Barmack Neal H, Qian Zuyuan, Yakhnitsa Vadim
Department of Physiology and Pharmacology, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA
Department of Physiology and Pharmacology, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA.
Philos Trans R Soc Lond B Biol Sci. 2014 Sep 26;369(1652). doi: 10.1098/rstb.2013.0508.
Synaptic activation of central neurons is often evoked by electrical stimulation leading to post-tetanic potentiation, long-term potentiation or long-term depression. Even a brief electrical tetanus can induce changes in as many as 100 proteins. Since climbing fibre activity is often associated with cerebellar behavioural plasticity, we used horizontal optokinetic stimulation (HOKS) to naturally increase synaptic input to floccular Purkinje cells in mice for hours, not minutes, and investigated how this activity influenced the transcription of microRNAs, small non-coding nucleotides that reduce transcripts of multiple, complementary mRNAs. A single microRNA can reduce the translation of as many as 30 proteins. HOKS evoked increases in 12 microRNA transcripts in floccular Purkinje cells. One of these microRNAs, miR335, increased 18-fold after 24 h of HOKS. After HOKS stopped, miR335 transcripts decayed with a time constant of approximately 2.5 h. HOKS evoked a 28-fold increase in pri-miR335 transcripts compared with an 18-fold increase in mature miR335 transcripts, confirming that climbing fibre-evoked increases in miR335 could be attributed to increases in transcription. We used three screens to identify potential mRNA targets for miR335 transcripts: (i) nucleotide complementarity, (ii) detection of increased mRNAs following microinjection of miR335 inhibitors into the cerebellum, and (iii) detection of decreased mRNAs following HOKS. Two genes, calbindin and 14-3-3-θ, passed these screens. Transfection of N2a cells with miR335 inhibitors or precursors inversely regulated 14-3-3-θ transcripts. Immunoprecipitation of 14-3-3-θ co-immunoprecipitated PKC-γ and GABAAγ2. Knockdown of either 14-3-3-θ or PKC-γ decreased the serine phosphorylation of GABAAγ2, suggesting that 14-3-3-θ and PKC-γ under the control of miR335 homeostatically regulate the phosphorylation and insertion of GABAAγ2 into the Purkinje cell post-synaptic membrane.
中枢神经元的突触激活通常由电刺激诱发,进而导致强直后增强、长时程增强或长时程抑制。即使是短暂的电强直也能诱导多达100种蛋白质发生变化。由于攀缘纤维活动常与小脑行为可塑性相关,我们利用水平视动刺激(HOKS)在数小时而非数分钟内自然增加小鼠绒球浦肯野细胞的突触输入,并研究这种活动如何影响微小RNA(一种能减少多种互补mRNA转录本的小非编码核苷酸)的转录。单个微小RNA能减少多达30种蛋白质的翻译。HOKS使绒球浦肯野细胞中12种微小RNA转录本增加。其中一种微小RNA,即miR335,在HOKS处理24小时后增加了18倍。HOKS停止后,miR335转录本以约2.5小时的时间常数衰减。与成熟miR335转录本增加18倍相比,HOKS使初级miR335转录本增加了28倍,证实攀缘纤维诱发的miR335增加可归因于转录增加。我们通过三个筛选来确定miR335转录本的潜在mRNA靶点:(i)核苷酸互补性,(ii)向小脑微量注射miR335抑制剂后检测mRNA增加情况,以及(iii)HOKS后检测mRNA减少情况。两个基因,即钙结合蛋白和14-3-3-θ,通过了这些筛选。用miR335抑制剂或前体转染N2a细胞可反向调节14-3-·θ转录本。14-3-3-θ的免疫沉淀共沉淀了PKC-γ和GABAAγ2。敲低14-3-3-θ或PKC-γ均可降低GABAAγ2的丝氨酸磷酸化,这表明在miR335的控制下,14-3-3-θ和PKC-γ稳态调节GABAAγ2的磷酸化及其插入浦肯野细胞突触后膜的过程。