98%
921
2 minutes
20
Interest in the common marmoset is growing due to evolutionarily proximity to humans compared to laboratory mice, necessitating a comparison of mouse and marmoset brain architectures, including connectivity and cell type distributions. Creating an actionable comparative platform is challenging since these brains have distinct spatial organizations and expert neuroanatomists disagree. We propose a general theoretical framework to relate named atlas compartments across taxa and use it to establish a detailed correspondence between marmoset and mice brains. Contrary to conventional wisdom that brain structures may be easier to relate at higher levels of the atlas hierarchy, we find that finer parcellations at the leaf levels offer greater reconcilability despite naming discrepancies. Utilizing existing atlases and associated literature, we created a list of leaf-level structures for both species and establish five types of correspondence between them. One-to-one relations were found between 43% of the structures in mouse and 47% in marmoset, whereas 25% of mouse and 10% of marmoset structures were not relatable. The remaining structures show a set of more complex mappings which we quantify. Implementing this correspondence with volumetric atlases of the two species, we make available a computational tool for querying and visualizing relationships between the corresponding brains. Our findings provide a foundation for computational comparative analyses of mesoscale connectivity and cell type distributions in the laboratory mouse and the common marmoset.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11142350 | PMC |
http://dx.doi.org/10.21203/rs.3.rs-4373678/v1 | DOI Listing |
Front Aging Neurosci
August 2025
Research Center for Global Agromedicine, Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Japan.
The aim of this study was to explore and discuss efficient and effective mammalian models for Alzheimer's disease (AD). In this study, efficient AD models are characterized by a small body size, a short lifespan, and rapid development of the main pathology including amyloid plaque formation. Effective AD models are expected to exhibit not only the main pathology, but also co-pathology associated with other neurodegenerative diseases (e.
View Article and Find Full Text PDFStructural changes involving new neurons can occur through stem cell-driven neurogenesis, and through incorporation of late-maturing "immature" neurons into networks, namely undifferentiated neuronal precursors frozen in a state of arrested maturation. The latter have been found in the cerebral cortex and are particularly abundant in large-brained mammals, covarying with the size of the brain and cortex. Similar cells have been described in the amygdala of some species, although their features and interspecies variation remain poorly understood.
View Article and Find Full Text PDFJMA J
July 2025
Department of Otorhinolaryngology-Head and Neck Surgery, Keio University School of Medicine, Tokyo, Japan.
Recent advances in molecular biology have led to significant progress in the fields of otology and audiology. Rodents, particularly genetically modified mice, have traditionally served as the primary model for inner ear research. However, growing evidence highlights inter-species differences in hearing research.
View Article and Find Full Text PDFbioRxiv
June 2025
School of Psychological Sciences, Monash University, Clayton, Victoria, Australia.
Neural fluctuations exhibit rich spectral profiles that reflects both local dynamics and structural (or anatomical) embedding. Yet, standard models of resting-state effective connectivity neglect structural embedding and assume uniformity in the timescales of regions' endogenous fluctuations. We introduce a chromatic dynamic causal model (DCM) in which structural valency (or degree) modulates the spectral 'color' of endogenous fluctuations.
View Article and Find Full Text PDFbioRxiv
August 2025
Department of Neuroscience, Del Monte Institute for Neuroscience, University of Rochester Medical Center, Rochester, NY 14642, USA.
The primate cerebral cortex relies on long-range connections to integrate information across spatially distributed and functionally specialized areas, yet tools for selectively modulating these pathways remain limited. Here, we present an optimized intersectional viral and optogenetic strategy for precisely exciting and inhibiting projection-specific neurons in the common marmoset. Building on a mouse-to-marmoset pipeline, we first validated that optogenetic activation of inhibitory neurons (via AAV9-Dlx-ChR2) enables robust local cortical inhibition.
View Article and Find Full Text PDF