Gorelik E, Duty L, Anaraki F, Galili U
Pittsburgh Cancer Institute, University of Pittsburgh, Pennsylvania 15213, USA.
Cancer Res. 1995 Sep 15;55(18):4168-73.
Three melanomas of C57BL/6 mice (BL6, JB/MS, and JB/RH) share several phenotypic properties. All these cells contain melanoma-specific ecotropic C-type retrovirus that encodes melanoma-associated antigen recognizable by MM2-9B6 mAb. They do not express H-2Kb molecules, and the alpha-galactosyl epitopes (Gal alpha 1-3Gal beta 1-4GlcNAc-R) they fail to react with soybean agglutinin (SBA), peanut agglutinin (PNA), and vicia villosa (VV) lectins. Previously, we found that failure of BL6 melanoma cells to express alpha-galactosyl epitopes is due to down-regulation of alpha 1,3 galactosyltransferase (alpha 1,3GT) gene expression. To evaluate the possible role of alpha-galactosyl cell membrane carbohydrates in regulation of metastatic properties, individual clones isolated from BL6, JB/MS, and JB/RH melanomas were transfected with alpha 1,3GT cDNA. This resulted in appearance of alpha-galactosyl epitopes, as well as of carbohydrates reacting with SBA, PNA, or VV lectins, but did not affect expression of H-2 class I molecules or melanoma-associated antigen. Appearance of SBA, PNA, and VV lectin binding carbohydrates in the alpha 1,3GT gene-transfected melanoma cells is a result of reduction of cell membrane sialylation and unmasking of these carbohydrates. Reduction in cell membrane sialylation in the alpha 1,3GT gene-transfected melanoma cells is probably due to the competition between alpha 1,3GT with alpha 2,3 sialyltransferase or alha 2,6 sialyltransferase for the common acceptor N-acetyllactosamine in the Golgi apparatus. As a result of this competition, cell membranes of alpha 1,3GT gene-transfected melanoma cells became galactosylated and less sialylated. In parallel with alteration of cell membrane carbohydrates, transfection of the alpha 1,3GT gene leads to the loss of metastatic properties of the transfected melanoma cells in the immunocompetent and immunosuppressed C57BL/6 mice. Thus, the use of specific glycosyltransferase cDNA transfection presents direct experimental confirmation of the importance of cell membrane carbohydrates in the regulation of metastatic properties of tumor cells.
C57BL/6小鼠的三种黑色素瘤(BL6、JB/MS和JB/RH)具有若干表型特性。所有这些细胞都含有黑色素瘤特异性嗜亲性C型逆转录病毒,该病毒编码可被MM2 - 9B6单克隆抗体识别的黑色素瘤相关抗原。它们不表达H - 2Kb分子,其α - 半乳糖基表位(Galα1 - 3Galβ1 - 4GlcNAc - R)不能与大豆凝集素(SBA)、花生凝集素(PNA)和绒毛豌豆(VV)凝集素发生反应。此前,我们发现BL6黑色素瘤细胞未能表达α - 半乳糖基表位是由于α1,3半乳糖基转移酶(α1,3GT)基因表达下调。为了评估α - 半乳糖基细胞膜碳水化合物在转移特性调节中的可能作用,从BL6、JB/MS和JB/RH黑色素瘤中分离出的单个克隆用α1,3GT cDNA进行转染。这导致了α - 半乳糖基表位以及与SBA、PNA或VV凝集素发生反应的碳水化合物的出现,但不影响H - 2 I类分子或黑色素瘤相关抗原的表达。α1,3GT基因转染的黑色素瘤细胞中出现SBA、PNA和VV凝集素结合碳水化合物是细胞膜唾液酸化减少以及这些碳水化合物暴露的结果。α1,3GT基因转染的黑色素瘤细胞中细胞膜唾液酸化的减少可能是由于α1,3GT与α2,3唾液酸转移酶或α2,6唾液酸转移酶在高尔基体中对共同受体N - 乙酰乳糖胺的竞争。由于这种竞争,α1,3GT基因转染的黑色素瘤细胞的细胞膜变得半乳糖基化且唾液酸化程度降低。与细胞膜碳水化合物的改变同时发生的是,α1,3GT基因的转染导致转染的黑色素瘤细胞在免疫活性和免疫抑制的C57BL/6小鼠中失去转移特性。因此,使用特异性糖基转移酶cDNA转染直接实验证实了细胞膜碳水化合物在肿瘤细胞转移特性调节中的重要性。