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Layer 1 (L1) of the neocortex integrates bottom-up and top-down signals. Inputs to L1, however, remain incompletely characterized. L1 of the auditory cortex (ACX) receives ascending inputs from the medial geniculate body (MGB) subdivisions and the surrounding posterior thalamic nuclei (PTN). The precise manner in which these structures innervate L1 is not fully understood. Here we examined the distribution of axon terminals from MGB/PTN subdivisions in L1 of the mouse ACX using virus-based axonal labeling. A bulk injection into the entire MGB and its adjacent PTN (referred to as W) confirmed their projection to upper L1, in addition to other layers. However, we observed multiple vertical axon bundles with irregular inter-bundle intervals in L2 in coronal sections. To identify their origin, we first applied a retrograde tracer to the surface of the ACX and found labeled cell bodies across MGB/PTN subdivisions. The distribution of labeled cells could be dichotomously divided into a dorsomedial (DM) region, primarily encompassing the dorsal and medial nuclei of MGB, and a ventrolateral (VL) region, primarily containing the marginal zone (MZ) of PTN. Sparsely labeled neurons in the caudal part of the ventral MGB (MGv) were also observed. We then injected the virus tracer into the DM region containing the dorsomedial subdivisions of MGB and the dorsomedial MGv (dmMGB), and into the VL region containing the MZ and the ventrolateral MGv, for anterograde labeling of axons. A DM injection resulted in strong, uniform labeling of axons in upper L1, without apparent axon bundles in L2, while a VL injection produced clear axon bundles in L2, as well as labeling in upper L1. The bundle density and inter-bundle interval were not significantly different between the W and VL injection cases, suggesting that the MZ is the primary origin of the axon bundles in L2. Interestingly, axons labeled by VL injections had a higher density at locations where the axon bundles reached upper L1, resulting in a clustered distribution of axons in this layer. Coherence analyses confirmed that axon density in upper L1 varied in phase with that in L2 for the VL injection cases. In tangential sections, axons labeled by W injections in lower L1 appeared to distribute in a square grid-like pattern, with expanded nodes. Quantitative analysis revealed that the axon bundles in coronal sections predominantly corresponded to the grid nodes in the tangential sections. Taken together, our results suggest a strong, uniform distribution of dmMGB axon terminals and a square grid-like distribution of MZ axon terminals in cortical upper L1. These two ascending inputs may exert differential influences on the function of L1 in the ACX.
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http://dx.doi.org/10.1016/j.heares.2025.109275 | DOI Listing |
Anat Sci Int
August 2025
Department of Anatomy and Neurobiology, National Defense Medical College, Tokorozawa, Saitama, 359-8513, Japan.
Numerous neuroanatomical tract-tracing techniques have been reported to demonstrate the origin, course, and termination of neural pathways. New techniques have been developed to achieve higher specificity and efficiency. Early tract-tracing studies at the microscopic level used non-specific staining, for example, by tracing fiber bundles of normal nervous tissue using myelin staining.
View Article and Find Full Text PDFImaging Neurosci (Camb)
March 2025
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, United States.
Anatomic tracing is the gold standard tool for delineating brain connections and for validating more recently developed imaging approaches such as diffusion MRI tractography. A key step in the analysis of data from tracer experiments is the careful, manual charting of fiber trajectories on histological sections. This is a very time-consuming process, which limits the amount of annotated tracer data that are available for validation studies.
View Article and Find Full Text PDFImaging Neurosci (Camb)
June 2025
Department of Biomedical Engineering, McGill University, Montreal, QC, Canada.
The g-ratio of a myelinated axon is defined as the ratio of the inner-to-outer diameter of the myelin sheath and modulates conduction speed of action potentials along axons. This g-ratio can be mappedat the macroscopic scale across the entire human brain using multi-modal MRI and sampled along white matter streamlines reconstructed from diffusion-weighted images to derive the g-ratio of a white matter tract. This tractometry approach has shown spatiotemporal variations in g-ratio across white matter tracts and networks.
View Article and Find Full Text PDFImaging Neurosci (Camb)
November 2024
Department of Medical Biophysics, Schulich School of Medicine and Dentistry, Western University, London, ON, Canada.
Surgical resection is the method of choice for treating drug-resistant focal temporal lobe epilepsy (TLE). Postsurgical outcomes are better when magnetic resonance imaging (MRI) findings can localize the seizure focus for resection. However, many patients are MR-negative, meaning the focus cannot be differentiated from normal tissue in relaxation-weighted MRI.
View Article and Find Full Text PDFbioRxiv
July 2025
Laboratory of Sensory Neuroscience, The Rockefeller University, New York, NY 10065, USA.
Peripheral nerve regeneration requires precise selection of the appropriate targets of innervation, often in an environment that differs from that during the developmental wiring of the neural circuit. Severed axons of the zebrafish posterior lateral line nerve have the capacity to reinnervate mechanosensory hair cells clustered in neuromast organs. Regeneration represents a balance between fasciculated regrowth of the axonal bundle and defasciculation of individual axons into the epidermis where neuromasts reside.
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