotoxic and unfolded protein response pathways to resolve cellular stress or induce apoptosis in damaged cells. However, the responses of individual tissues to proteotoxic stress and evoking cell death program have not been extensively explored in vivo. Here, we show that a reduction in Nascent polypeptide-associated complex protein alpha subunit (Nacα) specifically and progressively induces cell death in Drosophila fat body cells. Nacα mutants disrupt both ER integrity and the proteasomal degradation system, resulting in caspase activation through JNK and p53. Although forced activation of the JNK and p53 pathways was insufficient to induce cell death in the fat body, the reduction of Nacα sensitized fat body cells to intrinsic and environmental stresses. Reducing overall protein synthesis by mTor inhibition or Minute mutants alleviated the cell death phenotype in Nacα mutant fat body cells. Our work revealed that Nacα is crucial for protecting the fat body from cell death by maintaining cellular proteostasis, thus demonstrating the coexistence of a unique vulnerability and cell death resistance in the fat body.
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spelling pubmed-104741262023-09-03 Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila Yamada, Takayuki Yoshinari, Yuto Tobo, Masayuki Habara, Okiko Nishimura, Takashi Nat Commun Article Protein homeostasis (proteostasis) is crucial for the maintenance of cellular homeostasis. Impairment of proteostasis activates proteotoxic and unfolded protein response pathways to resolve cellular stress or induce apoptosis in damaged cells. However, the responses of individual tissues to proteotoxic stress and evoking cell death program have not been extensively explored in vivo. Here, we show that a reduction in Nascent polypeptide-associated complex protein alpha subunit (Nacα) specifically and progressively induces cell death in Drosophila fat body cells. Nacα mutants disrupt both ER integrity and the proteasomal degradation system, resulting in caspase activation through JNK and p53. Although forced activation of the JNK and p53 pathways was insufficient to induce cell death in the fat body, the reduction of Nacα sensitized fat body cells to intrinsic and environmental stresses. Reducing overall protein synthesis by mTor inhibition or Minute mutants alleviated the cell death phenotype in Nacα mutant fat body cells. Our work revealed that Nacα is crucial for protecting the fat body from cell death by maintaining cellular proteostasis, thus demonstrating the coexistence of a unique vulnerability and cell death resistance in the fat body. Nature Publishing Group UK 2023-09-01 /pmc/articles/PMC10474126/ /pubmed/37658058 http://dx.doi.org/10.1038/s41467-023-41103-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yamada, Takayuki
Yoshinari, Yuto
Tobo, Masayuki
Habara, Okiko
Nishimura, Takashi
Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila
title Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila
title_full Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila
title_fullStr Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila
title_full_unstemmed Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila
title_short Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila
title_sort nacα protects the larval fat body from cell death by maintaining cellular proteostasis in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474126/
https://www.ncbi.nlm.nih.gov/pubmed/37658058
http://dx.doi.org/10.1038/s41467-023-41103-1
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