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

Author

Listed:
  • Takayuki Yamada

    (Laboratory for Growth Control Signaling, RIKEN Center for Biosystems Dynamics Research (BDR))

  • Yuto Yoshinari

    (Gunma University)

  • Masayuki Tobo

    (Gunma University)

  • Okiko Habara

    (Laboratory for Growth Control Signaling, RIKEN Center for Biosystems Dynamics Research (BDR))

  • Takashi Nishimura

    (Laboratory for Growth Control Signaling, RIKEN Center for Biosystems Dynamics Research (BDR)
    Gunma University)

Abstract

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.

Suggested Citation

  • Takayuki Yamada & Yuto Yoshinari & Masayuki Tobo & Okiko Habara & Takashi Nishimura, 2023. "Nacα protects the larval fat body from cell death by maintaining cellular proteostasis in Drosophila," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41103-1
    DOI: 10.1038/s41467-023-41103-1
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    References listed on IDEAS

    as
    1. Jianli Tao & Qi Wang & Carlos Mendez-Dorantes & Kathleen H. Burns & Roberto Chiarle, 2022. "Frequency and mechanisms of LINE-1 retrotransposon insertions at CRISPR/Cas9 sites," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    2. Emi Murayama & Milka Sarris & Michael Redd & Dorothée Le Guyader & Catherine Vivier & Wyatt Horsley & Nikolaus Trede & Philippe Herbomel, 2015. "NACA deficiency reveals the crucial role of somite-derived stromal cells in haematopoietic niche formation," Nature Communications, Nature, vol. 6(1), pages 1-14, December.
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