葡萄糖转运蛋白-2对男性和女性下丘脑星形胶质细胞MAPK表达和激活的调节:葡萄糖的影响

MadhuBabu Pasula, Sagor C Roy, Khaggeswar Bheemanapally, Paul W Sylvester, Karen P Briski
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摘要

质膜葡萄糖转运蛋白(GLUT)-2在GLUT家族蛋白中是独特的,因为它也具有葡萄糖传感器的功能。GLUT2通过未知机制对下丘脑星形胶质细胞葡萄糖储存和分解代谢施加性别二态控制。丝裂原活化蛋白激酶(MAPK)信号级联在应激敏感信号转导途径中运作。目前的研究采用建立的原代星形胶质细胞培养模型和基因敲低工具来研究三个主要MAP激酶家族中的一个或多个是否受GLUT2调控。GLUT2基因敲除导致葡萄糖供应的男性和女性星形胶质细胞中ERK1/2总蛋白的相反调节,增加或降低这些性别中44和42 kDa变异的平均磷酸化/总蛋白比率。葡萄糖剥夺放大了这两种ERK1/2变异的比例,尽管在男性中幅度更大;GLUT2 siRNA仅在雄性中加剧了这种刺激反应。GLUT2敲低可上调雄性星形胶质细胞中磷酸化/总p38 MAPK蛋白的比例,而雌性星形胶质细胞中没有。在GLUT2基因沉默后,葡萄糖剥夺的星形胶质细胞在这一比例上没有变化(雄性)或减少(雌性)。当葡萄糖存在时,GLUT2 siRNA增加了两性中54和46 kDa SAPK/JNK蛋白的磷酸化/总蛋白比率。然而,葡萄糖戒断抑制(男性)或放大(女性)这些比率,而GLUT2敲低则减弱这些反向反应。结果表明,GLUT2在雄性中抑制ERK1/2、p38和SAPK/JNK MAPK的活性,但在雌性下丘脑星形胶质细胞中刺激和抑制这些信号通路的活性存在差异。葡萄糖活化诱导星形胶质细胞p38 MAPK和SAPK/JNK活性的不同调节。研究结果表明,在葡萄糖缺乏的雌性星形胶质细胞中,GLUT2在p38 MAPK激活中具有刺激作用,但在葡萄糖缺乏的雄性和雌性胶质细胞中,GLUT2分别可以作为SAPK/JNK激活的抑制剂或诱导剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glucose Transporter-2 Regulation of Male versus Female Hypothalamic Astrocyte MAPK Expression and Activation: Impact of Glucose.

The plasma membrane glucose transporter (GLUT)-2 is unique among GLUT family proteins in that it also functions as a glucose sensor. GLUT2 imposes sex-dimorphic control of hypothalamic astrocyte glucose storage and catabolism by unknown mechanisms. Mitogen-activated protein kinase (MAPK) signaling cascades operate within stress-sensitive signal transduction pathways. Current research employed an established primary astrocyte culture model and gene knockdown tools to investigate whether one or more of the three primary MAP kinase families are regulated by GLUT2. GLUT2 gene knockdown caused opposing adjustments in total ERK1/2 proteins in glucose-supplied male versus female astrocytes, augmenting or reducing the mean phosphorylated/total protein ratio for 44 and 42 kDa variants in these sexes. Glucose deprivation amplified this ratio for both ERK1/2 variants, albeit by a larger magnitude in male; GLUT2 siRNA exacerbated this stimulatory response in males only. Phosphorylated/total p38 MAPK protein ratios were up-regulated by GLUT2 knockdown in male, but not female astrocytes. Glucose-deprived astrocytes exhibited no change (male) or reduction (female) in this ratio after GLUT2 gene silencing. GLUT2 siRNA increased the phosphorylated/total protein ratio for 54 and 46 kDa SAPK/JNK proteins in each sex when glucose was present. However, glucose withdrawal suppressed (male) or amplified (female) these ratios, while GLUT2 knockdown attenuated these inverse responses. Results show that GLUT2 inhibits ERK1/2, p38, and SAPK/JNK MAPK activity in male, but differentially stimulates and inhibits activity of these signaling pathways in female hypothalamic astrocytes. Glucoprivation induces divergent adjustments in astrocyte p38 MAPK and SAPK/JNK activities. The findings demonstrate a stimulatory role for GLUT2 in p38 MAPK activation in glucose-starved female astrocytes, but can act as either an inhibitor or inducer of SAPK/JNK activation in glucose-deprived male versus female glial cells, respectively.

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