A Portable Live-Cell Imaging System With an Invert-Upright-Convertible Architecture and a Mini-Bioreactor for Long-Term Simultaneous Cell Imaging, Chemical Sensing, and Electrophysiological Recording

被引:15
作者
Rajan, Dhanesh Kattipparambil [1 ,2 ]
Kreutzer, Joose [1 ,2 ]
Valimaki, Hannu [1 ,2 ]
Pekkanen-Mattila, Mari [3 ]
Ahola, Antti [1 ,2 ]
Skogberg, Anne [1 ,2 ]
Aalto-Setala, Katriina [3 ,4 ]
Ihalainen, Heimo [1 ,2 ]
Kallio, Pasi [1 ,2 ]
Lekkala, Jukka [1 ,2 ]
机构
[1] Tampere Univ Technol, BioMediTech Inst, FI-33720 Tampere, Finland
[2] Tampere Univ Technol, Fac Biomed Sci & Engn, FI-33720 Tampere, Finland
[3] Univ Tampere, Fac Med & Life Sci, BioMediTech, FI-33100 Tampere, Finland
[4] Tampere Univ Hosp, Heart Hosp, FI-33521 Tampere, Finland
关键词
Portable compact microscope; label-free long-term live-cell imaging; modular portable microscope for in-situ in-vitro cell imaging; portable cell culture system; portable cell culture and measurement system; low-cost biosensor technology; ON-CHIP MICROSCOPY; A-CHIP; PIXEL SUPERRESOLUTION; DRUG DISCOVERY; CULTURE; ORGANS; INCUBATOR; PLATFORM; TISSUES; FOCUS;
D O I
10.1109/ACCESS.2018.2804378
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Cell culture in-vitro is a well-known method to develop cell and disease models for studying physiologically relevant mechanisms and responses for various applications in life sciences. Conventional methods for instance, using static culture flasks or well plates, have limitations, as these cannot provide accurate tractable models for advanced studies. However, microscale systems can overcome this since they mimic the cells' natural microenvironment adequately. We have developed a portable live-cell imaging system with an invert-upright-convertible architecture and a mini-bioreactor for long-term simultaneous cell imaging and analysis, chemical sensing and electrophysiological recording. Our system integrates biocompatible cell-friendly materials with modular measurement schemes and precise environment control and can be automated. High quality time-lapse cell imaging is hugely useful in cell/disease models. However, integration of advanced in-vitro systems into benchtop microscopes for in-situ imaging is tricky and challenging. This is especially true with device based biological systems, such as lab/organ/body-onchips, or mini-bioreactors/microfluidic systems. They face issues ranging from optical and physical geometry incompatibilities to difficulties in connectivity of flow and perfusion systems. However, the novel modular system we have developed either as an inverted or as an upright system can easily accommodate virtually any in-vitro devices. Furthermore, it can accept additional sensor or measurement devices quite freely. Cell characterization, differentiation, chemical sensing, drug screening, microelectrode-array-electrophysiological recordings, and cell stimulation can be carried out with simultaneous in-situ imaging and analysis. Moreover, our system can be configured to capture images from regions that are otherwise inaccessible by conventional microscopes, for example, cells cultured on physical or biochemical sensor systems. We demonstrate the system for video-based beating analysis of cardiomyocytes, cell orientation analysis on nanocellulose, and simultaneous long-term in-situ microscopy with pO(2) and temperature sensing. The compact microscope as such is comparable to standard phase-contrast-microscopes without any detectable aberrations and is useful practically for any in-situ microscopy demands.
引用
收藏
页码:11063 / 11075
页数:13
相关论文
共 61 条
[1]   Video image-based analysis of single human induced pluripotent stem cell derived cardiomyocyte beating dynamics using digital image correlation [J].
Ahola, Antti ;
Kiviaho, Anna L. ;
Larsson, Kim ;
Honkanen, Markus ;
Aalto-Setala, Katriina ;
Hyttinen, Jari .
BIOMEDICAL ENGINEERING ONLINE, 2014, 13
[2]   In vivo bioluminescence and reflectance imaging of multiple organs in bioluminescence reporter mice by bundled-fiber-coupled microscopy [J].
Ando, Yoriko ;
Sakurai, Takashi ;
Koida, Kowa ;
Tei, Hajime ;
Hida, Akiko ;
Nakao, Kazuki ;
Natsume, Mistuo ;
Numano, Rika .
BIOMEDICAL OPTICS EXPRESS, 2016, 7 (03) :963-978
[3]   Microfluidic organs-on-chips [J].
Bhatia, Sangeeta N. ;
Ingber, Donald E. .
NATURE BIOTECHNOLOGY, 2014, 32 (08) :760-772
[4]   Organ-on-a-chip platforms for studying drug delivery systems [J].
Bhise, Nupura S. ;
Ribas, Joao ;
Manoharan, Vijayan ;
Zhang, Yu Shrike ;
Polini, Alessandro ;
Massa, Solange ;
Dokmeci, Mehmet R. ;
Khademhosseini, Ali .
JOURNAL OF CONTROLLED RELEASE, 2014, 190 :82-93
[5]   Holographic pixel super-resolution in portable lensless on-chip microscopy using a fiber-optic array [J].
Bishara, Waheb ;
Sikora, Uzair ;
Mudanyali, Onur ;
Su, Ting-Wei ;
Yaglidere, Oguzhan ;
Luckhart, Shirley ;
Ozcan, Aydogan .
LAB ON A CHIP, 2011, 11 (07) :1276-1279
[6]   Lensfree on-chip microscopy over a wide field-of-view using pixel super-resolution [J].
Bishara, Waheb ;
Su, Ting-Wei ;
Coskun, Ahmet F. ;
Ozcan, Aydogan .
OPTICS EXPRESS, 2010, 18 (11) :11181-11191
[7]  
David Y., 2010, AFFINE OPTIC FLOW VE
[8]  
E. BioScience, 2016, REAL TIM QUANT LIV C
[9]   Cells on chips [J].
El-Ali, Jamil ;
Sorger, Peter K. ;
Jensen, Klavs F. .
NATURE, 2006, 442 (7101) :403-411
[10]  
Esch MB, 2011, ANNU REV BIOMED ENG, V13, P55, DOI [10.1146/annurev-bioeng-071910-124629, 10.1146/annurev-biocng-071910-124629]