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Thy1缺乏和膳食铁缺乏对小鼠纹状体多巴胺能特征影响的比较研究。

Comparative study of the influence of Thy1 deficiency and dietary iron deficiency on dopaminergic profiles in the mouse striatum.

作者信息

Connor James R, Wang Xin-Sheng, Neely Elizabeth B, Ponnuru Padmavathi, Morita Hokuto, Beard John

机构信息

Department of Neurosurgery, MS Hershey Medical Center, Penn State College of Medicine, Hershey, PA 17033, USA.

出版信息

J Neurosci Res. 2008 Nov 1;86(14):3194-202. doi: 10.1002/jnr.21758.

Abstract

Thy-1, a glycosyl-phosphatidylinositol (GPI)-linked integral membrane protein, may play a role in stabilizing synapses. Thy1 was identified in a gene expression analysis as iron responsive, and subsequent cell culture and animal models of iron deficiency expanded this finding to the protein. The importance of Thy1 in influencing neurotransmitter feedback mechanisms led to this study to determine the relative effects of Thy1 deficiency and dietary iron deficiency on the dopaminergic system in the mouse striatum. The model for this analysis was the Thy1 null mutant mouse in the presence or absence of dietary iron deficiency. The results revealed significant differences in dopaminergic profiles associated with Thy1 and iron deficiency and also a sex effect. For example, both iron deficiency and the absence of Thy1 are associated with increased dopamine in both sexes, but the dopamine transporter is increased in these experimental groups only in female mice. In male mice, the increase in dopamine transporter is found only in the Thy1 null mutants. Increases in vesicular monoamine transporter and phosphorylated tyrosine hydroxlyase are found only in iron-deficient mice. In contrast decreased release of dopamine from synaptosomes is found only in the Thy1 null mutant animals. In general, these results indicate that a loss of Thy1 can influence the dopaminergic profile in the striatum. Furthermore, the results reveal consistent differences in the dopaminergic profile in Thy1 knockout mice compared with iron-deficient mice, indicating that the effects of iron deficiency are not due only to a change in Thy1 expression.

摘要

Thy-1是一种糖基磷脂酰肌醇(GPI)连接的整合膜蛋白,可能在稳定突触方面发挥作用。在基因表达分析中,Thy1被确定为铁反应性蛋白,随后缺铁的细胞培养和动物模型将这一发现扩展到了该蛋白。Thy1在影响神经递质反馈机制方面的重要性促使开展这项研究,以确定Thy1缺乏和饮食缺铁对小鼠纹状体多巴胺能系统的相对影响。该分析的模型是存在或不存在饮食缺铁情况下的Thy1基因敲除突变小鼠。结果显示,与Thy1和缺铁相关的多巴胺能谱存在显著差异,且存在性别效应。例如,缺铁和Thy1缺失均与两性多巴胺增加有关,但仅在雌性小鼠的这些实验组中多巴胺转运体增加。在雄性小鼠中,仅在Thy1基因敲除突变体中发现多巴胺转运体增加。仅在缺铁小鼠中发现囊泡单胺转运体和磷酸化酪氨酸羟化酶增加。相反,仅在Thy1基因敲除突变动物中发现突触体多巴胺释放减少。总体而言,这些结果表明Thy1的缺失会影响纹状体中的多巴胺能谱。此外,结果显示Thy1基因敲除小鼠与缺铁小鼠的多巴胺能谱存在一致差异,表明缺铁的影响并非仅由Thy1表达的变化所致。

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