Allosteric modulation of metabotropic glutamate receptors by chloride ions. Issue 10 (26th June 2015)
- Record Type:
- Journal Article
- Title:
- Allosteric modulation of metabotropic glutamate receptors by chloride ions. Issue 10 (26th June 2015)
- Main Title:
- Allosteric modulation of metabotropic glutamate receptors by chloride ions
- Authors:
- Tora, Amélie S.
Rovira, Xavier
Dione, Ibrahima
Bertrand, Hugues‐Olivier
Brabet, Isabelle
De Koninck, Yves
Doyon, Nicolas
Pin, Jean‐Philippe
Acher, Francine
Goudet, Cyril - Abstract:
- ABSTRACT: Metabotropic glutamate receptors (mGluRs) play key roles in the modulation of many synapses. Chloride (Cl ‐ ) is known to directly bind and regulate the function of different actors of neuronal activity, and several studies have pointed to the possible modulation of mGluRs by Cl ‐ . Herein, we demonstrate that Cl ‐ behaves as a positive allosteric modulator of mGluRs. For example, whereas glutamate potency was 3.08 ± 0.33 μM on metabotropic glutamate (mGlu) 4 receptors in high‐Cl ‐ buffer, signaling activity was almost abolished in low Cl _ in cell‐based assays. Cl ‐ potency was 78.6 ± 3.5 mM. Cl ‐ possesses a high positive cooperativity with glutamate (Hill slope ã6 on mGlu4), meaning that small variations in [Cl ‐ ] lead to large variations in glutamate action. Using molecular modeling and mutagenesis, we have identified 2 well‐conserved Cl ‐ binding pockets in the extracellular domain of mGluRs. Moreover, modeling of activity‐dependent Cl ‐ variations at GABAergic synapses suggests that these variations may be compatible with a dynamic modulation of the most sensitive mGluRs present in these synapses. Taken together, these data reveal a necessary role of Cl ‐ for the glutamate activation of manymGluRs. Exploiting Cl ‐ binding pockets may yield to the development of innovative regulators of mGluR activity.—Tora, A. S., Rovira, X., Dione, I., Bertrand, H.‐O., Brabet, I., De Koninck, Y., Doyon, N., Pin, J.P., Acher, F., Goudet, C. Allosteric modulation ofABSTRACT: Metabotropic glutamate receptors (mGluRs) play key roles in the modulation of many synapses. Chloride (Cl ‐ ) is known to directly bind and regulate the function of different actors of neuronal activity, and several studies have pointed to the possible modulation of mGluRs by Cl ‐ . Herein, we demonstrate that Cl ‐ behaves as a positive allosteric modulator of mGluRs. For example, whereas glutamate potency was 3.08 ± 0.33 μM on metabotropic glutamate (mGlu) 4 receptors in high‐Cl ‐ buffer, signaling activity was almost abolished in low Cl _ in cell‐based assays. Cl ‐ potency was 78.6 ± 3.5 mM. Cl ‐ possesses a high positive cooperativity with glutamate (Hill slope ã6 on mGlu4), meaning that small variations in [Cl ‐ ] lead to large variations in glutamate action. Using molecular modeling and mutagenesis, we have identified 2 well‐conserved Cl ‐ binding pockets in the extracellular domain of mGluRs. Moreover, modeling of activity‐dependent Cl ‐ variations at GABAergic synapses suggests that these variations may be compatible with a dynamic modulation of the most sensitive mGluRs present in these synapses. Taken together, these data reveal a necessary role of Cl ‐ for the glutamate activation of manymGluRs. Exploiting Cl ‐ binding pockets may yield to the development of innovative regulators of mGluR activity.—Tora, A. S., Rovira, X., Dione, I., Bertrand, H.‐O., Brabet, I., De Koninck, Y., Doyon, N., Pin, J.P., Acher, F., Goudet, C. Allosteric modulation of metabotropic glutamate receptors by chloride ions. FASEB J. 29, 4174‐4188 (2015). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 29:Issue 10(2015)
- Journal:
- FASEB journal
- Issue:
- Volume 29:Issue 10(2015)
- Issue Display:
- Volume 29, Issue 10 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 10
- Issue Sort Value:
- 2015-0029-0010-0000
- Page Start:
- 4174
- Page End:
- 4188
- Publication Date:
- 2015-06-26
- Subjects:
- allostery -- GABA -- GPCR -- PAM -- anion
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.14-269746 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13227.xml