Heng Boon Chin, Clement Marie Veronique, Cao Tong
Stem Cell Laboratory, Faculty of Dentistry, National University of Singapore, Singapore, Singapore.
Biosci Rep. 2007 Oct;27(4-5):257-64. doi: 10.1007/s10540-007-9051-2.
Previous study demonstrated that the low survival of human embryonic stem cells (hESC) under conventional slow-cooling cryopreservation protocols is predominantly due to apoptosis rather than cellular necrosis. Hence, this study investigated whether a synthetic broad-spectrum irreversible inhibitor of caspase enzymes, Z-VAD-FMK can be used to enhance the post-thaw survival rate of hESC. About 100 mM Z-VAD-FMK was supplemented into either the freezing solution, the post-thaw culture media or both. Intact and adherent hESC colonies were cryopreserved so as to enable subsequent quantitation of the post-thaw cell survival rate through the MTT assay, which can only be performed with adherent cells. Exposure to 100 mM Z-VAD-FMK in the freezing solution alone did not significantly enhance the post-thaw survival rate (10.2% vs. 9.9%, p > 0.05). However, when 100 mM Z-VAD-FMK was added to the post-thaw culture media, there was a significant enhancement in the survival rate from 9.9% to 14.4% (p < 0.05), which was further increased to 18.7% when Z-VAD-FMK was also added to the freezing solution as well (p < 0.01). Spontaneous differentiation of hESC after cryopreservation was assessed by morphological observations under bright-field microscopy, and by immunocytochemical staining for the pluripotency markers SSEA-3 and TRA-1-81. The results demonstrated that exposure to Z-VAD-FMK did not significantly enhance the spontaneous differentiation of hESC within post-thaw culture.
先前的研究表明,在传统的慢速冷冻保存方案下,人类胚胎干细胞(hESC)的低存活率主要是由于细胞凋亡而非细胞坏死。因此,本研究调查了一种合成的广谱不可逆半胱天冬酶抑制剂Z-VAD-FMK是否可用于提高hESC解冻后的存活率。将约100 mM的Z-VAD-FMK添加到冷冻溶液、解冻后培养基或两者中。完整且贴壁的hESC集落被冷冻保存,以便随后通过MTT法对解冻后的细胞存活率进行定量,该方法只能用于贴壁细胞。仅在冷冻溶液中暴露于100 mM Z-VAD-FMK并不能显著提高解冻后的存活率(10.2%对9.9%,p>0.05)。然而,当在解冻后培养基中添加100 mM Z-VAD-FMK时,存活率从9.9%显著提高到14.4%(p<0.05),当Z-VAD-FMK也添加到冷冻溶液中时,存活率进一步提高到18.7%(p<0.01)。通过明场显微镜下的形态学观察以及对多能性标志物SSEA-3和TRA-1-81的免疫细胞化学染色,评估冷冻保存后hESC的自发分化。结果表明,暴露于Z-VAD-FMK并没有显著提高解冻后培养中hESC的自发分化。