首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Pancreatic carcinomas deposit laminin-5 preferably adhere to laminin-5 and migrate on the newly deposited basement membrane.
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Pancreatic carcinomas deposit laminin-5 preferably adhere to laminin-5 and migrate on the newly deposited basement membrane.

机译:胰腺癌沉积层粘连蛋白5优选粘附在层粘连蛋白5上并在新沉积的基底膜上迁移。

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摘要

We studied the adhesion mechanism of pancreatic carcinoma using in vitro adhesion and migration assays of stable cell lines and tumors grown from these cell lines in nude mice. We also compared the results with the expression profiles of laminins and their receptors in pancreatic carcinomas to evaluate the relevance of these mechanisms in vivo. All of the cell lines preferably adhered to laminin-5, irrespective of their capability to synthesize laminin-5. Cell migration was studied in the presence of hepatocyte growth factor, as it increased the speed of migration manyfold. Herbimycin A treatment and antibodies against the beta 1 and alpha 3 integrin subunits and laminin alpha 3 chain almost entirely blocked cell migration of the BxPC-3 cell line, whereas migration was nearly unaffected by RGD peptide and only moderately inhibited by antibody against the alpha 6 integrin subunit. Indirect immunofluorescence microscopy of wounded BxPC-3 cells suggested a rapid endocytosis of alpha 3 integrin subunit in the cells at the margin of the wound and a rapid, polarized rearrangement of the alpha 6 beta 4 integrin. Especially HGF-treated cultures showed a prominent cytoplasmic reaction for laminin-5 at the margin of the wound. Xenografted cells formed tumors that produced and deposited the same laminin chains as the in vitro cultures. Frozen sections of human pancreatic carcinomas showed reactivity for laminin chains suggestive for expression of laminin-1 and laminin-5. Both xenografted tumors and human pancreatic carcinomas also showed stromal reactivity for laminin-5. Electron microscopy of the human tumors suggested that this was due to an abundant reduplication the basement-membrane-like material around the nests of malignant cells. Our results suggest that pancreatic carcinomas synthesize and deposit laminin-5 in the basement membrane in an abnormal manner. Invading cells adhere to this newly produced basement membrane and migrate on it by using the alpha 3 beta 1 integrin receptor recognizing laminin-5.
机译:我们使用体外细胞黏附和迁移实验研究了胰腺癌的黏附机制,稳定细胞系和裸鼠从这些细胞系中生长的肿瘤均通过体外黏附和迁移分析。我们还将结果与层粘连蛋白及其受体在胰腺癌中的表达谱进行了比较,以评估这些机制在体内的相关性。优选所有细胞系都粘附于层粘连蛋白5,而不管它们合成层粘连蛋白5的能力如何。在存在肝细胞生长因子的情况下研究了细胞迁移,因为它使迁移速度提高了许多倍。除草霉素A处理剂和针对beta 1和alpha 3整联蛋白亚基的抗体以及层粘连蛋白alpha 3链几乎完全阻止了BxPC-3细胞系的细胞迁移,而迁移几乎不受RGD肽的影响,而仅受到针对α6的抗体的中度抑制整联蛋白亚基。受伤的BxPC-3细胞的间接免疫荧光显微镜检查表明,伤口边缘的细胞中α3整联蛋白亚基快速内吞,α6β4整联蛋白快速极化发生重排。特别是HGF处理的培养物在伤口边缘显示了层粘连蛋白5的显着细胞质反应。异种移植的细胞形成了与体外培养物产生并沉积相同层粘连蛋白链的肿瘤。人类胰腺癌的冷冻切片显示对层粘连蛋白链的反应性,提示了层粘连蛋白-1和层粘连蛋白5的表达。异种移植肿瘤和人胰腺癌也都显示层粘连蛋白5的基质反应性。人类肿瘤的电子显微镜表明,这是由于大量复制了恶性细胞巢周围的基底膜样物质。我们的结果表明,胰腺癌以异常的方式合成并在基底膜中沉积层粘连蛋白5。侵入的细胞粘附在这种新产生的基底膜上,并通过使用识别层粘连蛋白5的alpha 3 beta 1整联蛋白受体在其上迁移。

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