In Situ Formation of Microgel Array Via Patterned Electrospun Nanofibers Promotes 3D Cell Culture and Drug Testing in a Microphysiological System

Author(s):  
Minhua Liang ◽  
Fan Lei ◽  
Yang Liu ◽  
Dongxu Lan ◽  
Hanhao Huang ◽  
...  
2020 ◽  
Vol 31 (6) ◽  
pp. 762-780 ◽  
Author(s):  
Zhiping Fan ◽  
Ping Cheng ◽  
Gaowei Yin ◽  
Zhengping Wang ◽  
Jun Han

2020 ◽  
Author(s):  
Cheng-Guang Wu ◽  
Francesca Chiovaro ◽  
Alessandra Curioni ◽  
Ruben Casanova ◽  
Alex Soltermann

Abstract Background Malignant serous effusion (MSE) denotes a manifestation of metastatic disease with typical high concentrations of both cancer and immune cells, making them an ideal resource for in vitro cytologic studies. Hence, the aim of the study was to investigate the features of 2D and 3D MSE culture systems as well as their feasibilities for in vitro drug screening. Methods Pleural and peritoneal effusions from 8 patients were collected and processed for 2D monolayer and 3D hanging drop cell culture into GravityPLUS™ plates. Representative markers for cell components, proliferation rate and tumour classification were investigated by immunohistochemistry, followed by absolute quantification using a digitalised image analysis approach. Further, we implemented another 3D cell culture model based on a low attachment method for in vitro drug sensitivity testing of carboplatin, pemetrexed and pembrolizumab for 5 patients. Results Monolayer cell culture was favourable for the growth of mesothelial cells, while hanging drop culture in GravityPLUS™ plates showed better ability for preserving cancer cells, inducing positive diagnostic markers expression and restraining the growth of mesothelial cells. For in vitro drug testing, MSE from five patients presented various drug sensitivities, and one case showed strong response to PD-1 checkpoint inhibition (pembrolizumab). For some patients, the application of combinatorial drugs had better therapeutic responses compared to monotherapy. Conclusions Digitalised quantification of data offers a better understanding of different MSE culture models. More importantly, the proposed platforms are practical and amenable for performing in vitro chemo-/immunotherapeutic drug testing by using routine cytologic MSE in a personalised manner. Next to cell blocks, our work demonstrates the prognostic and predictive value of cytologic effusion samples.


2015 ◽  
Vol 10 (11) ◽  
pp. 1682-1688 ◽  
Author(s):  
Jonghoon Choi ◽  
Eun Kyu Lee ◽  
Jaebum Choo ◽  
Junhan Yuh ◽  
Jong Wook Hong

Biosensors ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 509
Author(s):  
Chengxun Su ◽  
Yon Jin Chuah ◽  
Hong Boon Ong ◽  
Hui Min Tay ◽  
Rinkoo Dalan ◽  
...  

Incorporation of extracellular matrix (ECM) and hydrogel in microfluidic 3D cell culture platforms is important to create a physiological microenvironment for cell morphogenesis and to establish 3D co-culture models by hydrogel compartmentalization. Here, we describe a simple and scalable ECM patterning method for microfluidic cell cultures by achieving hydrogel confinement due to the geometrical expansion of channel heights (stepped height features) and capillary burst valve (CBV) effects. We first demonstrate a sequential “pillar-free” hydrogel patterning to form adjacent hydrogel lanes in enclosed microfluidic devices, which can be further multiplexed with one to two stepped height features. Next, we developed a novel “spheroid-in-gel” culture device that integrates (1) an on-chip hanging drop spheroid culture and (2) a single “press-on” hydrogel confinement step for rapid ECM patterning in an open-channel microarray format. The initial formation of breast cancer (MCF-7) spheroids was achieved by hanging a drop culture on a patterned polydimethylsiloxane (PDMS) substrate. Single spheroids were then directly encapsulated on-chip in individual hydrogel islands at the same positions, thus, eliminating any manual spheroid handling and transferring steps. As a proof-of-concept to perform a spheroid co-culture, endothelial cell layer (HUVEC) was formed surrounding the spheroid-containing ECM region for drug testing studies. Overall, this developed stepped height-based hydrogel patterning method is simple to use in either enclosed microchannels or open surfaces and can be readily adapted for in-gel cultures of larger 3D cellular spheroids or microtissues.


2020 ◽  
Author(s):  
Ambica Baru ◽  
Saumyabrata Mazumdar ◽  
Prabuddha Kundu ◽  
Swati Sharma ◽  
Biswa Pratim Das Purakayastha ◽  
...  

AbstractThe formation of three-dimensional spheroid tumor model using the scaffold-based platforms has been demonstrated over many years now. 3D tumor models are generated mainly in non-scalable culture systems, using synthetic and biological scaffolds. Many of these models fail to reflect the complex tumor microenvironment and do not allow long-term monitoring of tumor progression. This has resulted in inconsistent data in drug testing assays during preclinical and clinical studies. To overcome these limitations, we have developed 3D tissueoids model by using novel AXTEX-4D™ platform. Cancer 3D tissueoids demonstrated the basic features of 3D cell culture with rapid attachment, proliferation, and longevity with contiguous cytoskeleton and hypoxic core. This study also demonstrated greater drug resistance in 3D-MCF-7 tissueoids in comparison to 2D monolayer cell culture and the collagen-based 3D system. In conclusion, 3D-tissueoids are more responsive than 2D-cultured cells in simulating important tumor characteristics, anti-apoptotic features, and their resulting drug resistance.


2020 ◽  
Author(s):  
Cheng-Guang Wu ◽  
Francesca Chiovaro ◽  
Alessandra Curioni ◽  
Ruben Casanova ◽  
Alex Soltermann

Abstract Background Malignant serous effusion (MSE) denotes a manifestation of metastatic disease with typical high concentrations of both cancer and immune cells, making them an ideal resource for in vitro cytologic studies. Hence, the aim of the study was to investigate the features of 2D and 3D MSE culture systems as well as their feasibilities for in vitro drug screening. Methods Pleural and peritoneal effusions from 8 patients were collected and processed for 2D monolayer and 3D hanging drop cell culture into GravityPLUS™ plates. Representative markers for cell components, proliferation rate and tumour classification were investigated by immunohistochemistry, followed by absolute quantification using a digitalised image analysis approach. Further, we implemented another 3D cell culture model based on a low attachment method for in vitro drug sensitivity testing of carboplatin, pemetrexed and pembrolizumab for 5 patients. Results Monolayer cell culture was favourable for the growth of mesothelial cells, while hanging drop culture in GravityPLUS™ plates showed better ability for preserving cancer cells, inducing positive diagnostic markers expression and restraining the growth of mesothelial cells. For in vitro drug testing, MSE from five patients presented various drug sensitivities, and one case showed strong response to PD-1 checkpoint inhibition (pembrolizumab). For some patients, the application of combinatorial drugs had better therapeutic responses compared to monotherapy. Conclusions Digitalised quantification of data offers a better understanding of different MSE culture models. More importantly, the proposed platforms are practical and amenable for performing in vitro chemo-/immunotherapeutic drug testing by using routine cytologic MSE in a personalised manner. Next to cell blocks, our work demonstrates the prognostic and predictive value of cytologic effusion samples.


The Analyst ◽  
2019 ◽  
Vol 144 (1) ◽  
pp. 290-298 ◽  
Author(s):  
Naricha Pupinyo ◽  
Moragot Chatatikun ◽  
Anchalee Chiabchalard ◽  
Wanida Laiwattanapaisal

Recently, paper has gained traction in the biotechnology research field due to its ability to be a substrate for 3D cell culture.


2019 ◽  
Vol 10 (23) ◽  
pp. 3180-3193 ◽  
Author(s):  
Sam C. P. Norris ◽  
Stephanie M. Delgado ◽  
Andrea M. Kasko

Highly conjugated, hydrophobically modified gelatin hydrogels were synthesized, polymerized and degraded with orthogonal wavelengths of light.


2020 ◽  
Vol 237 ◽  
pp. 116092 ◽  
Author(s):  
Mulazim Hussain Asim ◽  
Stefanie Silberhumer ◽  
Iram Shahzadi ◽  
Aamir Jalil ◽  
Barbara Matuszczak ◽  
...  

2010 ◽  
Vol 35 (9) ◽  
pp. 1374 ◽  
Author(s):  
Jong-ryul Choi ◽  
Jong Hwan Sung ◽  
Michael Louis Shuler ◽  
Donghyun Kim

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