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Fyn酪氨酸激酶可提高载脂蛋白E受体2的水平并使其磷酸化。

Fyn tyrosine kinase increases Apolipoprotein E Receptor 2 levels and phosphorylation.

作者信息

Burrell Teal C, Divekar Shailaja D, Weeber Edwin J, Rebeck G William

机构信息

Department of Neuroscience, Georgetown University Medical Center, Washington, District of Columbia, United States of America.

Department of Molecular Pharmacology and Physiology, University of South Florida Health Byrd Alzheimer's Institute, University of South Florida, Tampa, Florida, United States of America.

出版信息

PLoS One. 2014 Oct 23;9(10):e110845. doi: 10.1371/journal.pone.0110845. eCollection 2014.

Abstract

Apolipoprotein E Receptor 2 (ApoER2) and the tyrosine kinase Fyn are both members of the Reelin pathway, a signaling pathway essential for the laminar formation of the cortex during development and proper dendritic spine density and long-term potential (LTP) in the adult brain. In the presence of extracellular Reelin, ApoER2 binds the intracellular protein Dab1, an adaptor protein that is phosphorylated by Fyn. However, direct interactions between ApoER2 and Fyn are not well defined. Here, we show that total levels of ApoER2 and surface levels of ApoER2 are increased by active Fyn. Via a separate mechanism, ApoER2 is also phosphorylated by Fyn, an event that peaks in the postnatal cortex at day 5 and can occur at multiple ApoER2 tyrosine residues. Dab1 is also involved in this phosphorylation, promoting the phosphorylation of ApoER2 by Fyn when it is itself phosphorylated. These results elucidate some of the intracellular mechanisms that give rise to a functional Reelin pathway.

摘要

载脂蛋白E受体2(ApoER2)和酪氨酸激酶Fyn都是Reelin信号通路的成员,该信号通路对于发育过程中皮质的分层形成以及成人大脑中适当的树突棘密度和长时程增强(LTP)至关重要。在细胞外Reelin存在的情况下,ApoER2与细胞内蛋白Dab1结合,Dab1是一种由Fyn磷酸化的衔接蛋白。然而,ApoER2与Fyn之间的直接相互作用尚未明确界定。在这里,我们表明活性Fyn会增加ApoER2的总水平和表面水平。通过一种独立的机制,ApoER2也会被Fyn磷酸化,这一事件在出生后第5天的皮质中达到峰值,并且可以发生在多个ApoER2酪氨酸残基上。Dab1也参与了这种磷酸化过程,当其自身被磷酸化时,会促进Fyn对ApoER2的磷酸化。这些结果阐明了一些产生功能性Reelin信号通路的细胞内机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc6a/4207760/3b05f123f0ac/pone.0110845.g001.jpg

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