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DEAE微载体的离子交换能力决定了培养细胞的生长模式。

Ion exchange capacity of DEAE microcarriers determined the growth pattern of cells in culture.

作者信息

Kotler M, Reuveny S, Mizrahi A, Shahar A

出版信息

Dev Biol Stand. 1985;60:255-61.

PMID:3899787
Abstract

Transformed embryonic avian and mammalian cells, as well as cells from established cell lines grow as a monolayer on DEAE-cellulose based microcarriers (MC): the DE-52 and DE-53 MC. Normal, non-transformed, embryonic avian and mammalian cells do not grow on DE-52 MC (having an exchange capacity of 1 meq/g dry material) but grow well on DE-53 MC (having an exchange capacity of 2 meq/g dry material). On DE-53 MC embryonic non-transformed cells grow in multilayers, while embryonic viral-transformed cells and cells from established cell lines grow in a monolayer form. Possible explanations for the differences in cell growth on various MC and variation in the mode of growth in monolayer vs multilayer are discussed. These differences may serve as a valuable tool for separation and distinction between normal and transformed cells. In addition, the described novel MC culturing system provides a support for tridimensional growth on which cell growth mimics the in vivo growth conditions. Therefore, this system is suitable for the study of cell recognition, cell to cell connection and cell orientation.

摘要

转化的胚胎禽细胞和哺乳动物细胞,以及来自已建立细胞系的细胞,能在基于二乙氨基乙基纤维素(DEAE - 纤维素)的微载体(MC)上形成单层生长,即DE - 52和DE - 53微载体。正常的、未转化的胚胎禽细胞和哺乳动物细胞不在DE - 52微载体(干物质交换容量为1 meq/g)上生长,但能在DE - 53微载体(干物质交换容量为2 meq/g)上良好生长。在DE - 53微载体上,未转化的胚胎细胞呈多层生长,而胚胎病毒转化细胞和来自已建立细胞系的细胞则呈单层生长。文中讨论了不同微载体上细胞生长差异以及单层生长与多层生长模式变化的可能原因。这些差异可能成为区分正常细胞和转化细胞的有价值工具。此外,所描述的新型微载体培养系统为三维生长提供了支持,细胞生长在此系统中模拟体内生长条件。因此,该系统适用于细胞识别、细胞间连接和细胞定向的研究。

相似文献

1
Ion exchange capacity of DEAE microcarriers determined the growth pattern of cells in culture.DEAE微载体的离子交换能力决定了培养细胞的生长模式。
Dev Biol Stand. 1985;60:255-61.
2
Cell and virus propagation on cylindrical cellulose based microcarriers.细胞和病毒在基于圆柱形纤维素的微载体上的增殖。
Dev Biol Stand. 1981;50:115-23.
3
A new cellulose-based microcarrier culturing system.一种新型的基于纤维素的微载体培养系统。
Dev Biol Stand. 1980;46:137-45.
4
Differentiation of myoblasts with nerve cells on microcarriers in culture.培养物中微载体上成肌细胞与神经细胞的分化
Dev Biol Stand. 1985;60:263-8.
5
DE-52 and DE-53 cellulose microcarriers. I. Growth of primary and established anchorage-dependent cells.
In Vitro. 1982 Feb;18(2):92-8. doi: 10.1007/BF02796400.
6
Role of substrata in determining the growth topology of transformed and nontransformed cells in culture.基质在确定培养中转化细胞和未转化细胞生长拓扑结构中的作用。
Cell Biol Int Rep. 1984 Jul;8(7):539-49. doi: 10.1016/0309-1651(84)90053-5.
7
Newly developed microcarrier culturing systems--an overview.新开发的微载体培养系统——综述。
Dev Biol Stand. 1985;60:243-53.
8
Agarose-polyacrolein microsphere beads: a new microcarrier culturing system.琼脂糖-聚丙烯醛微球珠:一种新型微载体培养系统。
Dev Biol Stand. 1985;60:457-65.
9
Utilisation of DEAE-cellulose as a microcarrier material.
Dev Biol Stand. 1980;46:147-9.
10
[Investigation of Soviet microcarriers for cell cultivation].[苏联用于细胞培养的微载体研究]
Tsitologiia. 1986 Apr;28(4):465-9.

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Cytotechnology. 1995 Jan;18(3):193-206. doi: 10.1007/BF00767767.
2
Evaluation of anchorage-dependent cell propagation systems for production of human acetylcholinesterase by recombinant 293 cells.评估用于重组293细胞生产人乙酰胆碱酯酶的锚定依赖性细胞增殖系统。
Cytotechnology. 1993;13(2):115-23. doi: 10.1007/BF00749938.
3
Mammalian cell culture. Patents and literature.哺乳动物细胞培养。专利与文献。
Appl Biochem Biotechnol. 1986 Oct;13(2):167-74. doi: 10.1007/BF02798909.
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Evaluation of a microcarrier process for large-scale cultivation of attenuated hepatitis A.
Cytotechnology. 1992;9(1-3):173-87. doi: 10.1007/BF02521745.