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CD30抗原的双重作用:抗CD30抗体诱导Ki-1淋巴瘤细胞凋亡并分泌白细胞介素-8

Dual action of CD30 antigen: anti-CD30 antibody induced apoptosis and interleukin-8 secretion in Ki-1 lymphoma cells.

作者信息

Masuda M, Ishida C, Arai Y, Okamura T, Ohsawa M, Shimakage M, Mizoguchi H

机构信息

Department of Hematology, Tokyo Women's Medical College, Japan.

出版信息

Int J Hematol. 1998 Apr;67(3):257-65. doi: 10.1016/s0925-5710(98)00006-1.

Abstract

CD30 is a member of the tumor necrosis factor superfamily. In this study, we examined the effect of four anti-CD30 (aCD30) antibodies (Abs) on CD30-positive anaplastic large cell lymphoma-derived cell line, Ki-JK. The aCD30 Abs suppressed [3H]thymidine (TdR) incorporation. With a TdT mediated dUTP-biotin nick end labeling method, apoptosis was detected in Ki-JK cells at day 5 after the addition of aCD30 Ab to the culture. Genistein, an inhibitor of protein tyrosine kinase, had no effect on aCD30 Ab-induced apoptosis. The aCD30 Ab simultaneously induced interleukin-8 (IL-8) secretion in the Ki-JK cells. In culture of the Ki-JK cells with aCD30 Ab for 5 days, the IL-8 concentration of the cell free-supernatant increased to 240 +/- 16 pg/ml, though the concentration was < 12.5 pg/ml without aCD30 Ab. In combination with aCD30 Ab, genistein decreased the concentration of IL-8 in day 5 supernatants. Although, doxorubicin and herbimycin-A suppressed [3H]TdR incorporation and induced apoptosis in the Ki-JK cells, they did not induce IL-8 secretion. Only aCD30 Ab-induced apoptosis was accompanied by IL-8 secretion. IL-8 mRNA was not detected in the Ki-JK cells by reverse transcription-polymerase chain reaction assay. IL-8 mRNA was detected 5 days after adding aCD30 Ab to the culture.

摘要

CD30是肿瘤坏死因子超家族的一员。在本研究中,我们检测了四种抗CD30(aCD30)抗体对CD30阳性间变性大细胞淋巴瘤衍生细胞系Ki-JK的作用。aCD30抗体抑制了[3H]胸腺嘧啶核苷(TdR)的掺入。采用TdT介导的dUTP生物素缺口末端标记法,在向培养物中添加aCD30抗体后第5天,在Ki-JK细胞中检测到凋亡。蛋白酪氨酸激酶抑制剂染料木黄酮对aCD30抗体诱导的凋亡没有影响。aCD30抗体同时诱导Ki-JK细胞分泌白细胞介素-8(IL-8)。在用aCD30抗体培养Ki-JK细胞5天时,无细胞上清液中的IL-8浓度增加到240±16 pg/ml,而在无aCD30抗体时该浓度<12.5 pg/ml。与aCD30抗体联合使用时,染料木黄酮降低了第5天上清液中IL-8的浓度。虽然阿霉素和除草霉素A抑制了Ki-JK细胞中[3H]TdR的掺入并诱导了凋亡,但它们没有诱导IL-8分泌。只有aCD30抗体诱导的凋亡伴有IL-8分泌。通过逆转录-聚合酶链反应分析在Ki-JK细胞中未检测到IL-8 mRNA。在向培养物中添加aCD30抗体5天后检测到IL-8 mRNA。

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