Kerr William G
Immunology Program, Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Methods Mol Biol. 2008;430:87-99. doi: 10.1007/978-1-59745-182-6_6.
Analysis of apoptosis can be used to assess aging and survival in the hematopoietic stem cell (HSC) compartment in the context of disease, therapeutic manipulation, or genetic mutation. Two different methods to assess the frequency of apoptosis in the HSC compartment are presented. The first method utilizes an intracellular TUNEL assay that detects DNA strand breaks, a late apoptotic event. The second method relies on an extracellular stain with recombinant AnnexinV that detects flipping of phosphatidylserine groups to the outer membrane leaflet, an early apoptotic event. Both methods involve an initial magnetic enrichment or sorting of hematopoietic stem/progenitor cells from whole bone marrow (BM). Magnetic sorting is followed by polychromatic antibody (Ab) stains that detect AnnexinV or TUNEL staining in the KFTLS or KTLS HSC phenotypes, respectively. Because of the intracellular detection required for the TUNEL assay, that procedure also includes cell fixation and permeabilization. Electronic gating strategies to assess the frequency of AnnexinV+ or TUNEL+ cells in KFTLS or KTLS HSC phenotypes are also described along with representative examples.
在疾病、治疗干预或基因突变的背景下,细胞凋亡分析可用于评估造血干细胞(HSC)区室的衰老和存活情况。本文介绍了两种评估HSC区室中细胞凋亡频率的不同方法。第一种方法利用细胞内TUNEL检测法,该方法可检测DNA链断裂,这是一种晚期凋亡事件。第二种方法依赖于用重组膜联蛋白V进行细胞外染色,该方法可检测磷脂酰丝氨酸基团外翻至外膜小叶,这是一种早期凋亡事件。两种方法都涉及从全骨髓(BM)中初步磁性富集或分选造血干/祖细胞。磁性分选之后是多色抗体(Ab)染色,分别检测KFTLS或KTLS HSC表型中的膜联蛋白V或TUNEL染色。由于TUNEL检测需要细胞内检测,该程序还包括细胞固定和通透处理。本文还描述了评估KFTLS或KTLS HSC表型中膜联蛋白V+或TUNEL+细胞频率的电子门控策略以及代表性实例。