Neurons with dopamine-like immunoreactivity target mushroom body Kenyon cell somata in the brain of some hymenopteran insects

1999 ◽  
Vol 28 (3) ◽  
pp. 203-210 ◽  
Author(s):  
Wolfgang Blenau ◽  
Manfred Schmidt ◽  
Daniel Faensen ◽  
Friedrich-Wilhelm Schürmann
Keyword(s):  
Mushroom Body ◽  
Kenyon Cell ◽  
The Brain ◽  
Cell Somata ◽  
Hymenopteran Insects

scholarly journals Early Development of Mushroom Bodies in the Brain of the Honeybee Apis mellifera as Revealed by BrdU Incorporation and Ablation Experiments

1998 ◽  
Vol 5 (1) ◽  
pp. 90-101 ◽  
Author(s):  
Dagmar Malun
Keyword(s):  
Stem Cells ◽  
Larval Stage ◽  
Mushroom Body ◽  
Brdu Incorporation ◽  
Homogeneous Distribution ◽  
Mushroom Bodies ◽  
Kenyon Cell ◽  
Cell Clusters ◽  
Stage 1 ◽  
The Brain

In the honeybee the mushroom bodies are prominent neuropil structures arranged as pairs in the dorsal protocerebrum of the brain. Each mushroom body is composed of a medial and a lateral subunit. To understand their development, the proliferation pattern of mushroom body intrinsic cells, the Kenyon cells, were examined during larval and pupal stages using the bromodeoxyuridine (BrdU) technique and chemical ablation with hydroxyurea.By larval stage 1, ∼40 neuroblasts are located in the periphery of the protocerebrum. Many of these stem cells divide asymmetrically to produce a chain of ganglion mother cells. Kenyon cell precursors underly a different proliferation pattern. With the beginning of larval stage 3, they are arranged in two large distinct cell clusters in each side of the brain. BrdU incorporation into newly synthesized DNA and its immunohistochemical detection show high mitotic activity in these cell clusters that lasts until mid-pupal stages. The uniform diameter of cells, the homogeneous distribution of BrdU-labeled nuclei, and the presence of equally dividing cells in these clusters indicate symmetrical cell divisions of Kenyon cell precursors.Hydroxyurea applied to stage 1 larvae caused the selective ablation of mushroom bodies. Within these animals a variety of defects were observed. In the majority of brains exhibiting mushroom body defects, either one mushroom body subunit on one or on both sides, or three or four subunits (e.g., complete mushroom body ablation) were missing. In contrast, partial ablation of mushroom body subunits resulting in small Kenyon cell clusters and peduncles was observed very rarely. These findings indicate that hydroxyurea applied during larval stage 1 selectively deletes Kenyon stem cells. The results also show that each mushroom body subunit originates from a very small number of stem cells and develops independently of its neighboring subunit.

scholarly journals Calcium in Kenyon Cell Somata as a Substrate for an Olfactory Sensory Memory in Drosophila

2018 ◽  
Vol 12 ◽  
Author(s):  
Alja Lüdke ◽  
Georg Raiser ◽  
Johannes Nehrkorn ◽  
Andreas V. M. Herz ◽  
C. Giovanni Galizia ◽  
...  
Keyword(s):  
Sensory Memory ◽  
Kenyon Cell ◽  
Cell Somata

scholarly journals Corrigendum: Calcium in Kenyon Cell Somata as a Substrate for an Olfactory Sensory Memory in Drosophila

2018 ◽  
Vol 12 ◽  
Author(s):  
Alja Lüdke ◽  
Georg Raiser ◽  
Johannes Nehrkorn ◽  
Andreas V. M. Herz ◽  
C. Giovanni Galizia ◽  
...  
Keyword(s):  
Sensory Memory ◽  
Kenyon Cell ◽  
Cell Somata

scholarly journals Avoidance response to CO2 in the lateral horn

2018 ◽  
Author(s):  
Nélia Varela ◽  
Miguel Gaspar ◽  
Sophie Dias ◽  
Maria Luísa Vasconcelos
Keyword(s):  
Calcium Imaging ◽  
Mushroom Body ◽  
Antennal Lobe ◽  
Functional Role ◽  
Direct Evidence ◽  
Physiological Responses ◽  
Lateral Horn ◽  
The One ◽  
The Brain

ABSTRACTIn flies, the olfactory information is carried from the first relay in the brain, the antennal lobe, to the mushroom body (MB) and the lateral horn (LH). Olfactory associations are formed in the MB. The LH was ascribed a role in innate responses based on the stereotyped connectivity with the antennal lobe, stereotyped physiological responses to odors and MB silencing experiments. Direct evidence for the functional role of the LH is still missing. Here we investigate the behavioral role of the LH neurons directly, using the CO2 response as a paradigm. Our results show the involvement of the LH in innate responses. Specifically, we demonstrate that activity in two sets of neurons is required for the full behavioral response to CO2. Using calcium imaging we observe that the two sets of neurons respond to CO2 in different manners. Using independent manipulation and recording of the two sets of neurons we find that the one that projects to the SIP also outputs to the local neurons within the LH. The design of simultaneous output at the LH and the SIP, an output of the MB, allows for coordination between innate and learned responses.

scholarly journals Rhythmic expression of Neurofibromin 1 in mushroom body neurons mediates circadian wake drive through activating cAMP−PKA signaling

2020 ◽  
Author(s):  
Pedro Machado Almeida ◽  
Blanca Lago Solis ◽  
Alexis Feidler ◽  
Emi Nagoshi
Keyword(s):  
Mushroom Body ◽  
Regulation Of Gene Expression ◽  
Neurofibromatosis Type ◽  
Rna Seq ◽  
Sleep Regulation ◽  
Rhythmic Expression ◽  
Cognitive States ◽  
Neurofibromin 1 ◽  
The Brain

SUMMARYVarious behavioral and cognitive states exhibit circadian variations in animals across phyla including Drosophila, in which only ∼0.1% of the entire brain neurons contain circadian clocks. This suggests that clock neurons communicate with a plethora of non-clock neurons to transmit the timing information to gate various behavioral outputs in Drosophila. Here, we address the molecular underpinning of this phenomenon by performing circadian RNA-seq analysis of non-clock neurons that constitute the mushroom body (MB), the center of information processing and sleep regulation. We identify hundreds of genes rhythmically expressed in the MB, including the Drosophila ortholog of Neurofibromin 1 (Nf1), the gene responsible for neurofibromatosis type 1 (NF1). Rhythmic expression of Nf1 promotes daytime wakefulness by activating cAMP−PKA signaling and increasing excitability of the MB. These findings reveal the pervasive, non-cell-autonomous circadian regulation of gene expression in the brain and its role in sleep, with implications in the pathology of NF1.

scholarly journals Drosophila mef2 is essential for normal mushroom body and wing development

2018 ◽  
Author(s):  
Jill R. Crittenden ◽  
Efthimios M. C. Skoulakis ◽  
Elliott. S. Goldstein ◽  
Ronald L. Davis
Keyword(s):  
Nuclear Localization ◽  
Mushroom Body ◽  
Normal Development ◽  
Cell Types ◽  
Mushroom Bodies ◽  
Wing Development ◽  
Myocyte Enhancer Factor 2 ◽  
Multiple Cell ◽  
The Brain ◽  
Enhancer Factor

ABSTRACTMEF2 (myocyte enhancer factor 2) transcription factors are found in the brain and muscle of insects and vertebrates and are essential for the differentiation of multiple cell types. We show that in the fruitfly Drosophila, MEF2 is essential for normal development of wing veins, and for mushroom body formation in the brain. In embryos mutant for D-mef2, there was a striking reduction in the number of mushroom body neurons and their axon bundles were not detectable. D-MEF2 expression coincided with the formation of embryonic mushroom bodies and, in larvae, expression onset was confirmed to be in post-mitotic neurons. With a D-mef2 point mutation that disrupts nuclear localization, we find that D-MEF2 is restricted to a subset of Kenyon cells that project to the α/β, and γ axonal lobes of the mushroom bodies, but not to those forming the α’/β’ lobes. Our findings that ancestral mef2 is specifically important in dopamine-receptive neurons has broad implications for its function in mammalian neurocircuits.

scholarly journals Inhibitory muscarinic acetylcholine receptors enhance aversive olfactory conditioning in adult Drosophila

2018 ◽  
Author(s):  
Noa Bielopolski ◽  
Hoger Amin ◽  
Anthi A. Apostolopoulou ◽  
Eyal Rozenfeld ◽  
Hadas Lerner ◽  
...  
Keyword(s):  
Mushroom Body ◽  
Acetylcholine Receptors ◽  
Physiological Function ◽  
Muscarinic Acetylcholine Receptors ◽  
Kenyon Cell ◽  
Olfactory Conditioning ◽  
Muscarinic Acetylcholine ◽  
Kenyon Cells ◽  
Output Neurons ◽  
Adult Drosophila

AbstractOlfactory associative learning inDrosophilais mediated by synaptic plasticity between the Kenyon cells of the mushroom body and their output neurons. Both Kenyon cells and their inputs are cholinergic, yet little is known about the physiological function of muscarinic acetylcholine receptors in learning in adult flies. Here we show that aversive olfactory learning in adult flies requires type A muscarinic acetylcholine receptors (mAChR-A) specifically in the gamma subtype of Kenyon cells. Surprisingly, mAChR-A inhibits odor responses in both Kenyon cell dendrites and axons. Moreover, mAChR-A knockdown impairs the learning-associated depression of odor responses in a mushroom body output neuron. Our results suggest that mAChR-A is required at Kenyon cell presynaptic terminals to depress the synapses between Kenyon cells and their output neurons, and may suggest a role for the recently discovered axo-axonal synapses between Kenyon cells.

Sign in / Sign up

Export Citation Format

Share Document