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微小RNA-8调节细胞骨架调节因子,以影响果蝇翅膀中的细胞存活和上皮组织。

miR-8 modulates cytoskeletal regulators to influence cell survival and epithelial organization in Drosophila wings.

作者信息

Bolin Kelsey, Rachmaninoff Nicholas, Moncada Kea, Pula Katharine, Kennell Jennifer, Buttitta Laura

机构信息

University of Michigan, Department of Molecular, Cellular and Developmental Biology, Ann Arbor, MI 48109, United States.

Vassar College, Department of Biology, Poughkeepsie, NY 12604, United States.

出版信息

Dev Biol. 2016 Apr 1;412(1):83-98. doi: 10.1016/j.ydbio.2016.01.041. Epub 2016 Feb 21.

Abstract

The miR-200 microRNA family plays important tumor suppressive roles. The sole Drosophila miR-200 ortholog, miR-8 plays conserved roles in Wingless, Notch and Insulin signaling - pathways linked to tumorigenesis, yet homozygous null animals are viable and often appear morphologically normal. We observed that wing tissues mosaic for miR-8 levels by genetic loss or gain of function exhibited patterns of cell death consistent with a role for miR-8 in modulating cell survival in vivo. Here we show that miR-8 levels impact several actin cytoskeletal regulators that can affect cell survival and epithelial organization. We show that loss of miR-8 can confer resistance to apoptosis independent of an epithelial to mesenchymal transition while the persistence of cells expressing high levels of miR-8 in the wing epithelium leads to increased JNK signaling, aberrant expression of extracellular matrix remodeling proteins and disruption of proper wing epithelial organization. Altogether our results suggest that very low as well as very high levels of miR-8 can contribute to hallmarks associated with cancer, suggesting approaches to increase miR-200 microRNAs in cancer treatment should be moderate.

摘要

miR-200微小RNA家族发挥着重要的肿瘤抑制作用。果蝇中唯一的miR-200直系同源物miR-8在与肿瘤发生相关的无翅、Notch和胰岛素信号通路中发挥保守作用,但纯合缺失的动物是存活的,且通常在形态上看起来正常。我们观察到,通过基因功能丧失或获得使miR-8水平呈嵌合状态的翅组织表现出细胞死亡模式,这与miR-8在体内调节细胞存活的作用一致。在此我们表明,miR-8水平影响几种肌动蛋白细胞骨架调节因子,这些调节因子可影响细胞存活和上皮组织。我们表明,miR-8的缺失可赋予细胞对凋亡的抗性,且不依赖于上皮-间质转化,而在翅上皮中持续表达高水平miR-8的细胞会导致JNK信号增加、细胞外基质重塑蛋白的异常表达以及翅上皮组织的正常结构破坏。总之,我们的结果表明,极低和极高水平的miR-8都可能促成与癌症相关的特征,这表明在癌症治疗中增加miR-200微小RNA的方法应该适度。

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