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光触发发育中大鼠视网膜中对 philanthotoxin 不敏感的 Ca2+ 通透型 AMPA 受体的表达。

Light triggers expression of philanthotoxin-insensitive Ca2+-permeable AMPA receptors in the developing rat retina.

作者信息

Osswald Ingrid K, Galan Alba, Bowie Derek

机构信息

Department of Pharmacology & Therapeutics, McIntyre Medical Sciences Building, Room 1317, McGill University, Montreal, Québec, Canada H3A 1Y6.

出版信息

J Physiol. 2007 Jul 1;582(Pt 1):95-111. doi: 10.1113/jphysiol.2007.127894. Epub 2007 Apr 12.

Abstract

Ca2+-permeable AMPA receptors (AMPARs) are expressed throughout the adult CNS but yet their role in development is poorly understood. In the developing retina, most investigations have focused on Ca2+ influx through NMDARs in promoting synapse maturation and not on AMPARs. However, NMDARs are absent from many retinal cells suggesting that other Ca2+-permeable glutamate receptors may be important to consider. Here we show that inhibitory horizontal and AII amacrine cells lack NMDARs but express Ca2+-permeable AMPARs. Before eye-opening, AMPARs were fully blocked by philanthotoxin (PhTX), a selective antagonist of Ca2+-permeable AMPARs. After eye-opening, however, a subpopulation of Ca2+-permeable AMPARs were unexpectedly PhTX resistant. Furthermore, Joro spider toxin (JSTX) and IEM-1460 also failed to antagonize, demonstrating that this novel pharmacology is shared by several AMPAR channel blockers. Interestingly, PhTX-insensitive AMPARs failed to express in retinae from dark-reared animals demonstrating that light entering the eye triggers their expression. Eye-opening coincides with the consolidation of inhibitory cell connections suggesting that the developmental switch to a Ca2+-permeable AMPAR with novel pharmacology may be critical to synapse maturation in the mammalian retina.

摘要

Ca2+通透型AMPA受体(AMPARs)在整个成年中枢神经系统中均有表达,但其在发育过程中的作用却鲜为人知。在发育中的视网膜中,大多数研究都集中在通过NMDARs的Ca2+内流对促进突触成熟的作用上,而不是AMPARs。然而,许多视网膜细胞中不存在NMDARs,这表明其他Ca2+通透型谷氨酸受体可能也值得关注。在此我们表明,抑制性水平细胞和AII无长突细胞缺乏NMDARs,但表达Ca2+通透型AMPARs。在睁眼之前,AMPARs被 philanthotoxin(PhTX)完全阻断,PhTX是Ca2+通透型AMPARs的选择性拮抗剂。然而,在睁眼之后,一个Ca2+通透型AMPARs亚群出人意料地对PhTX具有抗性。此外,Joro蜘蛛毒素(JSTX)和IEM-1460也无法拮抗,这表明这种新的药理学特性为几种AMPAR通道阻滞剂所共有。有趣的是,对PhTX不敏感的AMPARs在黑暗饲养动物的视网膜中未能表达,这表明进入眼睛的光线会触发它们的表达。睁眼与抑制性细胞连接的巩固同时发生,这表明向具有新药理学特性的Ca2+通透型AMPAR的发育转变可能对哺乳动物视网膜中的突触成熟至关重要。

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