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免疫磁珠过滤:一种用于肿瘤细胞分离和增殖的新方法。

Immunobead filtration: a novel approach for the isolation and propagation of tumor cells.

作者信息

Rye P D, Høifødt H K, Overli G E, Fodstad O

机构信息

Department of Tumor Biology, Norwegian Radium Hospital, Oslo, Norway.

出版信息

Am J Pathol. 1997 Jan;150(1):99-106.

Abstract

We have developed a method to facilitate the isolation and expansion of tumor cells from body fluids and tissue biopsies. Antibody-conjugated magnetic beads (immunobeads) were used to isolate tumor cells from blood, bone marrow, ascitic/pleural fluids, and enzyme-digested tissue biopsies. Filtration of the resulting cell suspension through a 20-micron nylon monofilament filter secured to the base of polystyrene 96-well strips purged the bead-rosetting cell fraction of contaminating normal cells and unbound beads. Tumor cells that bound the magnetic beads were retained on the membrane due to their increased size and concentrated into a small area (0.332 cm2), thus maintaining a high cell density. The filters provided a stable and uniform three-dimensional matrix for cell growth, with a total surface area of 1.42 cm2 available for cell attachment. The filters could be easily removed from the base of the 96-well strips to facilitate handling and transfer between culture vessels. Tumor cells grown on the filters could subsequently be harvested using trypsin/EDTA or left in situ for immunostaining with conventional immunohistochemical procedures. Filter-grown cells have shown extended passage in conventional cell culture in six cases. In two of five cases, the orthotopic implantation of confluent filters that contained approximately 10(4) cells/8 x 8 mm filter successfully produced tumors in nude mice after only 4 weeks. Our new approach may be of value in improving the success rate of generating long-term cultures from previously unproductive sources of tumor cells and thus may yield a greater variety of cell lines/strains for the study of malignant disease.

摘要

我们已经开发出一种方法,以促进从体液和组织活检中分离和扩增肿瘤细胞。使用抗体偶联磁珠(免疫磁珠)从血液、骨髓、腹水/胸水以及酶消化的组织活检中分离肿瘤细胞。将所得细胞悬液通过固定在聚苯乙烯96孔板底部的20微米尼龙单丝过滤器进行过滤,可清除与磁珠结合的细胞部分中的污染正常细胞和未结合的磁珠。与磁珠结合的肿瘤细胞因其体积增大而保留在膜上,并浓缩到一个小区域(0.332平方厘米),从而保持高细胞密度。这些过滤器为细胞生长提供了稳定且均匀的三维基质,有1.42平方厘米的总表面积可供细胞附着。过滤器可轻松从96孔板底部移除,便于在培养容器之间进行处理和转移。在过滤器上生长的肿瘤细胞随后可用胰蛋白酶/乙二胺四乙酸进行收获,或留在原位用传统免疫组织化学方法进行免疫染色。在6例中,过滤器上生长的细胞在传统细胞培养中显示出延长的传代。在5例中的2例中,含有约10(4)个细胞/8×8毫米过滤器的汇合过滤器原位植入裸鼠后,仅4周就成功产生了肿瘤。我们的新方法可能有助于提高从以前无法产生肿瘤细胞的来源生成长期培养物的成功率,从而可能产生更多种类的细胞系/菌株用于恶性疾病的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c673/1858507/5f81d7fc931e/amjpathol00025-0099-a.jpg

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