Sun Xuerong, Dong Zhizhang, Deng Fei, Hu Huiling, Ge Jian
Institute of Aging Research, Key Laboratory for Medical Molecular Diagnostics of Guangdong Province, Guangdong Medical College, Dongguan 523000, China.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2013 Feb;30(1):125-30.
BrdU (5-Bromo-2'-deoxyuridine) is usually used to label the mitotic cells as well as to trace reagent in cell transplation. However, BrdU could also exert some side effect on cellular biological characteristics upon inappropriate use. To explore the appropriate concentration of BrdU for labelling retinal progenitor cells (RPCs), we co-cultured Embryonic day (E) 17. 5 RPCs with different concentrations of BrdU, which were 0.2, 1, 5 and 10 micromol/L, respectively. After 48 hours, the RPCs were proliferation- or differentiation-cultured. Immunofluorescence was used to detect the BrdU-positive ratio and differentiation potential. Cell count was used to evaluate proliferation ability, and lactate dehydrogenase (LDH) release assay was used to monitor cytotoxicity. The results showed that 0.2 micromol/ L BrdU could not label RPCs clearly, while BrdU of 1, 5 or 10 micromol/L could label the RPCs with similar ratios. 1 micromol/L BrdU displayed no obvious cytotoxicity and showed no obvious effect on the proliferation and differentiation ability. However, 5 micromol/L or 10 micromol/L BrdU could evidently inhibit RPCs proliferation, partly due to the cytotoxicity effect. Furthermore, 10 micromol/L BrdU could inhibit the differentiation of RPCs towards MAP2-positive nerve cells, but showed no influence on the differentiation of RPCs towards GFAP- and glutamine synthetase positive glial cells. This study suggested that 1 micromol/L BrdU could be an appropriate concentration for RPCs labelling and could efficiently label RPCs without obvious side effect.
5-溴脱氧尿苷(BrdU)通常用于标记有丝分裂细胞以及在细胞移植中追踪试剂。然而,使用不当的话,BrdU也可能对细胞生物学特性产生一些副作用。为了探索用于标记视网膜祖细胞(RPCs)的BrdU的合适浓度,我们将胚胎第17.5天的RPCs与不同浓度的BrdU共同培养,这些浓度分别为0.2、1、5和10微摩尔/升。48小时后,对RPCs进行增殖培养或分化培养。采用免疫荧光法检测BrdU阳性率和分化潜能。通过细胞计数评估增殖能力,采用乳酸脱氢酶(LDH)释放试验监测细胞毒性。结果显示,0.2微摩尔/升的BrdU不能清晰地标记RPCs,而1、5或10微摩尔/升的BrdU能以相似的比例标记RPCs。1微摩尔/升的BrdU没有明显的细胞毒性,对增殖和分化能力也没有明显影响。然而,5微摩尔/升或10微摩尔/升的BrdU能明显抑制RPCs的增殖,部分原因是细胞毒性作用。此外,10微摩尔/升的BrdU能抑制RPCs向微管相关蛋白2(MAP2)阳性神经细胞的分化,但对RPCs向胶质纤维酸性蛋白(GFAP)和谷氨酰胺合成酶阳性神经胶质细胞的分化没有影响。本研究表明,1微摩尔/升的BrdU可能是标记RPCs的合适浓度,能够有效标记RPCs且无明显副作用。