{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Nishiyama M"],"funding":["NINDS NIH HHS"],"pagination":["676-85"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3395591"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13(6)"],"pubmed_abstract":["Polarized neurites (axons and dendrites) form the functional circuitry of the nervous system. Secreted guidance cues often control the polarity of neuron migration and neurite outgrowth by regulating ion channels. Here, we show that secreted semaphorin 3A (Sema3A) induces the neurite identity of Xenopus spinal commissural interneurons (xSCINs) by activating Ca(V)2.3 channels (Ca(V)2.3). Sema3A treatment converted the identity of axons of cultured xSCINs to that of dendrites by recruiting functional Ca(V)2.3. Inhibition of Sema3A signalling prevented both the expression of Ca(V)2.3 and acquisition of the dendrite identity, and inhibition of Ca(V)2.3 function resulted in multiple axon-like neurites of xSCINs in the spinal cord. Furthermore, Sema3A-triggered cGMP production and PKG activity i"],"journal":["Nature cell biology"],"pubmed_title":["Semaphorin 3A induces CaV2.3 channel-dependent conversion of axons to dendrites."],"pmcid":["PMC3395591"],"funding_grant_id":["R01 NS064671","NS042823","NS064671","R01 NS042823"],"pubmed_authors":["von Schimmelmann MJ","Maeda S","Goshima Y","Hong K","Nishiyama M","Lim CS","Togashi K","Yamashita N","Ishii S"],"additional_accession":[]},"is_claimable":false,"name":"Semaphorin 3A induces CaV2.3 channel-dependent conversion of axons to dendrites.","description":"Polarized neurites (axons and dendrites) form the functional circuitry of the nervous system. Secreted guidance cues often control the polarity of neuron migration and neurite outgrowth by regulating ion channels. Here, we show that secreted semaphorin 3A (Sema3A) induces the neurite identity of Xenopus spinal commissural interneurons (xSCINs) by activating Ca(V)2.3 channels (Ca(V)2.3). Sema3A treatment converted the identity of axons of cultured xSCINs to that of dendrites by recruiting functional Ca(V)2.3. Inhibition of Sema3A signalling prevented both the expression of Ca(V)2.3 and acquisition of the dendrite identity, and inhibition of Ca(V)2.3 function resulted in multiple axon-like neurites of xSCINs in the spinal cord. Furthermore, Sema3A-triggered cGMP production and PKG activity i","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011 Jun","modification":"2025-04-18T16:16:34.786Z","creation":"2019-03-27T00:55:32Z"},"accession":"S-EPMC3395591","cross_references":{"pubmed":["21602796"],"doi":["10.1038/ncb2255"]}}