Inamura Mihoko, Itakura Makoto, Okamoto Hirotsugu, Hoka Sumio, Mizoguchi Akira, Fukazawa Yugo, Shigemoto Ryuichi, Yamamori Saori, Takahashi Masami
Department of Anesthesiology, Kitasato University School of Medicine, Sagamihara, Kanagawa 228-8555, Japan.
Neurosci Res. 2006 May;55(1):45-53. doi: 10.1016/j.neures.2006.01.004. Epub 2006 Mar 3.
Transmembrane AMPA receptor regulatory proteins (TARPs), including stargazin/gamma-2, are associated with AMPA receptors and participate in their surface delivery and anchoring at the postsynaptic membrane. TARPs may also act as a positive modulator of the AMPA receptor ion channel function; however, little is known about other TARP members except for stargazin/gamma-2. We examined the synaptic localization of stargazin/gamma-2 and gamma-8 by immunoelectron microscopy and biochemical analysis. The analysis of sodium dodecyl sulfate-digested freeze-fracture replica labeling revealed that stargazin/gamma-2 was concentrated in the postsynaptic area, whereas gamma-8 was distributed both in synaptic and extra-synaptic plasma membranes of the hippocampal neuron. When a synaptic plasma membrane-enriched brain fraction was treated with Triton X-100 and separated by sucrose density gradient ultracentrifugation, a large proportion of NMDA receptor and stargazin/gamma-2 was accumulated in raft-enriched fractions, whereas AMPA receptor and gamma-8 were distributed in both the raft-enriched fractions and other Triton-insoluble fractions. Phosphorylation of stargazin/gamma-2 and gamma-8 was regulated by different sets of kinases and phosphatases in cultured cortical neurons. These results suggested that stargazin/gamma-2 and gamma-8 have distinct roles in postsynaptic membranes under the regulation of different intracellular signaling pathways.
跨膜AMPA受体调节蛋白(TARPs),包括stargazin/γ-2,与AMPA受体相关,并参与其在突触后膜的表面转运和锚定。TARPs也可能作为AMPA受体离子通道功能的正向调节剂;然而,除了stargazin/γ-2之外,对其他TARP成员知之甚少。我们通过免疫电子显微镜和生化分析研究了stargazin/γ-2和γ-8的突触定位。十二烷基硫酸钠消化的冷冻断裂复制品标记分析表明,stargazin/γ-2集中在突触后区域,而γ-8分布在海马神经元的突触和突触外质膜中。当用Triton X-100处理富含突触质膜的脑部分并用蔗糖密度梯度超速离心分离时,大部分NMDA受体和stargazin/γ-2积累在富含筏的部分中,而AMPA受体和γ-8分布在富含筏的部分和其他Triton不溶性部分中。在培养的皮质神经元中,stargazin/γ-2和γ-8的磷酸化受不同组的激酶和磷酸酶调节。这些结果表明,在不同的细胞内信号通路调节下,stargazin/γ-2和γ-8在突触后膜中具有不同的作用。