4.8 Article

Heterotypic Signals from Neural HSF-1 Separate Thermotolerance from Longevity

Journal

CELL REPORTS
Volume 12, Issue 7, Pages 1196-1204

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2015.07.026

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Funding

  1. NIH-Office of Research Infrastructure Programs [P40 OD010440]
  2. NIH [R37AG024365, R01AG042679, R01ES021667, T32AG000266, R01AG025549, R01AG043080]
  3. NIH/NIA [1K99AG042495]
  4. George E. Hewitt Foundation for Medical Research
  5. Salk Center for Nutritional Genomics from the Leona M. & Harry B. Helmsley Charitable Trust
  6. Glenn Foundation for Medical Research

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Integrating stress responses across tissues is essential for the survival of multicellular organisms. The metazoan nervous system can sense protein-misfolding stress arising in different subcellular compartments and initiate cytoprotective transcriptional responses in the periphery. Several subcellular compartments possess a homotypic signal whereby the respective compartment relies on a single signaling mechanism to convey information within the affected cell to the same stress-responsive pathway in peripheral tissues. In contrast, we find that the heat shock transcription factor, HSF-1, specifies its mode of transcellular protection via two distinct signaling pathways. Upon thermal stress, neural HSF-1 primes peripheral tissues through the thermosensory neural circuit to mount a heat shock response. Independent of this thermosensory circuit, neural HSF-1 activates the FOXO transcription factor, DAF-16, in the periphery and prolongs lifespan. Thus a single transcription factor can coordinate different stress response pathways to specify its mode of protection against changing environmental conditions.

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