Neurosteroid binding to the amino terminal and glutamate binding domains of ionotropic glutamate receptors

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• 作者：Krasnodara Cameron^a ; Emily Bartle^a ; Ryan Roark^a ; David Fanelli^a ; Melissa Pham^a ; Beth Pollard^a ; Brian Borkowski^a ; Sarah Rhoads^a ; Joon Kim^a ; Monica Rocha^a ; Martha Kahlson^a ; Melinda Kangala^b ; Lisa Gentile^a ; ^{lgentile@richmond.edu}
• 关键词：iGluR ; Amino terminal domain ; Pregnenolone sulfate ; Pregnanolone sulfate
• 刊名：Steroids
• 出版年：2012
• 出版时间：June, 2012
• 年：2012
• 卷：77
• 期：7
• 页码：774-779
• 全文大小：445 K

文摘

The endogenous neurosteroids, pregnenolone sulfate (PS) and 3¦Á-hydroxy-5¦Â-pregnan-20-one sulfate (PREGAS), have been shown to differentially regulate the ionotropic glutamate receptor (iGluR) family of ligand-gated ion channels. Upon binding to these receptors, PREGAS decreases current flow through the channels. Upon binding to non-NMDA or NMDA receptors containing an GluN2C or GluN2D subunit, PS also decreases current flow through the channels, however, upon binding to NMDA receptors containing an GluN2A or GluN2B subunit, flow through the channels increases. To begin to understand this differential regulation, we have cloned the S1S2 and amino terminal domains (ATD) of the NMDA GluN2B and GluN2D and AMPA GluA2 subunits. Here we present results that show that PS and PREGAS bind to different sites in the ATD of the GluA2 subunit, which when combined with previous results from our lab, now identifies two binding domains for each neurosteroid. We also show both neurosteroids bind only to the ATD of the GluN2D subunit, suggesting that this binding is distinct from that of the AMPA GluA2 subunit, with both leading to iGluR inhibition. Finally, we provide evidence that both PS and PREGAS bind to the S1S2 domain of the NMDA GluN2B subunit. Neurosteroid binding to the S1S2 domain of NMDA subunits responsible for potentiation of iGluRs and to the ATD of NMDA subunits responsible for inhibition of iGluRs, provides an interesting option for therapeutic design.