Garofalo Tina, Matarrese Paola, Manganelli Valeria, Marconi Matteo, Tinari Antonella, Gambardella Lucrezia, Faggioni Alberto, Misasi Roberta, Sorice Maurizio, Malorni Walter
a Department of Experimental Medicine , Sapienza University , Rome , Italy.
b Section of Cell Aging and Degeneration, Department of Drug Research and Evaluation, Istituto Superiore di Sanita' , Rome , Italy.
Autophagy. 2016 Jun 2;12(6):917-35. doi: 10.1080/15548627.2016.1160971. Epub 2016 Apr 28.
Mitochondria-associated membranes (MAMs) are subdomains of the endoplasmic reticulum (ER) that interact with mitochondria. This membrane scrambling between ER and mitochondria appears to play a critical role in the earliest steps of autophagy. Recently, lipid microdomains, i.e. lipid rafts, have been identified as further actors of the autophagic process. In the present work, a series of biochemical and molecular analyses has been carried out in human fibroblasts with the specific aim of characterizing lipid rafts in MAMs and to decipher their possible implication in the autophagosome formation. In fact, the presence of lipid microdomains in MAMs has been detected and, in these structures, a molecular interaction of the ganglioside GD3, a paradigmatic "brick" of lipid rafts, with core-initiator proteins of autophagy, such as AMBRA1 and WIPI1, was revealed. This association seems thus to take place in the early phases of autophagic process in which MAMs have been hypothesized to play a key role. The functional activity of GD3 was suggested by the experiments carried out by knocking down ST8SIA1 gene expression, i.e., the synthase that leads to the ganglioside formation. This experimental condition results in fact in the impairment of the ER-mitochondria crosstalk and the subsequent hindering of autophagosome nucleation. We thus hypothesize that MAM raft-like microdomains could be pivotal in the initial organelle scrambling activity that finally leads to the formation of autophagosome.
线粒体相关膜(MAMs)是内质网(ER)与线粒体相互作用的亚结构域。内质网和线粒体之间的这种膜紊乱似乎在自噬的最早阶段起着关键作用。最近,脂质微区,即脂筏,已被确定为自噬过程的进一步参与者。在本研究中,我们对人成纤维细胞进行了一系列生化和分子分析,具体目的是表征MAMs中的脂筏,并解读它们在自噬体形成中的可能作用。事实上,已检测到MAMs中存在脂质微区,并且在这些结构中,揭示了神经节苷脂GD3(脂筏的典型“组成部分”)与自噬的核心起始蛋白(如AMBRA1和WIPI1)之间的分子相互作用。因此,这种关联似乎发生在自噬过程的早期阶段,在这个阶段中,MAMs被认为起着关键作用。通过敲低ST8SIA1基因表达(即导致神经节苷脂形成的合酶)所进行的实验表明了GD3的功能活性。这种实验条件实际上导致内质网 - 线粒体相互作用受损,进而阻碍自噬体的成核。因此,我们假设MAM类脂筏微区可能在最终导致自噬体形成的初始细胞器紊乱活动中起关键作用。