血小板来源的凋亡小泡通过APOA2调节脂质代谢改善非酒精性脂肪肝(1/2025)

Yuhe Jiang, Yike Liao, Zeying Wang, Lei Zhu, Yunsong Liu, Ping Zhang, Yuan Zhu, Wenyue Li, Yongsheng Zhou, Xiao Zhang
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引用次数: 0

摘要

我们的封面设计选用红色为主色调。图片中央是部分恶化为脂肪肝的肝脏。左下角的紫色球体是凋亡囊泡(apoVs),而右边的细胞是血小板,说明了血小板释放凋亡囊泡的过程。apoVs中的绿色物质代表APOA2蛋白。apoVs包埋在脂肪肝中显示凋亡囊泡被摄取到肝脏中,而右侧健康肝脏显示凋亡囊泡被摄取后脂肪肝的改善。总的来说,覆盖设计的三个主要元素是脂肪肝、载脂蛋白和血小板,这是我们研究中最重要的组成部分。我们研究的中心思想是,通过APOA2吸收血小板释放的apoVs后,脂肪肝有改善的潜力,这可以通过这个封面设计直观地理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Platelet-Derived Apoptotic Vesicles Ameliorate Nonalcoholic Fatty Liver Disease by Regulating Lipid Metabolism via APOA2 (1/2025)

Platelet-Derived Apoptotic Vesicles Ameliorate Nonalcoholic Fatty Liver Disease by Regulating Lipid Metabolism via APOA2 (1/2025)

Our cover design chooses red as the dominant hue. In the center of the picture is a liver that has partially deteriorated into fatty liver. The purple sphere in the lower left corner are apoptotic vesicles (apoVs), while the cells on the right are platelets, illustrating the process of releasing apoptotic vesicles from platelets. The green substance in apoVs represents APOA2 protein. The embedding of apoVs into fatty liver demonstrates the uptake of apoptotic vesicles into the liver, while the healthy liver on the right shows the amelioration of fatty liver after the uptake of apoptotic vesicles. Overall, the three main elements in the cover design are fatty liver, apoVs and platelets, which are the most significant components in our research. The central idea of our research is that fatty liver has the potential to be ameliorated after uptaking the apoVs released by platelets via APOA2, which can be intuitively comprehended through this cover design.

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