Present address: Y. Driege, VIB Department for Molecular Biomedical Research, Ghent University, UGent-VIB Research Building FSVM, Technologiepark 927, 9052 GENT, BELGIUM.
DILP-producing median neurosecretory cells in the Drosophila brain mediate the response of lifespan to nutrition
Article first published online: 12 FEB 2010
© 2010 The Authors. Journal compilation © Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland 2010
Volume 9, Issue 3, pages 336–346, June 2010
How to Cite
Broughton, S. J., Slack, C., Alic, N., Metaxakis, A., Bass, T. M., Driege, Y. and Partridge, L. (2010), DILP-producing median neurosecretory cells in the Drosophila brain mediate the response of lifespan to nutrition. Aging Cell, 9: 336–346. doi: 10.1111/j.1474-9726.2010.00558.x
- Issue published online: 18 MAY 2010
- Article first published online: 12 FEB 2010
- Accepted for publication 1 February 2010
Vol. 9, Issue 5, 930, Article first published online: 16 SEP 2010
- dietary restriction;
- insulin-like peptide
Dietary restriction extends lifespan in diverse organisms, but the gene regulatory mechanisms and tissues mediating the increased survival are still unclear. Studies in worms and flies have revealed a number of candidate mechanisms, including the target of rapamycin and insulin/IGF-like signalling (IIS) pathways and suggested a specific role for the nervous system in mediating the response. A pair of sensory neurons in Caenorhabditis elegans has been found to specifically mediate DR lifespan extension, but a neuronal focus in the Drosophila nervous system has not yet been identified. We have previously shown that reducing IIS via the partial ablation of median neurosecretory cells in the Drosophila adult brain, which produce three of the seven fly insulin-like peptides, extends lifespan. Here, we show that these cells are required to mediate the response of lifespan to full feeding in a yeast dilution DR regime and that they appear to do so by mechanisms that involve both altered IIS and other endocrine effects. We also present evidence of an interaction between these mNSCs, nutrition and sleep, further emphasising the functional homology between the DILP-producing neurosecretory cells in the Drosophila brain and the hypothalamus of mammals in their roles as integration sites of many inputs for the control of lifespan and behaviour.