scholarly journals Role of motoneuron-derived neurotrophin 3 in survival and axonal projection of sensory neurons during neural circuit formation

Development ◽  
2012 ◽  
Vol 139 (6) ◽  
pp. 1125-1132 ◽  
Author(s):  
N. Usui ◽  
K. Watanabe ◽  
K. Ono ◽  
K. Tomita ◽  
N. Tamamaki ◽  
...  
Keyword(s):  
Sensory Neurons ◽  
Neural Circuit ◽  
Axonal Projection ◽  
Neurotrophin 3 ◽  
Circuit Formation

Role of microRNAs in Semaphorin function and neural circuit formation

2013 ◽  
Vol 24 (3) ◽  
pp. 146-155 ◽  
Author(s):  
Marie-Laure Baudet ◽  
Anaïs Bellon ◽  
Christine E. Holt
Keyword(s):  
Neural Circuit ◽  
Circuit Formation

scholarly journals Neurotrophin, p75, and Trk Signaling Module in the Developing Nervous System of the Marine AnnelidPlatynereis dumerilii

2016 ◽  
Vol 2016 ◽  
pp. 1-12 ◽  
Author(s):  
Antonella Lauri ◽  
Paola Bertucci ◽  
Detlev Arendt
Keyword(s):  
Nervous System ◽  
Neuronal Development ◽  
Neural Circuit ◽  
Circuit Development ◽  
Circuit Formation ◽  
Neurotrophic Signaling ◽  
High Degree ◽  
Developing Nervous System

In vertebrates, neurotrophic signaling plays an important role in neuronal development, neural circuit formation, and neuronal plasticity, but its evolutionary origin remains obscure. We found and validated nucleotide sequences encoding putative neurotrophic ligands (neurotrophin, NT) and receptors (Trk and p75) in two annelids,Platynereis dumerilii(Errantia) andCapitella teleta(Sedentaria, for which some sequences were found recently by Wilson, 2009). Predicted protein sequences and structures ofPlatynereisneurotrophic molecules reveal a high degree of conservation with the vertebrate counterparts; some amino acids signatures present in the annelid Trk sequences are absent in the basal chordate amphioxus, reflecting secondary loss in the cephalochordate lineage. In addition, expression analysis of NT, Trk, and p75 duringPlatynereisdevelopment by whole-mount mRNAin situhybridization supports a role of these molecules in nervous system and circuit development. These annelid data corroborate the hypothesis that the neurotrophic signaling and its involvement in shaping neural networks predate the protostome-deuterostome split and were present in bilaterian ancestors.

scholarly journals The role of lineage, hemilineage and temporal identity in establishing neuronal connectivity in the Drosophila larval CNS

2019 ◽  
Author(s):  
Brandon Mark ◽  
Sen-Lin Lai ◽  
Aref Arzan Zarin ◽  
Laurina Manning ◽  
Albert Cardona ◽  
...  
Keyword(s):  
Sensory Processing ◽  
Neural Circuit ◽  
Neuronal Morphology ◽  
Neural Progenitors ◽  
Neuronal Diversity ◽  
Developmental Mechanism ◽  
Temporal Identity ◽  
Circuit Formation ◽  
Synapse Targeting

AbstractThe mechanisms specifying neuronal diversity are well-characterized, yet it remains unclear how or if these mechanisms regulate neuronal morphology and connectivity. Here we map the developmental origin of 78 bilateral pairs of interneurons from seven identified neural progenitors (neuroblasts) within a complete TEM reconstruction of the Drosophila newly-hatched larval CNS. This allows us to correlate developmental mechanism with neuronal projections, synapse targeting, and connectivity. We find that clonally-related neurons from project widely in the neuropil, without preferential circuit formation. In contrast, the two NotchON/NotchOFF hemilineages from each neuroblast project to either dorsal motor neuropil (NotchON) or ventral sensory neuropil (NotchOFF). Thus, each neuroblast contributes both motor and sensory processing neurons. Lineage-specific constitutive Notch transforms sensory to motor hemilineages, showing hemilineage identity determines neuronal targeting. Within a hemilineage, temporal cohorts target processes and synapses to different sub-domains of the neuropil, effectively “tiling” the hemilineage neuropil, and hemilineage/temporal cohorts are enriched for shared connectivity. Thus, neuroblast lineage, hemilineage, and temporal identity progressively restrict neuropil targeting, synapse localization, and connectivity. We propose that mechanisms generating neural diversity are also determinants of neural circuit formation.

scholarly journals Trans-Axonal Signaling in Neural Circuit Wiring

2020 ◽  
Vol 21 (14) ◽  
pp. 5170 ◽  
Author(s):  
Olivia Spead ◽  
Fabienne E. Poulain
Keyword(s):  
Molecular Mechanisms ◽  
Neural Circuits ◽  
Neural Circuit ◽  
Target Selection ◽  
Synaptic Connectivity ◽  
Recent Advances ◽  
Complex Process ◽  
Circuit Formation

The development of neural circuits is a complex process that relies on the proper navigation of axons through their environment to their appropriate targets. While axon–environment and axon–target interactions have long been known as essential for circuit formation, communication between axons themselves has only more recently emerged as another crucial mechanism. Trans-axonal signaling governs many axonal behaviors, including fasciculation for proper guidance to targets, defasciculation for pathfinding at important choice points, repulsion along and within tracts for pre-target sorting and target selection, repulsion at the target for precise synaptic connectivity, and potentially selective degeneration for circuit refinement. This review outlines the recent advances in identifying the molecular mechanisms of trans-axonal signaling and discusses the role of axon–axon interactions during the different steps of neural circuit formation.

scholarly journals A9 DORSAL ROOT GANGLIA NEURONAL RESPONSES AND SUBSTANCE P PRODUCTION ARE HIGHER IN MALE MICE

2021 ◽  
Vol 4 (Supplement_1) ◽  
pp. 10-11
Author(s):  
J Pujo ◽  
G De Palma ◽  
J Lu ◽  
S M Collins ◽  
P Bercik
Keyword(s):  
Abdominal Pain ◽  
Substance P ◽  
Gut Microbiota ◽  
Sensory Neurons ◽  
Dorsal Root ◽  
Neuronal Response ◽  
Neuronal Responses ◽  
Visceral Sensitivity ◽  
Germ Free

Abstract Background Abdominal pain is a common complaint in patients with chronic gastrointestinal disorders. Accumulating evidence suggests that gut microbiota is an important determinant of gut function, including visceral sensitivity. Germ-free (GF) mice have been shown to display visceral hypersensitivity, which normalizes after colonization. Sex also appears to play a key role in visceral sensitivity, as women report more abdominal pain than men. Thus, both gut bacteria and sex are important in the regulation of gut nociception, but the underlying mechanisms remain poorly understood. Aims To investigate the role of gut microbiota and sex in abdominal pain. Methods We used primary cultures of sensory neurons from dorsal root ganglia (DRG) of female and male conventionally raised (SPF) or germ-free (GF) mice (7–18 weeks old). To study the visceral afferent activity in vitro, calcium mobilization in DRG sensory neurons was measured by inverted fluorescence microscope using a fluorescent calcium probe Fluo-4 (1mM). Two parameters were considered i) the percentage of responding neurons ii) the intensity of the neuronal response. First, DRG sensory neurons were stimulated by a TRPV1 agonist capsaicin (12.5nM, 125nM and 1.25µM) or by a mixture of G-protein coupled receptors agonist (GPCR: bradykinin, histamine and serotonin; 1µM, 10µM and 100µM). We next measured the neuronal production of substance P and calcitonin gene-related peptide (CGRP), two neuropeptides associated with nociception, in response to capsaicin (1.25µM) or GPCR agonists (100µM) by ELISA and EIA, respectively. Results The percentage of neurons responding to capsaicin and GPCR agonists was similar in male and female SPF and GF mice. However, the intensity of the neuronal response was higher in SPF male compared to SPF female in response to capsaicin (125nM: p=0.0336; 1.25µM: p=0.033) but not to GPCR agonists. Neuronal activation was similar in GF and SPF mice of both sexes after administration of capsaicin or GPCR agonists. Furthermore, substance P and CGRP production by sensory neurons induced by capsaicin or GPCR agonists was similar in SPF and GF mice, regardless of sex. However, while the response to capsaicin was similar, the GPCR agonists-induced production of substance P was higher in SPF male mice compared to SPF females (p=0.003). The GPCR agonists-induced production of CGRP was similar in SPF male and female mice. Conclusions Our data suggest that at the level of DRG neurons, the absence of gut microbiota does not predispose to visceral hypersensitivity. The intensity of DRG neuronal responses to capsaicin and the GPCR agonists-induced production of substance P are higher in male compared to female mice, in contrast to previously published studies in various models of acute and chronic pain. Further studies are thus needed to investigate the role of sex in visceral sensitivity. Funding Agencies CIHR

scholarly journals Implications of Extended Inhibitory Neuron Development

2021 ◽  
Vol 22 (10) ◽  
pp. 5113
Author(s):  
Jae-Yeon Kim ◽  
Mercedes F. Paredes
Keyword(s):  
Neural Circuit ◽  
Inhibitory Neuron ◽  
Postnatal Period ◽  
Specific Pattern ◽  
Inhibitory Neurons ◽  
Gabaergic Interneuron ◽  
Gabaergic Interneurons ◽  
Neuron Development ◽  
Cortical Regions ◽  
Circuit Formation

A prolonged developmental timeline for GABA (γ-aminobutyric acid)-expressing inhibitory neurons (GABAergic interneurons) is an amplified trait in larger, gyrencephalic animals. In several species, the generation, migration, and maturation of interneurons take place over several months, in some cases persisting after birth. The late integration of GABAergic interneurons occurs in a region-specific pattern, especially during the early postnatal period. These changes can contribute to the formation of functional connectivity and plasticity, especially in the cortical regions responsible for higher cognitive tasks. In this review, we discuss GABAergic interneuron development in the late gestational and postnatal forebrain. We propose the protracted development of interneurons at each stage (neurogenesis, neuronal migration, and network integration), as a mechanism for increased complexity and cognitive flexibility in larger, gyrencephalic brains. This developmental feature of interneurons also provides an avenue for environmental influences to shape neural circuit formation.

Optical survey of neural circuit formation in the embryonic chick vagal pathway

2004 ◽  
Vol 19 (5) ◽  
pp. 1217-1225 ◽  
Author(s):  
Katsushige Sato ◽  
Naohisa Miyakawa ◽  
Yoko Momose-Sato
Keyword(s):  
Neural Circuit ◽  
Embryonic Chick ◽  
Vagal Pathway ◽  
Circuit Formation

Perinatal Development of the Medial Nucleus of the Trapezoid Body

2018 ◽  
pp. 244-272
Author(s):  
Shobhana Sivaramakrishnan ◽  
Ashley Brandebura ◽  
Paul Holcomb ◽  
Daniel Heller ◽  
Douglas Kolson ◽  
...  
Keyword(s):  
Axon Guidance ◽  
Neural Circuit ◽  
Neural Cells ◽  
Calyx Of Held ◽  
Medial Nucleus ◽  
Target Neuron ◽  
Circuit Formation ◽  
Key Events ◽  
The Brain ◽  
Trapezoid Body

Bushy cells (BC) of the cochlear nucleus mono-innervate their target neuron, the principal cell of the medial nucleus of the trapezoid body (MNTB), via the calyx of Held (CH) terminal, which is a typically mammalian structure and perhaps the largest nerve terminal in the brain. CH:MNTB innervation has become an attractive model to study neural circuit formation because it forms quickly, passing through stages of competition in mice within 2–4 days. BCs innervate MNTB neurons by E17, but CHs do not begin to grow for another five days (P3). Progress has been made to identify molecular factors for axon guidance, CH growth, and physiological maturation of synaptic partners, but important details remain to be discovered. We summarize key events in CH formation and highlight unresolved issues in molecular and physiological signaling, roles for non-neural cells, and the nature of competition during the first postnatal week.

scholarly journals Protective Effects of Acupuncture Against Gentamicin-Induced Ototoxicity in Rats: Possible Role of Neurotrophin-3

2017 ◽  
Vol 23 ◽  
pp. 446-451
Author(s):  
Ping Zhou ◽  
Weijun Ma ◽  
Ying Sheng ◽  
Maoli Duan ◽  
Xiaotong Zhang
Keyword(s):  
Protective Effects ◽  
Neurotrophin 3
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