SPR Imaging Sensor for Visualization of Individual Cell Activation and Clinical Diagnosis of Allergy

Author(s):  
Y. Yanase ◽  
T. Kawaguchi ◽  
K. Ishii ◽  
M. Hide
2013 ◽  
Vol 62 (2) ◽  
pp. 163-169 ◽  
Author(s):  
Yuhki Yanase ◽  
Takaaki Hiragun ◽  
Tetsuji Yanase ◽  
Tomoko Kawaguchi ◽  
Kaori Ishii ◽  
...  

2014 ◽  
Vol 2 ◽  
pp. 43-48 ◽  
Author(s):  
Yuhki Yanase ◽  
Takaaki Hiragun ◽  
Tetsuji Yanase ◽  
Tomoko Kawaguchi ◽  
Kaori Ishii ◽  
...  

2007 ◽  
Vol 19 (5) ◽  
pp. 519-523 ◽  
Author(s):  
Masayasu Suzuki ◽  
◽  
Toyohiro Ohshima ◽  
Shintaro Hane ◽  
Yasunori Iribe ◽  
...  

Evaluating cell activity and functions in different-sized cell chambers requires multiscale sensing. We have been developing multiscale biosensing applied from 10 µm to 1 mm. We measured mouse IgG in micro wells using a high-resolution two-dimensional surface plasmon resonance (SPR) imaging affinity sensor. This sensor uses high refractive optics, a 1X to 7X microscopic lens, and a cooled CCD camera. The micro-well array was prepared with a PDMS film on gold sensor film. Protein A immobilized on sensor film was used for IgG recognition. SPR sensitivity was dramatically decreased with 10 and 8.5 µm microwells. To improve sensor sensitivity, we optimized the sensor’s measurement angle and exposure time, enabling mouse IgG to be detected in wells of 1 mm, 30 µm, and 10 µm using the same 2D-SPR imaging sensor and measurement protocol. These results show the feasibility of multiscale biosensing use in antibody production in a micro well or a cell chamber.


2019 ◽  
Vol 58 (25) ◽  
pp. 6942
Author(s):  
Shuang Liang ◽  
Chen Cai ◽  
Ran Gao ◽  
Mengying Zhang ◽  
Ning Xue ◽  
...  

Sensors ◽  
2019 ◽  
Vol 19 (9) ◽  
pp. 2067 ◽  
Author(s):  
Yuhki Yanase ◽  
Kyohei Yoshizaki ◽  
Kaiken Kimura ◽  
Tomoko Kawaguchi ◽  
Michihiro Hide ◽  
...  

Label-free evaluation and monitoring of living cell conditions or functions by means of chemical and/or physical sensors in a real-time manner are increasingly desired in the field of basic research of cells and clinical diagnosis. In order to perform multi-parametric analysis of living cells on a chip, we here developed a surface plasmon resonance (SPR) imaging (SPRI)-impedance sensor that can detect both refractive index (RI) and impedance changes on a sensor chip with comb-shaped electrodes. We then investigated the potential of the sensor for label-free and real-time analysis of living cell reactions in response to stimuli. We cultured rat basophilic leukemia (RBL)-2H3 cells on the sensor chip, which was a glass slide coated with comb-shaped electrodes, and detected activation of RBL-2H3 cells, such as degranulation and morphological changes, in response to a dinitro-phenol-conjugated human serum albumin (DNP-HSA) antigen. Moreover, impedance analysis revealed that the changes of impedance derived from RBL-2H3 cell activation appeared in the range of 1 kHz–1 MHz. Furthermore, we monitored living cell-derived RI and impedance changes simultaneously on a sensor chip using the SPRI-impedance sensor. Thus, we developed a new technique to monitor both impedance and RI derived from living cells by using a comb-shaped electrode sensor chip. This technique may enable us to clarify complex living cell functions which affect the RI and impedance and apply this to medical applications, such as accurate clinical diagnosis of type I allergy.


2016 ◽  
Vol 680 ◽  
pp. 012031
Author(s):  
Bing Zhang ◽  
Kai Pang ◽  
Chunfei Shi ◽  
Yi Sun ◽  
Wei Dong ◽  
...  
Keyword(s):  

2021 ◽  
Vol 121 ◽  
pp. 111484
Author(s):  
Maneesh Kumar Singh ◽  
Vipin Kumar Verma ◽  
Sarika Pal ◽  
Yogendra Kumar Prajapati ◽  
J.P. Saini

1989 ◽  
Vol 256 (4) ◽  
pp. F590-F595
Author(s):  
W. A. Kachadorian ◽  
J. Muller ◽  
V. A. DiScala

The hydrosmotic response of toad bladder to antidiuretic hormone (ADH) is quantitatively linked to the induced fusion of aggrephores with, and the appearance of aggregates of tightly packed intramembrane particles in the luminal membrane of granular cells. We used these morphological indexes of hormonally induced cell activation 1) to assess the variability of individual cell responsiveness to a maximally stimulating concentration of ADH and 2) to compare cell response patterns in paired tissues where the extent of whole tissue stimulation, as evidenced by transtissue water flow, was either maximal or submaximal. The results indicate that individual cell responsiveness within the same tissue to standardized maximal ADH treatment varies between two- and sevenfold, depending on the morphological endpoint measured. Furthermore, based on skewness in endpoint distribution, this variability appears to reflect inherent heterogeneity of granular cell reactivity to hormone. In relation to proportional tissue responses elicited by different stimulating concentrations of ADH, our observations of luminal membrane aggregate incidence suggest that the responding cells, whatever their sensitivity, participate in a graded, rather than "all-or-none," "on-off" manner.


2016 ◽  
Author(s):  
Y. Yanase ◽  
T. Kawaguchi ◽  
K. Sakamoto ◽  
M. Hide

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