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使用位点特异性抗体鉴定和表征抗抑郁药敏感的血清素转运蛋白

Identification and characterization of antidepressant-sensitive serotonin transporter proteins using site-specific antibodies.

作者信息

Qian Y, Melikian H E, Rye D B, Levey A I, Blakely R D

机构信息

Graduate Program in Neuroscience, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

J Neurosci. 1995 Feb;15(2):1261-74. doi: 10.1523/JNEUROSCI.15-02-01261.1995.

Abstract

Serotonin (5HT) transporters (SERTs) are responsible for clearance of synaptic and plasma 5HT and are molecular targets for multiple therapeutic and addictive compounds. Recently brain and peripheral SERT cDNAs have been cloned and characterized functionally in transfected cells. Antipeptide (S365) and anti-fusion protein (CT-2) antibodies, directed at epitopes poorly conserved among other Na+/Cl- cotransporters, have been prepared to facilitate the identification and characterization of SERT proteins in native and transfected cells. Immunoprecipitations and immunoblots of rat/human SERT-transfected HeLa cells reveal specific SERT-immunoreactive glycoproteins absent from extracts of vector-transfected cells and absent when incubations were conducted using peptide- or fusion protein-absorbed antibody. In SDS-PAGE of membranes prepared from rat midbrain and cortex, SERTs migrate as single 76 kDa polypeptides with a relative abundance consistent with the known distribution of 5HT neurons and axonal projections. SERT-immunoreactive proteins are also detectable in platelet and pulmonary membranes, sites of peripheral 5HT uptake, but not in liver. Our studies also indicate that brain and platelet SERTs are formed from identical polypeptides differing significantly in their extent of N-linked glycosylation. Immunocytochemistry performed on rat brain sections with CT-2 antibody revealed SERT expression associated with brainstem raphe nuclei in a pattern virtually identical to that obtained by labeling adjacent sections with 5HT antisera. SERT-immunoreactive fibers were found to be widely distributed throughout the rodent brain, with highest density in forebrain regions known to receive a dense serotonergic innervation. In a similar manner, CT-2 antibody also detects endogenous expression of human SERT proteins, providing an opportunity for future studies on the modulation of transporter protein expression in neurologic and psychiatric disorders.

摘要

血清素(5HT)转运体(SERTs)负责清除突触和血浆中的5HT,是多种治疗性和成瘾性化合物的分子靶点。最近,脑和外周SERT的cDNA已被克隆并在转染细胞中进行了功能表征。针对其他Na+/Cl-共转运体中保守性较差的表位制备了抗肽(S365)和抗融合蛋白(CT-2)抗体,以促进在天然细胞和转染细胞中鉴定和表征SERT蛋白。对大鼠/人SERT转染的HeLa细胞进行免疫沉淀和免疫印迹分析,结果显示载体转染细胞提取物中不存在特异性的SERT免疫反应性糖蛋白,并且当使用肽或融合蛋白吸附抗体进行孵育时也不存在。在大鼠中脑和皮质制备的膜的SDS-PAGE分析中,SERTs以单一的76 kDa多肽形式迁移,其相对丰度与5HT神经元和轴突投射的已知分布一致。在血小板和肺膜(外周5HT摄取部位)中也可检测到SERT免疫反应性蛋白,但在肝脏中未检测到。我们的研究还表明,脑和血小板SERTs由相同的多肽形成,它们在N-连接糖基化程度上有显著差异。用CT-2抗体对大鼠脑切片进行免疫细胞化学分析,结果显示SERT表达与脑干中缝核相关,其模式与用5HT抗血清标记相邻切片所获得的模式几乎相同。发现SERT免疫反应性纤维广泛分布于整个啮齿动物脑内,在前脑已知接受密集5-羟色胺能神经支配的区域密度最高。以类似的方式,CT-2抗体也能检测到人SERT蛋白的内源性表达,为未来研究神经和精神疾病中转运蛋白表达的调节提供了机会。

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