Gras Christelle, Vinatier Jacqueline, Amilhon Bénédicte, Guerci Aline, Christov Christo, Ravassard Philippe, Giros Bruno, El Mestikawy Salah
INSERM, U 513, Faculté de Médecine, Neurobiologie et Psychiatrie, 8 rue du Général Sarrail, 94010 Créteil Cedex, France.
Neuropharmacology. 2005 Nov;49(6):901-11. doi: 10.1016/j.neuropharm.2005.07.023. Epub 2005 Sep 21.
Three subtypes of vesicular glutamate transporters, named VGLUT1-3, accumulate glutamate into synaptic vesicles. In this study, the post-natal expression of VGLUT3 was determined with specific probes and antiserums in the rat brain and compared with that of VGLUT1 and VGLUT2. The expression of VGLUT1 and VGLUT2 increases linearly during post-natal development. In contrast, VGLUT3 developmental pattern appears to have a more or less biphasic profile. A first peak of expression is centered around post-natal day 10 (P10) while the second one is reached in the adult brain. Between P1 and P15, VGLUT3 is observed in the frontal brain (striatum, accumbens, and hippocampus) and in the caudal brain (colliculi, pons and cerebellum). During a second phase extending from P15 to adulthood, the labeling of the caudal brain fades away. The adult pattern is reached at P21. We further analyzed the transient expression of VGLUT3 in the cerebellum and found it to correspond to a temporary expression in Purkinje cells. At P10 VGLUT3 immunoreactivity was present both in the soma and terminals of Purkinje cells (PC), where it colocalized with the vesicular inhibitory amino acid transporter (VIAAT). In agreement with data from the literature [Gillespie, D.C., Kim, G., Kandler, K., 2005. Inhibitory synapses in the developing auditory system are glutamatergic. Nat. Neurosci. 8, 332-338], our results suggest that during the first 2 weeks of post-natal life PC may have the potential to transiently release simultaneously GABA and glutamate.
囊泡谷氨酸转运体有三种亚型,分别命名为VGLUT1 - 3,它们将谷氨酸积累到突触小泡中。在本研究中,用特异性探针和抗血清测定了大鼠脑中VGLUT3的出生后表达,并与VGLUT1和VGLUT2进行了比较。VGLUT1和VGLUT2的表达在出生后发育过程中呈线性增加。相比之下,VGLUT3的发育模式似乎或多或少呈双相分布。第一个表达峰值集中在出生后第10天(P10)左右,而第二个峰值出现在成年大脑中。在P1到P15之间,在额叶脑区(纹状体、伏隔核和海马体)以及尾脑区(丘、脑桥和小脑)观察到VGLUT3。在从P15到成年的第二阶段,尾脑区的标记逐渐消失。在P21时达到成年模式。我们进一步分析了VGLUT3在小脑中的瞬时表达,发现它对应于浦肯野细胞中的临时表达。在P10时,VGLUT3免疫反应性存在于浦肯野细胞(PC)的胞体和终末,在那里它与囊泡抑制性氨基酸转运体(VIAAT)共定位。与文献数据一致[Gillespie, D.C., Kim, G., Kandler, K., 2005. 发育中的听觉系统中的抑制性突触是谷氨酸能的。《自然神经科学》8, 332 - 338],我们的结果表明,在出生后生命的前2周,浦肯野细胞可能有同时瞬时释放GABA和谷氨酸的潜力。