内膜系统
内吞作用
内吞循环
生长素
细胞生物学
布雷菲尔德A
网格蛋白
内化
化学
高尔基体
生物
生物化学
内体
细胞内
细胞
基因
作者
Madhumitha Narasimhan,Michelle Gallei,Shutang Tan,Alexander D. Johnson,Inge Verstraeten,Lanxin Li,Lesia Rodriguez,Huibin Han,Ellie Himschoot,Ren Wang,Steffen Vanneste,Judit Sánchez-Simarro,Fernando Aniento,Maciek Adamowski,Jiří Friml
出处
期刊:Plant Physiology
[Oxford University Press]
日期:2021-06-11
卷期号:186 (2): 1122-1142
被引量:23
标识
DOI:10.1093/plphys/kiab134
摘要
Abstract The phytohormone auxin and its directional transport through tissues are intensively studied. However, a mechanistic understanding of auxin-mediated feedback on endocytosis and polar distribution of PIN auxin transporters remains limited due to contradictory observations and interpretations. Here, we used state-of-the-art methods to reexamine the auxin effects on PIN endocytic trafficking. We used high auxin concentrations or longer treatments versus lower concentrations and shorter treatments of natural indole-3-acetic acid (IAA) and synthetic naphthalene acetic acid (NAA) auxins to distinguish between specific and nonspecific effects. Longer treatments of both auxins interfere with Brefeldin A-mediated intracellular PIN2 accumulation and also with general aggregation of endomembrane compartments. NAA treatment decreased the internalization of the endocytic tracer dye, FM4-64; however, NAA treatment also affected the number, distribution, and compartment identity of the early endosome/trans-Golgi network, rendering the FM4-64 endocytic assays at high NAA concentrations unreliable. To circumvent these nonspecific effects of NAA and IAA affecting the endomembrane system, we opted for alternative approaches visualizing the endocytic events directly at the plasma membrane (PM). Using total internal reflection fluorescence microscopy, we saw no significant effects of IAA or NAA treatments on the incidence and dynamics of clathrin foci, implying that these treatments do not affect the overall endocytosis rate. However, both NAA and IAA at low concentrations rapidly and specifically promoted endocytosis of photo-converted PIN2 from the PM. These analyses identify a specific effect of NAA and IAA on PIN2 endocytosis, thus, contributing to its polarity maintenance and furthermore illustrate that high auxin levels have nonspecific effects on trafficking and endomembrane compartments.
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