Department of Experimental Medicine, Sapienza University, Rome, Italy.
Oncology Unit, Center for Gender-Specific Medicine, Istituto Superiore di Sanità, Rome, Italy.
Autophagy. 2021 Sep;17(9):2528-2548. doi: 10.1080/15548627.2020.1834207. Epub 2020 Oct 23.
Mitochondria-associated membranes (MAMs) are essential communication subdomains of the endoplasmic reticulum (ER) that interact with mitochondria. We previously demonstrated that, upon macroautophagy/autophagy induction, AMBRA1 is recruited to the BECN1 complex and relocalizes to MAMs, where it regulates autophagy by interacting with raft-like components. ERLIN1 is an endoplasmic reticulum lipid raft protein of the prohibitin family. However, little is known about its association with the MAM interface and its involvement in autophagic initiation. In this study, we investigated ERLIN1 association with MAM raft-like microdomains and its interaction with AMBRA1 in the regulation of the autophagic process. We show that ERLIN1 interacts with AMBRA1 at MAM raft-like microdomains, which represents an essential condition for autophagosome formation upon nutrient starvation, as demonstrated by knocking down gene expression. Moreover, this interaction depends on the "integrity" of key molecules, such as ganglioside GD3 and MFN2. Indeed, knocking down ST8SIA1/GD3-synthase or MFN2 expression impairs AMBRA1-ERLIN1 interaction at the MAM level and hinders autophagy. In conclusion, AMBRA1-ERLIN1 interaction within MAM raft-like microdomains appears to be pivotal in promoting the formation of autophagosomes. ACSL4/ACS4: acyl-CoA synthetase long chain family member 4; ACTB/β-actin: actin beta; AMBRA1: autophagy and beclin 1 regulator 1; ATG14: autophagy related 14; BECN1: beclin 1; CANX: calnexin; Cy5: cyanine 5; ECL: enhanced chemiluminescence; ER: endoplasmic reticulum; ERLIN1/KE04: ER lipid raft associated 1; FB1: fumonisin B1; FE: FRET efficiency; FRET: Förster/fluorescence resonance energy transfer; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GD3: aNeu5Ac(2-8)aNeu5Ac(2-3)bDGalp(1-4)bDGlcp(1-1)ceramide; HBSS: Hanks' balanced salt solution; HRP: horseradish peroxidase; LMNB1: lamin B1; mAb: monoclonal antibody; MAMs: mitochondria-associated membranes; MAP1LC3B/LC3: microtubule associated protein 1 light chain 3 beta; MFN2: mitofusin 2; MTOR: mechanistic target of rapamycin kinase; MYC/cMyc: proto-oncogene, bHLH transcription factor; P4HB: prolyl 4-hydroxylase subunit beta; pAb: polyclonal antibody; PE: phycoerythrin; SCAP/SREBP: SREBF chaperone; SD: standard deviation; ST8SIA1: ST8 alpha-N-acetyl-neuraminide alpha-2,8 sialyltransferase 1; SQSTM1/p62: sequestosome 1; TOMM20: translocase of outer mitochondrial membrane 20; TUBB/beta-tubulin: tubulin beta class I; ULK1: unc-51 like autophagy activating kinase 1; VDAC1/porin: voltage dependent anion channel 1.
线粒体相关膜 (MAMs) 是内质网 (ER) 的重要通讯亚区,与线粒体相互作用。我们之前的研究表明,在巨自噬/自噬诱导后,AMBRA1 被招募到 BECN1 复合物并重新定位到 MAMs,在那里它通过与筏样成分相互作用来调节自噬。ERLIN1 是一种内质网脂筏蛋白,属于抑制素家族。然而,人们对它与 MAM 界面的关联及其在自噬起始中的作用知之甚少。在这项研究中,我们研究了 ERLIN1 与 MAM 筏样微区的关联及其在调节自噬过程中与 AMBRA1 的相互作用。我们表明,ERLIN1 在 MAM 筏样微区与 AMBRA1 相互作用,这是营养饥饿时形成自噬体的必要条件,如基因表达敲低所示。此外,这种相互作用依赖于关键分子的“完整性”,如神经节苷脂 GD3 和 MFN2。事实上,敲低 ST8SIA1/GD3-合成酶或 MFN2 表达会损害 MAM 水平上的 AMBRA1-ERLIN1 相互作用,并阻碍自噬。总之,AMBRA1-ERLIN1 相互作用似乎在促进自噬体的形成中起着关键作用。ACSL4/ACS4:酰基辅酶 A 合成酶长链家族成员 4;ACTB/β-肌动蛋白:肌动蛋白β;AMBRA1:自噬和 beclin 1 调节 1;ATG14:自噬相关 14;BECN1:beclin 1;CANX:钙网蛋白;Cy5:青Cy5;ECL:增强化学发光;ER:内质网;ERLIN1/KE04:与 ER 脂筏相关 1;FB1:伏马菌素 B1;FE:FRET 效率;FRET:Förster/荧光共振能量转移;GAPDH:甘油醛-3-磷酸脱氢酶;GD3:aNeu5Ac(2-8)aNeu5Ac(2-3)bDGalp(1-4)bDGlcp(1-1)神经酰胺;HBSS:汉克斯平衡盐溶液;HRP:辣根过氧化物酶;LMNB1:核纤层蛋白 B1;mAb:单克隆抗体;MAMs:线粒体相关膜;MAP1LC3B/LC3:微管相关蛋白 1 轻链 3β;MFN2:线粒体融合蛋白 2;MTOR:雷帕霉素机制靶蛋白激酶;MYC/cMyc:原癌基因,bHLH 转录因子;P4HB:脯氨酰 4-羟化酶亚基β;pAb:多克隆抗体;PE:藻红蛋白;SCAP/SREBP:SREBF 伴侣;SD:标准差;ST8SIA1:ST8α-N-乙酰神经氨酸α-2,8 唾液酸转移酶 1;SQSTM1/p62:自噬体 1;TOMM20:外线粒体膜 20 转位酶;TUBB/β-微管蛋白:微管蛋白β I 类;ULK1:UNC-51 样自噬激活激酶 1;VDAC1/porin:电压依赖性阴离子通道 1。