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蛋白激酶A对RIM1α的磷酸化作用可触发小脑平行纤维突触的突触前长时程增强。

Phosphorylation of RIM1alpha by PKA triggers presynaptic long-term potentiation at cerebellar parallel fiber synapses.

作者信息

Lonart György, Schoch Susanne, Kaeser Pascal S, Larkin C Jenny, Südhof Thomas C, Linden David J

机构信息

Center for Basic Neuroscience, Department of Molecular Genetics and Howard Hughes Medical Institute, UT Southwestern Medical Center, 6000 Harry Hines Boulevard, Dallas, TX 75390, USA.

出版信息

Cell. 2003 Oct 3;115(1):49-60. doi: 10.1016/s0092-8674(03)00727-x.

Abstract

Presynaptic activation of protein kinase A (PKA) induces LTP in cerebellar parallel fiber synapses. Presynaptic LTP is known to require the active zone protein RIM1alpha, but the underlying induction mechanism remains unclear. We now show that PKA directly phosphorylates RIM1alpha at two sites. Using paired recordings from cultured cerebellar granule and Purkinje neurons, we demonstrate that LTP is absent in neurons from RIM1alpha KO mice but is rescued by presynaptic expression of RIM1alpha. Mutant RIM1alpha lacking the N-terminal phosphorylation site is unable to rescue LTP in RIM1alpha knockout neurons but selectively suppresses LTP in wild-type neurons. Our findings suggest that PKA-mediated phosphorylation of the active zone protein RIM1alpha at a single N-terminal site induces presynaptic LTP.

摘要

蛋白激酶A(PKA)的突触前激活可诱导小脑平行纤维突触产生长时程增强(LTP)。已知突触前LTP需要活性区蛋白RIM1α,但潜在的诱导机制仍不清楚。我们现在发现,PKA可直接在两个位点磷酸化RIM1α。利用培养的小脑颗粒神经元和浦肯野神经元的配对记录,我们证明RIM1α基因敲除(KO)小鼠的神经元中不存在LTP,但通过突触前表达RIM1α可使其恢复。缺乏N端磷酸化位点的突变型RIM1α无法挽救RIM1α基因敲除神经元中的LTP,但能选择性抑制野生型神经元中的LTP。我们的研究结果表明,PKA介导的活性区蛋白RIM1α在单个N端位点的磷酸化可诱导突触前LTP。

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