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Gender-specific effects of transthyretin on neural stem cell fate in the subventricular zone of the adult mouse

机译:Transthyretin对成人小鼠凹陷区神经干细胞命运的性别特异性效果

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Choroid plexus epithelial cells produce and secrete transthyretin (TTR). TTR binds and distributes thyroid hormone (TH) to brain cells via the cerebrospinal fluid. The adult murine subventricular zone (SVZ) is in close proximity to the choroid plexus. In the SVZ, TH determines neural stem cell (NSC) fate towards a neuronal or a glial cell. We investigated whether the loss of TTR also disrupted NSC fate choice. Our results show a decreased neurogenic versus oligodendrogenic balance in the lateroventral SVZ of Ttr knockout mice. This balance was also decreased in the dorsal SVZ, but only in Ttr knockout male mice, concomitant with an increased oligodendrocyte precursor density in the corpus callosum. Quantitative RTqPCR analysis following FACS-dissected SVZs, or marked-coupled microbeads sorting of in vitro neurospheres, showed elevated Ttr mRNA levels in neuronal cells, as compared to uncommitted precursor and glial cells. However, TTR protein was undetectable in vivo using immunostaining, and this despite the presence of Ttr mRNA-expressing SVZ cells. Altogether, our data demonstrate that TTR is an important factor in SVZ neuro- and oligodendrogenesis. They also reveal important gender-specific differences and spatial heterogeneity, providing new avenues for stimulating endogenous repair in neurodegenerative diseases.
机译:Choroid Plexus上皮细胞产生和分泌Transthyretin(TTR)。 TTR通过脑脊髓液将甲状腺激素(TH)与脑细胞结合并分发。成人鼠子内腔(SVZ)紧邻脉络丛。在SVZ中,将神经干细胞(NSC)命中朝向神经元或胶质细胞确定。我们调查了TTR的损失也扰乱了NSC命运选择。我们的结果表明,在TTR敲除小鼠的后病程SVZ中,神经发生与寡突增寡平均值下降。背部SVZ也降低了这种平衡,但仅在TTR敲除雄性小鼠中,伴随着胼callosum中的少突胶质细胞前体密度增加。与未提交的前体和神经胶质细胞相比,在体外神经球中,在体外神经球中进行定量RTQPCR分析或标记偶联的微生物分选,在神经元细胞中显示出升高的TTR mRNA水平。然而,在体内使用免疫染色而在体内不可检测到TTR蛋白,尽管存在TTR mRNA表达的SVZ细胞。完全,我们的数据表明,TTR是SVZ神经和少偶突的重要因素。他们还揭示了重要的性别特异性差异和空间异质性,为新的途径提供了新的途径,用于刺激神经变性疾病的内源性修复。

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