scholarly journals Suppression of a Novel Vitellogenesis-Inhibiting Hormone Significantly Increases Ovarian Vitellogenesis in the Black Tiger Shrimp, Penaeus monodon

2021 ◽  
Vol 12 ◽  
Author(s):  
Phaivit Laphyai ◽  
Thanapong Kruangkum ◽  
Charoonroj Chotwiwatthanakun ◽  
Wanita Semchuchot ◽  
Prawporn Thaijongrak ◽  
...  
Keyword(s):  
Nerve Cord ◽  
Ventral Nerve Cord ◽  
Penaeus Monodon ◽  
Fold Increase ◽  
Type Ii ◽  
Stomatogastric Nervous System ◽  
Eyestalk Ablation ◽  
Reading Frame ◽  
The Brain

In this study, a novel Crustacean Hyperglycemic Hormone-type II gene (CHH-type II) was identified and biologically characterized in a shrimp, Penaeus monodon. Based on its structure and function, this gene was named P. monodon vitellogenesis-inhibiting hormone (PemVIH). The complete cDNA sequence of PemVIH consisted of 1,022 nt with an open reading frame (ORF) of 339 nt encoding a polypeptide of 112 amino acids. It was classified as a member of the CHH-type II family based on conserved cysteine residues, a characteristically positioned glycine residue, and the absence of CHH precursor-related peptide (CPRP) domain. The deduced mature PemVIH shared the highest sequence similarities with giant river prawn sinus gland peptide A. Unlike P. monodon gonad-inhibiting hormone (PemGIH), PemVIH was expressed only in the brain and ventral nerve cord, but not the eyestalks. Whole mount immunofluorescence using a newly generated PemVIH antiserum detected positive signals in neuronal cluster 9/11 and 17 of the brain, commissural ganglion (CoG), and neuronal clusters of ventral nerve cord. The presence of PemVIH-positive neurons in CoG, a part of stomatogastric nervous system, suggested a potential mechanism for crosstalk between nutritional and reproductive signaling. The role of PemVIH in vitellogenesis was evaluated using RNA interference technique. Temporal knockdown of PemVIH in female subadults resulted in a 3-fold increase in ovarian vitellogenin expression, suggesting an inhibitory role of PemVIH in vitellogenesis. This study provided novel insight into the control of vitellogenesis and additional strategies for improving ovarian maturation in P. monodon without the current harmful practice of eyestalk ablation.

scholarly journals The AP2 clathrin adaptor protein complex regulates the abundance of GLR-1 glutamate receptors in the ventral nerve cord of Caenorhabditis elegans

2015 ◽  
Vol 26 (10) ◽  
pp. 1887-1900 ◽  
Author(s):  
Steven D. Garafalo ◽  
Eric S. Luth ◽  
Benjamin J. Moss ◽  
Michael I. Monteiro ◽  
Emily Malkin ◽  
...  
Keyword(s):  
Caenorhabditis Elegans ◽  
Nerve Cord ◽  
Ventral Nerve Cord ◽  
Secretory Pathway ◽  
Adaptor Protein ◽  
Intracellular Compartments ◽  
Clathrin Adaptor ◽  
Strength And Plasticity

Regulation of glutamate receptor (GluR) abundance at synapses by clathrin-mediated endocytosis can control synaptic strength and plasticity. We take advantage of viable, null mutations in subunits of the clathrin adaptor protein 2 (AP2) complex in Caenorhabditis elegans to characterize the in vivo role of AP2 in GluR trafficking. In contrast to our predictions for an endocytic adaptor, we found that levels of the GluR GLR-1 are decreased at synapses in the ventral nerve cord (VNC) of animals with mutations in the AP2 subunits APM-2/μ2, APA-2/α, or APS-2/σ2. Rescue experiments indicate that APM-2/μ2 functions in glr-1–expressing interneurons and the mature nervous system to promote GLR-1 levels in the VNC. Genetic analyses suggest that APM-2/μ2 acts upstream of GLR-1 endocytosis in the VNC. Consistent with this, GLR-1 accumulates in cell bodies of apm-2 mutants. However, GLR-1 does not appear to accumulate at the plasma membrane of the cell body as expected, but instead accumulates in intracellular compartments including Syntaxin-13– and RAB-14–labeled endosomes. This study reveals a novel role for the AP2 clathrin adaptor in promoting the abundance of GluRs at synapses in vivo, and implicates AP2 in the regulation of GluR trafficking at an early step in the secretory pathway.

scholarly journals Neuronal spreading and plaque induction of intracellular Aβ and its disruption of Aβ homeostasis

2021 ◽  
Author(s):  
Tomas T. Roos ◽  
Megg G. Garcia ◽  
Isak Martinsson ◽  
Rana Mabrouk ◽  
Bodil Israelsson ◽  
...  
Keyword(s):  
Brain Homogenate ◽  
Fold Increase ◽  
Amyloid Beta Peptide ◽  
Intracellular Accumulation ◽  
Brain Areas ◽  
Cellular Models ◽  
Beta Peptide ◽  
The Brain

AbstractThe amyloid-beta peptide (Aβ) is thought to have prion-like properties promoting its spread throughout the brain in Alzheimer’s disease (AD). However, the cellular mechanism(s) of this spread remains unclear. Here, we show an important role of intracellular Aβ in its prion-like spread. We demonstrate that an intracellular source of Aβ can induce amyloid plaques in vivo via hippocampal injection. We show that hippocampal injection of mouse AD brain homogenate not only induces plaques, but also damages interneurons and affects intracellular Aβ levels in synaptically connected brain areas, paralleling cellular changes seen in AD. Furthermore, in a primary neuron AD model, exposure of picomolar amounts of brain-derived Aβ leads to an apparent redistribution of Aβ from soma to processes and dystrophic neurites. We also observe that such neuritic dystrophies associate with plaque formation in AD-transgenic mice. Finally, using cellular models, we propose a mechanism for how intracellular accumulation of Aβ disturbs homeostatic control of Aβ levels and can contribute to the up to 10,000-fold increase of Aβ in the AD brain. Our data indicate an essential role for intracellular prion-like Aβ and its synaptic spread in the pathogenesis of AD.

Upregulation of γ-aminobutyric acid transporter expression: role of alkylated γ-aminobutyric acid derivatives

2001 ◽  
Vol 29 (6) ◽  
pp. 736-741 ◽  
Author(s):  
T. L. Whitworth ◽  
M. W. Quick
Keyword(s):  
Plasma Membrane ◽  
Tyrosine Kinases ◽  
Fold Increase ◽  
Aminobutyric Acid ◽  
Gaba Uptake ◽  
Prolonged Incubation ◽  
Gaba Derivatives ◽  
Brain Gaba ◽  
The Brain

Pregabalin [(S)-(+)-3-isobutylgaba] and gabapentin [1-(aminomethyl)cyclohexane acetic acid] are γ-aminobutyric acid (GABA) derivatives that are effective in the treatment of behavioural disorders, convulsions, epilepsy and hyperalgesia. The mechanisms underlying the diverse actions of these compounds in the brain have not been well elucidated. To test the hypothesis that these compounds exert some of their effects on GABA-ergic systems in the brain, we examined their role in regulating the rat brain GABA transporter GAT1, a plasma membrane protein involved in regulating synaptic transmitter levels. Prolonged incubation of hippocampal cultures, which endogenously express GAT1, with gabapentin and pregabalin caused a 2-fold increase in subsequent GABA uptake, which was concentration- and time-dependent. This increase in uptake was correlated with a redistribution of GAT1 protein from intracellular locations to the plasma membrane. Further experiments also suggested that the signal transduction cascade that modulates pregabalin-mediated GAT1 redistribution may involve pathways activated by specific GAT1 substrates and antagonists but does not involve protein kinase C and tyrosine kinases, two other pathways known to regulate GAT1 redistribution. These data suggest that pregabalin and gabapentin may exert some of their actions in the brain by altering GABAergic signalling.

scholarly journals Identification and Expression Analysis of Tryptophan Hydroxylase in the Brain and Ventral Nerve Cord of RagwormNeanthes japonica(Polychaeta, Annelida)

2016 ◽  
Vol 300 (2) ◽  
pp. 415-424
Author(s):  
Shun Wang ◽  
Zhe Dong ◽  
Shen Li ◽  
Haotian Yin ◽  
Zhifu Zhao ◽  
...  
Keyword(s):  
Expression Analysis ◽  
Nerve Cord ◽  
Ventral Nerve Cord ◽  
Tryptophan Hydroxylase ◽  
The Brain

First detection of serotonin in the nervous system of the marine calanoid copepod Centropages typicus

2005 ◽  
Vol 85 (1) ◽  
pp. 71-72 ◽  
Author(s):  
D. Benzid ◽  
C. Morris ◽  
R.-M. Barthélémy
Keyword(s):  
Nervous System ◽  
Nerve Cord ◽  
Ventral Nerve Cord ◽  
Calanoid Copepod ◽  
Marine Species ◽  
Biological Processes ◽  
Calanoid Copepods ◽  
The Brain ◽  
Serotoninergic Nervous System ◽  
Centropages Typicus

This investigation constitutes the first study of the serotoninergic nervous system in calanoid copepods (crustaceans). Serotonin (5-HT), a neurotransmitter which plays a part in many biological processes, has been detected by immunofluorescence in the brain, the circumoesophageal collar and the ventral nerve cord of the marine species Centropages typicus.

Role of antioxidant treatment on DNA and lipid damage in the brain of rats subjected to a chemically induced chronic model of tyrosinemia type II

2017 ◽  
Vol 435 (1-2) ◽  
pp. 207-214 ◽  
Author(s):  
Emilio L. Streck ◽  
Samira D. T. De Prá ◽  
Paula Ronsani Ferro ◽  
Milena Carvalho-Silva ◽  
Lara M. Gomes ◽  
...  
Keyword(s):  
Type Ii ◽  
Antioxidant Treatment ◽  
Tyrosinemia Type Ii ◽  
Lipid Damage ◽  
Chemically Induced ◽  
Chronic Model ◽  
The Brain

scholarly journals Whole-central nervous system functional imaging in larval Drosophila

2015 ◽  
Vol 6 (1) ◽  
Author(s):  
William C. Lemon ◽  
Stefan R. Pulver ◽  
Burkhard Höckendorf ◽  
Katie McDole ◽  
Kristin Branson ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Nerve Cord ◽  
Ventral Nerve Cord ◽  
Activity Patterns ◽  
Network Activity ◽  
Imaging Data ◽  
Spatiotemporal Resolution ◽  
Functional Connections ◽  
The Brain

Abstract Understanding how the brain works in tight concert with the rest of the central nervous system (CNS) hinges upon knowledge of coordinated activity patterns across the whole CNS. We present a method for measuring activity in an entire, non-transparent CNS with high spatiotemporal resolution. We combine a light-sheet microscope capable of simultaneous multi-view imaging at volumetric speeds 25-fold faster than the state-of-the-art, a whole-CNS imaging assay for the isolated Drosophila larval CNS and a computational framework for analysing multi-view, whole-CNS calcium imaging data. We image both brain and ventral nerve cord, covering the entire CNS at 2 or 5 Hz with two- or one-photon excitation, respectively. By mapping network activity during fictive behaviours and quantitatively comparing high-resolution whole-CNS activity maps across individuals, we predict functional connections between CNS regions and reveal neurons in the brain that identify type and temporal state of motor programs executed in the ventral nerve cord.

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