Department of Dermatology, Medical University of Vienna, 1090 Vienna, Austria.
Christian Doppler Laboratory for Skin Multimodal Imaging of Aging and Senescence-SKINMAGINE, 1090 Vienna, Austria.
Cells. 2024 Oct 10;13(20):1675. doi: 10.3390/cells13201675.
The epidermis of the skin and skin appendages, such as nails, hair and sebaceous glands, depend on a balance of cell proliferation and terminal differentiation in order to fulfill their functions at the interface of the body and the environment. The differentiation of epithelial cells of the skin, commonly referred to as keratinocytes, involves major remodeling processes that generate metabolically inactive cell remnants serving as building blocks of the epidermal stratum corneum, nail plates and hair shafts. Only sebaceous gland differentiation results in cell disintegration and holocrine secretion. A series of studies performed in the past decade have revealed that the lysosome-dependent intracellular degradation mechanism of autophagy is active during keratinocyte differentiation, and the blockade of autophagy significantly alters the properties of the differentiation products. Here, we present a model for the autophagy-mediated degradation of organelles and cytosolic proteins as an important contributor to cellular remodeling in keratinocyte differentiation. The roles of autophagy are discussed in comparison to alternative intracellular degradation mechanisms and in the context of programmed cell death as an integral end point of epithelial differentiation.
皮肤表皮及其附属物(如指甲、毛发和皮脂腺)的功能依赖于细胞增殖和终末分化之间的平衡,以实现其在身体与环境界面的功能。皮肤上皮细胞(通常称为角质形成细胞)的分化涉及主要的重塑过程,这些过程产生代谢不活跃的细胞残片,作为表皮角质层、指甲板和毛发轴的构建块。只有皮脂腺分化导致细胞解体和全浆分泌。过去十年中的一系列研究表明,自噬的溶酶体依赖性细胞内降解机制在角质形成细胞分化过程中是活跃的,自噬的阻断会显著改变分化产物的特性。在这里,我们提出了一个模型,即自噬介导的细胞器和细胞质蛋白降解是角质形成细胞分化中细胞重塑的重要贡献者。自噬的作用与替代的细胞内降解机制进行了比较,并在程序性细胞死亡的背景下进行了讨论,程序性细胞死亡是上皮细胞分化的一个完整终点。