a Cell Biology Department , Institut Necker-Enfants Malades (INEM) , INSERM U1151-CNRS UMR 8253, Paris , France.
b Université Paris Descartes-Sorbonne Paris Cité , Paris , France .
Autophagy. 2017 Sep 2;13(9):1602-1612. doi: 10.1080/15548627.2017.1341465. Epub 2017 Aug 16.
Phosphatidylinositol 3-phosphate (PtdIns3P) is a key player of membrane trafficking regulation, mostly synthesized by the PIK3C3 lipid kinase. The presence of PtdIns3P on endosomes has been demonstrated; however, the role and dynamics of the pool of PtdIns3P dedicated to macroautophagy/autophagy remains elusive. Here we addressed this question by studying the mobilization of PtdIns3P in time and space during autophagosome biogenesis. We compared different dyes known to specifically detect PtdIns3P by fluorescence microscopy analysis, based on PtdIns3P-binding FYVE and PX domains, and show that these transfected dyes induce defects in endosomal dynamics as well as artificial and sustained autophagosome formation. In contrast, indirect use of recombinant FYVE enabled us to track and discriminate endosomal and autophagosomal pools of PtdIns3P. We used this method to analyze localization and dynamics of PtdIns3P subdomains on the endoplasmic reticulum, at sites of pre-autophagosome associated protein recruitment such as the PtdIns3P-binding ZFYVE1/DFCP1 and WIPI2 autophagy regulators. This approach thus revealed the presence of a specific pool of PtdIns3P at the site where autophagosome assembly is initiated.
磷脂酰肌醇 3-磷酸 (PtdIns3P) 是膜运输调节的关键参与者,主要由 PIK3C3 脂质激酶合成。内体上存在 PtdIns3P 已得到证实;然而,专门用于巨自噬/自噬的 PtdIns3P 池的作用和动力学仍然难以捉摸。在这里,我们通过研究自噬体生物发生过程中 PtdIns3P 在时间和空间上的动员来解决这个问题。我们通过荧光显微镜分析比较了基于 PtdIns3P 结合 FYVE 和 PX 结构域的不同染料,这些染料专门用于检测 PtdIns3P,并表明这些转染的染料会导致内体动力学缺陷以及人工和持续的自噬体形成。相比之下,重组 FYVE 的间接使用使我们能够跟踪和区分内体和自噬体的 PtdIns3P 池。我们使用该方法分析了内质网上 PtdIns3P 亚区在与前自噬体相关蛋白募集相关的部位(如 PtdIns3P 结合 ZFYVE1/DFCP1 和 WIPI2 自噬调节剂)的定位和动力学。这种方法揭示了在自噬体组装起始部位存在特定的 PtdIns3P 池。