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Characterization of an A-Kinase Anchoring Protein in Human Ciliary Axonemes

机译:人睫状轴突中A激酶锚定蛋白的表征

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摘要

Although protein kinase A (PKA) activation is known to increase ciliary beat frequency in humans the molecular mechanisms involved are unknown. We demonstrate that PKA is associated with ciliary axonemes where it specifically phosphorylates a 23-kDa protein. Because PKA is often localized to subcellular compartments in proximity to its substrate(s) via interactions with A-kinase–anchoring proteins (AKAPs), we investigated whether an AKAP was also associated with ciliary axonemes. This study has identified a novel 28 kDa AKAP (AKAP28)that is highly enriched in airway axonemes. The mRNA for AKAP28 is up-regulated as primary airway cells differentiate and is specifically expressed in tissues containing cilia and/or flagella. Additionally, both Western blot and immunostaining data show that AKAP28 is enriched in airway cilia. These data demonstrate that we have identified the first human axonemal AKAP, a protein that likely plays a role in the signaling necessary for efficient modulation of ciliary beat frequency.
机译:尽管已知蛋白激酶A(PKA)激活会增加人的纤毛搏动频率,但所涉及的分子机制尚不清楚。我们证明,PKA与纤毛轴突联系在一起,在那里它特异性磷酸化23 kDa蛋白。由于PKA通常通过与A激酶锚定蛋白(AKAP)的相互作用而定位于其底物附近的亚细胞区室,因此我们调查了AKAP是否也与睫状轴突相关。这项研究确定了一种新型的28 kDa AKAP(AKAP28),它在气道轴突中含量很高。随着原代气道细胞的分化,AKAP28的mRNA上调,并在含有纤毛和/或鞭毛的组织中特异性表达。此外,蛋白质印迹和免疫染色数据均表明AKAP28富含气道纤毛。这些数据表明,我们已经鉴定出第一个人类轴突AKAP,这种蛋白质可能在有效调节睫状心跳频率所需的信号传导中起作用。

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