Chow Jeremy Pak Hong, Fujikawa Akihiro, Shimizu Hidetada, Noda Masaharu
Division of Molecular Neurobiology, National Institute for Basic Biology, 5-1 Higashiyama, Myodaiji-cho, Okazaki, Aichi 444-8787, Japan.
Neurosci Lett. 2008 Sep 19;442(3):208-12. doi: 10.1016/j.neulet.2008.07.028. Epub 2008 Jul 16.
Protein tyrosine phosphatase receptor type Z (Ptprz, also known as PTPzeta or RPTPbeta) is preferentially expressed in the CNS as a major chondroitin sulfate proteoglycan (CSPG). Ptprz interacts with the PSD95 family through its intracellular carboxyl-terminal PDZ-binding motif in the postsynaptic density. Ptprz-deficient adult mice display impairments in spatial and contextual learning. Here, we identified the proteolytic processing of Ptprz by plasmin in the mouse brain, which is markedly enhanced after kainic acid (KA)-induced seizures. We mapped plasmin cleavage sites in the extracellular region of Ptprz by cell-based assays and in vitro digestion experiments with recombinant proteins. These findings indicate that Ptprz is a physiological target for activity-dependent proteolytic processing by the tPA/plasmin system, and suggest that the proteolytic cleavage is involved in the functional processes of the synapses during learning and memory.
蛋白酪氨酸磷酸酶Z型受体(Ptprz,也称为PTPzeta或RPTPbeta)作为一种主要的硫酸软骨素蛋白聚糖(CSPG),在中枢神经系统中优先表达。Ptprz通过其位于突触后致密区的细胞内羧基末端PDZ结合基序与PSD95家族相互作用。Ptprz基因缺失的成年小鼠在空间和情境学习方面存在障碍。在此,我们确定了小鼠脑中纤溶酶对Ptprz的蛋白水解加工,在 kainic acid(KA)诱导的癫痫发作后,这种加工显著增强。我们通过基于细胞的实验和重组蛋白的体外消化实验,绘制了Ptprz细胞外区域的纤溶酶切割位点。这些发现表明,Ptprz是tPA/纤溶酶系统进行活性依赖性蛋白水解加工的生理靶点,并提示蛋白水解切割参与了学习和记忆过程中突触的功能过程。