首页> 美国卫生研究院文献>other >Fluid Shear Stress Upregulates E-Tmod41 via miR-23b-3p and Contributes to F-Actin Cytoskeleton Remodeling during Erythropoiesis
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Fluid Shear Stress Upregulates E-Tmod41 via miR-23b-3p and Contributes to F-Actin Cytoskeleton Remodeling during Erythropoiesis

机译:流体剪切应力通过miR-23b-3p上调E-Tmod41并在促红细胞生成过程中促进F-肌动蛋白细胞骨架重塑

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摘要

The membrane skeleton of mature erythrocyte is formed during erythroid differentiation. Fluid shear stress is one of the main factors that promote embryonic hematopoiesis, however, its effects on erythroid differentiation and cytoskeleton remodeling are unclear. Erythrocyte tropomodulin of 41 kDa (E-Tmod41) caps the pointed end of actin filament (F-actin) and is critical for the formation of hexagonal topology of erythrocyte membrane skeleton. Our study focused on the regulation of E-Tmod41 and its role in F-actin cytoskeleton remodeling during erythroid differentiation induced by fluid shear stress. Mouse erythroleukemia (MEL) cells and embryonic erythroblasts were subjected to fluid shear stress (5 dyn/cm2) and erythroid differentiation was induced in both cells. F-actin content and E-Tmod41 expression were significantly increased in MEL cells after shearing. E-Tmod41 overexpression resulted in a significant increase in F-actin content, while the knockdown of E-Tmod41 generated the opposite result. An E-Tmod 3’UTR targeting miRNA, miR-23b-3p, was found suppressed by shear stress. When miR-23b-3p level was overexpressed / inhibited, both E-Tmod41 protein level and F-actin content were reduced / augmented. Furthermore, among the two alternative promoters of E-Tmod, PE0 (upstream of exon 0), which mainly drives the expression of E-Tmod41, was found activated by shear stress. In conclusion, our results suggest that fluid shear stress could induce erythroid differentiation and F-actin cytoskeleton remodeling. It upregulates E-Tmod41 expression through miR-23b-3p suppression and PE0 promoter activation, which, in turn, contributes to F-actin cytoskeleton remodeling.
机译:成熟的红细胞的膜骨架是在红系分化过程中形成的。流体剪切应力是促进胚胎造血作用的主要因素之一,但是,其对红系分化和细胞骨架重塑的影响尚不清楚。 41 kDa的红细胞原代调节蛋白(E-Tmod41)覆盖了肌动蛋白丝(F-actin)的尖端,对于形成红细胞膜骨架的六边形拓扑结构至关重要。我们的研究集中于E-Tmod41的调控及其在流体剪切应力诱导的类红细胞分化过程中F-肌动蛋白细胞骨架重塑中的作用。小鼠红白血病(MEL)细胞和胚胎成红细胞受到流体剪切应力(5 dyn / cm 2 )的作用,并在两种细胞中诱导红系分化。剪切后,MEL细胞中的F-肌动蛋白含量和E-Tmod41表达显着增加。 E-Tmod41过表达导致F-肌动蛋白含量显着增加,而敲除E-Tmod41则产生相反的结果。发现靶向E-Tmod 3’UTR的miRNA miR-23b-3p被剪切应力抑制。当miR-23b-3p水平过表达/被抑制时,E-Tmod41蛋白水平和F-肌动蛋白含量均降低/升高。此外,发现在E-Tmod的两个替代启动子中,主要驱动E-Tmod41表达的PE0(外显子0的上游)被剪切应力激活。总之,我们的结果表明,流体剪切应力可以诱导红系分化和F-肌动蛋白细胞骨架重塑。它通过miR-23b-3p抑制和PE0启动子激活来上调E-Tmod41的表达,进而促进F-肌动蛋白的细胞骨架重塑。

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