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Sci. Signal., 1 December 2009 EDITORS' CHOICE
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Neuroscience Controlling SynaptogenesisWei Wong Science Signaling, AAAS, Washington, DC 20005, USA
Lim et al. investigated the biological functions of the brain-specific protein tyrosine phosphatase receptor–type T (PTPRT). Hippocampal neurons overexpressing wild-type PTPRT (WT-RT) showed increased numbers of dendritic spines, excitatory synapses, and inhibitory synapses compared with those expressing a control plasmid. Conversely, knockdown of PTPRT by small interfering RNA (siRNA) in neurons reduced spine density and synapse formation. Mass spectrometry of PTPRT immunoprecipitates from brain extract identified the neuroligin and neurexin families of cell adhesion proteins as PTPRT binding partners; coimmunoprecipitation assays in transfected cells showed that neuroligin-1 and neurexin-2 S. H. Lim, S.-K. Kwon, M. K. Lee, J. Moon, D. G. Jeong, E. Park, S. J. Kim, B. C. Park, S. C. Lee, S.-E. Ryu, D.-Y. Yu, B. H. Chung, E. Kim, P.-K. Myung, J.-R. Lee, Synapse formation regulated by protein tyrosine phosphatase receptor T through interaction with cell adhesion molecules and Fyn. EMBO J. 28, 3564–3578 (2009). [PubMed]
Citation: W. Wong, Controlling Synaptogenesis. Sci. Signal. 2, ec384 (2009). The editors suggest the following Related Resources on Science sites:In Science Signaling
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Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882