Characterization of an optic lobe circadian pacemaker by in situ and in vitro recording of neural activity in the cricket, Gryllus bimaculatus

1992 ◽  
Vol 171 (1) ◽  
Author(s):  
Kenji Tomioka ◽  
Yoshihiko Chiba
Keyword(s):  
Neural Activity ◽  
Optic Lobe ◽  
Circadian Pacemaker ◽  
Gryllus Bimaculatus

scholarly journals Enlisting the Ixodes scapularis Embryonic ISE6 Cell Line to Investigate the Neuronal Basis of Tick—Pathogen Interactions

Pathogens ◽  
2021 ◽  
Vol 10 (1) ◽  
pp. 70
Author(s):  
Lourdes Mateos-Hernández ◽  
Natália Pipová ◽  
Eléonore Allain ◽  
Céline Henry ◽  
Clotilde Rouxel ◽  
...  
Keyword(s):  
Cell Line ◽  
Peripheral Nerves ◽  
Ixodes Scapularis ◽  
Embryonic Cell ◽  
Cell Subpopulation ◽  
In Vivo Experiments

Neuropeptides are small signaling molecules expressed in the tick central nervous system, i.e., the synganglion. The neuronal-like Ixodes scapularis embryonic cell line, ISE6, is an effective tool frequently used for examining tick–pathogen interactions. We detected 37 neuropeptide transcripts in the I. scapularis ISE6 cell line using in silico methods, and six of these neuropeptide genes were used for experimental validation. Among these six neuropeptide genes, the tachykinin-related peptide (TRP) of ISE6 cells varied in transcript expression depending on the infection strain of the tick-borne pathogen, Anaplasma phagocytophilum. The immunocytochemistry of TRP revealed cytoplasmic expression in a prominent ISE6 cell subpopulation. The presence of TRP was also confirmed in A. phagocytophilum-infected ISE6 cells. The in situ hybridization and immunohistochemistry of TRP of I. scapularis synganglion revealed expression in distinct neuronal cells. In addition, TRP immunoreaction was detected in axons exiting the synganglion via peripheral nerves as well as in hemal nerve-associated lateral segmental organs. The characterization of a complete Ixodes neuropeptidome in ISE6 cells may serve as an effective in vitro tool to study how tick-borne pathogens interact with synganglion components that are vital to tick physiology. Therefore, our current study is a potential stepping stone for in vivo experiments to further examine the neuronal basis of tick–pathogen interactions.

Serotonin sets the day state in the neurons that control coupling between the optic lobe circadian pacemakers in the cricketGryllus bimaculatus

2002 ◽  
Vol 205 (9) ◽  
pp. 1305-1314 ◽  
Author(s):  
A. S. M. Saifullah ◽  
Kenji Tomioka
Keyword(s):  
Neural Activity ◽  
Receptor Agonist ◽  
Serotonin Receptor ◽  
Optic Lobe ◽  
Neural Pathway ◽  
Gryllus Bimaculatus ◽  
Dependent Inhibition ◽  
Serotonin Receptor Antagonist ◽  
Time Dependent Inhibition ◽  
Circadian Pacemakers

SUMMARYThe bilaterally paired optic lobe circadian pacemakers of the cricket Gryllus bimaculatus mutually exchange photic and circadian information to keep their activity synchronized. The information is mediated by a neural pathway, consisting of the so-called medulla bilateral neurons,connecting the medulla areas of the two optic lobes. We investigated the effects of serotonin on the neural activity in this coupling pathway. Spontaneous and light-induced electrical activity of the neurons in the coupling pathway showed daily variations, being more intense during the night than the day. Microinjection of serotonin or a serotonin-receptor agonist,quipazine, into the optic lobe caused a dose- and time-dependent inhibition of spontaneous and light-induced responses, mimicking the day state. The amount of suppression was greater and the recovery from the suppression occurred faster during the night. Application of metergoline, a non-selective serotonin-receptor antagonist, increased spontaneous activity and light-evoked responses during both the day and the night, with higher effect during the day. In addition, metergoline effectively attenuated the effects of serotonin. These facts suggest that in the cricket's optic lobe, serotonin is released during the daytime and sets the day state in the neurons regulating coupling between the bilaterally paired optic lobe circadian pacemakers.

In vitro characterization of an injectable in situ forming composite system for bone reconstruction

2015 ◽  
Vol 119 ◽  
pp. 151-158 ◽  
Author(s):  
R. Dorati ◽  
C. Colonna ◽  
I. Genta ◽  
A. De Trizio ◽  
T. Modena ◽  
...  
Keyword(s):  
Composite System ◽  
Bone Reconstruction ◽  
In Situ Forming ◽  
In Vitro Characterization

Characterization of distinct mesenchymal-like cell populations from human skeletal muscle in situ and in vitro

2010 ◽  
Vol 316 (15) ◽  
pp. 2513-2526 ◽  
Author(s):  
Séverine Lecourt ◽  
Jean-Pierre Marolleau ◽  
Olivia Fromigué ◽  
Karine Vauchez ◽  
Rina Andriamanalijaona ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Human Skeletal Muscle ◽  
Cell Populations

scholarly journals Characterization of the Exoglucanase-Encoding Gene PaEXG2 and Study of Its Role in the Biocontrol Activity of Pichia anomala Strain K

2003 ◽  
Vol 93 (9) ◽  
pp. 1145-1152 ◽  
Author(s):  
Cathy Grevesse ◽  
Philippe Lepoivre ◽  
Mohamed Haïssam Jijakli
Keyword(s):  
Marker Gene ◽  
Glycosylation Site ◽  
Pichia Anomala ◽  
Gene Encoding ◽  
Biocontrol Activity ◽  
Monophosphate Decarboxylase ◽  
Uracil Auxotroph

The PaEXG2 gene, encoding an exo-β-1,3-glucanase, was isolated from the biocontrol agent Pichia anomala strain K. PaEXG2 has the capacity for coding an acidic protein of 427 amino acids with a predicted molecular weight of 45.7 kDa, a calculated pI of 4.7, and one potential N-glycosylation site. PaEXG2 was disrupted by the insertion of the URA3 marker gene, encoding orotidine monophosphate decarboxylase in strain KU1, a uracil auxotroph derived from strain K. Strain KU1 showed inferior biocontrol activity and colonization of wounds on apples, compared to the prototrophic strain. Antagonism and colonization were recovered after the restoration of prototrophy by transformation with the URA3 gene. Integrative transformation was shown to be mostly ectopic in strain K descendants (only 4% of integration by homologous recombination). PaEXG2 disruption abolished all detectable extracellular exo-β-1,3-glucanase activity in vitro and in situ but did not affect biocontrol of Botrytis cinerea on wounded apples.

Characterization of the tomato (Lycopersicon esculentum) genome using in vitro and in situ DNA reassociation

Genome ◽  
1998 ◽  
Vol 41 (3) ◽  
pp. 346-356 ◽  
Author(s):  
Daniel G. Peterson ◽  
William R. Pearson ◽  
Stephen M. Stack
Keyword(s):  
Lycopersicon Esculentum ◽  
Dna Reassociation

Platelet-rich gel-incorporated silk scaffold promotes meniscus regeneration in a rabbit total meniscectomy model

2019 ◽  
Vol 14 (8) ◽  
pp. 753-768 ◽  
Author(s):  
Yifan Wu ◽  
Jianqiao Hong ◽  
Guangyao Jiang ◽  
Sihao Li ◽  
Shiming Chen ◽  
...  
Keyword(s):  
Cartilage Degeneration ◽  
Functional Regeneration ◽  
Scaffold Materials ◽  
Silk Scaffold ◽  
Meniscus Regeneration ◽  
Tgf Β1

Aim: To investigate whether platelet-rich gel (PRG) incorporation could promote meniscal regeneration of the silk scaffold. Materials & methods: A PRG-incorporated silk sponge was fabricated for reconstruction of the meniscus in a rabbit meniscectomy model. Subsequently, characterization of the scaffold, as well as the in vitro cytocompatibility and in vivo function was evaluated. Results: Our results showed that the PRG-incorporated silk scaffold provided a sustained release of TGF-β1 over 1 week. The PRG enhanced the cytocompatibility in vitro and cell infiltration in vivo of the silk sponge. Meanwhile, the implantation of the composite in situ ameliorated the cartilage degeneration in knee at 3 months. Conclusion: These findings indicated that PRG-incorporated silk scaffold could promote functional regeneration of the meniscus and effectively prevented subsequent osteoarthritis after meniscectomy.

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