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代谢型谷氨酸受体和γ-氨基丁酸受体在新皮质谷氨酸能和γ-氨基丁酸能轴突终末的差异表达。

Differential expression of metabotropic glutamate and GABA receptors at neocortical glutamatergic and GABAergic axon terminals.

作者信息

Bragina Luca, Bonifacino Tiziana, Bassi Silvia, Milanese Marco, Bonanno Giambattista, Conti Fiorenzo

机构信息

Section of Neuroscience and Cell Biology, Department of Experimental and Clinical Medicine, Università Politecnica delle Marche Ancona, Italy ; Center for Neurobiology of Aging, Istituto Nazionale di Riposo e Cura per Anziani - Istituto di Ricovero e Cura a Carattere Scientifico Ancona, Italy.

Department of Pharmacy, Unit of Pharmacology and Toxicology, University of Genoa Genoa, Italy.

出版信息

Front Cell Neurosci. 2015 Sep 4;9:345. doi: 10.3389/fncel.2015.00345. eCollection 2015.

Abstract

Metabotropic glutamate (Glu) receptors (mGluRs) and GABAB receptors are highly expressed at presynaptic sites. To verify the possibility that the two classes of metabotropic receptors contribute to axon terminals heterogeneity, we studied the localization of mGluR1α, mGluR5, mGluR2/3, mGluR7, and GABAB1 in VGLUT1-, VGLUT2-, and VGAT- positive terminals in the cerebral cortex of adult rats. VGLUT1-positive puncta expressed mGluR1α (∼5%), mGluR5 (∼6%), mGluR2/3 (∼22%), mGluR7 (∼17%), and GABAB1 (∼40%); VGLUT2-positive terminals expressed mGluR1α (∼10%), mGluR5 (∼11%), mGluR2/3 (∼20%), mGluR7 (∼28%), and GABAB1 (∼25%); whereas VGAT-positive puncta expressed mGluR1α (∼27%), mGluR5 (∼24%), mGluR2/3 (∼38%), mGluR7 (∼31%), and GABAB1 (∼19%). Control experiments ruled out the possibility that postsynaptic mGluRs and GABAB1 might have significantly biased our results. We also performed functional assays in synaptosomal preparations, and showed that all agonists modify Glu and GABA levels, which return to baseline upon exposure to antagonists. Overall, these findings indicate that mGluR1α, mGluR5, mGluR2/3, mGluR7, and GABAB1 expression differ significantly between glutamatergic and GABAergic axon terminals, and that the robust expression of heteroreceptors may contribute to the homeostatic regulation of the balance between excitation and inhibition.

摘要

代谢型谷氨酸(Glu)受体(mGluRs)和GABAB受体在突触前位点高度表达。为了验证这两类代谢型受体是否导致轴突终末的异质性,我们研究了成年大鼠大脑皮层中VGLUT1、VGLUT2和VGAT阳性终末中mGluR1α、mGluR5、mGluR2/3、mGluR7和GABAB1的定位。VGLUT1阳性小点表达mGluR1α(约5%)、mGluR5(约6%)、mGluR2/3(约22%)、mGluR7(约17%)和GABAB1(约40%);VGLUT2阳性终末表达mGluR1α(约10%)、mGluR5(约11%)、mGluR2/3(约20%)、mGluR7(约28%)和GABAB1(约25%);而VGAT阳性小点表达mGluR1α(约27%)、mGluR5(约24%)、mGluR2/3(约38%)、mGluR7(约31%)和GABAB1(约19%)。对照实验排除了突触后mGluRs和GABAB1可能显著影响我们结果的可能性。我们还在突触体制备物中进行了功能测定,并表明所有激动剂都会改变Glu和GABA水平,在暴露于拮抗剂后这些水平会恢复到基线。总体而言,这些发现表明mGluR1α、mGluR5、mGluR2/3、mGluR7和GABAB1在谷氨酸能和GABA能轴突终末之间的表达存在显著差异,并且异受体的强烈表达可能有助于对兴奋与抑制之间平衡的稳态调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/417d/4559644/62dad37dc23e/fncel-09-00345-g001.jpg

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