Cell Damage Evaluation of Thermal Inkjet Printed Chinese Hamster Ovary Cells

被引:273
作者
Cui, Xiaofeng [1 ,2 ]
Dean, Delphine [1 ]
Ruggeri, Zaverio M. [2 ]
Boland, Thomas [1 ,3 ]
机构
[1] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
[2] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[3] Univ Texas El Paso, Dept Met & Mat Engn, El Paso, TX 79968 USA
基金
美国国家科学基金会;
关键词
inkjet printing; apoptosis; cell membrane; gene delivery; Chinese hamster ovary cells; EXPRESSION; PRINTHEAD;
D O I
10.1002/bit.22762
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 ; 0836 ; 090102 ; 100705 ;
摘要
Thermal inkjet printing technology has been applied successfully to cell printing. However, there are concerns that printing process may cause cell damages or death. We conducted a comprehensive study of thermal inkjet printed Chinese hamster ovary (CHO) cells by evaluating cell viability and apoptosis, and possible cell membrane damages. Additionally, we studied the cell concentration of bio-ink and found optimum printing of concentrations around 8 million cells per mL. Printed cell viability was 89% and only 3.5% apoptotic cells were observed after printing. Transient pores were developed in the cell membrane of printed cells. Cells were able to repair these pores within 2 h after printing. Green fluorescent protein (GFP) DNA plasmids were delivered to CHO-S cells by co-printing. The transfection efficiency is above 30%. We conclude that thermal inkjet printing technology can be used for precise cell seeding with minor effects and damages to the printed mammalian cells. The printing process causes transient pores. in cell membranes, a process which has promising applications for gene and Mactopartides delivery to induce the biocompatibility or growth of engineered tissues. Biotechnol. Bioeng. 2010;106: 963-969. (C) 2010 Wiley Periodicals, Inc.
引用
收藏
页码:963 / 969
页数:7
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