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1.
Elife ; 102021 09 15.
Artículo en Inglés | MEDLINE | ID: mdl-34523418

RESUMEN

Insects have evolved diverse and remarkable strategies for navigating in various ecologies all over the world. Regardless of species, insects share the presence of a group of morphologically conserved neuropils known collectively as the central complex (CX). The CX is a navigational center, involved in sensory integration and coordinated motor activity. Despite the fact that our understanding of navigational behavior comes predominantly from ants and bees, most of what we know about the underlying neural circuitry of such behavior comes from work in fruit flies. Here, we aim to close this gap, by providing the first comprehensive map of all major columnar neurons and their projection patterns in the CX of a bee. We find numerous components of the circuit that appear to be highly conserved between the fly and the bee, but also highlight several key differences which are likely to have important functional ramifications.


Bumblebees forage widely for pollen and nectar from flowers, sometimes travelling kilometers away from their nest, but they can somehow always find their way home in a nearly straight line. These insects have been known to return to their nest from new locations almost 10 kilometers away. This homing ability is a complex neurological feat and requires the brain to combine several processes, including observing the external world, controlling bodily movements and drawing on memory. While the navigational behavior of bees has been well-studied, the neuronal circuitry behind it has not. Unfortunately, most of what is known about insects' brain activity comes from studies in species such as locusts or fruit flies. In these species, a region of the brain known as the central complex has been shown to have an essential role in homing behaviors. However, it is unknown how similar the central complex of bumblebees might be to fruit flies' or locusts', or how these differences may affect navigational abilities. Sayre et al. obtained images of thin slices of the bumblebee central complex using a technique called block-face electron microscopy, which produces high-resolution image volumes. These images were used to obtain a three-dimensional map of over 1300 neurons. This cellular atlas showed that key aspects of the central complex are nearly identical between flies and bumblebees, including the internal compass that monitors what direction the insect is travelling in. However, hundreds of millions of years of independent evolution have resulted in some differences. These were found in neurons possibly involved in forming memories of the directions and lengths of travelled paths, and in the circuits that use such vector memories to steer the insects towards their targets. Sayre et al. propose that these changes underlie bees' impressive ability to navigate. These results help explain how the structure of insects' brains can determine homing abilities. The insights gained could be used to develop efficient autonomous navigation systems, which are challenging to build and require a lot more processing power than offered by a small part of an insect brain.


Asunto(s)
Abejas/fisiología , Conducta Animal , Conectoma , Vuelo Animal , Vías Nerviosas/fisiología , Neurópilo/fisiología , Conducta Espacial , Animales , Abejas/ultraestructura , Drosophila melanogaster/fisiología , Drosophila melanogaster/ultraestructura , Vías Nerviosas/ultraestructura , Neurópilo/ultraestructura , Especificidad de la Especie
2.
Arthropod Struct Dev ; 60: 101024, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-33383276

RESUMEN

Only a few studies have examined the central visual system of Solifugae until now. To get new insights suitable for phylogenetic analysis we studied the R-cell (or retinula cell) projections and visual neuropils of Galeodes granti using various methods. G. granti possesses large median eyes and rudimentary lateral eyes. In this study, only the R-cells and neuropils of the median eyes were successfully stained. The R-cells terminate in two distinct visual neuropils. The first neuropil is located externally to the protocerebrum directly below the retina, the second neuropil lies in the cell body rind of the protocerebrum, and immediately adjacent is the arcuate body. This layout of the median eye visual system differs from Arachnopulmonata (Scorpiones + Tetrapulmonata). However, there are several similarities with Opiliones. In both, (1) the R-cells are connected to a first and second visual neuropil and not to any other region of the brain, (2) the first neuropil is not embedded in the cell body rind of the protocerebrum, it is rather external to the protocerebrum, (3) the second visual neuropil is embedded in the cell body rind, and (4) the second neuropil abuts the arcuate body. These findings may provide important new characters for the discussion on arachnid phylogeny.


Asunto(s)
Arácnidos/anatomía & histología , Animales , Arácnidos/ultraestructura , Ojo/anatomía & histología , Ojo/ultraestructura , Microscopía , Microscopía Electrónica de Transmisión , Neurópilo/citología , Neurópilo/ultraestructura , Vías Visuales/anatomía & histología , Vías Visuales/ultraestructura
3.
Cereb Cortex ; 31(1): 410-425, 2021 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-32887978

RESUMEN

The entorhinal cortex (EC) is a brain region that has been shown to be essential for memory functions and spatial navigation. However, detailed three-dimensional (3D) synaptic morphology analysis and identification of postsynaptic targets at the ultrastructural level have not been performed before in the human EC. In the present study, we used Focused Ion Beam/Scanning Electron Microscopy to perform a 3D analysis of the synapses in the neuropil of medial EC in layers II and III from human brain autopsies. Specifically, we studied synaptic structural parameters of 3561 synapses, which were fully reconstructed in 3D. We analyzed the synaptic density, 3D spatial distribution, and type (excitatory and inhibitory), as well as the shape and size of each synaptic junction. Moreover, the postsynaptic targets of synapses could be clearly determined. The present work constitutes a detailed description of the synaptic organization of the human EC, which is a necessary step to better understand the functional organization of this region in both health and disease.


Asunto(s)
Corteza Entorrinal/ultraestructura , Imagenología Tridimensional , Neurópilo/ultraestructura , Sinapsis/ultraestructura , Adulto , Anciano , Enfermedad de Alzheimer/patología , Humanos , Imagenología Tridimensional/métodos , Masculino , Persona de Mediana Edad , Neuronas/ultraestructura
4.
Arthropod Struct Dev ; 58: 100971, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-32755758

RESUMEN

Locusts, like other insects, partly rely on a sun compass mechanism for spatial orientation during seasonal migrations. To serve as a useful guiding cue throughout the day, however, the sun's apparent movement has to be accounted for. In locusts, a neural pathway from the accessory medulla, the circadian pacemaker, via the posterior optic tubercle, to the protocerebral bridge, part of the internal sky compass, has been proposed to mediate the required time compensation. Toward a better understanding of neural connectivities within the posterior optic tubercle, we investigated this neuropil using light and electron microscopy. Based on vesicle content, four types of synaptic profile were distinguished within the posterior optic tubercle. Immunogold labeling showed that pigment-dispersing hormone immunoreactive neurons from the accessory medulla, containing large dense-core vesicles, have presynaptic terminals in the posterior optic tubercle. Ultrastructural examination of two Neurobiotin-injected tangential neurons of the protocerebral bridge revealed that these neurons are postsynaptic in the posterior optic tubercle. Our data, therefore, support a role of the posterior optic tubercles in mediating circadian input to the insect sky compass.


Asunto(s)
Saltamontes/anatomía & histología , Neurópilo/ultraestructura , Animales , Femenino , Saltamontes/ultraestructura , Inmunohistoquímica , Masculino , Microscopía Inmunoelectrónica
5.
Arthropod Struct Dev ; 54: 100902, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31991325

RESUMEN

Copepoda is one of the crustacean taxa with still unresolved phylogenetic relationships within Tetraconata. Recent phylogenomic studies place them close to Malacostraca and Cirripedia. Little is known about the morphological details of the copepod nervous system, and the available data are sometimes contradictory. We investigated several representatives of the subgroup Calanoida using immunohistochemical labeling against alpha-tubulin and various neuroactive substances, combining this with confocal laser scanning analysis and 3D reconstruction. Our results show that the studied copepods exhibit only a single anterior protocerebral neuropil which is connected to the nerves of two protocerebral sense organs: the frontal filament organ and a photoreceptor known as the Gicklhorn's organ. We suggest, on the basis of its position and the innervation it provides, that Gicklhorn's organ is homologous to the compound eye in arthropods. With regard to the frontal filament organ, we reveal detailed innervation to the lateral protocerebrum and the appearance of spherical bodies that stain intensely against alpha tubulin. A potential homology of these bodies to the onion bodies in malacostacan crustaceans and in Mystacocarida is suggested. The nauplius eye in all the examined calanoids shows the same basic pattern of innervation with the middle cup sending its neurites into the median nerve, while the axons of the lateral cups proceed into both the median and the lateral nerves. The early development of the axonal scaffold of the nauplius eye neuropil from the proximal parts of the nauplius eye nerves follows the same pattern as in other crustaceans. In our view, this specific innervation pattern is a further feature supporting the homology of the nauplius eye in crustaceans.


Asunto(s)
Ojo Compuesto de los Artrópodos/anatomía & histología , Copépodos/anatomía & histología , Animales , Encéfalo/anatomía & histología , Encéfalo/ultraestructura , Ojo Compuesto de los Artrópodos/ultraestructura , Copépodos/ultraestructura , Microscopía Confocal , Microscopía Electrónica de Rastreo , Neurópilo/citología , Neurópilo/ultraestructura , Órganos de los Sentidos/anatomía & histología , Órganos de los Sentidos/ultraestructura
6.
Science ; 366(6469)2019 11 29.
Artículo en Inglés | MEDLINE | ID: mdl-31649140

RESUMEN

The dense circuit structure of mammalian cerebral cortex is still unknown. With developments in three-dimensional electron microscopy, the imaging of sizable volumes of neuropil has become possible, but dense reconstruction of connectomes is the limiting step. We reconstructed a volume of ~500,000 cubic micrometers from layer 4 of mouse barrel cortex, ~300 times larger than previous dense reconstructions from the mammalian cerebral cortex. The connectomic data allowed the extraction of inhibitory and excitatory neuron subtypes that were not predictable from geometric information. We quantified connectomic imprints consistent with Hebbian synaptic weight adaptation, which yielded upper bounds for the fraction of the circuit consistent with saturated long-term potentiation. These data establish an approach for the locally dense connectomic phenotyping of neuronal circuitry in the mammalian cortex.


Asunto(s)
Conectoma , Corteza Somatosensorial/ultraestructura , Animales , Axones/ultraestructura , Imagenología Tridimensional , Masculino , Ratones , Ratones Endogámicos C57BL , Microscopía Electrónica , Neuronas/ultraestructura , Neurópilo/ultraestructura , Sinapsis/ultraestructura
7.
Methods Mol Biol ; 2034: 83-95, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31392679

RESUMEN

Immunohistochemical electron microscopy (EM) allows the identification of microglial cell bodies and processes, which are otherwise difficult to recognize based on their ultrastructural features. The technique has been essential in defining, at high spatial resolution, microglial interactions with neurons and synapses, thus providing, among other discoveries, important insights into their roles in synaptic pruning and stripping. In this protocol, we describe the preparation of mouse brain tissue for EM, the immunocytochemical staining against ionized calcium binding adaptor molecule 1, the imaging of microglial cell bodies and processes, and the analysis of microglial relationships with the synaptic neuropil.


Asunto(s)
Microglía , Neuronas , Neurópilo , Coloración y Etiquetado , Sinapsis , Animales , Inmunohistoquímica , Ratones , Microglía/metabolismo , Microglía/ultraestructura , Neuronas/metabolismo , Neuronas/ultraestructura , Neurópilo/metabolismo , Neurópilo/ultraestructura , Sinapsis/metabolismo , Sinapsis/ultraestructura
8.
Neuron ; 103(1): 118-132.e7, 2019 07 03.
Artículo en Inglés | MEDLINE | ID: mdl-31147153

RESUMEN

Animals use global image motion cues to actively stabilize their position by compensatory movements. Neurons in the zebrafish pretectum distinguish different optic flow patterns, e.g., rotation and translation, to drive appropriate behaviors. Combining functional imaging and morphological reconstruction of single cells, we revealed critical neuroanatomical features of this sensorimotor transformation. Terminals of direction-selective retinal ganglion cells (DS-RGCs) are located within the pretectal retinal arborization field 5 (AF5), where they meet dendrites of pretectal neurons with simple tuning to monocular optic flow. Translation-selective neurons, which respond selectively to optic flow in the same direction for both eyes, are intermingled with these simple cells but do not receive inputs from DS-RGCs. Mutually exclusive populations of pretectal projection neurons innervate either the reticular formation or the cerebellum, which in turn control motor responses. We posit that local computations in a defined pretectal circuit transform optic flow signals into neural commands driving optomotor behavior. VIDEO ABSTRACT.


Asunto(s)
Flujo Optico/fisiología , Vías Visuales/citología , Animales , Cerebelo/citología , Cerebelo/fisiología , Dendritas/fisiología , Neurópilo/fisiología , Neurópilo/ultraestructura , Terminales Presinápticos/fisiología , Formación Reticular/citología , Formación Reticular/fisiología , Células Ganglionares de la Retina/fisiología , Colículos Superiores/citología , Colículos Superiores/fisiología , Visión Binocular/fisiología , Visión Monocular/fisiología , Vías Visuales/anatomía & histología , Pez Cebra/fisiología
9.
Sci Rep ; 9(1): 6941, 2019 05 06.
Artículo en Inglés | MEDLINE | ID: mdl-31061452

RESUMEN

The gastrointestinal tract is constructed with an intrinsic series of interconnected ganglia that span its entire length, called the enteric nervous system (ENS). The ENS exerts critical local reflex control over many essential gut functions; including peristalsis, water balance, hormone secretions and intestinal barrier homeostasis. ENS ganglia exist as a collection of neurons and glia that are arranged in a series of plexuses throughout the gut: the myenteric plexus and submucosal plexus. While it is known that enteric ganglia are derived from a stem cell population called the neural crest, mechanisms that dictate final neuropil plexus organization remain obscure. Recently, the vertebrate animal, zebrafish, has emerged as a useful model to understand ENS development, however knowledge of its developing myenteric plexus architecture was unknown. Here, we examine myenteric plexus of the maturing zebrafish larval fish histologically over time and find that it consists of a series of tight axon layers and long glial cell processes that wrap the circumference of the gut tube to completely encapsulate it, along all levels of the gut. By late larval stages, complexity of the myenteric plexus increases such that a layer of axons is juxtaposed to concentric layers of glial cells. Ultrastructurally, glial cells contain glial filaments and make intimate contacts with one another in long, thread-like projections. Conserved indicators of vesicular axon profiles are readily abundant throughout the larval plexus neuropil. Together, these data extend our understanding of myenteric plexus architecture in maturing zebrafish, thereby enabling functional studies of its formation in the future.


Asunto(s)
Sistema Nervioso Entérico/metabolismo , Sistema Nervioso Entérico/ultraestructura , Neurópilo/metabolismo , Neurópilo/ultraestructura , Animales , Axones/metabolismo , Axones/ultraestructura , Biomarcadores , Tracto Gastrointestinal/inervación , Tracto Gastrointestinal/metabolismo , Inmunohistoquímica , Larva , Neurogénesis , Neuroglía/metabolismo , Neuroglía/ultraestructura , Pez Cebra
10.
J Histochem Cytochem ; 67(3): 185-202, 2019 03.
Artículo en Inglés | MEDLINE | ID: mdl-30562121

RESUMEN

Electron microscopy (EM) studies of the postmortem human brain provide a level of resolution essential for understanding brain function in both normal and disease states. However, processes associated with death can impair the cellular and organelle ultrastructural preservation required for quantitative EM studies. Although postmortem interval (PMI), the time between death and preservation of tissue, is thought to be the most influential factor of ultrastructural quality, numerous other factors may also influence tissue preservation. The goal of the present study was to assess the effects of pre- and postmortem factors on multiple components of ultrastructure in the postmortem human prefrontal cortex. Tissue samples from 30 subjects were processed using standard EM histochemistry. The primary dependent measure was number of identifiable neuronal profiles, and secondary measures included presence and/or integrity of synapses, mitochondria, and myelinated axonal fibers. Number of identifiable neuronal profiles was most strongly affected by the interaction of PMI and pH, such that short PMIs and neutral pH values predicted the best preservation. Secondary measures were largely unaffected by pre- and postmortem factors. Together, these data indicate that distinct components of the neuropil are differentially affected by PMI and pH in postmortem human brain.


Asunto(s)
Histocitoquímica/normas , Fibras Nerviosas Mielínicas/ultraestructura , Neuronas/ultraestructura , Neurópilo/ultraestructura , Corteza Prefrontal/ultraestructura , Sinapsis/ultraestructura , Adulto , Enfermedades Cardiovasculares/patología , Estudios de Casos y Controles , Causas de Muerte , Femenino , Histocitoquímica/métodos , Humanos , Concentración de Iones de Hidrógeno , Masculino , Trastornos Mentales/patología , Persona de Mediana Edad , Mitocondrias/ultraestructura , Cambios Post Mortem , Corteza Prefrontal/anatomía & histología , Corteza Prefrontal/patología , Trastornos Relacionados con Sustancias/patología , Factores de Tiempo , Conservación de Tejido/métodos
11.
J Comp Neurol ; 527(7): 1261-1277, 2019 05 01.
Artículo en Inglés | MEDLINE | ID: mdl-30592041

RESUMEN

Animals are active at different times of the day. Each temporal niche offers a unique light environment, which affects the quality of the available visual information. To access reliable visual signals in dim-light environments, insects have evolved several visual adaptations to enhance their optical sensitivity. The extent to which these adaptations reflect on the sensory processing and integration capabilities within the brain of a nocturnal insect is unknown. To address this, we analyzed brain organization in congeneric species of the Australian bull ant, Myrmecia, that rely predominantly on visual information and range from being strictly diurnal to strictly nocturnal. Weighing brains and optic lobes of seven Myrmecia species, showed that after controlling for body mass, the brain mass was not significantly different between diurnal and nocturnal ants. However, the optic lobe mass, after controlling for central brain mass, differed between day- and night-active ants. Detailed volumetric analyses showed that the nocturnal ants invested relatively less in the primary visual processing regions but relatively more in both the primary olfactory processing regions and in the integration centers of visual and olfactory sensory information. We discuss how the temporal niche occupied by each species may affect cognitive demands, thus shaping brain organization among insects active in dim-light conditions.


Asunto(s)
Hormigas/fisiología , Encéfalo/anatomía & histología , Ritmo Circadiano/fisiología , Ojo Compuesto de los Artrópodos/fisiología , Animales , Hormigas/anatomía & histología , Australia , Tamaño Corporal , Mapeo Encefálico , Luz , Locomoción/fisiología , Neurópilo/fisiología , Neurópilo/ultraestructura , Visión Nocturna , Lóbulo Óptico de Animales no Mamíferos/anatomía & histología , Lóbulo Óptico de Animales no Mamíferos/fisiología , Tamaño de los Órganos , Olfato/fisiología , Especificidad de la Especie
12.
Behav Brain Res ; 360: 279-285, 2019 03 15.
Artículo en Inglés | MEDLINE | ID: mdl-30550949

RESUMEN

The energy deficit hypothesis of attention-deficit/hyperactivity disorder (ADHD) suggests that low lactate production by brain astrocytes causes the symptoms of the disorder. Astrocytes are the main producers of lactate in the brain; however, skeletal muscles can produce the most lactate in the body. The lactate production by skeletal muscles increases with physical activity, as does the expression of the lactate transporter monocarboxylate transporter 1 (MCT1) at the blood-brain barrier (BBB). We hypothesise that children with ADHD, by being hyperactive, increase lactate production by skeletal muscles and transport it into the brain to compensate for low supply by astrocytes. The aim of this study was to explore whether the level of MCT1 is altered in the brain in an animal model of ADHD. The MCT1 expression was quantified on hippocampal brain sections from the best available rat model of ADHD, i.e., the spontaneously hypertensive rat (SHR) (n = 12), and the relevant control, the Wistar Kyoto rat (WKY) (n = 12), by the use of quantitative immunofluorescence laser scanning microscopy and postembedding immunogold electron microscopy. The results revealed significantly higher levels of hippocampal MCT1 immunoreactivity in SHR compared to WKY, particularly at the BBB. These results indicate that lactate flux through MCT1 between the body and the brain could be upregulated in children with ADHD. This study adds to previous research suggesting hyperactivity may be beneficial in ADHD; Children with ADHD possibly display a hyperactive behaviour in order to raise skeletal muscle lactate production, MCT1 expression and flux over the BBB to supply the brain with lactate.


Asunto(s)
Trastorno por Déficit de Atención con Hiperactividad/patología , Barrera Hematoencefálica/metabolismo , Transportadores de Ácidos Monocarboxílicos/metabolismo , Regulación hacia Arriba/fisiología , Animales , Trastorno por Déficit de Atención con Hiperactividad/genética , Barrera Hematoencefálica/ultraestructura , Modelos Animales de Enfermedad , Masculino , Microscopía Confocal , Microscopía Inmunoelectrónica , Transportadores de Ácidos Monocarboxílicos/genética , Transportadores de Ácidos Monocarboxílicos/ultraestructura , Neurópilo/metabolismo , Neurópilo/ultraestructura , Ratas , Ratas Endogámicas SHR , Ratas Endogámicas WKY , Análisis de Regresión , Especificidad de la Especie , Regulación hacia Arriba/genética
13.
Front Neural Circuits ; 12: 103, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30546298

RESUMEN

The central complex (CX) is a midline-situated collection of neuropil compartments in the arthropod central brain, implicated in higher-order processes such as goal-directed navigation. Here, we provide a systematic genetic-neuroanatomical analysis of the ellipsoid body (EB), a compartment which represents a major afferent portal of the Drosophila CX. The neuropil volume of the EB, along with its prominent input compartment, called the bulb, is subdivided into precisely tessellated domains, distinguishable based on intensity of the global marker DN-cadherin. EB tangential elements (so-called ring neurons), most of which are derived from the DALv2 neuroblast lineage, predominantly interconnect the bulb and EB domains in a topographically organized fashion. Using the DN-cadherin domains as a framework, we first characterized this connectivity by Gal4 driver lines expressed in different DALv2 ring neuron (R-neuron) subclasses. We identified 11 subclasses, 6 of which correspond to previously described projection patterns, and 5 novel patterns. These subclasses both spatially (based on EB innervation pattern) and numerically (cell counts) summate to the total EB volume and R-neuron cell number, suggesting that our compilation of R-neuron subclasses approaches completion. EB columnar elements, as well as non-DALv2 derived extrinsic ring neurons (ExR-neurons), were also incorporated into this anatomical framework. Finally, we addressed the connectivity between R-neurons and their targets, using the anterograde trans-synaptic labeling method, trans-Tango. This study demonstrates putative interactions of R-neuron subclasses and reveals general principles of information flow within the EB network. Our work will facilitate the generation and testing of hypotheses regarding circuit interactions within the EB and the rest of the CX.


Asunto(s)
Red Nerviosa/fisiología , Red Nerviosa/ultraestructura , Plasticidad Neuronal/fisiología , Neurópilo/fisiología , Neurópilo/ultraestructura , Animales , Animales Modificados Genéticamente , Drosophila , Femenino , Red Nerviosa/citología , Neuronas/fisiología , Neuronas/ultraestructura
14.
J Neurosci ; 38(31): 6933-6948, 2018 08 01.
Artículo en Inglés | MEDLINE | ID: mdl-30012687

RESUMEN

Animals use binocular information to guide many behaviors. In highly visual arthropods, complex binocular computations involved in processing panoramic optic flow generated during self-motion occur in the optic neuropils. However, the extent to which binocular processing of object motion occurs in these neuropils remains unknown. We investigated this in a crab, where the distance between the eyes and the extensive overlapping of their visual fields advocate for the use of binocular processing. By performing in vivo intracellular recordings from the lobula (third optic neuropil) of male crabs, we assessed responses of object-motion-sensitive neurons to ipsilateral or contralateral moving objects under binocular and monocular conditions. Most recorded neurons responded to stimuli seen independently with either eye, proving that each lobula receives profuse visual information from both eyes. The contribution of each eye to the binocular response varies among neurons, from those receiving comparable inputs from both eyes to those with mainly ipsilateral or contralateral components, some including contralateral inhibition. Electrophysiological profiles indicated that a similar number of neurons were recorded from their input or their output side. In monocular conditions, the first group showed shorter response delays to ipsilateral than to contralateral stimulation, whereas the second group showed the opposite. These results fit well with neurons conveying centripetal and centrifugal information from and toward the lobula, respectively. Intracellular and massive stainings provided anatomical support for this and for direct connections between the two lobulae, but simultaneous recordings failed to reveal such connections. Simplified model circuits of interocular connections are discussed.SIGNIFICANCE STATEMENT Most active animals became equipped with two eyes, which contributes to functions like depth perception, objects spatial location, and motion processing, all used for guiding behaviors. In visually active arthropods, binocular neural processing of the panoramic optic flow generated during self-motion happens already in the optic neuropils. However, whether binocular processing of single-object motion occurs in these neuropils remained unknown. We investigated this in a crab, where motion-sensitive neurons from the lobula can be recorded in the intact animal. Here we demonstrate that different classes of neurons from the lobula compute binocular information. Our results provide new insight into where and how the visual information acquired by the two eyes is first combined in the brain of an arthropod.


Asunto(s)
Braquiuros/fisiología , Percepción de Movimiento/fisiología , Neuronas/fisiología , Neurópilo/fisiología , Visión Binocular/fisiología , Vías Visuales/fisiología , Animales , Dominancia Cerebral , Masculino , Neurópilo/ultraestructura , Técnicas de Placa-Clamp , Estimulación Luminosa , Tiempo de Reacción , Visión Monocular/fisiología
15.
J Comp Neurol ; 526(14): 2301-2318, 2018 10 01.
Artículo en Inglés | MEDLINE | ID: mdl-30004590

RESUMEN

The central complex is a group of midline-crossing neuropils in the insect brain involved in head direction coding, sky compass navigation, and spatial visual memory. To compare the neuroarchitecture and neurochemistry of the central complex in insects that differ in locomotion, ways of orientation, time of activity (diurnal, nocturnal), and evolutionary history, we studied the distribution of γ-aminobutyric acid (GABA) immunostaining in the central complex of 29 species, ranging from Zygentoma to Diptera. In all species, the lower division of the central body was densely innervated by GABA-immunoreactive tangential neurons. These neurons had additional arborizations in the bulb, a distinct region of synaptic complexes in the lateral complex, and somata in a cell cluster mediodorsally to the antennal lobe. Differences in the appearance of GABA immunostaining in the lower division of the central body corresponded to differences in neuropil architecture, such as transformation of the lower division into a toroid in certain Diptera and Heteroptera. In nearly all species two additional systems of tangential neuron of the upper division of the central body were GABA-immunoreactive. One of these systems diffusely invaded a superior layer, while the second system showed fan-like projections in an inferior layer. Sparse immunostaining in the protocerebral bridge was detected in cockroaches, a cricket, and two hemipteran species. The data show that three systems of GABA-immunoreactive tangential neurons of the central body are highly conserved and suggest that the layered organization of the upper division of the central body is, likewise, largely maintained from basal to advanced species.


Asunto(s)
Sistema Nervioso Central/metabolismo , Sistema Nervioso Central/fisiología , Insectos/fisiología , Ácido gamma-Aminobutírico/metabolismo , Animales , Antenas de Artrópodos/crecimiento & desarrollo , Antenas de Artrópodos/inervación , Evolución Biológica , Inmunohistoquímica , Neuronas/metabolismo , Neurópilo/metabolismo , Neurópilo/ultraestructura , Especificidad de la Especie , Sinapsis/metabolismo
16.
Cereb Cortex ; 28(10): 3673-3684, 2018 10 01.
Artículo en Inglés | MEDLINE | ID: mdl-30060007

RESUMEN

Mitochondria play a key role in energy production and calcium buffering, among many other functions. They provide most of the energy required by neurons, and they are transported along axons and dendrites to the regions of higher energy demands. We have used focused ion beam milling and scanning electron microscopy (FIB/SEM) to obtain stacks of serial sections from the somatosensory cortex of the juvenile rat. We have estimated the volume fraction occupied by mitochondria and their distribution between dendritic, axonal, and nonsynaptic processes. The volume fraction of mitochondria increased from layer I (4.59%) to reach its maximum in layer IV (7.74%) and decreased to its minimum in layer VI (4.03%). On average, 44% of mitochondrial volume was located in dendrites, 15% in axons and 41% in nonsynaptic elements. Given that dendrites, axons, and nonsynaptic elements occupied 38%, 23%, and 39% of the neuropil, respectively, it can be concluded that dendrites are proportionally richer in mitochondria with respect to axons, supporting the notion that most energy consumption takes place at the postsynaptic side. We also found a positive correlation between the volume fraction of mitochondria located in neuronal processes and the density of synapses.


Asunto(s)
Mitocondrias/ultraestructura , Neurópilo/ultraestructura , Corteza Somatosensorial/ultraestructura , Animales , Axones/ultraestructura , Vasos Sanguíneos/ultraestructura , Dendritas/ultraestructura , Metabolismo Energético , Ratas , Ratas Wistar
17.
PLoS One ; 13(7): e0198131, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29966021

RESUMEN

This study has used dense reconstructions from serial EM images to compare the neuropil ultrastructure and connectivity of aged and adult mice. The analysis used models of axons, dendrites, and their synaptic connections, reconstructed from volumes of neuropil imaged in layer 1 of the somatosensory cortex. This shows the changes to neuropil structure that accompany a general loss of synapses in a well-defined brain region. The loss of excitatory synapses was balanced by an increase in their size such that the total amount of synaptic surface, per unit length of axon, and per unit volume of neuropil, stayed the same. There was also a greater reduction of inhibitory synapses than excitatory, particularly those found on dendritic spines, resulting in an increase in the excitatory/inhibitory balance. The close correlations, that exist in young and adult neurons, between spine volume, bouton volume, synaptic size, and docked vesicle numbers are all preserved during aging. These comparisons display features that indicate a reduced plasticity of cortical circuits, with fewer, more transient, connections, but nevertheless an enhancement of the remaining connectivity that compensates for a generalized synapse loss.


Asunto(s)
Envejecimiento/patología , Neurópilo/ultraestructura , Corteza Somatosensorial/ultraestructura , Sinapsis/ultraestructura , Animales , Axones/ultraestructura , Humanos , Imagenología Tridimensional , Ratones , Microscopía Electrónica , Neuronas/patología , Neuronas/ultraestructura , Neurópilo/patología , Corteza Somatosensorial/irrigación sanguínea , Corteza Somatosensorial/patología , Sinapsis/patología
18.
J Comp Neurol ; 526(8): 1307-1328, 2018 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-29427506

RESUMEN

The peptidergic Pigment-dispersing factor (PDF)-Tri neurons are a group of non-clock neurons that appear transiently around the time of adult ecdysis (=eclosion) in the fruit fly Drosophila melanogaster. This specific developmental pattern points to a function of these neurons in eclosion or other processes that are active around pupal-adult transition. As a first step to understand the role of these neurons, we here characterize the anatomy of the PDF-Tri neurons. In addition, we describe a further set of peptidergic neurons that have been associated with eclosion behavior, eclosion hormone (EH), and crustacean cardioactive peptide (CCAP) neurons, to single cell level in the pharate adult brain. PDF-Tri neurons as well as CCAP neurons co-express a classical transmitter indicated by the occurrence of small clear vesicles in addition to dense-core vesicles containing the peptides. In the tritocerebrum, gnathal ganglion and the superior protocerebrum PDF-Tri neurites contain peptidergic varicosities and both pre- and postsynaptic sites, suggesting that the PDF-Tri neurons represent modulatory rather than pure interneurons that connect the subesophageal zone with the superior protocerebrum. The extensive overlap of PDF-Tri arborizations with neurites of CCAP- and EH-expressing neurons in distinct brain regions provides anatomical evidence for a possible function of the PDF-Tri neurons in eclosion behavior.


Asunto(s)
Agaricales/metabolismo , Proteínas de Drosophila/metabolismo , Neuronas/metabolismo , Neuropéptidos/metabolismo , Agaricales/citología , Animales , Animales Modificados Genéticamente , Drosophila , Proteínas de Drosophila/genética , Proteínas de Drosophila/ultraestructura , Drosophila melanogaster , Hormonas de Insectos , Proteínas Luminiscentes/genética , Proteínas Luminiscentes/metabolismo , Microscopía Electrónica , Neuronas/ultraestructura , Neuropéptidos/genética , Neurópilo/metabolismo , Neurópilo/ultraestructura , Fracciones Subcelulares/metabolismo , Fracciones Subcelulares/ultraestructura , Sinapsinas/metabolismo , Sinapsinas/ultraestructura , Factores de Transcripción/metabolismo
19.
Brain Struct Funct ; 222(7): 3025-3042, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28243762

RESUMEN

The present study is the first to describe quantitatively the patterns of synaptic connections made by the patchy network of pyramidal cell axons in the superficial layers of cat V1 in relation to the orientation map. Intrinsic signal imaging of the orientation map was combined with 3D morphological reconstructions of physiologically-characterized neurons at light and electron microscope levels. A Similarity Index (SI) expressed the similarity of the orientation domain of a given bouton cluster to that of its parent dendritic tree. Six pyramidal cells whose axons had a wide range of SIs were examined. Boutons were sampled from five local and five distal clusters, and from the linear segments that link the clusters. The synaptic targets were reconstructed by serial section electron microscopy. Of the 233 synapses examined, 182 synapses were formed with spiny neurons, the remainder with smooth neurons. The proportion of smooth neurons that were synaptic targets varied greatly (from 0 to 50%) between the cluster samples, but was not correlated with the SI. The postsynaptic density sizes were similar for synapses in local and distal clusters, regardless of their SI. This heterogeneity in the synaptic targets of single cells within the superficial layers is a network feature well-suited for context-dependent processing.


Asunto(s)
Axones/fisiología , Mapeo Encefálico , Neurópilo/fisiología , Células Piramidales/citología , Sinapsis/fisiología , Corteza Visual/anatomía & histología , Animales , Axones/ultraestructura , Gatos , Dendritas/fisiología , Dendritas/ultraestructura , Microscopía Electrónica , Modelos Anatómicos , Neurópilo/ultraestructura , Terminales Presinápticos/ultraestructura , Células Piramidales/metabolismo , Células Piramidales/ultraestructura , Sinapsis/ultraestructura
20.
J Comp Neurol ; 525(9): 2175-2191, 2017 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-28256708

RESUMEN

The excitatory glutamatergic synapse is the principal site of communication between cortical pyramidal neurons and their targets, a key locus of action of many drugs, and highly vulnerable to dysfunction and loss in neurodegenerative disease. A detailed knowledge of the structure of these synapses in distinct cortical areas and across species is a prerequisite for understanding the anatomical underpinnings of cortical specialization and, potentially, selective vulnerability in neurological disorders. We used serial electron microscopy to assess the ultrastructural features of excitatory (asymmetric) synapses in the layers 2-3 (L2-3) neuropil of visual (V1) and frontal (FC) cortices of the adult mouse and compared findings to those in the rhesus monkey (V1 and lateral prefrontal cortex [LPFC]). Analyses of multiple ultrastructural variables revealed four organizational features. First, the density of asymmetric synapses does not differ between frontal and visual cortices in either species, but is significantly higher in mouse than in monkey. Second, the structural properties of asymmetric synapses in mouse V1 and FC are nearly identical, by stark contrast to the significant differences seen between monkey V1 and LPFC. Third, while the structural features of postsynaptic entities in mouse and monkey V1 do not differ, the size of presynaptic boutons are significantly larger in monkey V1. Fourth, both presynaptic and postsynaptic entities are significantly smaller in the mouse FC than in the monkey LPFC. The diversity of synaptic ultrastructural features demonstrated here have broad implications for the nature and efficacy of glutamatergic signaling in distinct cortical areas within and across species.


Asunto(s)
Lóbulo Frontal/ultraestructura , Macaca mulatta/anatomía & histología , Ratones/anatomía & histología , Sinapsis/ultraestructura , Corteza Visual/ultraestructura , Análisis de Varianza , Animales , Femenino , Lóbulo Frontal/metabolismo , Imagenología Tridimensional , Masculino , Microscopía Inmunoelectrónica , Neuronas/metabolismo , Neuronas/ultraestructura , Neurópilo/metabolismo , Neurópilo/ultraestructura , Terminales Presinápticos/ultraestructura , Especificidad de la Especie , Sinapsis/clasificación , Sinapsis/metabolismo , Corteza Visual/metabolismo
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