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酪氨酸羟化酶-Gal4 驱动的质膜 Ca ATP 酶下调可独立于神经元中的作用降低果蝇寿命。

Downregulation of Plasma Membrane Ca ATPase driven by tyrosine hydroxylase-Gal4 reduces Drosophila lifespan independently of effects in neurons.

机构信息

Instituto de Investigaciones Bioquímicas de Buenos Aires (IIBBA)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.

Fundación Instituto Leloir, Buenos Aires, Argentina.

出版信息

Fly (Austin). 2023 Dec;17(1):2192457. doi: 10.1080/19336934.2023.2192457.

Abstract

In , several Gal4 drivers are used to direct gene/RNAi expression to different dopaminergic neuronal clusters. We previously developed a fly model of Parkinson's disease, in which dopaminergic neurons had elevated cytosolic Ca due to the expression of a Plasma Membrane Ca ATPase (PMCA) RNAi under the thyroxine hydroxylase (TH)-Gal4 driver. Surprisingly, TH-Gal4>PMCA flies died earlier compared to controls and showed swelling in the abdominal area. Flies expressing the PMCA under other TH drivers also showed such swelling and shorter lifespan. Considering that TH-Gal4 is also expressed in the gut, we proposed to suppress the expression specifically in the nervous system, while maintaining the activation in the gut. Therefore, we expressed Gal80 under the direction of the panneuronal synaptobrevin (nSyb) promoter in the context of TH-Gal4. nSyb-Gal80; TH-Gal4>PMCA flies showed the same reduction of survival as TH-Gal4>PMCA flies, meaning that the phenotype of abdomen swelling and reduced survival could be due to the expression of the PMCA in the gut. In stages TH-Gal4>PMCA guts had alteration in the proventriculi and crops. The proventriculi appeared to lose cells and collapse on itself, and the crop increased its size several times with the appearance of cellular accumulations at its entrance. No altered expression or phenotype was observed in flies expressing PMCA in the dopaminergic PAM cluster (PAM-Gal4>PMCA). In this work we show the importance of checking the global expression of each promoter and the relevance of the inhibition of PMCA expression in the gut.

摘要

在这项研究中,使用了几种 Gal4 驱动子将基因/RNAi 表达导向不同的多巴胺能神经元簇。我们之前开发了一种帕金森病的果蝇模型,其中由于在甲状腺素羟化酶(TH)-Gal4 驱动子下表达了质膜 Ca ATP 酶(PMCA)RNAi,多巴胺能神经元的细胞质 Ca 升高。令人惊讶的是,与对照相比,TH-Gal4>PMCA 果蝇更早死亡,并表现出腹部肿胀。在其他 TH 驱动子下表达 PMCA 的果蝇也表现出这种肿胀和寿命缩短。考虑到 TH-Gal4 也在肠道中表达,我们提议特异性地在神经系统中抑制其表达,同时保持在肠道中的激活。因此,我们在 TH-Gal4 的背景下,通过神经元突触融合蛋白(nSyb)启动子表达 Gal80。nSyb-Gal80;TH-Gal4>PMCA 果蝇的存活率与 TH-Gal4>PMCA 果蝇一样降低,这意味着腹部肿胀和存活率降低的表型可能是由于 PMCA 在肠道中的表达。在第 3 龄期,TH-Gal4>PMCA 果蝇的前胃和前肠发生了改变。前胃似乎失去了细胞并自行塌陷,而前肠的体积增加了数倍,其入口处出现了细胞堆积。在表达 PMCA 的多巴胺能 PAM 簇(PAM-Gal4>PMCA)的果蝇中,没有观察到 PMCA 表达的改变或表型。在这项工作中,我们展示了检查每个启动子的全局表达的重要性,以及抑制 PMCA 在肠道中表达的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cc/10038040/f1a2320efccf/KFLY_A_2192457_F0001_OC.jpg

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