Interfaculty Institute for Biochemistry, University of Tübingen, Tübingen, Germany.
Cell Cycle. 2013 Jun 15;12(12):1922-7. doi: 10.4161/cc.24944. Epub 2013 May 13.
Due to its role in aging and antitumor defense, cellular senescence has recently attracted increasing interest. However, there is currently no single specific marker that can unequivocally detect senescent cells. Here, we identified α-L-fucosidase (α-Fuc) as a novel sensitive biomarker for cellular senescence. Regardless of the stress stimulus and cell type, α-Fuc activity was induced in all canonical types of cellular senescence, including replicative, DNA damage- and oncogene-induced senescence. Strikingly, in most models the degree of α-Fuc upregulation was higher than the induction of senescence-associated β-galactosidase (SA-β-Gal), the current gold standard for senescence detection. As α-Fuc is convenient and easy to measure, we suggest its utility as a valuable marker, in particular in cells with low SA-β-Gal activity.
由于其在衰老和抗肿瘤防御中的作用,细胞衰老最近引起了越来越多的关注。然而,目前还没有单一的特定标志物可以明确检测衰老细胞。在这里,我们确定α-L-岩藻糖苷酶(α-Fuc)是一种新的敏感的细胞衰老生物标志物。无论应激刺激和细胞类型如何,α-Fuc 活性在所有典型的细胞衰老类型中都被诱导,包括复制性、DNA 损伤和致癌基因诱导的衰老。引人注目的是,在大多数模型中,α-Fuc 的上调程度高于衰老相关β-半乳糖苷酶(SA-β-Gal)的诱导,SA-β-Gal 是目前检测衰老的金标准。由于 α-Fuc 方便且易于测量,我们建议将其用作有价值的标志物,特别是在 SA-β-Gal 活性低的细胞中。