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血清源性α2巨球蛋白在培养细胞中的定位及莫洛尼肉瘤病毒转化后的减少

Localization of serum-derived alpha 2 macroglobulin in cultured cells and decrease after Moloney sarcoma virus transformation.

作者信息

Pastan I, Willingham M, Anderson W, Gallo M

出版信息

Cell. 1977 Nov;12(3):609-17. doi: 10.1016/0092-8674(77)90261-6.

Abstract

NRK cells and many other cultured fibroblasts were found to contain the protease inhibitor, alpha 2 macroglobulin (alpha 2M). This alpha 2M is present as a result of uptake of alpha 2M from the calf serum in the culture medium. Some of this alpha 2M is released back into the medium. In radiolabeling experiments with 14C-amino acids, no radioactivity was detected in intracellular or extracellular alpha 2M. Fluorescence microscopy of fixed cells using rhodamine-labeled antibodies indicated that alpha 2M is present in vesicular organelles different from primary lysosomes. Fluorescence microscopy of living cells shows that rhodamine-labeled alpha 2M (rhodamine-alpha 2M) is taken up into similar structures. Of the many cell lines examined, Moloney sarcoma virus-transformed cells had the lowest amounts of alpha 2M. Some of the effects of serum on the behavior of cultured cells could be a consequence of inhibition of cellular proteases by alpha 2M.

摘要

研究发现,NRK细胞和许多其他培养的成纤维细胞含有蛋白酶抑制剂α2巨球蛋白(α2M)。这种α2M是由于从培养基中的小牛血清摄取α2M而存在的。其中一些α2M会释放回培养基中。在用14C -氨基酸进行的放射性标记实验中,在细胞内或细胞外的α2M中均未检测到放射性。使用罗丹明标记抗体对固定细胞进行荧光显微镜检查表明,α2M存在于与初级溶酶体不同的囊泡细胞器中。对活细胞进行荧光显微镜检查显示,罗丹明标记的α2M(罗丹明-α2M)被摄取到类似的结构中。在所检测的众多细胞系中,莫洛尼肉瘤病毒转化的细胞中α2M的含量最低。血清对培养细胞行为的一些影响可能是α2M抑制细胞蛋白酶的结果。

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