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Lehman, J.

Publications and source records attributed to Lehman, J..

3 recordsLinked to original sources

The modular nature of long-association pathways in the human brain

Human brain functions are organized within large-scale networks, yet the long-range structural pathways that support them remain only partly understood. Diffusion MRI tractography has enabled non-invasive mapping of these connections but its low resolution has also contributed to a view of white matter association bundles as monolithic entities linking distant cortical regions. This contrasts with anatomical studies in non-human primates and humans, which show these bundles act as conduits for complex systems of short- and long-range projections. Here we investigate the dorsal branch of the superior longitudinal fasciculus (SLF-I), the proposed structural backbone of the dorsal attention network, whose anatomy in humans is debated. Using anatomic tracing, polarization-sensitive optical coherence tomography, and in vivo and ex vivo diffusion MRI, we reconstruct the SLF-I across species, modalities, and scales. High resolution tractography (<750 m), consistent with tracer and PS-OCT data, reveals multiple fiber systems of varying lengths rather than uniform parieto-frontal connections observed at more conventional resolution (1.5 mm). Comparative analyses show a consistent organization: the SLF-I carries short-range cortico-cortical projections rostral to area 6 and longer, layered connections extending to parietal regions, while direct parieto-frontal connectivity is mostly supported by the adjacent cingulum bundle. These findings reconcile our understanding of the SLF-I across the scales of non-invasive neuroimaging and invasive anatomic studies and provide an updated framework for future investigations of large-scale networks in health and disease.

neuroscience↗

The rostral zona incerta: a subcortical integrative hub and potential DBS target for OCD

BackgroundThe zona incerta (ZI) is involved in mediating survival behaviors and is connected to a wide range of cortical and subcortical structures, including key basal ganglia nuclei. Based on these connections and their links to behavioral modulation, we propose the ZI is a connectional hub for in mediating between top-down and bottom-up control and a possible target for deep brain stimulation for obsessive compulsive disorder. MethodsWe analyzed the trajectory of cortical fibers to the ZI in nonhuman and human primates, based on tracer injections in monkeys and high-resolution diffusion MRI in humans. The organization of cortical and subcortical connections with the ZI were identified in the nonhuman primate studies. ResultsMonkey anatomic data and human dMRI data showed a similar trajectory of fibers/streamlines to the ZI. PFC/ACC terminals all converge within the rostral ZI (ZIr), with dorsal and lateral areas most prominent. Motor areas terminate caudally. Dense subcortical reciprocal connections included the thalamus, medial hypothalamus, substantia nigra/ventral tegmental area, reticular formation, and pedunculopontine nucleus and a dense nonreciprocal projection to the lateral habenula (LHb). Additional connections included amygdala, dorsal raphe nucleus, and periaqueductal grey. ConclusionsDense connections with dorsal and lateral PFC/ACC cognitive control areas and LHb and SN/VTA coupled with inputs from the amygdala, hypothalamus, and brainstem, suggests that the ZIr is a subcortical hub positioned to modulate between top-down and bottom-up control. A DBS electrode placed in the ZIr would involve both connections common to other DBS sites, but also would capture several critically distinctive connections.

neuroscience↗

Allelic variation in Class I HLA determines pre-existing memory responses to SARS-CoV-2 that shape the CD8+ T cell repertoire upon viral exposure

Effective presentation of antigens by HLA class I molecules to CD8+ T cells is required for viral elimination and generation of long-term immunological memory. In this study, we applied a single-cell, multi-omic technology to generate the first unified ex vivo characterization of the CD8+ T cell response to SARS-CoV-2 across 4 major HLA class I alleles. We found that HLA genotype conditions key features of epitope specificity, TCR /{beta} sequence diversity, and the utilization of pre-existing SARS-CoV-2 reactive memory T cell pools. Single-cell transcriptomics revealed functionally diverse T cell phenotypes of SARS-CoV-2-reactive T cells, associated with both disease stage and epitope specificity. Our results show that HLA variations influence pre-existing immunity to SARS-CoV-2 and shape the immune repertoire upon subsequent viral exposure. One-Sentence SummaryWe perform a unified, multi-omic characterization of the CD8+ T cell response to SARS-CoV-2, revealing pre-existing immunity conditioned by HLA genotype.

immunology↗