Weber P J, Eckhard C P, Gonser S, Otto H, Folkers G, Beck-Sickinger A G
Department of Pharmacy, Swiss Federal Institute of Technology, Zürich.
Biol Chem. 1999 Jun;380(6):653-60. doi: 10.1515/BC.1999.081.
Thymopoietins (TMPOs) are a group of ubiquitously expressed nuclear proteins. They are suggested to play an important role in nuclear envelope organization and cell cycle control, as has been shown for lamina-associated polypeptides 2 alpha and beta, which are the rat homologs of human TMPOalpha and TMPObeta, respectively. The recent isolation and characterization of seven mouse TMPO mRNA transcripts named TMPO-alpha, beta, beta', gamma, epsilon delta and zeta, suggest that more than the three previously reported transcripts, alpha, beta, and gamma forms, may exist in humans. Here we report on the demonstration of putative human TMPOdelta and epsilon by immunoblotting of human cell lines using a newly prepared polyclonal antiserum against the common N-terminal region of TMPO. Furthermore, we prepared the first truly TMPO-beta-specific, affinity-purified polyclonal antiserum, using a part of the human analog of the beta-specific domain of mouse TMPO 220-259 for immunization. We showed that human TMPObeta is highly expressed in all cancerous cells tested, while hardly any cross-reactivities with other proteins could be detected. In contrast to the high expression of human TMPObeta in the cancer-derived neuroblastoma cell lines SK-N-MC and SMS-KAN, we found very low expression of human TMPObeta in low-proliferative nerve tissue. These data led us to the assumption that expression of TMPObeta may correlate with the occurrence of cancer, and therefore may serve as a new tumor marker, or even as a new target for cancer therapy.
胸腺生成素(TMPOs)是一组广泛表达的核蛋白。它们被认为在核膜组织和细胞周期控制中发挥重要作用,正如层粘连相关多肽2α和β所显示的那样,它们分别是人类TMPOα和TMPOβ的大鼠同源物。最近分离和鉴定出七种小鼠TMPO mRNA转录本,命名为TMPO-α、β、β'、γ、ε、δ和ζ,这表明人类中可能存在的转录本不止之前报道的α、β和γ三种形式。在这里,我们报告了使用新制备的针对TMPO共同N端区域的多克隆抗血清,通过对人类细胞系进行免疫印迹来证明推定的人类TMPOδ和ε。此外,我们使用小鼠TMPO 220-259β特异性结构域的人类类似物的一部分进行免疫,制备了第一种真正的TMPO-β特异性亲和纯化多克隆抗血清。我们发现人类TMPOβ在所有测试的癌细胞中高表达,而几乎检测不到与其他蛋白质的交叉反应。与人类TMPOβ在癌症来源的神经母细胞瘤细胞系SK-N-MC和SMS-KAN中的高表达相反,我们发现在低增殖性神经组织中人类TMPOβ的表达非常低。这些数据使我们推测TMPOβ的表达可能与癌症的发生相关,因此可能作为一种新的肿瘤标志物,甚至作为癌症治疗的新靶点。