van Niekerk C C, Poels L G
Department of Cell Biology and Histology, Faculty of Medical Sciences, University of Nijmegen, The Netherlands.
Cancer Lett. 1999 Mar 22;137(1):61-73. doi: 10.1016/s0304-3835(98)00344-9.
Based on LOH studies protein tyrosine phosphatasegamma (PTPgamma) has been suggested as a candidate tumor suppressor gene involved in the oncogenesis of lung and renal cancers. In order to assess the involvement of PTPgamma in tumor development we developed a PTPgamma-specific monoclonal antibody (gammaTL1) (IgM isotype) by immunization with a synthetic peptide of 15 amino acids corresponding to the amino acid sequence nos. 1423-1438 just outside the phosphatase domain-II. In line with the fact that the antibody was raised to an intracellular domain of the PTPgamma molecule the antibody labeled the cell membrane of fixed cells but did not stain the outside of the cell membrane in the immunofluorescence assay. The Mab gammaTL1 recognized a full-length baculovirus recombinant PTPgamma protein of 185 kDa, in addition to putative cleavage products of 120 kDa, 114/110 kDa and 80 kDa, on Western blots of lysates of PTPgamma-gene transfected Sf9 insect cells but not of tumor cell lysates. Based on immunoperoxidase and immunofluorescence assays on cryostat sections, however, PTPgamma was expressed in more than 90% of both normal, human tissue samples and in the (non-) tumor cells of carcinoma samples. However, PTPgamma was not found in 28% of the overall lung tumor samples, i.e. in 50% of the lung adenocarcinoma samples, while the expression was weak and heterogeneous in 71% of squamous lung cell carcinomas. PTPgamma was not suppressed in the normal cells between the lung carcinoma cells. The presence of PTPgamma, assayed by immunofluorescence in lung tumor cell lines (H69, H128, H82, C3) was confirmed by RT-PCR assay. Interestingly, the 90% expression score of PTPgamma protein in normal ovarian tissue samples was reduced dramatically to 44 and 38% in both the non-tumorous and tumorous cells, respectively, in ovarian tumor samples. PTPgamma was absent in the HT29 human colon carcinoma cell line both by immunofluorescence and RT-PCR assay. In summary, we have developed a PTPgamma-specific monoclonal antibody, that demonstrated that the expression of PTPgamma is severely reduced (>50%) in lung tumors and ovarian tumors.
基于杂合性缺失(LOH)研究,蛋白酪氨酸磷酸酶γ(PTPγ)被认为是一种候选肿瘤抑制基因,参与肺癌和肾癌的肿瘤发生过程。为了评估PTPγ在肿瘤发展中的作用,我们通过用一段15个氨基酸的合成肽进行免疫,该合成肽对应于磷酸酶结构域II外的氨基酸序列编号1423 - 1438,从而制备了一种PTPγ特异性单克隆抗体(γTL1)(IgM亚型)。鉴于该抗体是针对PTPγ分子的细胞内结构域产生的,在免疫荧光测定中,该抗体标记了固定细胞的细胞膜,但未对细胞膜外进行染色。单克隆抗体γTL1在PTPγ基因转染的Sf9昆虫细胞裂解物的蛋白质印迹上识别出185 kDa的全长杆状病毒重组PTPγ蛋白,此外还有120 kDa、114/110 kDa和80 kDa的假定裂解产物,但在肿瘤细胞裂解物中未识别到。然而,基于对冰冻切片的免疫过氧化物酶和免疫荧光测定,PTPγ在超过90%的正常人体组织样本以及癌样本的(非)肿瘤细胞中均有表达。然而,在28%的总体肺肿瘤样本中未发现PTPγ,即在50%的肺腺癌样本中未发现,而在71%的肺鳞状细胞癌中表达较弱且不均匀。肺癌细胞之间的正常细胞中PTPγ未被抑制。通过免疫荧光在肺肿瘤细胞系(H69、H128、H82、C3)中检测到的PTPγ的存在,通过逆转录聚合酶链反应(RT-PCR)测定得到了证实。有趣的是,在正常卵巢组织样本中PTPγ蛋白90%的表达率在卵巢肿瘤样本的非肿瘤细胞和肿瘤细胞中分别急剧降至44%和38%。通过免疫荧光和RT-PCR测定,HT29人结肠癌细胞系中均不存在PTPγ。总之,我们制备了一种PTPγ特异性单克隆抗体,该抗体表明PTPγ在肺肿瘤和卵巢肿瘤中的表达严重降低(>50%)。