Schendzielorz P, Froelich K, Rak K, Gehrke T, Scherzad A, Hagen R, Radeloff A
Comprehensive Hearing Center, Department of Otorhinolaryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, University of Würzburg, Josef-Schneider-Strasse 11, 97080 Würzburg, Germany.
Stem Cells Int. 2016;2016:6549347. doi: 10.1155/2016/6549347. Epub 2016 Jun 8.
Adipose-derived stem cells (ASCs) have been extensively studied in the field of stem cell research and possess numerous clinical applications. Cell labeling is an essential component of various experimental protocols and Hoechst 33342 (H33342) represents a cost-effective and easy methodology for live staining. The purpose of this study was to evaluate the labeling of rat ASCs with two different concentrations of H33342 (0.5 μg/mL and 5 μg/mL), with particular regard to usability, interference with cell properties, and potential DNA damage. Hoechst 33342 used at a low concentration of 0.5 μg/mL did not significantly affect cell proliferation, viability, or differentiation potential of the ASCs, nor did it cause any significant DNA damage as measured by the olive tail moment. High concentrations of 5 μg/mL H33342, however, impaired the proliferation and viability of the ASCs, and considerable DNA damage was observed. Undesirable colabeling of unlabeled cocultivated cells was seen in particular with higher concentrations of H33342, independent of varying washing procedures. Hence, H33342 labeling with lower concentrations represents a usable method, which does not affect the tested cell properties. However, the colabeling of adjacent cells is a drawback of the technique.
脂肪来源干细胞(ASCs)在干细胞研究领域已得到广泛研究,并具有众多临床应用。细胞标记是各种实验方案的重要组成部分,而Hoechst 33342(H33342)是一种经济高效且简便的活细胞染色方法。本研究的目的是评估用两种不同浓度的H33342(0.5μg/mL和5μg/mL)对大鼠ASCs进行标记的情况,特别关注其可用性、对细胞特性的干扰以及潜在的DNA损伤。低浓度0.5μg/mL的Hoechst 33342对ASCs的细胞增殖、活力或分化潜能没有显著影响,通过橄榄尾矩测量也未引起任何显著的DNA损伤。然而,高浓度5μg/mL的H33342会损害ASCs的增殖和活力,并观察到相当程度的DNA损伤。特别是在较高浓度的H33342下,无论不同的洗涤程序如何,未标记的共培养细胞都会出现不希望的共标记现象。因此,较低浓度的H33342标记是一种可用的方法,不会影响所测试的细胞特性。然而,相邻细胞的共标记是该技术的一个缺点。