Study of cell-lipid film interaction by measuring heat shock proteins mRNA expression

被引:1
作者
Kishida, A
Matsuyama, T
Nakashima, M
Serizawa, T
Akashi, M
Sugimura, K
机构
[1] Kagoshima Univ, Fac Engn, Dept Bioengn, Kagoshima 8900065, Japan
[2] Kagoshima Univ, Fac Engn, Dept Appl Chem & Chem Engn, Kagoshima 8900065, Japan
关键词
D O I
10.1106/CKH2-73RB-CKJ2-YGAY
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
The adhesion and function of HeLa S3 cells on lipid films were investigated. The function of the cells adhering to lipid films was estimated by HSP 70B and HSP 47 mRNA expression using a reverse transcription-polymerase chain reaction (RT-PCR) analysis. It is apparent that HeLa S3 cells adhere to lipid films as well as tissue culture poly(styrene)(TCPS). HSPs mRNA expression on the lipid film depended on each lipid film. HeLa S3 cells adhered to the lipid films of DPPC, DPPE and DPPS expressed the same level HSPs mRNA as TCPS. High HSPs mRNA expressions were observed in the HeLa S3 cells adhering to films of synthetic lipids. The serum proteins affected the HSPs expression in the case of the synthetic lipids. These results imply that cell-material interactions are not simple and that mRNA expression is a powerful tool in the investigation of cell. function, especially the reaction by weak stimulus such as cell-material contact.
引用
收藏
页码:478 / 488
页数:11
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