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1.
Curr Biol ; 33(7): R274-R276, 2023 04 10.
Article in English | MEDLINE | ID: mdl-37040711

ABSTRACT

Insulin release has mostly been studied in the context of metabolic signals. An electrophysiology approach in Drosophila now reveals regulation of insulin-producing cell activity by neuronal circuits controlling locomotion. Even without actual movement, activating these circuits is sufficient to inhibit neuropeptide release.


Subject(s)
Drosophila Proteins , Insulin , Animals , Insulin/metabolism , Drosophila Proteins/metabolism , Drosophila/physiology , Neurons/metabolism , Locomotion/physiology
2.
Elife ; 102021 06 04.
Article in English | MEDLINE | ID: mdl-34085637

ABSTRACT

Neuroendocrine systems in animals maintain organismal homeostasis and regulate stress response. Although a great deal of work has been done on the neuropeptides and hormones that are released and act on target organs in the periphery, the synaptic inputs onto these neuroendocrine outputs in the brain are less well understood. Here, we use the transmission electron microscopy reconstruction of a whole central nervous system in the Drosophila larva to elucidate the sensory pathways and the interneurons that provide synaptic input to the neurosecretory cells projecting to the endocrine organs. Predicted by network modeling, we also identify a new carbon dioxide-responsive network that acts on a specific set of neurosecretory cells and that includes those expressing corazonin (Crz) and diuretic hormone 44 (Dh44) neuropeptides. Our analysis reveals a neuronal network architecture for combinatorial action based on sensory and interneuronal pathways that converge onto distinct combinations of neuroendocrine outputs.


Subject(s)
Connectome , Drosophila melanogaster/ultrastructure , Interneurons/ultrastructure , Neurosecretory Systems/ultrastructure , Sensory Receptor Cells/ultrastructure , Synapses/ultrastructure , Animals , Animals, Genetically Modified , Carbon Dioxide/metabolism , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Drosophila melanogaster/genetics , Drosophila melanogaster/metabolism , Insect Hormones/genetics , Insect Hormones/metabolism , Interneurons/metabolism , Microscopy, Electron, Transmission , Neuropeptides/genetics , Neuropeptides/metabolism , Neurosecretory Systems/metabolism , Sensory Receptor Cells/metabolism , Synapses/metabolism
3.
Nat Commun ; 11(1): 4491, 2020 09 08.
Article in English | MEDLINE | ID: mdl-32901033

ABSTRACT

The functionality of the nervous system requires transmission of information along axons with high speed and precision. Conductance velocity depends on axonal diameter whereas signaling precision requires a block of electrical crosstalk between axons, known as ephaptic coupling. Here, we use the peripheral nervous system of Drosophila larvae to determine how glia regulates axonal properties. We show that wrapping glial differentiation depends on gap junctions and FGF-signaling. Abnormal glial differentiation affects axonal diameter and conductance velocity and causes mild behavioral phenotypes that can be rescued by a sphingosine-rich diet. Ablation of wrapping glia does not further impair axonal diameter and conductance velocity but causes a prominent locomotion phenotype that cannot be rescued by sphingosine. Moreover, optogenetically evoked locomotor patterns do not depend on conductance speed but require the presence of wrapping glial processes. In conclusion, our data indicate that wrapping glia modulates both speed and precision of neuronal signaling.


Subject(s)
Drosophila melanogaster/physiology , Animals , Animals, Genetically Modified , Axons/physiology , Cell Differentiation , Drosophila Proteins/genetics , Drosophila Proteins/physiology , Drosophila melanogaster/cytology , Drosophila melanogaster/genetics , Larva/cytology , Larva/physiology , Locomotion/physiology , Models, Neurological , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/physiology , Neuroglia/cytology , Neuroglia/physiology , Optogenetics , Peripheral Nervous System/cytology , Peripheral Nervous System/physiology , Phenotype , Receptors, Fibroblast Growth Factor/physiology , Signal Transduction
4.
Elife ; 72018 12 11.
Article in English | MEDLINE | ID: mdl-30526854

ABSTRACT

We reconstructed, from a whole CNS EM volume, the synaptic map of input and output neurons that underlie food intake behavior of Drosophila larvae. Input neurons originate from enteric, pharyngeal and external sensory organs and converge onto seven distinct sensory synaptic compartments within the CNS. Output neurons consist of feeding motor, serotonergic modulatory and neuroendocrine neurons. Monosynaptic connections from a set of sensory synaptic compartments cover the motor, modulatory and neuroendocrine targets in overlapping domains. Polysynaptic routes are superimposed on top of monosynaptic connections, resulting in divergent sensory paths that converge on common outputs. A completely different set of sensory compartments is connected to the mushroom body calyx. The mushroom body output neurons are connected to interneurons that directly target the feeding output neurons. Our results illustrate a circuit architecture in which monosynaptic and multisynaptic connections from sensory inputs traverse onto output neurons via a series of converging paths.


Subject(s)
Central Nervous System/physiology , Drosophila melanogaster/physiology , Larva/physiology , Motor Neurons/physiology , Synapses/physiology , Synaptic Transmission/physiology , Animals , Central Nervous System/ultrastructure , Connectome/methods , Drosophila melanogaster/ultrastructure , Eating/physiology , Feeding Behavior/physiology , Interneurons/cytology , Interneurons/physiology , Larva/ultrastructure , Membrane Potentials/physiology , Motor Neurons/cytology , Mushroom Bodies/cytology , Mushroom Bodies/physiology , Nerve Net/physiology , Nerve Net/ultrastructure , Neuronal Plasticity/physiology , Synapses/ultrastructure
5.
Nat Commun ; 9(1): 3514, 2018 08 29.
Article in English | MEDLINE | ID: mdl-30158546

ABSTRACT

Specialized glial subtypes provide support to developing and functioning neural networks. Astrocytes modulate information processing by neurotransmitter recycling and release of neuromodulatory substances, whereas ensheathing glial cells have not been associated with neuromodulatory functions yet. To decipher a possible role of ensheathing glia in neuronal information processing, we screened for glial genes required in the Drosophila central nervous system for normal locomotor behavior. Shopper encodes a mitochondrial sulfite oxidase that is specifically required in ensheathing glia to regulate head bending and peristalsis. shopper mutants show elevated sulfite levels affecting the glutamate homeostasis which then act on neuronal network function. Interestingly, human patients lacking the Shopper homolog SUOX develop neurological symptoms, including seizures. Given an enhanced expression of SUOX by oligodendrocytes, our findings might indicate that in both invertebrates and vertebrates more than one glial cell type may be involved in modulating neuronal activity.


Subject(s)
Drosophila Proteins/metabolism , Neuroglia/metabolism , Sulfite Oxidase/metabolism , Animals , Astrocytes/metabolism , Drosophila , Drosophila Proteins/genetics , Glutamates/metabolism , Sulfite Oxidase/genetics , Sulfites/metabolism
6.
J Insect Physiol ; 106(Pt 1): 36-46, 2018 04.
Article in English | MEDLINE | ID: mdl-28735009

ABSTRACT

The functional organization of central motor circuits underlying feeding behaviors is not well understood. We have combined electrophysiological and genetic approaches to investigate the regulatory networks upstream of the motor program underlying food intake in the Drosophila larval central nervous system. We discovered that the serotonergic network of the CNS is able to set the motor rhythm frequency of pharyngeal pumping. Pharmacological experiments verified that modulation of the feeding motor pattern is based on the release of serotonin. Classical lesion and laser based cell ablation indicated that the serotonergic neurons in the subesophageal zone represent a redundant network for motor control of larval food intake.


Subject(s)
Drosophila/physiology , Eating/physiology , Serotonergic Neurons/physiology , Animals , Motor Activity
7.
Elife ; 52016 11 15.
Article in English | MEDLINE | ID: mdl-27845623

ABSTRACT

NeuromedinU is a potent regulator of food intake and activity in mammals. In Drosophila, neurons producing the homologous neuropeptide hugin regulate feeding and locomotion in a similar manner. Here, we use EM-based reconstruction to generate the entire connectome of hugin-producing neurons in the Drosophila larval CNS. We demonstrate that hugin neurons use synaptic transmission in addition to peptidergic neuromodulation and identify acetylcholine as a key transmitter. Hugin neuropeptide and acetylcholine are both necessary for the regulatory effect on feeding. We further show that subtypes of hugin neurons connect chemosensory to endocrine system by combinations of synaptic and peptide-receptor connections. Targets include endocrine neurons producing DH44, a CRH-like peptide, and insulin-like peptides. Homologs of these peptides are likewise downstream of neuromedinU, revealing striking parallels in flies and mammals. We propose that hugin neurons are part of an ancient physiological control system that has been conserved at functional and molecular level.


Subject(s)
Drosophila Proteins/metabolism , Drosophila/anatomy & histology , Drosophila/physiology , Eating , Neural Pathways/anatomy & histology , Neurons/metabolism , Neuropeptides/metabolism , Synaptic Transmission/drug effects , Acetylcholine/metabolism , Animals , Larva/anatomy & histology , Larva/physiology , Microscopy, Electron , Neurotransmitter Agents/metabolism
8.
Curr Biol ; 26(15): R701-R703, 2016 08 08.
Article in English | MEDLINE | ID: mdl-27505238

ABSTRACT

Which neurons in the brain become engaged when the body is deprived of food? A new study addresses this question using the vinegar fly Drosophila melanogaster, examining a group of neurons in the brain that show alterations in neural activity when flies are satiated or starved.


Subject(s)
Drosophila Proteins , Drosophila melanogaster , Animals , Brain , Hunger , Neurosciences
9.
PLoS One ; 10(8): e0135011, 2015.
Article in English | MEDLINE | ID: mdl-26252658

ABSTRACT

Motor systems can be functionally organized into effector organs (muscles and glands), the motor neurons, central pattern generators (CPG) and higher control centers of the brain. Using genetic and electrophysiological methods, we have begun to deconstruct the motor system driving Drosophila larval feeding behavior into its component parts. In this paper, we identify distinct clusters of motor neurons that execute head tilting, mouth hook movements, and pharyngeal pumping during larval feeding. This basic anatomical scaffold enabled the use of calcium-imaging to monitor the neural activity of motor neurons within the central nervous system (CNS) that drive food intake. Simultaneous nerve- and muscle-recordings demonstrate that the motor neurons innervate the cibarial dilator musculature (CDM) ipsi- and contra-laterally. By classical lesion experiments we localize a set of CPGs generating the neuronal pattern underlying feeding movements to the subesophageal zone (SEZ). Lesioning of higher brain centers decelerated all feeding-related motor patterns, whereas lesioning of ventral nerve cord (VNC) only affected the motor rhythm underlying pharyngeal pumping. These findings provide a basis for progressing upstream of the motor neurons to identify higher regulatory components of the feeding motor system.


Subject(s)
Central Pattern Generators/physiology , Drosophila melanogaster/embryology , Feeding Behavior , Motor Neurons/metabolism , Animals , Animals, Genetically Modified , Brain Mapping , Calcium/metabolism , Central Nervous System/physiology , Coloring Agents/chemistry , Electrophysiology , Glutamine/chemistry , Green Fluorescent Proteins/metabolism , Immunohistochemistry , Larva/physiology , Light , Neurons/metabolism , Pharynx/innervation , Temperature
10.
J Insect Physiol ; 69: 118-25, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24907674

ABSTRACT

The enteric nervous system is critical for coordinating diverse feeding-related behaviors and metabolism. We have characterized a cluster of four serotonergic neurons in Drosophila larval brain: cell bodies are located in the subesophageal ganglion (SOG) whose neuronal processes project into the enteric nervous system. Electrophysiological, calcium imaging and behavioral analyses indicate a functional role of these neurons in modulating foregut motility. We suggest that the axonal projections of this serotonergic cluster may be part of a brain-gut neural pathway that is functionally analogous to the vertebrate vagus nerve.


Subject(s)
Drosophila/metabolism , Serotonergic Neurons/metabolism , Serotonin/metabolism , Animals , Enteric Nervous System/metabolism , Gastrointestinal Motility , In Vitro Techniques , Neural Pathways
11.
PLoS Biol ; 12(6): e1001893, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24960360

ABSTRACT

Central mechanisms by which specific motor programs are selected to achieve meaningful behaviors are not well understood. Using electrophysiological recordings from pharyngeal nerves upon central activation of neurotransmitter-expressing cells, we show that distinct neuronal ensembles can regulate different feeding motor programs. In behavioral and electrophysiological experiments, activation of 20 neurons in the brain expressing the neuropeptide hugin, a homolog of mammalian neuromedin U, simultaneously suppressed the motor program for food intake while inducing the motor program for locomotion. Decreasing hugin neuropeptide levels in the neurons by RNAi prevented this action. Reducing the level of hugin neuronal activity alone did not have any effect on feeding or locomotion motor programs. Furthermore, use of promoter-specific constructs that labeled subsets of hugin neurons demonstrated that initiation of locomotion can be separated from modulation of its motor pattern. These results provide insights into a neural mechanism of how opposing motor programs can be selected in order to coordinate feeding and locomotive behaviors.


Subject(s)
Central Nervous System/physiology , Feeding Behavior/physiology , Locomotion/physiology , Animals
12.
J Morphol ; 271(8): 960-8, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20623655

ABSTRACT

An anatomical description is given by the muscles in the pro- and mesothorax, and those associated with the feeding apparatus (cephalopharyngeal skeleton, CPS) that participate in feeding behavior in third instar Calliphora larvae. The body wall muscles in the pro- and mesothoracic segments are organized in three layers: internal, intermedial, and external. The muscles were labeled with roman numerals according to the nomenclature in use for the abdominal segments. Muscles associated with the CPS are labeled according to their function. The prothorax bears five pairs of lateral symmetrically longitudinal segmental body wall muscles and lacks the transversal muscle group present in the mesothorax and abdominal segments. Additionally, four pairs of intersegmental muscles project from the prothorax to the second, fourth, and fifth segment. The mesothorax bears 15 pairs of segmental longitudinal and 18 pairs of transversal muscles. The accessory pharyngeal muscles span the CPS and the cuticle. Three pairs of protractors and retractors and two pairs of mouth hook accessors (MH(AC)) exist, which move the CPS relative to the body. The pharyngeal muscles are exclusively attached to the structures of the CPS. The mouth hook elevators and depressors, which mediate the hooks rotation are attached to the ventral arm of the CPS and project to a dorsal (elevators) or ventral (depressors) protuberance of the mouth hooks. The cibarial dilator muscles (CDM) span the dorsal arms of the CPS and the dorsal surface of the esophagus and mediate food ingestion. The labial retractors (LRs) lack antagonists and project from the ventral surface of the CPS to the unpaired labium. Contractions of these muscles open the mouth cavity.


Subject(s)
Diptera/anatomy & histology , Animals , Diptera/physiology , Feeding Behavior , Larva/anatomy & histology , Larva/physiology , Mouth/anatomy & histology , Muscles/anatomy & histology , Muscles/innervation
13.
J Morphol ; 271(8): 969-79, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20623656

ABSTRACT

We describe the anatomy of the nerves that project from the central nervous system (CNS) to the pro- and mesothoracic segments and the cephalopharyngeal skeleton (CPS) for third instar Calliphora larvae. Due to the complex branching pattern we introduce a nomenclature that labels side branches of first and second order. Two fine nerves that were not yet described are briefly introduced. One paired nerve projects to the ventral arms (VAs) of the CPS. The second, an unpaired nerve, projects to the ventral surface of the cibarial part of the esophagus (ES). Both nerves were tentatively labeled after the structures they innervate. The antennal nerve (AN) innervates the olfactory dorsal organ (DO). It contains motor pathways that project through the frontal connectives (FC) to the frontal nerve (FN) and innervate the cibarial dilator muscles (CDM) which mediate food ingestion. The maxillary nerve (MN) innervates the sensory terminal organ (TO), ventral organ (VO), and labial organ (LO) and comprises the motor pathways to the mouth hook (MH) elevator, MH depressor, and the labial retractor (LR) which opens the mouth cavity. An anastomosis of unknown function exists between the AN and MN. The prothoracic accessory nerve (PaN) innervates a dorsal protractor muscle of the CPS and sends side branches to the aorta and the bolwig organ (BO) (stemmata). In its further course, this nerve merges with the prothoracic nerve (PN). The architecture of the PN is extremely complex. It innervates a set of accessory pharyngeal muscles attached to the CPS and the body wall musculature of the prothorax. Several anastomoses exist between side branches of this nerve which were shown to contain motor pathways. The mesothoracic nerve (MeN) innervates a MH accessor and the longitudinal and transversal body wall muscles of the second segment.


Subject(s)
Diptera/anatomy & histology , Animals , Brain/anatomy & histology , Central Nervous System/anatomy & histology , Diptera/physiology , Efferent Pathways , Larva/anatomy & histology , Larva/physiology , Muscles/anatomy & histology , Muscles/innervation
14.
J Insect Physiol ; 56(7): 695-705, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20074578

ABSTRACT

To establish the existence of a central pattern generator for feeding in the larval central nervous system of two Drosophila species, the gross anatomy of feeding related muscles and their innervation is described, the motor units of the muscles identified and rhythmic motor output recorded from the isolated CNS. The cibarial dilator muscles that mediate food ingestion are innervated by the frontal nerve. Their motor pathway projects from the brain through the antennal nerves, the frontal connectives and the frontal nerve junction. The mouth hook elevator and depressor system is innervated by side branches of the maxillary nerve. The motor units of the two muscle groups differ in amplitude: the elevator is always activated by a small unit, the depressor by a large one. The dorsal protractors span the cephalopharyngeal skeleton and the body wall hence mediating an extension of the CPS. These muscles are innervated by the prothoracic accessory nerve. Rhythmic motor output produced by the isolated central nervous system can simultaneously be recorded from all three nerves. The temporal pattern of the identified motor units resembles the sequence of muscle contractions deduced from natural feeding behavior and is therefore considered as fictive feeding. Phase diagrams show an almost identical fictive feeding pattern is in both species.


Subject(s)
Brain/physiology , Drosophila/growth & development , Drosophila/physiology , Animals , Central Nervous System/physiology , Eating , Feeding Behavior , Larva/growth & development , Larva/physiology , Muscles/physiology
15.
J Insect Physiol ; 55(3): 218-30, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19100742

ABSTRACT

A description of the muscles and nerves involved in feeding of larval Calliphora vicina is given as a prerequisite to establish fictive feeding patterns recorded from the isolated central nervous system. Feeding Diptera larvae show a repetitive sequence of pro- and retraction of the cephalopharyngeal skeleton (CPS), elevation and depression of the mouth hooks and food ingestion. The corresponding pharyngeal muscles are protractors, mouth hook elevators and depressors, the labial retractor and cibarial dilator muscles. These muscles are innervated by the prothoracic accessory nerve (PaN), maxillary nerve (MN) and antennal nerve (AN) as shown electrophysiologically by recording action potentials from the respective nerve that correlate to post-synaptic potentials on the muscles. All three nerves show considerably more complex branching patterns than indicated in the literature. Extracellular recordings from the stumps of PaN, MN and AN connected to an isolated CNS show spontaneous rhythmic motor patterns that reflect the feeding sequence in intact larvae. Variability of the feeding pattern observed in behavioral experiments is also evident from the level of motor output from an isolated CNS. The data obtained from Calliphora will facilitate electrophysiological investigations dealing with the genetic background of feeding behavior in Drosophila larvae.


Subject(s)
Diptera , Electrophysiology/methods , Feeding Behavior/physiology , Pharyngeal Muscles/anatomy & histology , Pharyngeal Muscles/innervation , Animals , Biomechanical Phenomena , Larva/anatomy & histology , Larva/physiology
16.
J Morphol ; 269(3): 272-82, 2008 Mar.
Article in English | MEDLINE | ID: mdl-17960761

ABSTRACT

The stomatogastric nervous system (SNS) associated with the foregut was studied in 3rd instar larvae of Drosophila melanogaster and Calliphora vicina (blowfly). In both species, the foregut comprises pharynx, esophagus, and proventriculus. Only in Calliphora does the esophagus form a crop. The position of nerves and neurons was investigated with neuronal tracers in both species and GFP expression in Drosophila. The SNS is nearly identical in both species. Neurons are located in the proventricular and the hypocerebral ganglion (HCG), which are connected to each other by the proventricular nerve. Motor neurons for pharyngeal muscles are located in the brain not, as in other insect groups, in the frontal ganglion. The position of the frontal ganglion is taken by a nerve junction devoid of neurons. The junction is composed of four nerves: the frontal connectives that fuse with the antennal nerves (ANs), the frontal nerve innervating the cibarial dilator muscles and the recurrent nerve that innervates the esophagus and projects to the HCG. Differences in the SNS are restricted to a crop nerve only present in Calliphora and an esophageal ganglion that only exists in Drosophila. The ganglia of the dorsal organs give rise to the ANs, which project to the brain. The extensive conformity of the SNS of both species suggests functional parallels. Future electrophysiological studies of the motor circuits in the SNS of Drosophila will profit from parallel studies of the homologous but more accessible structures in Calliphora.


Subject(s)
Diptera/anatomy & histology , Drosophila melanogaster/anatomy & histology , Ganglia, Invertebrate/anatomy & histology , Neurons/cytology , Animals , Digestive System/cytology , Digestive System/innervation , Diptera/cytology , Drosophila melanogaster/cytology , Ganglia, Invertebrate/cytology , Larva/anatomy & histology , Larva/cytology , Nervous System/anatomy & histology , Nervous System/cytology
17.
J Insect Physiol ; 53(4): 349-60, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17306827

ABSTRACT

The anatomy and functionality of the stomatogastric nervous system (SNS) of third-instar larvae of Calliphora vicina was characterised. As in other insects, the Calliphora SNS consists of several peripheral ganglia involved in foregut movement regulation. The frontal ganglion gives rise to the frontal nerve and is connected to the brain via the frontal connectives and antennal nerves (ANs). The recurrent nerve connects the frontal- to the hypocerebral ganglion from which the proventricular nerve runs to the proventricular ganglion. Foregut movements include rhythmic contractions of the cibarial dilator muscles (CDM), wavelike movements of crop and oesophagus and contractions of the proventriculus. Transections of SNS nerves indicate mostly myogenic crop and oesophagus movements and suggest modulatory function of the associated nerves. Neural activity in the ANs, correlating with postsynaptic potentials on the CDM, demonstrates a motor pathway from the brain to CDM. Crop volume is monitored by putative stretch receptors. The respective sensory pathway includes the recurrent nerve and the proventricular nerve. The dorsal organs (DOs) are directly connected to the SNS. Mechanical stimulation of the DOs evokes sensory activity in the AN. This suggests the DOs can provide sensory input for temporal coordination of feeding behaviour.


Subject(s)
Diptera/physiology , Afferent Pathways/physiology , Animals , Digestive System/innervation , Digestive System Physiological Phenomena , Diptera/anatomy & histology , Diptera/growth & development , Efferent Pathways/physiology , Larva/anatomy & histology , Larva/physiology , Nervous System/anatomy & histology , Nervous System Physiological Phenomena , Neurons
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