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Isoform-specific expression of the Coxsackie and adenovirus receptor (CAR) in neuromuscular junction and cardiac intercalated discs

机译:柯萨奇和腺病毒受体(CAR)在神经肌肉接头和心脏插层盘中的同工型特异性表达

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摘要

BACKGROUND:The Coxsackie and adenovirus receptor (CAR) has a restricted expression pattern in the adult. In skeletal muscle, although CAR is expressed in immature fibers, its transcript levels are barely detectable in mature muscle. This is in contrast to the robust expression observed in the heart. However, both heart and skeletal muscle are susceptible to infection with the Coxsackie B virus which utilizes primarily CAR for cellular internalization. The specific point of viral entry in skeletal and heart muscle remains unknown.RESULTS:Using antibodies directed against the extracellular and the cytoplasmic domains of CAR, we show CAR in normal human and mouse skeletal muscle to be a novel component of the neuromuscular junction. In cardiac muscle, CAR immunoreactivity is observed at the level of intercalated discs. We demonstrate a single isoform of CAR to be expressed exclusively at the human neuromuscular junction whereas both predominant CAR isoforms are expressed at the intercalated discs of non-diseased human heart.CONCLUSION:The localization of CAR to these important junctional complexes suggests that CAR may play both a structural and a regulatory role in skeletal and cardiac muscle, and that these complexes may serve as a point of entry for Coxsackie B virus.
机译:背景:柯萨奇和腺病毒受体(CAR)在成人中的表达方式受到限制。在骨骼肌中,尽管CAR在未成熟的纤维中表达,但在成熟肌肉中几乎检测不到其转录水平。这与在心脏中观察到的强健表达相反。但是,心脏和骨骼肌都容易感染柯萨奇B病毒,该病毒主要利用CAR进行细胞内在化。结果:使用针对CAR的胞外和胞质结构域的抗体,我们可以证明正常人和小鼠骨骼肌中的CAR是神经肌肉接头的新组成部分。在心肌中,在插入椎间盘的水平观察到CAR免疫反应性。我们证明了CAR的单一同工型仅在人的神经肌肉连接处表达,而两种主要的CAR同工型均在未患病的人心脏的插层上表达。结论:CAR在这些重要的连接复合物上的定位表明CAR可能发挥作用在骨骼肌和心肌中都具有结构和调节作用,并且这些复合物可以作为柯萨奇B病毒的切入点。

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