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Effect of cytokines on the expression of cell adhesion molecule and on the adhesion of melanoma cells to endothelial cells

机译:细胞因子对细胞黏附分子表达和黑素瘤细胞与内皮细胞黏附的影响

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We examined the role of cell adhesion molecules (CAM) by which tumor cells bind to the endothelial cells using human umbilical vein endothelial cells (HUVEC) and cultured melanoma cells. Endothelial cells from human umbilical veins were isolated and examined for CAM expression and its modulation by tumor necrosis factor-alpha (TNF-alpha), interleukin-1 (IL-1), interleukin-6 (IL-6) or interferon-gamma (IFN-gamma). The expression of intercellular adhesion molecule 1 (ICAM-1) on HUVEC was increased by TNF-alpha, IL-1 and IFN-gamma when measured by ELISA or flow cytometric (FACS) analysis. IL-6 did not increase ICAM-1 expression on HUVEC. Two melanoma cell lines, Malme-3M and SK-Mel-28, showed increased expression of ICAM-1 after treatment with TNF-alpha, IL-1 and IFN-gamma in FACS analysis. IFN-gamma induced increased expression of HLA-DR only in SK-Mel-28 melanoma cells, not in Malme-3M melanoma cells. Neither HUVEC nor melanoma cells expressed lymphocyte function-associated antigen 1 (LFA-1) in either the basal (i.e., cytokine untreated) condition or the cytokine treated condition. Melanoma cells showed minimal increment in adhesion to TNF-alpha or IL-1 treated HUVEC than to cytokine untreated HUVEC. HUVEC and melanoma cells did not express LFA-1 and increased ICAM-1 expression by TNF-alpha, IL-1 and IFN-gamma treatment in FACS analysis did not coincide with minimal increase of melanoma cells adhesion to cytokine treated HUVEC. These results suggest that adhesion between melanoma cells and HUVEC is probably mediated by molecular interaction other than ICAM-1/LFA-1.
机译:我们检查了细胞黏附分子(CAM)的作用,使用人类脐静脉内皮细胞(HUVEC)和培养的黑素瘤细胞,肿瘤细胞通过黏附分子(CAM)与内皮细胞结合。分离人脐静脉内皮细胞,并通过肿瘤坏死因子-α(TNF-alpha),白细胞介素-1(IL-1),白细胞介素-6(IL-6)或干扰素-γ( IFN-γ)。通过ELISA或流式细胞术(FACS)分析测量时,TNF-α,IL-1和IFN-γ可增加HUVEC上的细胞间粘附分子1(ICAM-1)的表达。 IL-6不会增加HUVEC上ICAM-1的表达。两种黑色素瘤细胞系Malme-3M和SK-Mel-28在FACS分析中显示用TNF-α,IL-1和IFN-γ处理后,ICAM-1的表达增加。 IFN-γ仅在SK-Mel-28黑色素瘤细胞中诱导HLA-DR的表达增加,而在Malme-3M黑色素瘤细胞中则不诱导。 HUVEC和黑色素瘤细胞均未在基础(即未处理的细胞因子)或细胞因子治疗的条件下表达淋巴细胞功能相关抗原1(LFA-1)。黑色素瘤细胞与TNF-α或IL-1处理的HUVEC的粘附力比对未经细胞因子处理的HUVEC的粘附力最小。 HUVEC和黑色素瘤细胞不表达LFA-1,在FACS分析中通过TNF-α,IL-1和IFN-γ处理增加的ICAM-1表达与黑色素瘤细胞对细胞因子治疗的HUVEC粘附的最小增加不相符。这些结果表明,黑色素瘤细胞与HUVEC之间的粘附可能是由ICAM-1 / LFA-1以外的分子相互作用介导的。

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