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从培养基和血清中去除痕量金属用于体外缺乏研究。

Removal of trace metals from culture media and sera for in vitro deficiency studies.

作者信息

Messer H H, Murray E J, Goebel N K

出版信息

J Nutr. 1982 Apr;112(4):652-7. doi: 10.1093/jn/112.4.652.

Abstract

Culture media and sera contain substantial quantities of trace metals such as zinc and copper, so that they cannot be used for cell culture studies of trace metal deficiencies unless the element in question is first removed. By coupling the chelator iminodiacetate to an insoluble agarose matrix, we have been able to extract zinc selectively from both media and sera, without exposing cells directly to the chelator. The procedure reduced the zinc concentration of media to unmeasurably low levels, and serum zinc concentration by approximately 90%. The development of zinc deficiency in vitro was demonstrated by a reduced lymphocyte blastogenic response, which could be prevented by the addition of zinc to the extracted culture medium. The extraction procedure is potentially applicable to a range of trace elements (e.g., Zn, Cu, Mn, Fe) and to virtually any cell type that can be cultured.

摘要

培养基和血清含有大量的痕量金属,如锌和铜,因此除非首先去除相关元素,否则它们不能用于痕量金属缺乏的细胞培养研究。通过将螯合剂亚氨基二乙酸与不溶性琼脂糖基质偶联,我们能够从培养基和血清中选择性地提取锌,而无需将细胞直接暴露于螯合剂。该方法将培养基中的锌浓度降低到无法测量的低水平,血清锌浓度降低了约90%。体外锌缺乏的发展通过淋巴细胞增殖反应降低得到证明,向提取的培养基中添加锌可以预防这种情况。该提取方法可能适用于一系列痕量元素(如锌、铜、锰、铁)以及几乎任何可培养的细胞类型。

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