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NLP-12 engages different UNC-13 proteins to potentiate tonic and evoked release.
Hu, Zhitao; Vashlishan-Murray, Amy B; Kaplan, Joshua M.
Afiliação
  • Hu Z; Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, and.
  • Vashlishan-Murray AB; Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, and Department of Communication Sciences and Disorders, Emerson College, Boston, Massachusetts 02116.
  • Kaplan JM; Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, and kaplan@molbio.mgh.harvard.edu.
J Neurosci ; 35(3): 1038-42, 2015 Jan 21.
Article em En | MEDLINE | ID: mdl-25609620
ABSTRACT
A neuropeptide (NLP-12) and its receptor (CKR-2) potentiate tonic and evoked ACh release at Caenorhabditis elegans neuromuscular junctions. Increased evoked release is mediated by a presynaptic pathway (egl-30 Gαq and egl-8 PLCß) that produces DAG, and by DAG binding to short and long UNC-13 proteins. Potentiation of tonic ACh release persists in mutants deficient for egl-30 Gαq and egl-8 PLCß and requires DAG binding to UNC-13L (but not UNC-13S). Thus, NLP-12 adjusts tonic and evoked release by distinct mechanisms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropeptídeos / Acetilcolina / Proteínas de Transporte / Proteínas de Caenorhabditis elegans / Junção Neuromuscular Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropeptídeos / Acetilcolina / Proteínas de Transporte / Proteínas de Caenorhabditis elegans / Junção Neuromuscular Idioma: En Ano de publicação: 2015 Tipo de documento: Article