A trans-synaptic mechanism for the development and function of a neural circuit

dc.contributor.authorSilwal, Prabhisha
dc.contributor.examiningcommitteeHannila, Sari S (Human Anatomy and Cell Science) Stecina, Katinka (Physiology and Pathophysiology)en_US
dc.contributor.supervisorSiddiqui, Tabrez J (Physiology and Pathophysiology)en_US
dc.date.accessioned2020-04-02T15:51:32Z
dc.date.available2020-04-02T15:51:32Z
dc.date.copyright2020-04-02
dc.date.issued2020en_US
dc.date.submitted2020-04-02T15:17:17Zen_US
dc.degree.disciplinePhysiology and Pathophysiologyen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractSynapses are formed by high affinity trans-synaptic interactions between pre- and post- synaptic proteins. Any disturbance in these interactions may affect synaptogenesis. We assessed the consequences of disrupted trans-synaptic interaction between presynaptic neurexins and postsynaptic LRRTM4 proteins in vivo. We found that neurexins bind to LRRTM4 only in the presence of heparan sulfate (HS) chains. When HS binding site on LRRTM4 was mutated, they could not bind to neurexins. Analysis of brain collected from the knock-in mice with mutation in the functional HS binding domain of LRRTM4 showed reduction in excitatory synapses at dentate gyrus (DG). The binding of neurexins and LRRTM4 via HS chains recruited PTPσ to induce optimal presynaptic differentiation. The knock-in mice also revealed reduced levels of PTPσ and neurexins in the dentate gyrus lysates. Therefore, our results provide evidence that trans-synaptic interactions between neurexins and LRRTM4 via HS chains are required for excitatory synapse formation in the DG; and any disruption in their interaction impair excitatory synapse formation and development.en_US
dc.description.noteMay 2020en_US
dc.identifier.citationRoppongi, R.T., Dhume, S., Padmanabhan, N., Silwal, P., Zahra, N., Karimi, B., Bomkamp, C., Patil, C., Champagne-Jorgensen, K., Twilley, R.E., Zhang, P., Craig, A.M., Jackson, M.F., Siddiqui, T.J. (2020). LRRTMs organize synapses through differential engagement of neurexin and PTPσ. Neuron (in Press)en_US
dc.identifier.urihttp://hdl.handle.net/1993/34629
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectSynapseen_US
dc.subjectneurexinsen_US
dc.subjectLRRTMsen_US
dc.subjectcell adhesion moleculesen_US
dc.titleA trans-synaptic mechanism for the development and function of a neural circuiten_US
dc.typemaster thesisen_US
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