Co-labeling of Neuronal Cells Using DiI Neuronal Filling and Immunohistochemistry to Explore Metabotropic Glutamate Receptor Expression

Author(s):  
Jonna M. Leyrer-Jackson ◽  
Sade Spencer ◽  
Cassandra D. Gipson
2015 ◽  
Vol 93 (6) ◽  
pp. 964-972 ◽  
Author(s):  
Maria Ll. Valero ◽  
Elena Caminos ◽  
Jose M. Juiz ◽  
Juan R. Martinez-Galan

2017 ◽  
Author(s):  
David Moreno Delgado ◽  
Thor C Møller ◽  
Jeanne Ster ◽  
Jesús Giraldo ◽  
Damien Maurel ◽  
...  

2012 ◽  
Vol 204 (2) ◽  
pp. 221-226 ◽  
Author(s):  
Ramses Ayala ◽  
Lauren R. Kett ◽  
Tiffany L. Leach ◽  
Anne B. Young ◽  
Anthone W. Dunah ◽  
...  

2005 ◽  
Vol 10 (8) ◽  
pp. 841-848 ◽  
Author(s):  
Patrick. M. Downey ◽  
Gianluca Lozza ◽  
Roberta Petrò ◽  
Enrica Diodato ◽  
Chiara Foglia ◽  
...  

Stable and inducible expression of human metabotropic glutamate receptor types 2, 5, and 8 was achieved in HEK293 cells using the ecdysone inducible system. Treatment of the respective cell lines with ponasterone A resulted in time and concentration-dependent induction of receptor expression. In all cases, the functional activation of receptorswas determined bymeasuring increases in intracellular calcium. The physiologically G• i-coupled receptors mGluR2 andm GluR8 were successfully coupled to phospholipase Cactivation using the chimeric Gprotein G• q/o. The pharmacological properties of recombinant receptors were characterized and proved to be similar to native receptors. Our data suggest that the ecdysone system has a number of characteristics thatmake itwell suited for expressing mGluRs and that the combined use of this systemand chimeric G proteins allows receptors to be characterized using a rapid and straightforward Ca 2+assay.


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