A simple, low cost and reusable microfluidic gradient strategy and its application in modeling cancer invasion

被引:20
作者
Samandari, Mohamadmahdi [1 ,2 ]
Rafiee, Laleh [1 ]
Alipanah, Fatemeh [1 ]
Sanati-Nezhad, Amir [3 ,4 ]
Javanmard, Shaghayegh Haghjooy [1 ]
机构
[1] Isfahan Univ Med Sci, Cardiovasc Res Inst, Appl Physiol Res Ctr, Dept Physiol, Esfahan 8174673461, Iran
[2] Univ Connecticut, Hlth Ctr, Dept Biomed Engn, Farmington, CT 06030 USA
[3] Univ Calgary, Ctr Bioengn Res & Educ, Calgary, AB T2N 1N4, Canada
[4] Univ Calgary, Dept Mech & Mfg Engn, Calgary, AB T2N 1N4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
BREAST-CANCER; CELL-MIGRATION; CULTURE; 3D; CHEMOTAXIS; GENERATION; ANTIGEN; CHIP;
D O I
10.1038/s41598-021-89635-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Microfluidic chemical gradient generators enable precise spatiotemporal control of chemotactic signals to study cellular behavior with high resolution and reliability. However, time and cost consuming preparation steps for cell adhesion in microchannels as well as requirement of pumping facilities usually complicate the application of the microfluidic assays. Here, we introduce a simple strategy for preparation of a reusable and stand-alone microfluidic gradient generator to study cellular behavior. Polydimethylsiloxane (PDMS) is directly mounted on the commercial polystyrene-based cell culture surfaces by manipulating the PDMS curing time to optimize bonding strength. The stand-alone strategy not only offers pumpless application of this microfluidic device but also ensures minimal fluidic pressure and consequently a leakage-free system. Elimination of any surface treatment or coating significantly facilitates the preparation of the microfluidic assay and offers a detachable PDMS microchip which can be reused following to a simple cleaning and sterilization step. The chemotactic signal in our microchip is further characterized using numerical and experimental evaluations and it is demonstrated that the device can generate both linear and polynomial signals. Finally, the feasibility of the strategy in deciphering cellular behavior is demonstrated by exploring cancer cell migration and invasion in response to chemical stimuli. The introduced strategy can significantly decrease the complexity of the microfluidic chemotaxis assays and increase their throughput for various cellular and molecular studies.
引用
收藏
页数:11
相关论文
共 47 条
[1]   A tuneable microfluidic system for long duration chemotaxis experiments in a 3D collagen matrix [J].
Aizel, Koceila ;
Clark, Andrew G. ;
Simon, Anthony ;
Geraldo, Sara ;
Funfak, Anette ;
Vargas, Pablo ;
Bibette, Jerome ;
Vignjevic, Danijela Matic ;
Bremond, Nicolas .
LAB ON A CHIP, 2017, 17 (22) :3851-3861
[2]   OPINION Challenges in circulating tumour cell research [J].
Alix-Panabieres, Catherine ;
Pantel, Klaus .
NATURE REVIEWS CANCER, 2014, 14 (09) :623-631
[3]   The microfluidic palette: A diffusive gradient generator with spatio-temporal control [J].
Atencia, Javier ;
Morrow, Jayne ;
Locascio, Laurie E. .
LAB ON A CHIP, 2009, 9 (18) :2707-2714
[4]   Large-scale microfluidic gradient arrays reveal axon guidance behaviors in hippocampal neurons [J].
Bhattacharjee, Nirveek ;
Folch, Albert .
MICROSYSTEMS & NANOENGINEERING, 2017, 3
[5]   PROTEOLYTIC REMODELING OF EXTRACELLULAR-MATRIX [J].
BIRKEDALHANSEN, H .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (05) :728-735
[7]  
Brandenberg N., 2017, BIOL ENG STEM CELL N, P429, DOI 10.1016/B978-0-12-802734-9.00027-5
[8]  
Bruus H., 2008, Theoretical Microfluidics
[9]   Correlation between nanosecond X-ray flashes and stick-slip friction in peeling tape [J].
Camara, Carlos G. ;
Escobar, Juan V. ;
Hird, Jonathan R. ;
Putterman, Seth J. .
NATURE, 2008, 455 (7216) :1089-U7
[10]   Matrigel coated polydimethylsiloxane based microfluidic devices for studying metastatic and non-metastatic cancer cell invasion and migration [J].
Chaw, K. C. ;
Manimaran, M. ;
Tay, F. E. H. ;
Swaminathan, S. .
BIOMEDICAL MICRODEVICES, 2007, 9 (04) :597-602