Highly parallel introduction of nucleic acids into mammalian cells grown in microwell arrays

被引:20
作者
Jain, Tilak [1 ]
McBride, Ryan [2 ]
Head, Steven [2 ]
Saez, Enrique [1 ]
机构
[1] Scripps Res Inst, Dept Physiol Chem, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, DNA Array Core, La Jolla, CA 92037 USA
关键词
RNA INTERFERENCE; MICROARRAYS; ELECTROPORATION; TRANSFECTION; GENOME; CHIP; DNA;
D O I
10.1039/b913794g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High-throughput cell-based screens of genome-size collections of cDNAs and siRNAs have become a powerful tool to annotate the mammalian genome, enabling the discovery of novel genes associated with normal cellular processes and pathogenic states, and the unravelling of genetic networks and signaling pathways in a systems biology approach. However, the capital expenses and the cost of reagents necessary to perform such large screens have limited application of this technology. Efforts to miniaturize the screening process have centered on the development of cellular microarrays created on microscope slides that use chemical means to introduce exogenous genetic material into mammalian cells. While this work has demonstrated the feasibility of screening in very small formats, the use of chemical transfection reagents (effective only in a subset of cell lines and not on primary cells) and the lack of defined borders between cells grown in adjacent microspots containing different genetic material (to prevent cell migration and to aid spot location recognition during imaging and phenotype deconvolution) have hampered the spread of this screening technology. Here, we describe proof-of-principles experiments to circumvent these drawbacks. We have created microwell arrays on an electroporation-ready transparent substrate and established procedures to achieve highly efficient parallel introduction of exogenous molecules into human cell lines and primary mouse macrophages. The microwells confine cells and offer multiple advantages during imaging and phenotype analysis. We have also developed a simple method to load this 484-microwell array with libraries of nucleic acids using a standard microarrayer. These advances can be elaborated upon to form the basis of a miniaturized high-throughput functional genomics screening platform to carry out genome-size screens in a variety of mammalian cells that may eventually become a mainstream tool for life science research.
引用
收藏
页码:3557 / 3566
页数:10
相关论文
共 22 条
[1]   Identification of the tyrosine phosphatase PTP-MEG2 as an antagonist of hepatic insulin signaling [J].
Cho, Charles Y. ;
Koo, Seung-Hoi ;
Wang, Yan ;
Callaway, Scott ;
Hedrick, Susan ;
Mak, Puiying A. ;
Orth, Anthony P. ;
Peters, Eric C. ;
Saez, Enrique ;
Montminy, Marc ;
Schultz, Peter G. ;
Chanda, Surnit K. .
CELL METABOLISM, 2006, 3 (05) :367-378
[2]   Finishing the euchromatic sequence of the human genome [J].
Collins, FS ;
Lander, ES ;
Rogers, J ;
Waterston, RH .
NATURE, 2004, 431 (7011) :931-945
[3]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498
[4]   Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811
[5]   Unlocking the potential of the human genome with RNA interference [J].
Hannon, GJ ;
Rossi, JJ .
NATURE, 2004, 431 (7006) :371-378
[6]   Bio-chip for spatially controlled transfection of nucleic acid payloads into cells in a culture [J].
Jain, Tilak ;
Muthuswamy, Jit .
LAB ON A CHIP, 2007, 7 (08) :1004-1011
[7]   Transfection microarray of nonadherent cells on an oleyl poly(ethylene glycol) ether-modified glass slide [J].
Kato, K ;
Umezawa, K ;
Miyake, M ;
Miyake, J ;
Nagamune, T .
BIOTECHNIQUES, 2004, 37 (03) :444-+
[8]   Microscale electroporation: challenges and perspectives for clinical applications [J].
Lee, Won Gu ;
Demirci, Utkan ;
Khademhosseini, Ali .
INTEGRATIVE BIOLOGY, 2009, 1 (03) :242-251
[9]   5,000 RNAi experiments on a chip [J].
Lehner, B ;
Fraser, AG .
NATURE METHODS, 2004, 1 (02) :103-104
[10]   A microwell array system for stem cell culture [J].
Moeller, Hannes-Christian ;
Mian, Matthew K. ;
Shrivastava, Shamit ;
Chung, Bong Geun ;
Khademhosseini, Ali .
BIOMATERIALS, 2008, 29 (06) :752-763