Han K A, Jeon S, Um J W, Ko J
Department of Physiology and BK21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, South Korea.
Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Int Rev Cell Mol Biol. 2016;324:39-65. doi: 10.1016/bs.ircmb.2016.01.002. Epub 2016 Feb 8.
Leukocyte common antigen-related receptor tyrosine phosphatases (LAR-RPTPs) have emerged as key players that organize various aspects of neuronal development, including axon guidance, neurite extension, and synapse formation and function. Recent research has highlighted the roles of LAR-RPTPs at neuronal synapses in mediating distinct synaptic adhesion pathways through interactions with a host of extracellular ligands and in governing a variety of intracellular signaling cascades through binding to various scaffolds and signaling proteins. In this chapter, we review and update current research progress on the extracellular ligands of LAR-RPTPs, regulation of their extracellular interactions by alternative splicing and heparan sulfates, and their intracellular signaling machineries. In particular, we review structural insights on complexes of LAR-RPTPs with their various ligands. These studies lend support to general molecular mechanisms underlying LAR-RPTP-mediated synaptic adhesion and signaling pathways.
白细胞共同抗原相关受体酪氨酸磷酸酶(LAR - RPTPs)已成为神经元发育各个方面的关键参与者,包括轴突导向、神经突延伸以及突触形成和功能。最近的研究突出了LAR - RPTPs在神经元突触中的作用,它们通过与多种细胞外配体相互作用介导不同的突触粘附途径,并通过与各种支架和信号蛋白结合来调控多种细胞内信号级联反应。在本章中,我们回顾并更新了关于LAR - RPTPs细胞外配体、可变剪接和硫酸乙酰肝素对其细胞外相互作用的调节以及它们的细胞内信号传导机制的当前研究进展。特别是,我们回顾了LAR - RPTPs与其各种配体复合物的结构见解。这些研究为LAR - RPTP介导的突触粘附和信号通路的一般分子机制提供了支持。