Roles of type IIa receptor protein tyrosine phosphatases as synaptic organizers

被引:12
作者
Fukai, Shuya [1 ]
Yoshida, Tomoyuki [2 ]
机构
[1] Kyoto Univ, Grad Sch Sci, Dept Chem, Kyoto 6068502, Japan
[2] Univ Toyama, Dept Mol Neurosci, Grad Sch Med & Pharmaceut Sci, Toyama 9300194, Japan
关键词
cell adhesion; neuron; receptor protein tyrosine phosphatase; synapse; synaptic organizer; LIPRIN-ALPHA; PTP-SIGMA; MENTAL-RETARDATION; STRUCTURAL BASIS; IL1RAPL1; GENE; MICE LACKING; NEUROTRANSMITTER RELEASE; FAMILY PROTEINS; AXON GUIDANCE; ACTIVE ZONE;
D O I
10.1111/febs.15666
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurons establish circuits for brain functions such as cognition, emotion, learning, and memory. Their connections are mediated by synapses, which are specialized cell-cell adhesions responsible for neuronal signal transmission. During neurodevelopment, synapse formation is triggered by interactions of cell adhesion molecules termed synaptic organizers or synapse organizers. Type IIa receptor protein tyrosine phosphatases (IIa RPTPs; also known as leukocyte common antigen-related receptor tyrosine phosphatases or LAR-RPTPs) play important roles in axon guidance and neurite extension, and also serve as presynaptic organizers. IIa RPTPs transsynaptically interact with multiple sets of postsynaptic organizers, mostly in a splicing-dependent fashion. Here, we review and update research progress on IIa RPTPs, particularly regarding their functional roles in vivo demonstrated using conditional knockout approach and structural insights into their extracellular and intracellular molecular interactions revealed by crystallography and other biophysical techniques. Future directions in the research field of IIa RPTPs are also discussed, including recent findings of the molecular assembly mechanism underlying the formation of synapse-specific nanostructures essential for synaptic functions.
引用
收藏
页码:6913 / 6926
页数:14
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