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胰岛素受体底物 2(IRS2)缺乏对甲状腺的影响。

The influence of the lack of insulin receptor substrate 2 (IRS2) on the thyroid gland.

机构信息

Department of Physiology and Pharmacology, Faculty of Medicine, University of Salamanca, Salamanca, Spain.

Laboratory of Neuroendocrinology, Institute of Neurosciences of Castilla y León (INCyL), and Laboratory of Neuroendocrinology and Obesity, Institute of Biomedical Research of Salamanca (IBSAL), University of Salamanca, Salamanca, Spain.

出版信息

Sci Rep. 2019 Apr 5;9(1):5673. doi: 10.1038/s41598-019-42198-7.

Abstract

Involvement of IRS2 in the proliferative effects of IGF-I of follicular thyroid cells has been described, but there are no evidences for in vivo participation of IRS2. This study aimed to analyse the in vivo relevance of IRS2 in the proliferation and apoptosis of thyroid cells by immunocytochemical studies for PCNA, Ki67, and active-caspase-3 in thyroid cells of IRS2 knockout (IRS2-KO) mice, jointly to TUNEL assay. Thyroid hormones were lower in IRS2-KO mice than in their wild-type (WT) counterparts. Increases in the area, perimeter and diameter of thyroid follicles of IRS2-KO mice were observed, which also showed increased proliferation rate of follicular cells and decreased percentage of apoptotic cells that was more evident in the central than in the marginal region of the gland. Sex-related differences were also found, since the follicular epithelium height was higher in male than in female mice. The percentage of proliferating cells showed significant changes in male but not in female mice, and apoptotic cells were more abundant in female than in male IRS2-KO animals, without significant differences between WT-animals. Therefore, our results suggest that IRS2 could be involved in the maintenance of thyroid cells population and in the normal physiology of the thyroid gland.

摘要

IRS2 参与了 IGF-I 对滤泡甲状腺细胞的增殖作用,这已经得到了描述,但 IRS2 在体内的参与尚无证据。本研究旨在通过 IRS2 敲除(IRS2-KO)小鼠甲状腺细胞的增殖和凋亡的免疫细胞化学研究(针对 PCNA、Ki67 和活性 caspase-3)以及 TUNEL 检测,分析 IRS2 在甲状腺细胞增殖和凋亡中的体内相关性。IRS2-KO 小鼠的甲状腺激素水平低于其野生型(WT)对照。观察到 IRS2-KO 小鼠的甲状腺滤泡面积、周长和直径增加,并且滤泡细胞的增殖率增加,凋亡细胞的百分比减少,在腺体的中央区域比边缘区域更为明显。还发现了性别相关的差异,因为雄性小鼠的滤泡上皮高度高于雌性小鼠。增殖细胞的百分比在雄性小鼠中发生了显著变化,但在雌性小鼠中没有,并且雌性 IRS2-KO 动物中的凋亡细胞比雄性动物更为丰富,但 WT 动物之间没有差异。因此,我们的结果表明,IRS2 可能参与了甲状腺细胞群体的维持和甲状腺的正常生理功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0b4/6450905/27628262241a/41598_2019_42198_Fig1_HTML.jpg

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