Matches in SemOpenAlex for { <https://semopenalex.org/work/W2012082094> ?p ?o ?g. }
- W2012082094 endingPage "4199" @default.
- W2012082094 startingPage "4187" @default.
- W2012082094 abstract "Normal brain function requires balanced development of excitatory and inhibitory synapses. An imbalance in synaptic transmission underlies many brain disorders such as epilepsy, schizophrenia, and autism. Compared with excitatory synapses, relatively little is known about the molecular control of inhibitory synapse development. We used a genetic approach in mice to identify the Ig superfamily member IgSF9/Dasm1 as a candidate homophilic synaptic adhesion protein that regulates inhibitory synapse development. IgSF9 is expressed in pyramidal cells and subsets of interneurons in the CA1 region of hippocampus. Electrophysiological recordings of acute hippocampal slices revealed that genetic inactivation of the IgSF9 gene resulted in fewer functional inhibitory synapses; however, the strength of the remaining synapses was unaltered. These physiological abnormalities were correlated with decreased expression of inhibitory synapse markers in IgSF9(-/-) mice, providing anatomical evidence for a reduction in inhibitory synapse numbers, whereas excitatory synapse development was normal. Surprisingly, knock-in mice expressing a mutant isoform of IgSF9 lacking the entire cytoplasmic domain (IgSF9(ΔC/ΔC) mice) had no defects in inhibitory synapse development, providing genetic evidence that IgSF9 regulates synapse development via ectodomain interactions rather than acting itself as a signaling receptor. Further, we found that IgSF9 mediated homotypic binding and cell aggregation, but failed to induce synapse formation, suggesting that IgSF9 acts as a cell adhesion molecule (CAM) to maintain synapses. Juvenile IgSF9(-/-) mice exhibited increased seizure susceptibility indicative of an imbalance in synaptic excitation and inhibition. These results provide genetic evidence for a specific role of IgSF9 in inhibitory synapse development/maintenance, presumably by its CAM-like activity." @default.
- W2012082094 created "2016-06-24" @default.
- W2012082094 creator A5026565602 @default.
- W2012082094 creator A5040907200 @default.
- W2012082094 creator A5063529902 @default.
- W2012082094 creator A5074905460 @default.
- W2012082094 creator A5080050732 @default.
- W2012082094 creator A5086559537 @default.
- W2012082094 date "2014-03-19" @default.
- W2012082094 modified "2023-10-10" @default.
- W2012082094 title "Genetic Evidence for the Adhesion Protein IgSF9/Dasm1 to Regulate Inhibitory Synapse Development Independent of its Intracellular Domain" @default.
- W2012082094 cites W1510455972 @default.
- W2012082094 cites W1958828070 @default.
- W2012082094 cites W1978646107 @default.
- W2012082094 cites W1995352836 @default.
- W2012082094 cites W1996933817 @default.
- W2012082094 cites W2007487855 @default.
- W2012082094 cites W2013387085 @default.
- W2012082094 cites W2017808636 @default.
- W2012082094 cites W2022963868 @default.
- W2012082094 cites W2023179463 @default.
- W2012082094 cites W2023823207 @default.
- W2012082094 cites W2028057031 @default.
- W2012082094 cites W2028474009 @default.
- W2012082094 cites W2031755128 @default.
- W2012082094 cites W2041410072 @default.
- W2012082094 cites W2046165746 @default.
- W2012082094 cites W2047757988 @default.
- W2012082094 cites W2050465941 @default.
- W2012082094 cites W2053666202 @default.
- W2012082094 cites W2055720472 @default.
- W2012082094 cites W2070732190 @default.
- W2012082094 cites W2072151819 @default.
- W2012082094 cites W2072885702 @default.
- W2012082094 cites W2073015548 @default.
- W2012082094 cites W2074369549 @default.
- W2012082094 cites W2078380794 @default.
- W2012082094 cites W2096123613 @default.
- W2012082094 cites W2097394499 @default.
- W2012082094 cites W2107885885 @default.
- W2012082094 cites W2113939107 @default.
- W2012082094 cites W2114604503 @default.
- W2012082094 cites W2124506172 @default.
- W2012082094 cites W2127810309 @default.
- W2012082094 cites W2134236497 @default.
- W2012082094 cites W2143776576 @default.
- W2012082094 cites W2146350570 @default.
- W2012082094 cites W2147152912 @default.
- W2012082094 cites W2150314930 @default.
- W2012082094 cites W2150857690 @default.
- W2012082094 cites W2151686210 @default.
- W2012082094 doi "https://doi.org/10.1523/jneurosci.3671-13.2014" @default.
- W2012082094 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6608096" @default.
- W2012082094 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24647940" @default.
- W2012082094 hasPublicationYear "2014" @default.
- W2012082094 type Work @default.
- W2012082094 sameAs 2012082094 @default.
- W2012082094 citedByCount "24" @default.
- W2012082094 countsByYear W20120820942015 @default.
- W2012082094 countsByYear W20120820942016 @default.
- W2012082094 countsByYear W20120820942017 @default.
- W2012082094 countsByYear W20120820942018 @default.
- W2012082094 countsByYear W20120820942019 @default.
- W2012082094 countsByYear W20120820942020 @default.
- W2012082094 countsByYear W20120820942021 @default.
- W2012082094 countsByYear W20120820942023 @default.
- W2012082094 crossrefType "journal-article" @default.
- W2012082094 hasAuthorship W2012082094A5026565602 @default.
- W2012082094 hasAuthorship W2012082094A5040907200 @default.
- W2012082094 hasAuthorship W2012082094A5063529902 @default.
- W2012082094 hasAuthorship W2012082094A5074905460 @default.
- W2012082094 hasAuthorship W2012082094A5080050732 @default.
- W2012082094 hasAuthorship W2012082094A5086559537 @default.
- W2012082094 hasBestOaLocation W20120820941 @default.
- W2012082094 hasConcept C112592302 @default.
- W2012082094 hasConcept C127445978 @default.
- W2012082094 hasConcept C169760540 @default.
- W2012082094 hasConcept C170493617 @default.
- W2012082094 hasConcept C17077164 @default.
- W2012082094 hasConcept C200170125 @default.
- W2012082094 hasConcept C2777756961 @default.
- W2012082094 hasConcept C2777969728 @default.
- W2012082094 hasConcept C35599011 @default.
- W2012082094 hasConcept C515207424 @default.
- W2012082094 hasConcept C54355233 @default.
- W2012082094 hasConcept C65232495 @default.
- W2012082094 hasConcept C86803240 @default.
- W2012082094 hasConcept C95444343 @default.
- W2012082094 hasConcept C99223954 @default.
- W2012082094 hasConceptScore W2012082094C112592302 @default.
- W2012082094 hasConceptScore W2012082094C127445978 @default.
- W2012082094 hasConceptScore W2012082094C169760540 @default.
- W2012082094 hasConceptScore W2012082094C170493617 @default.
- W2012082094 hasConceptScore W2012082094C17077164 @default.
- W2012082094 hasConceptScore W2012082094C200170125 @default.
- W2012082094 hasConceptScore W2012082094C2777756961 @default.
- W2012082094 hasConceptScore W2012082094C2777969728 @default.
- W2012082094 hasConceptScore W2012082094C35599011 @default.