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用于人外周淋巴细胞生长的化学成分明确的无血清无蛋白培养基的研制。

Development of a chemically defined serum- and protein-free medium for growth of human peripheral lymphocytes.

作者信息

Shive W, Pinkerton F, Humphreys J, Johnson M M, Hamilton W G, Matthews K S

出版信息

Proc Natl Acad Sci U S A. 1986 Jan;83(1):9-13. doi: 10.1073/pnas.83.1.9.

Abstract

A chemically defined, protein-free medium (designated CFBI 1000, where CFBI = Clayton Foundation Biochemical Institute) that supports human peripheral lymphocyte proliferation has been developed. This medium allows exploration of individual metabolic differences by varying the medium composition as well as providing a base to explore further the mechanisms of lymphocyte activation in a system initially free of added macromolecular species other than mitogen. The peripheral blood lymphocyte is an ideal system for metabolic studies because it is easily obtained, is a primary resting cell that can be activated to proliferate, and presumably reflects both the genetic makeup and biochemical environmental history of the individual at the time the cells were formed. Examination of the role of various factors in lymphocyte activation and subsequent events may be simplified by the utilization of a medium that is protein-free and chemically defined. The CFBI 1000 medium supports the growth response of human peripheral lymphocytes to mitogen as measured by [3H]thymidine incorporation to an extent comparable to other media used widely in assessment of lymphocyte proliferation.

摘要

一种化学成分明确的无蛋白培养基(命名为CFBI 1000,其中CFBI代表克莱顿基金会生物化学研究所)已被开发出来,该培养基能够支持人外周血淋巴细胞增殖。这种培养基通过改变培养基成分,使得探索个体代谢差异成为可能,同时也为在最初除促有丝分裂原外无添加大分子物质的系统中进一步探索淋巴细胞激活机制提供了基础。外周血淋巴细胞是代谢研究的理想系统,因为它易于获取,是一种可被激活而增殖的原初静止细胞,并且大概反映了细胞形成时个体的基因组成和生化环境历史。利用一种无蛋白且化学成分明确的培养基,对各种因素在淋巴细胞激活及后续事件中的作用进行研究或许会变得更为简便。CFBI 1000培养基支持人外周血淋巴细胞对促有丝分裂原的生长反应,通过[³H]胸腺嘧啶核苷掺入法测定,其程度与广泛用于评估淋巴细胞增殖的其他培养基相当。

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