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用于人微血管内皮细胞克隆生长且血清含量最低的优化培养基。

Optimized medium for clonal growth of human microvascular endothelial cells with minimal serum.

作者信息

Knedler A, Ham R G

出版信息

In Vitro Cell Dev Biol. 1987 Jul;23(7):481-91. doi: 10.1007/BF02628418.

Abstract

An optimized basal nutrient medium, MCDB 131, has been developed that supports clonal growth of human microvascular endothelial cells (HMVEC) with as little as 0.7% dialyzed fetal bovine serum (dFBS) when also supplemented with 10 ng/ml epidermal growth factor (EGF) and 1 microgram/ml hydrocortisone. An extensive initial survey of available media showed that MCDB 402, a medium optimized for low-serum growth of Swiss 3T3 cells, supported the best clonal growth of HMVEC with 10% dFBS. Quantitative adjustment of the composition of MCDB 402 for improved clonal growth of HMVEC with reduced amounts of dFBS resulted in development of MCDB 131. Although many different adjustments contributed to the optimal properties of MCDB 131 for growth of HMVEC, the most unusual feature of this medium is its high magnesium concentration. A major benefit was achieved by increasing Mg2+ from 0.8 mM in MCDB 402 to 10.0 mM in MCDB 131. In the absence of defined supplements, MCDB 131 supports good clonal growth of HMVEC with 2% dFBS. This can be reduced to 0.7% by adding EGF and hydrocortisone, which act synergistically to improve growth with low levels of dFBS.

摘要

一种优化的基础培养基MCDB 131已被开发出来,当补充10 ng/ml表皮生长因子(EGF)和1 μg/ml氢化可的松时,该培养基仅需0.7%的透析胎牛血清(dFBS)就能支持人微血管内皮细胞(HMVEC)的克隆生长。对现有培养基进行的广泛初步调查表明,MCDB 402这种为瑞士3T3细胞低血清生长优化的培养基,在添加10% dFBS时能支持HMVEC的最佳克隆生长。对MCDB 402的成分进行定量调整以在减少dFBS用量的情况下改善HMVEC的克隆生长,从而开发出了MCDB 131。尽管许多不同的调整都促成了MCDB 131对HMVEC生长的最佳特性,但该培养基最不寻常的特点是其高镁浓度。通过将MCDB 402中的Mg2+从0.8 mM提高到MCDB 131中的10.0 mM,取得了一个主要的益处。在没有特定补充剂的情况下,MCDB 131能支持HMVEC在2% dFBS的条件下进行良好的克隆生长。通过添加EGF和氢化可的松,这一比例可降至0.7%,它们协同作用以在低水平dFBS条件下改善生长。

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