表达GFP-ATG8自噬体标记的拟南芥幼苗在非生物胁迫下的自噬分析

William Agbemafle, Vishadinie Jayasinghe, Diane C. Bassham
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引用次数: 0

摘要

植物自噬是一种分解代谢过程,其中细胞成分(如蛋白质聚集体和功能失调的细胞器)被降解和再循环,以维持体内平衡并促进应激恢复。自噬依赖于一种叫做自噬体的双膜囊泡,它将细胞货物运送到液泡中进行降解。拟南芥GFP-ATG8报告系是一种有价值的工具,广泛用于通过显微镜观察和量化自噬体,并通过免疫印迹法监测自噬降解。自噬活性的一致评估需要标准化的样品制备、成像和数据分析方案。在这里,我们提出了监测表达GFP-ATG8的拟南芥幼苗自噬的方案,包括诱导或抑制自噬通量的处理,以及成像和图像分析程序。这些方法能够可靠地评估自噬活性,并且可以适应不同的实验条件和基因型。©2025作者。基础方案1:非生物胁迫下拟南芥幼苗自噬的激活基础方案3:康那霉素A处理对空泡降解的抑制基础方案4:显微镜下定量拟南芥幼苗GFP-ATG8标记的自噬体基础方案5:免疫印迹法分析GFP-ATG8的自噬降解
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Analysis of Autophagy Under Abiotic Stress in Arabidopsis Seedlings Expressing the GFP-ATG8 Autophagosome Marker

Analysis of Autophagy Under Abiotic Stress in Arabidopsis Seedlings Expressing the GFP-ATG8 Autophagosome Marker

Plant autophagy is a catabolic process where cellular components such as protein aggregates and dysfunctional organelles are degraded and recycled to maintain homeostasis and facilitate stress resilience. Autophagy relies on a double-membrane vesicle called the autophagosome, which delivers cellular cargo to the vacuole for degradation. The Arabidopsis GFP-ATG8 reporter line is a valuable tool widely used to visualize and quantify autophagosomes via microscopy and monitor autophagic degradation via immunoblotting. Consistent assessment of autophagic activity requires standardized protocols for sample preparation, imaging, and data analysis. Here, we present protocols for monitoring autophagy in Arabidopsis seedlings expressing GFP-ATG8, including treatments to induce or inhibit autophagic flux, as well as imaging and image analysis procedures. These methods enable reliable evaluation of autophagic activity and can be adapted for diverse experimental conditions and genotypes. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Growth of Arabidopsis seedlings

Basic Protocol 2: Activation of autophagy in Arabidopsis seedlings by abiotic stresses

Basic Protocol 3: Inhibition of vacuolar degradation by concanamycin A treatment

Basic Protocol 4: Quantification of GFP-ATG8-labeled autophagosomes in Arabidopsis seedlings via microscopy

Basic Protocol 5: Analysis of autophagic degradation of GFP-ATG8 via immunoblotting

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