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细胞黏附调节剂类似物对黑色素瘤细胞与IV型胶原结合的抑制作用

Inhibition of melanoma cell binding to type IV collagen by analogs of cell adhesion regulator.

作者信息

Lauer J L, Furcht L T, Fields G B

机构信息

Department of Laboratory Medicine, University of Minnesota, Minneapolis 55455, USA.

出版信息

J Med Chem. 1997 Sep 12;40(19):3077-84. doi: 10.1021/jm970206j.

Abstract

Integrin-mediated tumor cell adhesion to type IV collagen is believed to play a role in the invasion of basement membrane proteins and the subsequent metastatic process. The cellular protein CAR (cell adhesion regulator) has been proposed to influence integrin-mediated binding to extracellular matrix proteins, including basement membrane (type IV) collagen. Three analogs of the CAR138-142 have been tested for activity. The first contains the 138-142 sequence (CAR138-142, Val-Glu-Ile-Leu-Tyr-NH2), the second contains the 138-142 sequence with a phosphorylated Tyr [pCAR138-142, Val-Glu-Ile-Leu-Tyr(PO3H2)-NH2], and the third contains the reversed 138-142 sequence (rCAR138-142, Tyr-Leu-Ile-Glu-Val-NH2). When added extracellularly, none of the analogs had a significant affect on cell adhesion to type IV collagen. Using a novel reversible cell permeabilization method, we found that intracellular incorporation of both CAR138-142 and pCAR138-142 resulted in inhibition of cell adhesion in a dose-dependent fashion. The IC50 values were approximately 90 and approximately 10 microM for CAR138-142 and pCAR138-142, respectively. Intracellular incorporation of the rCAR138-142 peptide had no affect on cell adhesion. Fluorescence microscopy of a fluorescein-labeled CAR138-142 peptide revealed that the reversible permeabilization procedure resulted in the peptides crossing the cell membrane. Affinity chromatography of melanoma cell lysates with pCAR138-142 or rCAR138-142 attached to a solid support of magnetic beads suggested that one protein was bound uniquely by pCAR138-142. Immunoprecipitation analysis identified vinculin, a protein associated with the actin cytoskeleton, as the protein specifically bound by pCAR138-142. Immunoprecipitation with pp125FAK- or beta 1-integrin-derived mAbs gave negative results. Our study suggests that a possible therapeutic approach for inhibition of melanoma cell adhesion adhesion to extracellular matrix proteins is the use of CAR peptide analogs intracellularly.

摘要

整合素介导的肿瘤细胞与IV型胶原的黏附被认为在基底膜蛋白的侵袭及随后的转移过程中发挥作用。细胞蛋白CAR(细胞黏附调节剂)被认为会影响整合素介导的与细胞外基质蛋白的结合,包括基底膜(IV型)胶原。已对CAR138 - 142的三种类似物进行了活性测试。第一种包含138 - 142序列(CAR138 - 142,缬氨酸 - 谷氨酸 - 异亮氨酸 - 亮氨酸 - 酪氨酸 - NH2),第二种包含带有磷酸化酪氨酸的138 - 142序列[pCAR138 - 142,缬氨酸 - 谷氨酸 - 异亮氨酸 - 亮氨酸 - 酪氨酸(PO3H2)-NH2],第三种包含反向的138 - 142序列(rCAR138 - 142,酪氨酸 - 亮氨酸 - 异亮氨酸 - 谷氨酸 - 缬氨酸 - NH2)。当在细胞外添加时,这些类似物均对细胞与IV型胶原的黏附无显著影响。使用一种新型的可逆细胞通透化方法,我们发现细胞内导入CAR138 - 142和pCAR138 - 142均导致细胞黏附受到剂量依赖性抑制。CAR138 - 142和pCAR138 - 142的IC50值分别约为90和约10微摩尔。细胞内导入rCAR138 - 142肽对细胞黏附无影响。对荧光素标记的CAR138 - 142肽进行荧光显微镜观察显示,可逆通透化过程导致肽穿过细胞膜。用附着于磁珠固体支持物上的pCAR138 - 142或rCAR138 - 142对黑色素瘤细胞裂解物进行亲和层析表明,一种蛋白质仅被pCAR138 - 142结合。免疫沉淀分析确定纽蛋白,一种与肌动蛋白细胞骨架相关的蛋白质,为被pCAR138 - 142特异性结合的蛋白质。用pp125FAK - 或β1 - 整合素衍生的单克隆抗体进行免疫沉淀得到阴性结果。我们的研究表明,抑制黑色素瘤细胞与细胞外基质蛋白黏附的一种可能的治疗方法是在细胞内使用CAR肽类似物。

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