ABSTRACT
Vision in humans and other primates enlists parallel processing streams in the dorsal and ventral visual cortex, known to support spatial and object processing, respectively. These streams are bridged, however, by a prominent white matter tract, the vertical occipital fasciculus (VOF), identified in both classical neuroanatomy and recent diffusion-weighted magnetic resonance imaging (dMRI) studies. Understanding the evolution of the VOF may shed light on its origin, function, and role in visually guided behaviors. To this end, we acquired high-resolution dMRI data from the brains of select mammalian species, including anthropoid and strepsirrhine primates, a tree shrew, rodents, and carnivores. In each species, we attempted to delineate the VOF after first locating the optic radiations in the occipital white matter. In all primate species examined, the optic radiation was flanked laterally by a prominent and coherent white matter fasciculus recognizable as the VOF. By contrast, the equivalent analysis applied to four non-primate species from the same superorder as primates (tree shrew, ground squirrel, paca, and rat) failed to reveal white matter tracts in the equivalent location. Clear evidence for a VOF was also absent in two larger carnivore species (ferret and fox). Although we cannot rule out the existence of minor or differently organized homologous fiber pathways in the non-primate species, the results suggest that the VOF has greatly expanded, or possibly emerged, in the primate lineage. This adaptation likely facilitated the evolution of unique visually guided behaviors in primates, with direct impacts on manual object manipulation, social interactions, and arboreal locomotion.
Subject(s)
Primates , Visual Cortex , White Matter , Animals , White Matter/diagnostic imaging , White Matter/anatomy & histology , Primates/anatomy & histology , Primates/physiology , Visual Cortex/physiology , Visual Cortex/diagnostic imaging , Visual Cortex/anatomy & histology , Visual Pathways/anatomy & histology , Visual Pathways/physiology , Visual Pathways/diagnostic imaging , Occipital Lobe/anatomy & histology , Occipital Lobe/physiology , Occipital Lobe/diagnostic imaging , Diffusion Magnetic Resonance Imaging , Carnivora/anatomy & histology , Carnivora/physiology , Species Specificity , Biological Evolution , Rodentia/anatomy & histology , Rodentia/physiologyABSTRACT
Brain development is a highly complex process regulated by numerous genes at the molecular and cellular levels. Brain tissue exhibits serial microstructural changes during the development process. High-resolution diffusion magnetic resonance imaging (dMRI) affords a unique opportunity to probe these changes in the developing brain non-destructively. In this study, we acquired multi-shell dMRI datasets at 32 µm isotropic resolution to investigate the tissue microstructure alterations, which we believe to be the highest spatial resolution dMRI datasets obtained for postnatal mouse brains. We adapted the Allen Developing Mouse Brain Atlas (ADMBA) to integrate quantitative MRI metrics and spatial transcriptomics. Diffusion tensor imaging (DTI), diffusion kurtosis imaging (DKI), and neurite orientation dispersion and density imaging (NODDI) metrics were used to quantify brain development at different postnatal days. We demonstrated that the differential evolutions of fiber orientation distributions contribute to the distinct development patterns in white matter (WM) and gray matter (GM). Furthermore, the genes enriched in the nervous system that regulate brain structure and function were expressed in spatial correlation with age-matched dMRI. This study is the first one providing high-resolution dMRI, including DTI, DKI, and NODDI models, to trace mouse brain microstructural changes in WM and GM during postnatal development. This study also highlighted the genotype-phenotype correlation of spatial transcriptomics and dMRI, which may improve our understanding of brain microstructure changes at the molecular level.
Subject(s)
Brain , Diffusion Magnetic Resonance Imaging , Transcriptome , Animals , Mice , Brain/growth & development , Brain/diagnostic imaging , Brain/anatomy & histology , Diffusion Magnetic Resonance Imaging/methods , Diffusion Tensor Imaging/methods , White Matter/growth & development , White Matter/diagnostic imaging , Gray Matter/growth & development , Gray Matter/diagnostic imaging , Gray Matter/anatomy & histology , Mice, Inbred C57BL , Male , FemaleABSTRACT
The Ophidiidae is a group of more than 300 species of fishes characterized by elongated, snake-like bodies and continuous dorsal, anal, and caudal fins. While describing a new species in the genus Monomitopus, we discovered a bilaterally paired fenestra on the dorsomedial surface of the neurocranium. We surveyed the distribution of this fenestra across species of Monomitopus and previously hypothesized allies in the genera Dannevigia, Dicrolene, Homostolus, Neobythites, and Selachophidium, finding variation in its presence and size. We also found a prominent bilaterally paired lateral fenestra and a posterior expansion of the exoccipital in the neurocrania of M. americanus and S. guentheri, with soft tissue connecting the back of the neurocranium to the first epineural and pectoral girdle in S. guentheri. In this study, we describe the distribution of and variation in these features. We integrate morphological characters and DNA data to generate a phylogeny of Monomitopus and allies to understand their relationships and trace the evolutionary history of these novel features. Our results call the monophyly of Monomitopus into question. The presence of the lateral neurocranial fenestra and posterior expansion of the exoccipital support the reclassification of M. americanus as a species of Selachophidium.
Subject(s)
Biological Evolution , Phylogeny , Skull , Animals , Skull/anatomy & histology , Fishes/anatomy & histologyABSTRACT
BACKGROUND: Autism Spectrum Disorder (ASD) is a group of neurodevelopmental disorders with higher incidence in males and is characterized by atypical verbal/nonverbal communication, restricted interests that can be accompanied by repetitive behavior, and disturbances in social behavior. This study investigated brain mechanisms that contribute to sociability deficits and sex differences in an ASD animal model. METHODS: Sociability was measured in C58/J and C57BL/6J mice using the 3-chamber social choice test. Bulk RNA-Seq and snRNA-Seq identified transcriptional changes in C58/J and C57BL/6J amygdala within which DMRseq was used to measure differentially methylated regions in amygdala. RESULTS: C58/J mice displayed divergent social strata in the 3-chamber test. Transcriptional and pathway signatures revealed immune-related biological processes differ between C58/J and C57BL/6J amygdala. Hypermethylated and hypomethylated genes were identified in C58/J versus C57BL/6J amygdala. snRNA-Seq data in C58/J amygdala identified differential transcriptional signatures within oligodendrocytes and microglia characterized by increased ASD risk gene expression and predicted impaired myelination that was dependent on sex and sociability. RNA velocity, gene regulatory network, and cell communication analysis showed diminished oligodendrocyte/microglia differentiation. Findings were verified using Bulk RNA-Seq and demonstrated oxytocin's beneficial effects on myelin gene expression. LIMITATIONS: Our findings are significant. However, limitations can be noted. The cellular mechanisms linking reduced oligodendrocyte differentiation and reduced myelination to an ASD phenotype in C58/J mice need further investigation. Additional snRNA-Seq and spatial studies would determine if effects in oligodendrocytes/microglia are unique to amygdala or if this occurs in other brain regions. Oxytocin's effects need further examination to understand its' potential as an ASD therapeutic. CONCLUSIONS: Our work demonstrates the C58/J mouse model's utility in evaluating the influence of sex and sociability on the transcriptome in concomitant brain regions involved in ASD. Our single-nucleus transcriptome analysis elucidates potential pathological roles of oligodendrocytes and microglia in ASD. This investigation provides details regarding regulatory features disrupted in these cell types, including transcriptional gene dysregulation, aberrant cell differentiation, altered gene regulatory networks, and changes to key pathways that promote microglia/oligodendrocyte differentiation. Our studies provide insight into interactions between genetic risk and epigenetic processes associated with divergent affiliative behavior and lack of positive sociability.
Subject(s)
Amygdala , Autism Spectrum Disorder , Mice, Inbred C57BL , Microglia , Oligodendroglia , Social Behavior , Animals , Male , Microglia/metabolism , Mice , Amygdala/metabolism , Female , Oligodendroglia/metabolism , Autism Spectrum Disorder/genetics , Autism Spectrum Disorder/pathology , Gene Expression Profiling/methods , Phenotype , Sex Characteristics , Transcriptome , Disease Models, Animal , Oxytocin/genetics , Oxytocin/metabolismABSTRACT
Purpose: To identify significant relationships between quantitative cytometric tissue features and quantitative MR (qMRI) intratumorally in preclinical undifferentiated pleomorphic sarcomas (UPS). Materials and methods: In a prospective study of genetically engineered mouse models of UPS, we registered imaging libraries consisting of matched multi-contrast in vivo MRI, three-dimensional (3D) multi-contrast high-resolution ex vivo MR histology (MRH), and two-dimensional (2D) tissue slides. From digitized histology we generated quantitative cytometric feature maps from whole-slide automated nuclear segmentation. We automatically segmented intratumoral regions of distinct qMRI values and measured corresponding cytometric features. Linear regression analysis was performed to compare intratumoral qMRI and tissue cytometric features, and results were corrected for multiple comparisons. Linear correlations between qMRI and cytometric features with p values of <0.05 after correction for multiple comparisons were considered significant. Results: Three features correlated with ex vivo apparent diffusion coefficient (ADC), and no features correlated with in vivo ADC. Six features demonstrated significant linear relationships with ex vivo T2*, and fifteen features correlated significantly with in vivo T2*. In both cases, nuclear Haralick texture features were the most prevalent type of feature correlated with T2*. A small group of nuclear topology features also correlated with one or both T2* contrasts, and positive trends were seen between T2* and nuclear size metrics. Conclusion: Registered multi-parametric imaging datasets can identify quantitative tissue features which contribute to UPS MR signal. T2* may provide quantitative information about nuclear morphology and pleomorphism, adding histological insights to radiological interpretation of UPS.
ABSTRACT
The appearance of evolutionary novelties is a central issue in biology. Since Darwin's theory, difficulties in explaining how novel intricate body parts arose have often been used by creationists and other deniers to challenge evolution. Here, we describe the gustatory stalk of the Remo flounder (Oncopterus darwinii), an anatomically and functionally complex organ presumably used as a chemoreceptor probe to detect prey buried in the substrate. We demonstrate that the gustatory stalk is derived from the first dorsal-fin ray, which acquired remarkable modifications in its external morphology, integument, skeleton, muscles, and nerves. Such structural innovations are echoed in both functional and ecological specializations. We reveal that the gustatory stalk arose through the gradual accumulation of changes that evolved at different levels of the phylogenetic tree of ray-finned fishes. At least five preconditions arose in nodes preceding Oncopterus darwinii. This finding constitutes an interesting example of how evolution can deeply remodel body parts to perform entirely new functions. In this case, a trivial support structure primitively used for swimming became a sophisticated sensory tool to uncover hidden prey.
Subject(s)
Biological Evolution , Flounder , Phylogeny , Animals , Flounder/genetics , Flounder/anatomy & histologyABSTRACT
We have combined MR histology and light sheet microscopy (LSM) of five postmortem C57BL/6J mouse brains in a stereotaxic space based on micro-CT yielding a multimodal 3D atlas with the highest spatial and contrast resolution yet reported. Brains were imaged in situ with multi gradient echo (mGRE) and diffusion tensor imaging (DTI) at 15 µm resolution (â¼ 2.4 million times that of clinical MRI). Scalar images derived from the average DTI and mGRE provide unprecedented contrast in 14 complementary 3D volumes, each highlighting distinct histologic features. The same tissues scanned with LSM and registered into the stereotaxic space provide 17 different molecular cell type stains. The common coordinate framework labels (CCFv3) complete the multimodal atlas. The atlas has been used to correct distortions in the Allen Brain Atlas and harmonize it with Franklin Paxinos. It provides a unique resource for stereotaxic labeling of mouse brain images from many sources.
ABSTRACT
Background: Autism Spectrum Disorder (ASD) is a group of neurodevelopmental disorders with higher incidence in males and is characterized by atypical verbal/nonverbal communication, restricted interests that can be accompanied by repetitive behavior, and disturbances in social behavior. This study investigated brain mechanisms that contribute to sociability deficits and sex differences in an ASD animal model. Methods: Sociability was measured in C58/J and C57BL/6J mice using the 3-chamber social choice test. Bulk RNA-Seq and snRNA-Seq identified transcriptional changes in C58/J and C57BL/6J amygdala within which DMRseq was used to measure differentially methylated regions in amygdala. Results: C58/J mice displayed divergent social strata in the 3-chamber test. Transcriptional and pathway signatures revealed immune-related biological processes differ between C58/J and C57BL/6J amygdala. Hypermethylated and hypomethylated genes were identified in C58/J versus C57BL/6J amygdala. snRNA-Seq data in C58/J amygdala identified differential transcriptional signatures within oligodendrocytes and microglia characterized by increased ASD risk gene expression and predicted impaired myelination that was dependent on sex and sociability. RNA velocity, gene regulatory network, and cell communication analysis showed diminished oligodendrocyte/microglia differentiation. Findings were verified using bulk RNA-Seq and demonstrated oxytocin's beneficial effects on myelin gene expression. Limitations: Our findings are significant. However, limitations can be noted. The cellular mechanisms linking reduced oligodendrocyte differentiation and reduced myelination to an ASD phenotype in C58/J mice need further investigation. Additional snRNA-Seq and spatial studies would determine if effects in oligodendrocytes/microglia are unique to amygdala or if this occurs in other brain regions. Oxytocin's effects need further examination to understand its potential as an ASD therapeutic. Conclusions: Our work demonstrates the C58/J mouse model's utility in evaluating the influence of sex and sociability on the transcriptome in concomitant brain regions involved in ASD. Our single-nucleus transcriptome analysis elucidates potential pathological roles of oligodendrocytes and microglia in ASD. This investigation provides details regarding regulatory features disrupted in these cell types, including transcriptional gene dysregulation, aberrant cell differentiation, altered gene regulatory networks, and changes to key pathways that promote microglia/oligodendrocyte differentiation. Our studies provide insight into interactions between genetic risk and epigenetic processes associated with divergent affiliative behavior and lack of positive sociability.
ABSTRACT
In 1985, Carter and Cohen noted that there are several yet-to-be described species of Monomitopus (Ophidiidae), including one from Hawaii. Recently, blackwater divers collected a larval fish off Kona, Hawaii, similar to the previously described larvae of M. kumae, but DNA sequence data from the larva does not match any of the six previously sequenced species within the genus. Within the Smithsonian Institutions National Museum of Natural History Ichthyology Collection, we find a single unidentified adult specimen of Monomitopus collected North of Maui, Hawaii in 1972 whose fin-ray and vertebral/myomere counts overlap those of the larval specimen. We describe this new Hawaiian species of Monomitopus based on larval and adult characters. Additionally, blackwater photographs of several species of Monomitopus show the larvae coiled into a tight ball, a novel behavior to be observed in cusk-eels. We describe this behavior, highlighting the importance of blackwater photography in advancing our understanding of marine larval fish biology.
Subject(s)
Fishes , Gadiformes , Animals , Hawaii , Eels , LarvaABSTRACT
Resumen El trasplante pulmonar implica una serie de desafíos, que como lo ha demostrado la historia, no sólo depende de un adecuado desarrollo de técnicas quirúrgicas, sino también de la comprensión de una serie de complejas interacciones inmunológicas celulares y humorales que serán las responsables del tipo de respuesta (innata y/o adquirida) fisiológica y que pudiesen desencadenar las complicaciones asociadas al trasplante (rechazo hiperagudo, agudo o crónico). Cada una de las cuales tiene su potencial prevención y/o tratamiento. El poder conocer esta serie de respuestas, permite al clínico anticiparse a algunos de estos eventos y evitar de mejor forma el daño y las consecuencias que pueden producir en los casos de trasplante pulmonar.
Lung transplantation involves a series of challenges, which as history has shown, depends not only on an adequate development of surgical techniques, but also on the understanding of a series of complex cellular and humoral immunological interactions that will be responsible for the type of physiological response (innate - acquired) and that could trigger the complications associated with transplantation (hyperacute, acute or chronic rejection). Each of which has its potential prevention and treatment. Being able to know this series of responses, allows the clinician to anticipate some of these events and to avoid in a better way the damage and the consequences that can occur in cases of lung transplantation.
Subject(s)
Humans , Transplantation Immunology/immunology , Lung Transplantation , Graft Rejection/immunology , T-Lymphocytes/immunology , Autoimmunity , Nuclear Factor 45 Protein , Graft Rejection/prevention & control , Immunity, Cellular , Immunity, Innate , Immunosuppressive AgentsABSTRACT
El objetivo de este artículo es presentar cuatro casos clínicos que requerían tratamiento protésico y/o periodontal y cómo la extrusión ortodóncica contribuye a un mejor resultado final e incluso evita la necesidad de realizar procedimientos periodontales complejos. La odontología restauradora actual encuentra cada vez con mayor frecuencia el reto de preservar dientes severamente destruidos o reemplazarlos de la manera más estética y funcional posible. Esto requiere procedimientos predecibles y de corta duración, funcionales, estéticos, económicos y no dolorosos, para la rehabilitación y/o reemplazo de dichos dientes...
Subject(s)
Dental Implantation , Periodontics , Tooth Movement Techniques , Dental Prosthesis , Dentistry , OrthodonticsSubject(s)
Blindness/epidemiology , Cataract , Glaucoma , Vision Disorders , Health Surveys , Mongolia , 28599 , Age FactorsABSTRACT
This study is part of a multi-year program aimed toward reducing earthquake risk for critical facility equipment and components. The program goal is to determine which equipment components are critical to life safety and normal operations, and how equipment systems have perfomed in past earthquakes. This report represents the dirst program phase, in which equipment data were collected and reviewed in the context of four sample facility types and six equipment systems. Subsequent program phases will: (i) develop a simplified method to assess and improve the reliability of equipment systems, (ii) apply the methodology to example building and component inventories, and (iii) disseminate component fragility and system reliability models in a format that can be used by codewriting bodies, emergency-response facility owners, and operators of economically valuable facilities.(AU)
Subject(s)
Earthquakes , Risk Assessment , Public Facilities , Engineering , EconomicsABSTRACT
A population-based prevalence survey of ocular disease was conducted in the Lower Shire Valley of Malawi in 1983. A total of 5;436 children less than 6 years of age and 1;664 persons greater than or equal to 6 years were examined. The prevalence of inflammatory trachoma peaked in the 1-2-year-old age group at 48.7 percent and declined rapidly with age to less than 5 percent by age 15. The prevalence of cicatricial trachoma was low in young children and climbed gradually with age to greater than 40 percent among those greater than or equal to 50 years. Risk factors for infLammatory disease in young children included low socioeconomic status of the family; long walking distance to the household's primary source of water; absence of a latrine in the family compound; and presence of trachoma among siblings. Indices of crowding practices were not associated with inflammatory disease. An apparent inverse association of facewashing and inflammatory trachoma in children did not hold up when adjusted for other risk factors