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在培养的小脑大神经元中抑制微管相关蛋白2(MAP2)会抑制小神经突的形成。

Suppression of MAP2 in cultured cerebellar macroneurons inhibits minor neurite formation.

作者信息

Caceres A, Mautino J, Kosik K S

机构信息

Instituto de Investigacion Medica Mercedes y Martin Ferreyra, Cordoba, Argentina.

出版信息

Neuron. 1992 Oct;9(4):607-18. doi: 10.1016/0896-6273(92)90025-9.

Abstract

We show here that antisense MAP2 oligonucleotides inhibit neurite outgrowth in cultured cerebellar macroneurons. Unlike control neurons, which first extend a lamellipodial veil followed by a consolidation phase during which the cells extend minor neurites, MAP2-suppressed cells persist with lamellipodia and later become rounded. The induction of microtubules containing tyrosinated tubulin, which parallels neurite outgrowth in control neurons, was blocked under antisense conditions. The small but significant increase in acetylated microtubules was not affected. In contrast, the suppression of tau, which selectively blocks axonal elongation, completely prevented the increase of acetylated microtubules, but did not modify the induction of labile microtubules. These results suggest that MAP2 and tau have different functions: the initial establishment of neurites depends upon MAP2, whereas further neurite elongation depends upon tau and microtubule stabilization.

摘要

我们在此表明,反义MAP2寡核苷酸可抑制培养的小脑大神经元的神经突生长。与对照神经元不同,对照神经元首先伸出片状伪足面纱,随后进入巩固阶段,在此期间细胞伸出细小神经突,而MAP2抑制的细胞则持续存在片状伪足,随后变圆。在反义条件下,含酪氨酸化微管蛋白的微管的诱导受到阻断,而这与对照神经元中的神经突生长平行。乙酰化微管虽有少量但显著的增加,却不受影响。相比之下,tau的抑制选择性地阻断轴突伸长,完全阻止了乙酰化微管的增加,但未改变不稳定微管的诱导。这些结果表明,MAP2和tau具有不同的功能:神经突的初始形成取决于MAP2,而神经突的进一步伸长取决于tau和微管稳定化。

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