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WI-38细胞在无血清、无生长因子、钙浓度升高的培养基中的生长情况。

The growth of WI-38 cells in a serum-free, growth factor-free, medium with elevated calcium concentrations.

作者信息

Praeger F C, Cristofalo V J

出版信息

In Vitro Cell Dev Biol. 1986 Jun;22(6):355-9. doi: 10.1007/BF02623410.

DOI:10.1007/BF02623410
PMID:3759791
Abstract

The growth of WI-38 cells in serum-free growth medium with and without hormone supplementation in the presence of elevated Ca2+ concentrations was investigated. At 5 mM CaCl2, WI-38 cells seeded at low density without serum or hormone supplementation showed up to a 12-fold increase in cell number at saturation density over that obtained at day 1. Saturation densities were comparable when either 5 mM CaCl2 or epidermal growth factor (1 mM CaCl2) was used in the presence of insulin, dexamethasone and transferrin. Combining suboptimal doses of epidermal growth factor and CaCl2 resulted in an additive effect on saturation density. Thus, normal human diploid cells are capable of substantial growth in serum-free, hormone-free growth medium. In contrast, confluent cultures refed with the same medium are not responsive to elevated Ca2+ concentrations. In fact, elevated Ca2+ concentrations inhibited the proliferative response of confluent cultures to epidermal growth factor, but enhanced their response to the combined treatment of insulin, transferrin and dexamethasone.

摘要

研究了WI-38细胞在添加和不添加激素的无血清生长培养基中,在Ca2+浓度升高的情况下的生长情况。在5 mM CaCl2条件下,低密度接种且不添加血清或激素的WI-38细胞在饱和密度时的细胞数量比第1天增加了12倍。在胰岛素、地塞米松和转铁蛋白存在的情况下,使用5 mM CaCl2或表皮生长因子(1 mM CaCl2)时,饱和密度相当。次优剂量的表皮生长因子和CaCl2联合使用对饱和密度产生累加效应。因此,正常人二倍体细胞能够在无血清、无激素的生长培养基中大量生长。相比之下,用相同培养基重新培养的汇合培养物对升高的Ca2+浓度没有反应。事实上,升高的Ca2+浓度抑制了汇合培养物对表皮生长因子的增殖反应,但增强了它们对胰岛素、转铁蛋白和地塞米松联合处理的反应。

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引用本文的文献

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本文引用的文献

1
Growth regulation of WI38 cells in s serum-free medium.WI38细胞在无血清培养基中的生长调控
Exp Cell Res. 1981 Aug;134(2):297-302. doi: 10.1016/0014-4827(81)90429-8.
2
Growth factor-induced proliferation of human fibroblasts in serum-free culture depends on cell density and extracellular calcium concentration.生长因子诱导的人成纤维细胞在无血清培养中的增殖取决于细胞密度和细胞外钙浓度。
J Cell Physiol. 1984 Feb;118(2):203-10. doi: 10.1002/jcp.1041180213.
3
Progressive loss of the proliferative response of senescing WI-38 cells to platelet-derived growth factor, epidermal growth factor, insulin, transferrin, and dexamethasone.
衰老的WI-38细胞对血小板衍生生长因子、表皮生长因子、胰岛素、转铁蛋白和地塞米松的增殖反应逐渐丧失。
J Gerontol. 1984 Jan;39(1):11-7. doi: 10.1093/geronj/39.1.11.
4
Calcium effects on epidermal growth factor receptor-mediated endocytosis in normal and SV40-transformed human fibroblasts.钙对正常及SV40转化的人成纤维细胞中表皮生长因子受体介导的内吞作用的影响。
J Cell Physiol. 1983 May;115(2):159-66. doi: 10.1002/jcp.1041150209.
5
[125I]EGF binding ability is stable throughout the replicative life-span of WI-38 cells.
J Cell Physiol. 1983 Mar;114(3):311-6. doi: 10.1002/jcp.1041140309.
6
Reversible ultrastructural changes in human fibroblasts grown in hepes buffered MCDB-104 supplemented with human serum.在补充了人血清的Hepes缓冲的MCDB - 104中培养的人成纤维细胞的可逆超微结构变化。
In Vitro. 1981 Nov;17(11):956-64. doi: 10.1007/BF02618420.
7
Epidermal growth factor-induced down-regulation of receptor does not occur in HeLa cells grown in defined medium.在限定培养基中培养的HeLa细胞中,表皮生长因子诱导的受体下调不会发生。
Proc Natl Acad Sci U S A. 1980 May;77(5):2735-9. doi: 10.1073/pnas.77.5.2735.
8
Assay and partial purification of factors from serum that control multiplication of human diploid fibroblasts.检测并部分纯化血清中控制人二倍体成纤维细胞增殖的因子。
Biochem Biophys Res Commun. 1978 Feb 28;80(4):1013-21. doi: 10.1016/0006-291x(78)91346-3.
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Hormonal growth control of cells in culture.培养细胞的激素生长调控。
In Vitro. 1978 Jan;14(1):23-30. doi: 10.1007/BF02618171.
10
Epidermal growth factor modulates extracellular Ca2+ requirement for multiplication of normal human skin fibroblasts.
Exp Cell Res. 1979 Oct 15;123(2):397-400. doi: 10.1016/0014-4827(79)90485-3.