analysis of adhesion molecules and basement membrane contributions to synaptic adhesion at the drosophila embryonic nmj分析粘附分子和基底膜对突触粘附在果蝇胚胎nmj的贡献.pdfVIP

analysis of adhesion molecules and basement membrane contributions to synaptic adhesion at the drosophila embryonic nmj分析粘附分子和基底膜对突触粘附在果蝇胚胎nmj的贡献.pdf

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analysis of adhesion molecules and basement membrane contributions to synaptic adhesion at the drosophila embryonic nmj分析粘附分子和基底膜对突触粘附在果蝇胚胎nmj的贡献

Analysis of Adhesion Molecules and Basement Membrane Contributions to Synaptic Adhesion at the Drosophila Embryonic NMJ 1¤ 2 1 Andre Koper , Annette Schenck , Andreas Prokop * 1 Faculty of Life Sciences, Wellcome Trust Centre for Cell-Matrix Research, Manchester, United Kingdom, 2 Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences, Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands Abstract Synapse formation and maintenance crucially underlie brain function in health and disease. Both processes are believed to depend on cell adhesion molecules (CAMs). Many different classes of CAMs localise to synapses, including cadherins, protocadherins, neuroligins, neurexins, integrins, and immunoglobulin adhesion proteins, and further contributions come from the extracellular matrix and its receptors. Most of these factors have been scrutinised by loss-of-function analyses in animal models. However, which adhesion factors establish the essential physical links across synaptic clefts and allow the assembly of synaptic machineries at the contact site in vivo is still unclear. To investigate these key questions, we have used the neuromuscular junction (NMJ) of Drosophila embryos as a genetically amenable model synapse. Our ultrastructural analyses of NMJs lacking different classes of CAMs revealed that loss of all neurexins, all classical cadherins or all glutamate receptors, as well as combinations between these or with a Laminin deficiency, failed to reveal structural phenotypes. These results are compatible with a view that these CAMs might have no structural role at this model synapse. However, we consider it far more likely that they operate in a redundan

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