髓鞘碱性蛋白mRNA在少突胶质细胞中的易位需要微管和运动蛋白。

J H Carson, K Worboys, K Ainger, E Barbarese
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引用次数: 126

摘要

髓鞘碱性蛋白(MBP) mRNA定位于少突胶质细胞的髓鞘膜。当外源性MBP mRNA微注射到培养的少突胶质细胞中时,它沿着过程运输并通过多步骤的细胞内RNA运输途径定位到髓鞘室。在这里描述的工作中,用影响细胞骨架的药物治疗少突胶质细胞,包括:诺可达唑,破坏微管;紫杉醇,稳定微管;细胞松弛素,破坏微丝;和激酶反义寡核苷酸,抑制激酶表达。将地高辛标记的MBP mRNA微注射到处理过的细胞中,用共聚焦显微镜检测微注射RNA的易位程度。诺可达唑、紫杉醇和激酶反义寡核苷酸抑制微注射MBP mRNA的易位,而细胞松弛素B和激酶寡核苷酸没有抑制作用。这些结果表明,MBP mRNA在少突胶质细胞中的易位需要完整的微管和激酶,而不需要完整的微丝。结果讨论了目前的多步骤模型的细胞内RNA运输在少突胶质细胞。
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Translocation of myelin basic protein mRNA in oligodendrocytes requires microtubules and kinesin.

Myelin basic protein (MBP) mRNA is localized to the myelin membranes of oligodendrocytes. When exogenous MBP mRNA is microinjected into oligodendrocytes in culture, it is transported along the processes and localized to the myelin compartment in a multistep intracellular RNA trafficking pathway. In the work described here, oligodendrocytes were treated with agents that affect the cytoskeleton including: nocodazole, to disrupt microtubules; taxol, to stabilize microtubules; cytochalasin, to disrupt microfilaments; and kinesin anti-sense oligonucleotide, to suppress kinesin expression. Digoxigenin-labeled MBP mRNA was microinjected into the treated cells and the extent of translocation of the microinjected RNA was determined by confocal microscopy. Nocodazole, taxol, and kinesin anti-sense oligonucleotide inhibited translocation of microinjected MBP mRNA, while cytochalasin B and kinesin sense oligonucleotide did not. These results indicate that translocation of MBP mRNA in oligodendrocytes requires intact microtubules and kinesin but does not require intact microfilaments. The results are discussed in relation to the current multistep model for intracellular RNA trafficking in oligodendrocytes.

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