A Gq-Ca2+ Axis Controls Circuit-Level Encoding of Circadian Time in the Suprachiasmatic Nucleus

被引:158
作者
Brancaccio, Marco [1 ]
Maywood, Elizabeth S. [1 ]
Chesham, Johanna E. [1 ]
Loudon, Andrew S. I. [2 ]
Hastings, Michael H. [1 ]
机构
[1] MRC, Mol Biol Lab, Div Neurobiol, Cambridge CB2 0QH, England
[2] Univ Manchester, Fac Life Sci, Manchester M13 9PL, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
VPAC(2) RECEPTOR; CELL AUTONOMY; RHYTHMICITY; SYNCHRONY; ROBUSTNESS; PACEMAKING; GENERATION; CLOCKWORK; DYNAMICS; NEURONS;
D O I
10.1016/j.neuron.2013.03.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The role of intracellular transcriptional/post-translational feedback loops (TTFL) within the circadian pacemaker of the suprachiasmatic nucleus (SCN) is well established. In contrast, contributions from G-coupled pathways and cytosolic rhythms to the intercellular control of SCN pacemaking are poorly understood. We therefore combined viral transduction of SCN slices with fluorescence/bioluminescence imaging to visualize GCaMP3-reported circadian oscillations of intracellular calcium [Ca2+](i) alongside activation of Ca2+/cAMP-responsive elements. We phase-mapped them to the TTFL, in time and SCN space, and demonstrated their dependence upon G-coupled vasoactive intestinal peptide (VIP) signaling. Pharmacogenetic manipulation revealed the individual contributions of Gq, Gs, and Gi to cytosolic and TTFL circadian rhythms. Importantly, activation of Gq-dependent (but not Gs or Gi) pathways in a minority of neurons reprogrammed [Ca2+](i) and TTFL rhythms across the entire SCN. This reprogramming was mediated by intrinsic VIPergic signaling, thus revealing a Gq/[Ca2+](i)-VIP leitmotif and unanticipated plasticity within network encoding of SCN circadian time.
引用
收藏
页码:714 / 728
页数:15
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