The present study is part of an ongoing project aimed at understanding the electrophysiologic properties of single amygdaloid neurons and their correlations with the morphology of the somata as well as axonal and dendritic trees. The axonal morphology of 14 three-dimensional, reconstructed spiny neurons (4 in the lateral and 10 in the basal nucleus) that were filled in vivo with intracellular injections of biocytin is described. Three-dimensional reconstruction was performed using Neurolucida software (MicroBrightField). Sholl analysis was used to assess the axonal length as well as the number of axonal varicosities and endings within concentric spherical shells placed at 50- micro m intervals from the soma. These data indicate that the same neuron can innervate several amygdaloid nuclear divisions or nuclei and extra-amygdaloid regions. This finding suggests that the same neuron can modulate various brain areas in parallel. Both the presumed intra-amygdaloid (all axonal branches within the amygdala) and extra-amygdaloid (axons also outside the amygdala) projection neurons have dense perisomatic axonal arborizations, and consequently, the intra-amygdaloid and extra-amygdaloid projection neurons are difficult to differentiate based on the analysis of perisomatic axonal morphology. Furthermore, the same extra-amygdaloid neuron can drive many neurons both locally as well as at extra-amygdaloid projection areas within a relatively short time. Finally, the axonal morphology of spiny neurons located in the lateral or basal nuclei was similar. These data provide baseline quantitative information about the axonal dimensions of amygdaloid neurons and can form the anatomic basis for modeling amygdaloid neuronal circuits when more quantitative data regarding neuronal numbers, size, and dendritic morphology become available.
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http://dx.doi.org/10.1111/j.1749-6632.2003.tb07069.x | DOI Listing |
Int J Mol Sci
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Neuroscience and Mental Health Innovation Institute, Cardiff University, Hadyn Ellis Building, Cardiff CF24 4HQ, UK.
Deletion and duplication in the human 16p11.2 chromosomal region are closely linked to neurodevelopmental disorders, specifically autism spectrum disorder. Data from neuroimaging studies suggest white matter microstructure aberrations across these conditions.
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View Article and Find Full Text PDFBiomolecules
January 2025
Department of Neurology, Christian-Doppler University Hospital, Paracelsus Medical University, 5020 Salzburg, Austria.
Intrathecal immunoglobulin A (IgA) synthesis in multiple sclerosis (MS) has long earned little attention, despite a potential significance in disease pathogenesis and prognosis. The presence of IgA-positive plasma cells in MS lesions and along damaged axons suggests a role in disease pathogenesis. Available clinical evidence about a potential positive or negative prognostic role is scarce and inconclusive.
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January 2025
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Myelination is a key biological process wherein glial cells such as oligodendrocytes wrap myelin around neuronal axons, forming an insulative sheath that accelerates signal propagation down the axon. A major obstacle to understanding myelination is the challenge of visualizing and reproducibly quantifying this inherently three-dimensional process in vitro. To this end, we previously developed artificial axons (AAs), a biocompatible platform consisting of 3D-printed hydrogel-based axon mimics designed to more closely recapitulate the micrometer-scale diameter and sub-kilopascal mechanical stiffness of biological axons.
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Department of Neurobiology, School of Biological Sciences, University of California San Diego, La Jolla, CA 92093.
The conserved MAP3K DLKs are widely known for their functions in synapse formation, axonal regeneration and degeneration, and neuronal survival, notably under traumatic injury and chronic disease conditions. In contrast, their roles in other neuronal compartments are much less explored. Through an unbiased forward genetic screening in C.
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