PMID- 20573882 OWN - NLM STAT- MEDLINE DCOM- 20100715 LR - 20220309 IS - 1529-2401 (Electronic) IS - 0270-6474 (Print) IS - 0270-6474 (Linking) VI - 30 IP - 25 DP - 2010 Jun 23 TI - Aplysia cell adhesion molecule and a novel protein kinase C activity in the postsynaptic neuron are required for presynaptic growth and initial formation of specific synapses. PG - 8353-66 LID - 10.1523/JNEUROSCI.0546-10.2010 [doi] AB - To explore the role of both Aplysia cell adhesion molecule (ApCAM) and activity of specific protein kinase C (PKC) isoforms in the initial formation of sensory neuron synapses with specific postsynaptic targets (L7 but not L11), we examined presynaptic growth, initial synapse formation, and the expression of the presynaptic neuropeptide sensorin following cell-specific reduction of ApCAM or of a novel PKC activity. Synapse formation between sensory neurons and L7 begins by 3 h after plating and is accompanied by a rapid accumulation of a novel PKC to sites of synaptic interaction. Reducing ApCAM expression specifically from the surface of L7 blocks presynaptic growth and initial synapse formation, target-induced increase of sensorin in sensory neuron cell bodies and the rapid accumulation of the novel PKC to sites of interaction. Selective blockade of the novel PKC activity in L7, but not in sensory neurons, with injection of a dominant negative construct that interferes with the novel PKC activity, produces the same actions as downregulating ApCAM; blockade of presynaptic growth and initial synapse formation, and the target-induced increase of sensorin in sensory neuron cell bodies. The results indicate that signals initiated by postsynaptic cell adhesion molecule ApCAM coupled with the activation of a novel PKC in the appropriate postsynaptic neuron produce the retrograde signals required for presynaptic growth associated with initial synapse formation, and the target-induced expression of a presynaptic neuropeptide critical for synapse maturation. FAU - Hu, Jiang-Yuan AU - Hu JY AD - Department of Neuroscience, Columbia University College of Physicians and Surgeons, New York State Psychiatric Institute, New York, New York 10032, USA. FAU - Chen, Yang AU - Chen Y FAU - Bougie, Joanna K AU - Bougie JK FAU - Sossin, Wayne S AU - Sossin WS FAU - Schacher, Samuel AU - Schacher S LA - eng GR - R01 NS042159-08/NS/NINDS NIH HHS/United States GR - R01 MH060387/MH/NIMH NIH HHS/United States GR - R01 NS042159/NS/NINDS NIH HHS/United States GR - R01 MH060387-11/MH/NIMH NIH HHS/United States GR - MH 60387/MH/NIMH NIH HHS/United States GR - P40 RR010294/RR/NCRR NIH HHS/United States GR - NS 42159/NS/NINDS NIH HHS/United States GR - MOP12046/CAPMC/CIHR/Canada PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PL - United States TA - J Neurosci JT - The Journal of neuroscience : the official journal of the Society for Neuroscience JID - 8102140 RN - 0 (Cell Adhesion Molecules) RN - 0 (Fluorescent Dyes) RN - 0 (Neuropeptides) RN - 0 (sensorin A protein, Aplysia) RN - EC 2.7.11.13 (Protein Kinase C) SB - IM MH - Analysis of Variance MH - Animals MH - Aplysia/growth & development/metabolism MH - Cell Adhesion Molecules/*metabolism MH - Cells, Cultured MH - Electrophysiology MH - Fluorescent Dyes MH - Ganglia, Invertebrate/metabolism MH - Immunohistochemistry MH - Microscopy, Fluorescence MH - Neurons/cytology/*metabolism MH - Neuropeptides/metabolism MH - Presynaptic Terminals/*metabolism MH - Protein Kinase C/*metabolism MH - Synapses/*metabolism MH - Synaptic Transmission/physiology PMC - PMC2908027 MID - NIHMS216044 EDAT- 2010/06/25 06:00 MHDA- 2010/07/16 06:00 PMCR- 2010/12/23 CRDT- 2010/06/25 06:00 PHST- 2010/06/25 06:00 [entrez] PHST- 2010/06/25 06:00 [pubmed] PHST- 2010/07/16 06:00 [medline] PHST- 2010/12/23 00:00 [pmc-release] AID - 30/25/8353 [pii] AID - 3607154 [pii] AID - 10.1523/JNEUROSCI.0546-10.2010 [doi] PST - ppublish SO - J Neurosci. 2010 Jun 23;30(25):8353-66. doi: 10.1523/JNEUROSCI.0546-10.2010.