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Image Search Results
Journal: STAR Protocols
Article Title: Engineering Elastic Nano- and Micro-Patterns and Textures for Directed Cell Motility
doi: 10.1016/j.xpro.2019.100013
Figure Lengend Snippet: Mechanical Rigidity of ICAM1 Nano-Topographies Controls T Cell On-Ridge Spreading and In-Groove Invasiveness Plasticity Balance (A) 3D super-resolution reconstruction of the ICAM1-functionalized PAA nano-topographic surface (G’=16 kPa). (B) Test super-resolution imaging (3D reconstruction) of human CD4+ T cells spreading and migrating along the ICAM1-coated nano-topographic surfaces on soft (16 kPa) and rigid (50 kPa) PAA surfaces. (C) Schematic of the T cell morphometric analysis and metrics: T cell height, projected area of spreading of entire cell interface ( S entire cell IF ) and projected area of in-groove invasive T cell interface ( S invasive IF ). (D and E) Mechanoregulation of T cell height, spreading area and invasiveness as indicated by T cell spreading assay on soft (G’=16 kPa) and rigid (G’=50 kPa) ICAM1 nano-textures. T cell spreading enhances on the rigid ICAM1, accompanied with T cell flattening, i.e. decrease of the T cell height. Results indicate a mechanically controlled dynamic balance between on-ridge T cell spreading and in-groove invasiveness, as shown on the schematic panel (E). I.e. T cell in-groove invasiveness structurally competes with on-ridge spreading, indicating that on-ridge spreading is mechanically enhanced and out-balances in-groove invasiveness on the rigid (G’=50 kPa) ICAM1 nano-topography. Alternatively, soft (G’=16 kPa) ICAM-1 nano-textures are unable to promote the mechanically sensitive on-ridge T cell spreading, shifting the balance towards steric in-groove T cell invasiveness. Data on the plots on (D) are as follows: boxes - means, Q1 and Q3; whiskers - max and min, X - medians; p values - one way ANOVA test. Experimental data collected in triplicates, total n>50.
Article Snippet:
Techniques: Imaging
Journal: STAR Protocols
Article Title: Engineering Elastic Nano- and Micro-Patterns and Textures for Directed Cell Motility
doi: 10.1016/j.xpro.2019.100013
Figure Lengend Snippet:
Article Snippet:
Techniques: Recombinant, Electrophoresis, Concentration Assay, Labeling, Saline, Modification, Cell Isolation, Derivative Assay, Software
Journal: International Journal of Cardiology. Heart & Vasculature
Article Title: Soluble CD54 induces human endothelial cells ex vivo expansion useful for cardiovascular regeneration and tissue engineering application
doi: 10.1016/j.ijcha.2015.01.004
Figure Lengend Snippet: Cell density of endothelial cells cultivated in the presence of soluble CD54. Endothelial cells cultivated in the presence of soluble CD54 (sCD54) were expanded for five splits. After the first (p1), second (p2) and fifth (p5) passages (as shown in the x-axis) the cellular densities were measured (y-axis) and compared between different growing conditions: in the presence of sCD54 alone, resulting in higher propagation rate, than cell culture treated with HUVEC-conditioned medium collected at p4 (CMP4) alone.
Article Snippet:
Techniques: Cell Culture
Journal: International Journal of Cardiology. Heart & Vasculature
Article Title: Soluble CD54 induces human endothelial cells ex vivo expansion useful for cardiovascular regeneration and tissue engineering application
doi: 10.1016/j.ijcha.2015.01.004
Figure Lengend Snippet: Capillary density. Tube formation occurred through an ordered sequence of events and was investigated with an inverted optical light microscope; (A) cells beginning to migrate and align themselves to close polygons beginning (B) to form complete tubules (C) of endothelial cells cultivated with the addition of sCD54. The histogram shows the data mean ± SD of the quantitative analysis of tube formation area; in the x-axis was reported capillary density in the presence of HUVEC-conditioned medium collected at p4 (CMP4), sCD54 and antibody direct against CD54 at the concentration of 15 ng/ml (y-axis). Scale bars: 200 μm.
Article Snippet:
Techniques: Sequencing, Light Microscopy, Concentration Assay
Journal: Physiological Genomics
Article Title: Gene expression profiling of the effects of organic dust in lung epithelial and THP-1 cells reveals inductive effects on inflammatory and immune response genes
doi: 10.1152/physiolgenomics.00096.2015
Figure Lengend Snippet: TaqMan gene expression IDs for target mRNAs
Article Snippet: ICAM-1 , intercellular adhesion molecule-1 ,
Techniques: Expressing
Journal: Physiological Genomics
Article Title: Gene expression profiling of the effects of organic dust in lung epithelial and THP-1 cells reveals inductive effects on inflammatory and immune response genes
doi: 10.1152/physiolgenomics.00096.2015
Figure Lengend Snippet: Some of the significantly induced transcripts in A549 cells by treatment with poultry dust extract
Article Snippet: ICAM-1 , intercellular adhesion molecule-1 ,
Techniques:
Journal: Physiological Genomics
Article Title: Gene expression profiling of the effects of organic dust in lung epithelial and THP-1 cells reveals inductive effects on inflammatory and immune response genes
doi: 10.1152/physiolgenomics.00096.2015
Figure Lengend Snippet: Some of the significantly induced transcripts in Beas2B cells by treatment with poultry dust extract
Article Snippet: ICAM-1 , intercellular adhesion molecule-1 ,
Techniques:
Journal: Physiological Genomics
Article Title: Gene expression profiling of the effects of organic dust in lung epithelial and THP-1 cells reveals inductive effects on inflammatory and immune response genes
doi: 10.1152/physiolgenomics.00096.2015
Figure Lengend Snippet: Some of the significantly induced transcripts in THP-1 cells by treatment with poultry dust extract
Article Snippet: ICAM-1 , intercellular adhesion molecule-1 ,
Techniques:
Journal: Physiological Genomics
Article Title: Gene expression profiling of the effects of organic dust in lung epithelial and THP-1 cells reveals inductive effects on inflammatory and immune response genes
doi: 10.1152/physiolgenomics.00096.2015
Figure Lengend Snippet: Effects of poultry DE on ICAM-1 levels in A549, Beas2B, and THP-1 cells. A549 and Beas2B cells were treated with medium alone or medium containing 0.25% DE for 3 h. THP-1 cells were treated with medium alone or medium containing 0.1% DE for 1 h. ICAM-1 levels in cell lysates were determined by Western immunoblotting. The same blot was probed for actin, which served as a loading and transfer control. Similar results were obtained in a 2nd independent experiment.
Article Snippet: ICAM-1 , intercellular adhesion molecule-1 ,
Techniques: Western Blot