TY - JOUR
T1 - Cell Culture of Nerve Cell and Immune Cell in CO2-Free Environment Based on Microfludic Chip
AU - Chen, Yu
AU - Zhang, Jing
AU - Cen, Junliang
AU - Sun, Feiyi
AU - Chen, Bo
AU - Deng, Yulin
AU - Ma, Hong
N1 - Publisher Copyright:
© 2017, Editorial Department of Transaction of Beijing Institute of Technology. All right reserved.
PY - 2017/6/1
Y1 - 2017/6/1
N2 - Space station is important to space biology and it is difficult to provide CO2 environment, a crucial element to cell culture. Meanwhile, a controllable and automatic method of cell culture is needed to perform the research in space station. Consequently, the establishment of cell culture based on microfluidic chip in a CO2-free environment is extremely important. Firstly, changed the component of medium (Initial pH of the medium was changed, then adding up exogenous CO2 into the medium, finally adding up buffer in culture medium), and performed the cell culture in CO2-free environment (the co-culture of U87 MG and SHSY-5Y and THP-1), then used MTS method to determine the cell viability. Secondly, after adding different proportions of HEPES, performed the cell culture in CO2-free environment, the cell viability was determinated by MTS method. Finally, according to the optimal proportion of HEPES, the cells were cultured in microfluidic chip. It was concluded that in CO2-free environment, cells in microfluidic chip would survive in the medium with 3% HEPES for 5 days.
AB - Space station is important to space biology and it is difficult to provide CO2 environment, a crucial element to cell culture. Meanwhile, a controllable and automatic method of cell culture is needed to perform the research in space station. Consequently, the establishment of cell culture based on microfluidic chip in a CO2-free environment is extremely important. Firstly, changed the component of medium (Initial pH of the medium was changed, then adding up exogenous CO2 into the medium, finally adding up buffer in culture medium), and performed the cell culture in CO2-free environment (the co-culture of U87 MG and SHSY-5Y and THP-1), then used MTS method to determine the cell viability. Secondly, after adding different proportions of HEPES, performed the cell culture in CO2-free environment, the cell viability was determinated by MTS method. Finally, according to the optimal proportion of HEPES, the cells were cultured in microfluidic chip. It was concluded that in CO2-free environment, cells in microfluidic chip would survive in the medium with 3% HEPES for 5 days.
KW - CO-free cell culture
KW - HEPES
KW - MTS
KW - Microfluidic Chip
UR - http://www.scopus.com/inward/record.url?scp=85033678083&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:85033678083
SN - 1001-0645
VL - 37
SP - 23
EP - 28
JO - Beijing Ligong Daxue Xuebao/Transaction of Beijing Institute of Technology
JF - Beijing Ligong Daxue Xuebao/Transaction of Beijing Institute of Technology
ER -