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Molecular and cellular neurosciences v.85, 2017년, pp.170 - 182   SCI SCIE
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Pituitary adenylate cyclase activating polypeptide induces long-term, transcription-dependent plasticity and remodeling at autonomic synapses

Starr, Eric R. (Corresponding author at: Department of Neurosciences, University of Toledo, College of Medicine & Life Sciences, 3000 Arlington Ave, Toledo, OH 43614, United States. ) ; Margiotta, Joseph F. ;
  • 초록  

    Abstract Pituitary adenylate cyclase activating polypeptide (PACAP) is a multifunctional neuropeptide, widely expressed in the nervous system (Vaudry et al., 2009; Starr and Margiotta, 2016). At neuronal synapses where transmission is mediated by nicotinic acetylcholine receptors (nAChRs) transient PACAP exposure increases the frequency and amplitude ( F S and A S ) of spontaneous excitatory postsynaptic currents (sEPSCs) within minutes. This short-term (ST) plasticity requires high-affinity PACAP receptor (PAC 1 R) signaling via adenylate cyclase (AC), cyclic AMP (cAMP), Protein kinase A (PKA) and obligatory nAChR-dependent stimulation of nitric oxide (NO) synthesis to retrogradely increase presynaptic ACh release (Pugh et al., 2010; Jayakar et al., 2014). Remarkably, synaptic changes persist 48h after transient PACAP exposure, featuring a similar increase in F S and an even larger increase in A S . Pharmacological studies reveal that this long-term (LT) plasticity requires PACAP/PAC 1 R signaling via AC and cAMP, but unlike ST plasticity, Phospholipase-C and new gene transcription are also necessary, whereas PKA, nAChR, impulse and NO synthase (NOS1) activities are dispensable. In accord with the increases in F S and A S characterizing LT plasticity, miniature EPSC (mEPSC) frequency, ACh release (quantal content), and mEPSC amplitude (quantal size) all increased in parallel. Consistent with these functional changes, imaging studies reveal that LT, but not ST, PACAP-induced plasticity is accompanied by increases in presynaptic terminal size, postsynaptic nAChR cluster size and density, and the size and density of co-localized pre- and post-synpatic sites. Thus PACAP/PAC 1 R signaling induces mechanistically distinct forms of synaptic plasticity, with a ST form arising from acute, membrane-delimited processes, and a LT form arising from transcription-dependent alterations in the function and structural arrangement of pre- and post-synaptic components. Highlights PACAP induces short- & long-term (ST & LT) plasticity at nAChR-mediated synapses. ST and LT forms of synaptic plasticity are mechanistically distinct and independent. The LT plasticity requires cAMP signaling but not protein kinase A activity. The LT synaptic plasticity requires new gene transcription. Functional and structural synaptic modifications accompany LT synaptic plasticity.


  • 주제어

    Neuropeptide .   Neuronal nicotinic acetylcholine receptor .   Excitatory postsynaptic current .   Synaptic plasticity .   Cell signaling .   Gene transcription.  

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