Lorenzen J, Alavaikko M, Hansmann M L
Institut für Pathologie, Universität zu Köln.
Pathologe. 1995 May;16(3):208-16. doi: 10.1007/s002920050093.
Previous studies have concentrated on the proliferative behaviour of the neoplastic cell compartment in Hodgkin's disease (HD). The aim of the current investigation was to analyse the frequency of programmed cell deaths in Hodgkin and Reed-Sternberg (HRS) cells in the different subtypes of HD and to correlate this phenomenon with the expression of the bcl-2 oncogene. For this purpose, we investigated paraffin-embedded material from 63 cases of HD. Oncogene expression was determined by immunohistochemistry with the monoclonal antibody bcl-2-124. The detection of apoptotic cells was facilitated by application of the in situ end-labelling (ISEL) technique. Our results confirmed that bcl-2 expression is low in the lymphocyte-predominant subtype of HD. Apoptotic cells were found in all subtypes to a variable extent and were not significantly associated with any particular subtype. Interestingly, there was no correlation of bcl-2 expression and the presence or absence of apoptotic HRS cells. Hence, other factors must be operative in the regulation of programmed cell death in HD. Such mechanisms have been described for lymphocytes under various conditions, such as negative selection in germinal centres and within the thymus, DNA damage due to irradiation, and cellular cytotoxicity.
以往的研究集中在霍奇金淋巴瘤(HD)肿瘤细胞区室的增殖行为上。本研究的目的是分析HD不同亚型中霍奇金和里德-斯腾伯格(HRS)细胞程序性细胞死亡的频率,并将这一现象与bcl-2癌基因的表达相关联。为此,我们研究了63例HD石蜡包埋材料。通过使用单克隆抗体bcl-2-124进行免疫组织化学测定癌基因表达。应用原位末端标记(ISEL)技术有助于检测凋亡细胞。我们的结果证实,bcl-2在HD淋巴细胞为主型亚型中的表达较低。在所有亚型中均发现了不同程度的凋亡细胞,且与任何特定亚型均无显著相关性。有趣的是,bcl-2表达与凋亡HRS细胞的存在与否无关。因此,在HD中程序性细胞死亡的调节中必定存在其他起作用的因素。在各种条件下,如生发中心和胸腺内的阴性选择、辐射引起的DNA损伤以及细胞毒性,淋巴细胞中已经描述了这样的机制。