Fujita K, Kawarada Y, Terada K, Sugiyama T, Ohyama H, Yamada T
Department of Biology, Toho University School of Medicine, Tokyo, Japan.
J Radiat Res. 2000 Jun;41(2):139-49. doi: 10.1269/jrr.41.139.
The quantitative detection of apoptotic cells in low frequency in the thymus of mice irradiated with X-rays using an anti-single-stranded DNA antibody was explored. The antibody against single-stranded DNA (anti-ssDNA) was obtained with rabbits hyperimmunized with complexes of alkaline-denatured calf thymus DNA. AKR female mice were irradiated with 10 to 100 cGy or 4 Gy X-rays; thereafter, thymus sections were prepared at various times after irradiation. The detection and counting of apoptotic cells in the section were performed after histochemical staining using an anti-ssDNA antibody. The results demonstrate that, although sensitive and quantitative detection of apoptotic cells in irradiated thymus using the anti-ssDNA antibody is possible, the sensitivity is lower compared to that of in situ end-labeling methods, such as TUNEL or ISEL. The antibodies could also be used for rat thymus and spleen. In addition, an increase in positively stained cells by both methods was detected as early as 6 min after the irradiation of mice.
探讨了使用抗单链DNA抗体对受X射线照射的小鼠胸腺中低频凋亡细胞进行定量检测。用碱性变性小牛胸腺DNA复合物对家兔进行超免疫,获得了抗单链DNA(anti-ssDNA)抗体。对AKR雌性小鼠照射10至100 cGy或4 Gy的X射线;此后,在照射后的不同时间制备胸腺切片。使用抗单链DNA抗体进行组织化学染色后,对切片中的凋亡细胞进行检测和计数。结果表明,尽管使用抗单链DNA抗体对受照射胸腺中的凋亡细胞进行灵敏且定量的检测是可行的,但与诸如TUNEL或ISEL等原位末端标记方法相比,其灵敏度较低。该抗体也可用于大鼠胸腺和脾脏。此外,在小鼠照射后最早6分钟就检测到两种方法阳性染色细胞均增加。