نتایج جستجو برای: 3d culture

تعداد نتایج: 461478  

2013
Sheng Feng Xinrui Duan Pang-Kuo Lo Shou Liu Xinfeng Liu Hexin Chen Qian Wang

a Cancer stem cells (CSCs) are hypothesized as tumor-initiating cells within tumors and main contributors of tumor growth, metastasis and recurrence. Mammary cancer cells, MCF-7 cells, were cultured on 3D polycaprolactone (PCL) fibrous scaffolds, showing an increased proportion of CSCs. The expression of stem cell markers, including OCT3/4 and SOX2, and breast CSC-specific markers, SOX4 and CD4...

Azoospermia is one of the challenging disorders affecting couples who are afflicted with infertility. Human testisderivedcells (hTCs) are suitable candidates for the initiation of in-vitro spermatogenesis for these types of patients.The current study aimed to assess the proliferation of hTCs through the cell culture on the three-dimensional (3D) porousscaffolds. Cells harveste...

2013
Hongzhou Huang Ying Ding Xiuzhi S. Sun Thu A. Nguyen

Three-dimensional (3D) cell culture plays an invaluable role in tumor biology by providing in vivo like microenviroment and responses to therapeutic agents. Among many established 3D scaffolds, hydrogels demonstrate a distinct property as matrics for 3D cell culture. Most of the existing pre-gel solutions are limited under physiological conditions such as undesirable pH or temperature. Here, we...

2016
Rajneesh Jha Qingling Wu Monalisa Singh Marcela K. Preininger Pengcheng Han Gouliang Ding Hee Cheol Cho Hanjoong Jo Kevin O. Maher Mary B. Wagner Chunhui Xu

Efficient generation of cardiomyocytes from human pluripotent stem cells is critical for their regenerative applications. Microgravity and 3D culture can profoundly modulate cell proliferation and survival. Here, we engineered microscale progenitor cardiac spheres from human pluripotent stem cells and exposed the spheres to simulated microgravity using a random positioning machine for 3 days du...

Journal: :Biochemical Society transactions 2010
Daniel J Maltman Stefan A Przyborski

Drug discovery programmes require accurate in vitro systems for drug screening and testing. Traditional cell culture makes use of 2D (two-dimensional) surfaces for ex vivo cell growth. In such environments, cells are forced to adopt unnatural characteristics, including aberrant flattened morphologies. Therefore there is a strong demand for new cell culture platforms which allow cells to grow an...

2016
Sabreen Khalil Nagwa El-Badri Mohamed El-Mokhtaar Saif Al-Mofty Mohamed Farghaly Radwa Ayman Dina Habib Noha Mousa

METHODS We utilized the hAM to provide the biological and the three dimensional (3D) topographic components of the prototype. The 3D nano-roughness of the hAM was characterized using surface electron microscopy and surface image analysis (ImageJ and SurfaceJ). We developed additional macro-scale and micro-scale versions of the platform which provided additional shear stress factors to simulate ...

2014

Mammalian cell culture has served as an invaluable tool in cell biology for several decades. Mono­ layers of adherent cells grown on flat and rigid two-dimensional (2D) substrates, such as polysty­ rene or glass, have evolved as the mainstay in conventional cell culture systems. Two-dimensional cell culture studies have played a pivotal role in furthering our understanding of developmental biol...

2016
Mario Luis Zuolo Alexandre Augusto Zaia

(AH Plus, Endomethasone N, EndoSequence BC, MTA Fillapex and Pulp Canal Sealer EWT) using a three-dimensional (3D) cell culture model. A conventional bi-dimensional (2D) cell culture model was used as reference technique for comparison. Balb/c 3T3 fibroblasts were cultured in conventional bi-dimensional cell culture and in rat-tail collagen type I three-dimensional cell culture models. Then, bo...

Journal: :American journal of physiology. Cell physiology 2005
Reza Jarrahy Weibiao Huang George H Rudkin Jane M Lee Kenji Ishida Micah D Berry Modar Sukkarieh Benjamin M Wu Dean T Yamaguchi Timothy A Miller

Osteogenic differentiation of osteoprogenitor cells in three-dimensional (3D) in vitro culture remains poorly understood. Using quantitative real-time RT-PCR techniques, we examined mRNA expression of alkaline phosphatase, osteocalcin, and vascular endothelial growth factor (VEGF) in murine preosteoblastic MC3T3-E1 cells cultured for 48 h and 14 days on conventional two-dimensional (2D) poly(l-...

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