Activation of GABAB receptors potentiates inward rectifying potassium currents in satellite glial cells from rat trigeminal ganglia: In vivo patch-clamp analysis

Neuroscience ◽  
2015 ◽  
Vol 288 ◽  
pp. 51-58 ◽  
Author(s):  
M. Takeda ◽  
M. Nasu ◽  
T. Kanazawa ◽  
Y. Shimazu
Pain ◽  
2011 ◽  
Vol 152 (9) ◽  
pp. 2147-2156 ◽  
Author(s):  
Mamoru Takeda ◽  
Masayuki Takahashi ◽  
Masanori Nasu ◽  
Shigeji Matsumoto

Pain ◽  
2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Zhiyong Chen ◽  
Qian Huang ◽  
Xiaodan Song ◽  
Neil C. Ford ◽  
Chi Zhang ◽  
...  

2020 ◽  
Vol 21 (8) ◽  
pp. 2938
Author(s):  
Timea Aczél ◽  
Angéla Kecskés ◽  
József Kun ◽  
Kálmán Szenthe ◽  
Ferenc Bánáti ◽  
...  

A large percentage of primary sensory neurons in the trigeminal ganglia (TG) contain neuropeptides such as tachykinins or calcitonin gene-related peptide. Neuropeptides released from the central terminals of primary afferents sensitize the secondary nociceptive neurons in the trigeminal nucleus caudalis (TNC), but also activate glial cells contributing to neuroinflammation and consequent sensitization in chronic orofacial pain and migraine. In the present study, we investigated the newest member of the tachykinin family, hemokinin-1 (HK-1) encoded by the Tac4 gene in the trigeminal system. HK-1 had been shown to participate in inflammation and hyperalgesia in various models, but its role has not been investigated in orofacial pain or headache. In the complete Freund’s adjuvant (CFA)-induced inflammatory orofacial pain model, we showed that Tac4 expression increased in the TG in response to inflammation. Duration-dependent Tac4 upregulation was associated with the extent of the facial allodynia. Tac4 was detected in both TG neurons and satellite glial cells (SGC) by the ultrasensitive RNAscope in situ hybridization. We also compared gene expression changes of selected neuronal and glial sensitization and neuroinflammation markers between wild-type and Tac4-deficient (Tac4-/-) mice. Expression of the SGC/astrocyte marker in the TG and TNC was significantly lower in intact and saline/CFA-treated Tac4-/- mice. The procedural stress-related increase of the SGC/astrocyte marker was also strongly attenuated in Tac4-/- mice. Analysis of TG samples with a mouse neuroinflammation panel of 770 genes revealed that regulation of microglia and cytotoxic cell-related genes were significantly different in saline-treated Tac4-/- mice compared to their wild-types. It is concluded that HK-1 may participate in neuron-glia interactions both under physiological and inflammatory conditions and mediate pain in the trigeminal system.


2010 ◽  
Vol 6 (3) ◽  
pp. 171-181 ◽  
Author(s):  
Paul L. Durham ◽  
F.G. Garrett

Cell bodies of trigeminal nerves, which are located in the trigeminal ganglion, are completely surrounded by satellite glial cells and together form a functional unit that regulates neuronal excitability. The goals of this study were to investigate the cellular organization of the rat trigeminal ganglia during postnatal development and correlate those findings with expression of proteins implicated in neuron–glia interactions. During postnatal development there was an increase in the volume of the neuronal cell body, which correlated with a steady increase in the number of glial cells associated with an individual neuron from an average of 2.16 at birth to 7.35 on day 56 in young adults. Interestingly, while the levels of the inwardly rectifying K+ channel Kir4.1 were barely detectable during the first week, its expression in satellite glial cells increased by day 9 and correlated with initial formation of functional units. Similarly, expression of the vesicle docking protein SNAP-25 and neuropeptide calcitonin gene-related peptide was readily detected beginning on day 9 and remained elevated throughout postnatal development. Based on our findings, we propose that the expression of proteins involved in facilitating neuron–glia interactions temporally correlates with the formation of mature functional units during postnatal development of trigeminal ganglion.


Neuroscience ◽  
2003 ◽  
Vol 120 (4) ◽  
pp. 969-977 ◽  
Author(s):  
M Weick ◽  
P.S Cherkas ◽  
W Härtig ◽  
T Pannicke ◽  
O Uckermann ◽  
...  

Open Medicine ◽  
2014 ◽  
Vol 9 (3) ◽  
pp. 500-504 ◽  
Author(s):  
Mugurel Rusu ◽  
Valentina Mănoiu ◽  
Nicolae Mirancea ◽  
Gheorghe Nini

AbstractSensory ganglia comprise functional units built up by neurons and satellite glial cells (SGCs). In animal species there was proven the presence of neuronoglial progenitor cells in adult samples. Such neural crest-derived progenitors were found in immunohistochemistry (IHC). These findings were not previously documented in transmission electron microscopy (TEM). It was thus aimed to assess in TEM if cells of the human adult trigeminal ganglion indeed have ultrastructural features to qualify for a progenitor, or quiescent phenotype. Trigeminal ganglia were obtained from fifteen adult donor cadavers. In TEM, cells with heterochromatic nuclei, a pancytoplasmic content of free ribosomes, few perinuclear mitochondria, poor developed endoplasmic reticulum, lack of Golgi complexes and membrane trafficking specializations, were found included in the neuronal envelopes built-up by SGCs. The ultrastructural pattern was strongly suggestive for these cells being quiescent progenitors. However, further experiments should correlate the morphologic and immune phenotypes of such cells.


2017 ◽  
Vol 47 (7) ◽  
pp. 1181-1187 ◽  
Author(s):  
Johanna G. Mitterreiter ◽  
Werner J. D. Ouwendijk ◽  
Monique van Velzen ◽  
Gijsbert P. van Nierop ◽  
Albert D. M. E. Osterhaus ◽  
...  

2016 ◽  
Vol 36 (suppl_1) ◽  
Author(s):  
Alison X Xie ◽  
Jakovin J Lee ◽  
Ken D McCarthy

The autonomic nervous system (ANS) exerts profound regulatory influence over cardiovascular physiology. The integrated network among autonomic nuclei in the central nervous system (CNS), as well as ganglionic innervation in the peripheral nervous system (PNS) are essential for homeostasis and for coordinating adaptive changes in physiology and behavior. In addition to neurons, the ANS contains large numbers of Glial Fibrillary Acidic Protein (GFAP) - expressing cells (GFAP + glial cells), which serve many functions in assisting neuronal network activity in both the CNS and the PNS. The present study explores the active role of GFAP + glial cells in regulating cardiovascular function in vivo . Using DREADD technology, we selectively activate Gq-GPCR signaling in satellite glial cells (SGCs) within sympathetic ganglia, which led to fast-acting, long-lasting increases in cardiac function and blood pressure in vivo . In addition, ganglionic SGCs likely increase postganglionic neuronal firing and subsequent norepinephrine release via a “local stimulatory effect“ on postganglionic neurons. Ongoing studies ex vivo using superior cervical ganglia cultures focus on identifying the mechanism underlying the interaction between sympathetic SGCs and postganglionic neurons.


2010 ◽  
Vol 6 (4) ◽  
pp. 237-243 ◽  
Author(s):  
Vitali Belzer ◽  
Nathanael Shraer ◽  
Menachem Hanani

Satellite glial cells (SGCs) are specialized cells that form a tight sheath around neurons in sensory ganglia. In recent years, there is increasing interest in SGCs and they have been studied in both intact ganglia and in tissue culture. Here we studied phenotypic changes in SGCs in cultured trigeminal ganglia from adult mice, containing both neurons and SGCs, using phase optics, immunohistochemistry and time-lapse photography. Cultures were followed for up to 14 days. After isolation virtually every sensory neuron is ensheathed by SGCs, as in the intact ganglia. After one day in culture, SGCs begin to migrate away from their parent neurons, but in most cases the neurons still retain an intact glial cover. At later times in culture, there is a massive migration of SGCs away from the neurons and they undergo clear morphological changes, and at 7 days they become spindle-shaped. At one day in culture SGCs express the glial marker glutamine synthetase, and also the purinergic receptor P2X7. From day 2 in culture the glutamine synthetase expression is greatly diminished, whereas that of P2X7 is largely unchanged. We conclude that SGCs retain most of their characteristics for about 24 h after culturing, but undergo major phenotypic changes at later times.


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