Umemura S, Yasuda M, Osamura R Y, Kawarada Y, Sugiyama T, Tsutsumi Y
Department of Pathology, Tokai University School of Medicine, Isehara, Japan.
J Histochem Cytochem. 1996 Feb;44(2):125-32. doi: 10.1177/44.2.8609368.
The TdT-mediated dUTP-biotin nick end-labeling (TUNEL) method has been employed widely to demonstrate apoptotic cells in routinely prepared paraffin sections. Because the apoptotic cells were reactive with the antibody to single-stranded DNA, we attempted to enhance the TUNEL positivity by pretreatment with single-stranded DNA digestion enzymes, S1 nuclease, and mung bean nuclease. When mung bean nuclease (5 U/50 microliter/section) was incubated at 37 degrees C for 30 min, the TUNEL reaction was most effectively enhanced. Pretreatment with S1 nuclease (0.25 U/50 microliter/section) at 37 degrees C for 45 min was less reliable. Compared with the conventional TUNEL sequence, the enhancement technique using mung bean nuclease enabled us to detect more apoptotic cells in human small intestine, colon, tonsil, thymus, endometrium, ovary, liver, kidney, and pancreas. The positivity was not affected by autolytic change. The mechanism of enhancement is discussed.
TdT介导的dUTP生物素缺口末端标记法(TUNEL法)已被广泛用于在常规制备的石蜡切片中显示凋亡细胞。由于凋亡细胞与单链DNA抗体有反应,我们试图通过用单链DNA消化酶、S1核酸酶和绿豆核酸酶进行预处理来增强TUNEL阳性。当绿豆核酸酶(5 U/50微升/切片)在37℃孵育30分钟时,TUNEL反应增强最为有效。在37℃用S1核酸酶(0.25 U/50微升/切片)预处理45分钟则不太可靠。与传统的TUNEL序列相比,使用绿豆核酸酶的增强技术使我们能够在人类小肠、结肠、扁桃体、胸腺、子宫内膜、卵巢、肝脏、肾脏和胰腺中检测到更多的凋亡细胞。阳性不受自溶变化的影响。文中讨论了增强的机制。