Institute of Musculoskeletal Medicine, Dept. Molecular Medicine, University Hospital Münster, Westfälische Wilhelms-Universität Münster, Münster, Germany.
Previous Address: Research Division of Biology and Pathobiology of the Skin, Department of Dermatology, Medical University of Vienna, Vienna, Austria.
Autophagy. 2020 May;16(5):932-945. doi: 10.1080/15548627.2019.1646552. Epub 2019 Aug 4.
In the adult mammalian skin, cells are constantly renewing, differentiating and moving upward, to finally die in a yet not fully understood manner. Here, we provide evidence that macroautophagy/autophagy has a dual role in the skin. In addition to its known catabolic protective role as an evolutionary conserved upstream regulator of lysosomal degradation, we show that autophagy induced cell death (CDA) occurs in epithelial lineage-derived organs, such as the inter-follicular epidermis, the sebaceous- and the Harderian gland. By utilizing GFP-LC3 transgenic and ATG7-deficient mice, we show that CDA is initiated during terminal differentiation at a stage when the cells have become highly resistant to apoptosis. In these transitional cells, the Golgi compartment expands, which accounts for the formation of primary lysosomes, and the nucleus starts to condense. During CDA a burst of autophagosome formation is observed, first the endoplasmic reticulum (ER) is phagocytosed followed by autophagy of the nucleus. By this selective form of cell death, most of the cytoplasmic organelles are degraded, but structural proteins remain intact. In the absence of autophagy, consequently, parts of the ER, ribosomes, and chromatin remain. A burst of autophagy was stochastically observed in single cells of the epidermis and collectively in larger areas of ductal cells, arguing for a coordinated induction. We conclude that autophagy is an integral part of cell death in keratinocyte lineage cells and participates in their terminal cell fate. Atg7: autophagy related 7; BECN1: beclin 1; CDA: cell death-induced autophagy; Cre: Cre-recombinase; DAPI: 4',6-diamidino-2-phenylindole; ER: endoplasmatic reticulum; GFP: green fluorescent protein; HaGl: haderian gland; IVL: involucrin; KRT14: keratin 14; LD: lipid droplet; LSM: laser scanning microscope; MAP1LC3/LC3: microtubule-associated protein 1 light chain 3; PN: perinuclear space; RB: residual body; rER: rough endoplasmatic reticulum; SB: sebum; SG-SC: stratum granulosum - stratum corneum; SGl: sebaceous gland; SQSTM1: sequestosome 1; TEM: transmission electron microscopy; TUNEL: terminal deoxynucleotidyl transferase dUTP nick end labelling.
在成年哺乳动物的皮肤中,细胞不断更新、分化并向上移动,最终以一种尚未完全阐明的方式死亡。在这里,我们提供证据表明,巨自噬/自噬在皮肤中有双重作用。除了作为进化上保守的溶酶体降解的上游调节剂的已知分解代谢保护作用外,我们还表明,自噬诱导的细胞死亡(CDA)发生在上皮谱系衍生的器官中,如毛囊间表皮、皮脂腺和哈德腺。通过利用 GFP-LC3 转基因和 ATG7 缺陷型小鼠,我们表明 CDA 是在细胞变得对细胞凋亡高度抵抗的终末分化阶段开始的。在这些过渡细胞中,高尔基体区室扩张,这导致初级溶酶体的形成,并且核开始浓缩。在 CDA 过程中,观察到自噬体形成的爆发,首先是内质网(ER)被吞噬,然后是核的自噬。通过这种选择性的细胞死亡形式,大部分细胞质细胞器被降解,但结构蛋白仍然完整。在没有自噬的情况下,因此,部分 ER、核糖体和染色质仍然存在。在表皮的单个细胞中随机观察到自噬的爆发,并且在更大的导管细胞区域中集体观察到自噬的爆发,这表明存在协调的诱导。我们得出结论,自噬是角质形成细胞谱系细胞死亡的一个组成部分,并参与其终末细胞命运。Atg7:自噬相关 7;BECN1:beclin 1;CDA:细胞死亡诱导的自噬;Cre:Cre 重组酶;DAPI:4',6-二脒基-2-苯基吲哚;ER:内质网;GFP:绿色荧光蛋白;HaGl:哈德腺;IVL: involucrin;KRT14:角蛋白 14;LD:脂滴;LSM:激光扫描显微镜;MAP1LC3/LC3:微管相关蛋白 1 轻链 3;PN:核周空间;RB:残余体;rER:粗糙内质网;SB:皮脂;SG-SC:颗粒层 - 角质层;SGl:皮脂腺;SQSTM1:sequestosome 1;TEM:透射电子显微镜;TUNEL:末端脱氧核苷酸转移酶 dUTP 缺口末端标记。