Highly integrated microfluidic device for cell pairing, fusion and culture

被引:21
作者
He, Weihua [1 ]
Huang, Liang [2 ]
Feng, Yongxiang [1 ]
Liang, Fei [1 ]
Ding, Wei [1 ]
Wang, Wenhui [1 ]
机构
[1] Tsinghua Univ, Dept Precis Instrument, State Key Lab Precis Measurement Technol & Instru, Beijing 100084, Peoples R China
[2] Hefei Univ Technol, Sch Instrument Sci & Optoelect Engn, Hefei 230009, Anhui, Peoples R China
来源
BIOMICROFLUIDICS | 2019年 / 13卷 / 05期
关键词
ELECTROFUSION PARAMETERS; OPTIMIZATION; HYBRIDOMA; ANTIBODY; GLYCOL; PEG;
D O I
10.1063/1.5124705
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we proposed a microfluidic device with compact structures integrating multiple modalities for cell capture, pairing, fusion, and culture. The microfluidic device is composed of upper and lower parts. The lower part configured with electrodes and capture wells is used for cell trapping/pairing/fusion, while the upper part configured with corresponding culture wells is used for cell culture. Dielectrophoresis is used to enable accurate cell trapping and pairing in capture wells. Moreover, the paired cells are fused flexibly by either electrical pulses or polyethylene glycol (PEG) buffer. The fused cells are then transferred to culture wells for on-chip culture simply by flipping the device. Using the device and HeLa cells, we demonstrated pairing efficiency of similar to 78% and fusion efficiencies of similar to 26% for electrical fusion or similar to 21% for PEG fusion, and successful cell proliferation and migration after 72 h on-chip culture. We believe that this multifunction-integrated but structure-simplified microfluidic device would largely facilitate cell fusion oriented tasks.
引用
收藏
页数:8
相关论文
共 46 条
  • [1] Protoplast fusion in banana (Musa spp.):: Comparison of chemical (PEG: Polyethylene glycol) and electrical procedure
    Assani, A
    Chabane, D
    Haïcour, R
    Bakry, F
    Wenzel, G
    Foroughi-Wehr, B
    [J]. PLANT CELL TISSUE AND ORGAN CULTURE, 2005, 83 (02) : 145 - 151
  • [2] Giant cell formation and function
    Brodbeck, William G.
    Anderson, James M.
    [J]. CURRENT OPINION IN HEMATOLOGY, 2009, 16 (01) : 53 - 57
  • [3] Nuclear reprogramming of somatic cells after fusion with human embryonic stem cells
    Cowan, CA
    Atienza, J
    Melton, DA
    Eggan, K
    [J]. SCIENCE, 2005, 309 (5739) : 1369 - 1373
  • [4] Dura B, 2015, METHODS MOL BIOL, P73, DOI 10.1007/978-1-4939-2703-6_5
  • [5] Deformability-based microfluidic cell pairing and fusion
    Dura, Burak
    Liu, Yaoping
    Voldman, Joel
    [J]. LAB ON A CHIP, 2014, 14 (15) : 2783 - 2790
  • [6] Triggering and visualizing the aggregation and fusion of lipid membranes in microfluidic chambers
    Estes, Daniel J.
    Lopez, Santiago R.
    Fuller, A. Oveta
    Mayer, Michael
    [J]. BIOPHYSICAL JOURNAL, 2006, 91 (01) : 233 - 243
  • [7] TEMPERATURE-DEPENDENCE OF CELL-CELL FUSION INDUCED BY THE ENVELOPE GLYCOPROTEIN OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1
    FREY, S
    MARSH, M
    GUNTHER, S
    PELCHENMATTHEWS, A
    STEPHENS, P
    ORTLEPP, S
    STEGMANN, T
    [J]. JOURNAL OF VIROLOGY, 1995, 69 (03) : 1462 - 1472
  • [8] Cell fusion: from hybridoma to dendritic cell-based vaccine
    Gong, Jianlin
    Koida, Shigeo
    Calderwood, Stuart K.
    [J]. EXPERT REVIEW OF VACCINES, 2008, 7 (07) : 1055 - 1068
  • [9] Guo WW, 1998, ACTA BOT SIN, V40, P417
  • [10] Nuclear Reprogramming in Cells
    Gurdon, J. B.
    Melton, D. A.
    [J]. SCIENCE, 2008, 322 (5909) : 1811 - 1815