No description available.

No description available.

Myosin VI, encoded by jaguar (jar) in Drosophila melanogaster, is the only member of the myosin superfamily of actin-based motor proteins known to move towards the minus ends of actin filaments. In vitro studies demonstrate that Myosin VI has the ability to perform distinct functions as a cargo transporter and anchor in the cell, however which of these roles Myosin VI plays in the nervous system has yet to be determined. A locomotor defect, observed as sluggish movement in severe jar mutant larvae, was confirmed by behavioural assays. As this can indicate problems at the neuromuscular synapse, microscopy and electrophysiology were used to investigate neuromuscular junction (NMJ) structure and function in jar loss of function mutants of varying severity. Confocal imaging studies revealed a decrease in NMJ length, a reduction in bouton number per NMJ, alterations to the microtubule cytoskeleton and mislocalization of the synaptic vesicle protein Synaptotagmin in jar mutant boutons. FM dye labeling was consistent with the immunostaining data revealing vesicles endocytosed following electrical stimulation occupy the bouton centre in jar mutants. The data is indicative of a function for Myosin VI in maintaining proper peripheral vesicle localization. Electrophysiological experiments revealed a role for Myosin VI in basal synaptic transmission, with a reduction in low frequency nerve-evoked responses and spontaneous release in severe jar mutants. Changes in short-term synaptic plasticity were also observed in Myosin VI mutants by using both paired-pulse experiments to examine release probability and high-frequency stimulation paradigms to recruit vesicles from different functional pools. Taken together, the data suggest that Myosin VI functions as an anchor to peripherally localize vesicles within the bouton enabling their efficient release during nerve stimulation. Synaptic vesicles are mobile at the Drosophila NMJ; thus if Myosin VI is acting as a vesicle tether, it would normally be expected to restrain vesicle mobility at the synapse. FRAP analysis revealed a significant increase in synaptic vesicle mobility in jar mutant boutons. This study elucidates novel roles for Myosin VI function in the nervous system via regulation of the synaptic microtubule architecture and localization of synaptic vesicles within the nerve terminal.

Myosin VI, encoded by jaguar (jar) in Drosophila melanogaster, is the only member of the myosin superfamily of actin-based motor proteins known to move towards the minus ends of actin filaments. In vitro studies demonstrate that Myosin VI has the ability to perform distinct functions as a cargo transporter and anchor in the cell, however which of these roles Myosin VI plays in the nervous system has yet to be determined. A locomotor defect, observed as sluggish movement in severe jar mutant larvae, was confirmed by behavioural assays. As this can indicate problems at the neuromuscular synapse, microscopy and electrophysiology were used to investigate neuromuscular junction (NMJ) structure and function in jar loss of function mutants of varying severity. Confocal imaging studies revealed a decrease in NMJ length, a reduction in bouton number per NMJ, alterations to the microtubule cytoskeleton and mislocalization of the synaptic vesicle protein Synaptotagmin in jar mutant boutons. FM dye labeling was consistent with the immunostaining data revealing vesicles endocytosed following electrical stimulation occupy the bouton centre in jar mutants. The data is indicative of a function for Myosin VI in maintaining proper peripheral vesicle localization. Electrophysiological experiments revealed a role for Myosin VI in basal synaptic transmission, with a reduction in low frequency nerve-evoked responses and spontaneous release in severe jar mutants. Changes in short-term synaptic plasticity were also observed in Myosin VI mutants by using both paired-pulse experiments to examine release probability and high-frequency stimulation paradigms to recruit vesicles from different functional pools. Taken together, the data suggest that Myosin VI functions as an anchor to peripherally localize vesicles within the bouton enabling their efficient release during nerve stimulation. Synaptic vesicles are mobile at the Drosophila NMJ; thus if Myosin VI is acting as a vesicle tether, it would normally be expected to restrain vesicle mobility at the synapse. FRAP analysis revealed a significant increase in synaptic vesicle mobility in jar mutant boutons. This study elucidates novel roles for Myosin VI function in the nervous system via regulation of the synaptic microtubule architecture and localization of synaptic vesicles within the nerve terminal.

No description available.

No description available.

This study has investigated the role of neurokinin receptors, in particular the NK-1 receptor, in the regulation of excitability of SPN using selective agonists and antagonists. The whole-cell patch clamp technique was used to record from SPN in transverse slices of neonatal rat spinal cord <I>in vitro</I>. Neurones were positively identified as SPN due to their characteristic electrophysiological and morphological properties. Perfusion of the selective NK-1 receptor agonist GR73632 (25 nM-5μM; 2-120 s) induced concentration-dependent depolarising responses in SPN. The response to GR73632 (67% of SPN responsive) was maintained in the presence of TTX (250-500 nM), suggesting that NK-1 receptors are located directly upon SPN. The depolarising response to GR73632 was associated with an increase in neuronal input resistance, reduced with increasing membrane hyperpolarisation, and blocked by two selective NK-1 receptor antagonists, CP-99,994 (1-3 μM) and GR82334 (250 nM-1 μM). Excitatory postsynaptic potentials and strychnine-sensitive inhibitory postsynaptic potentials were also induced by GR73632 in approximately 10% of neurones. Application of GR73632 to a subpopulation of silent SPN induced rhythmical oscillations in membrane potential. The induction of oscillations following NK-1 receptor activation can lead to synchronised action potential firing within groups of SPN. This study has presented preliminary evidence to suggest that a presynaptic NK-1 receptor may exist upon the terminals of neurones which descend from supraspinal centres in synapse upon SPN. Activation of this subtype of NK-1 receptor was found to exert an inhibitory influence upon glutamatergic synaptic transmission to SPN. The results from this study suggest that activation of the NK-1 receptor may have a major excitatory effect upon the activity of SPN, probably by causing the closure of potassium channels open at rest.

No description available.

The gastrocnemius muscle was removed from the hindlimb of female rodents, minced into 1mm3 fragments and autotransplanted. Experimental groups had the sural or tibial nerves laid in the mince as follows: both nerves (BN), sural only (SN), tibial only (TN) or no nerve (NN). Animals were sacrificed 45 days postsurgery and the regenerate and contralateral muscles studied for fiber composition and aerobic capacity. Regenerate mass and aerobic capacity were significantly less than control and followed the order BN > TN > SN > NN. The percentage of Types I, IIA and IIB fibers were also different between treatment groups. The data suggests (1) either a more rapid development of axons associated with IIA fibers following nerve transection or greater reinnervation capacity, and/or (2) a shift in the relative number of these axons in the regenerating nerve.

Synaptic inhibition in the vertebrate central nervous system is largely mediated by type A GABA receptors (GABA(_A)R). The clustering of (GABA(_A)R) at discrete and functionally significant domains on the nerve cell surface is an important determinant in the integration of synaptic inputs. To discern the role that specific GABA(_A)R subunits play in determining the receptor's cell surface topography and mobility, recombinant GABA(_A)Rs, comprising different GABA(_A)R subunit combinations, were transiently expressed in COS7, HEK293 and PC12 cells. In addition, a series of domain swapping experiments were performed in order to elucidate which regions of the protein are important in mobility/anchoring of receptors. The cellular localization and lateral mobility of the recombinantly expressed GABA(_A)Rs were determined by immunocytochemistry and Fluorescence Photobleach Recovery (FPR), respectively. The results presented in this thesis show that GABA(_A)R al subunits are recruited by the β3 subunits from an internally sequestered pool and assembled into a population of GABA(_A)Rs that are spatially segregated into clusters and also immobilised on the cell surface. FPR experiments on recombinant GABA(_A)R containing al-a6 subunits expressed in COS? cells showed restricted mobilities consistent with mobility constants determined for native GABA(_A)Rs expressed on cerebellar granule cells. Furthermore, the intracellular loop domain M3/M4 of the a1 subunits was found to be required for anchoring recombinantly expressed GABA(_A)Rs in C0S7 and cerebellar granule cells in culture, but not for GABA(_A)R clustering at the cell surface.