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Image Search Results
Journal: The Journal of Neuroscience
Article Title: Mitochondrial Dynamics and Bioenergetic Dysfunction Is Associated with Synaptic Alterations in Mutant SOD1 Motor Neurons
doi: 10.1523/JNEUROSCI.1233-11.2012
Figure Lengend Snippet: Impaired mitochondrial fusion in the soma and motor axons of G93A SOD1 motor neurons. A, Cell bodies from non-transgenic control and G93A SOD1 motor neurons containing mitoDendra-labeled mitochondria before (−1 min) and after (0 min) photo-activation. Subsets of mitochondria (green and red fluorescence) were followed over time (10, 40, 70, and 100 min) by live imaging microscopy. Note that the appearance of yellow fluorescence, as a result of the mixing between green and red mitochondria (i.e. fusion, indicated by arrows), was delayed in mutant SOD1 motor neurons. Scale bar, 10 μm. B, Fusion rates were obtained in single optical z-sections by measuring the colocalization (in %) of red over green fluorescent mitochondria at the indicated time points. The correlation coefficient (r) for each group is indicated. n (somas) = 8 non-transgenic, and 7 G93A. *P<0.05 by ANOVA with repeated measurements. C, In the inset, example of a time-lapse recording of axonal mitochondria (numbers indicate time in min) showing a fusion event (arrow). Scale bar, 5 μm. The graph shows the analysis of fusion (% of fusion events of total moving mitochondria) in control and G93A SOD1 motor axons. n (axons) = 24 non-transgenic, 28 WT and 16 G93A axonal segments. *P<0.05 versus non-transgenic. D, Time-lapse microscopy of mitochondrial transport in the soma of non-transgenic and G93A SOD1 motor neurons. All mitochondria in a ROI of the soma were photo-converted, while only non-photo-converted (green fluorescent) mitochondria were followed over time. Note a decrease of mobile mitochondria towards the ROI in mutant SOD1 motor neurons compared to controls. Scale bar, 10 μm. E, Analysis of the transport of green mitochondria over the photo-activated area (no green mitochondria present). The correlation coefficient (r) for each group is indicated. n (somas) = 8 non-transgenic, and 7 G93A. *P<0.05 by ANOVA with repeated measurements. F, Analysis of the transport of red mitochondria over the non-photo-activated area (no red mitochondria present). The correlation coefficient (r) for each group is indicated. n (somas) = 8 non-transgenic, and 7 G93A. *P<0.05 by ANOVA with repeated measurements. All data obtained from 3–5 independent experiments. The error bars represent ± SE.
Article Snippet:
Techniques: Transgenic Assay, Control, Labeling, Activation Assay, Fluorescence, Imaging, Microscopy, Mutagenesis, Time-lapse Microscopy
Journal: Journal of Food and Drug Analysis
Article Title: Pacific oyster-derived polysaccharides attenuate allergen-induced intestinal inflammation in a murine model of food allergy
doi: 10.1016/j.jfda.2015.08.006
Figure Lengend Snippet: Oyster-derived polysaccharides (OPS) restored the diminished ratio of villus length over crypt depth in the duodenum. Mice were treated as described in . Tissue sections of duodenum were prepared for standard hematoxylineosin (H&E) staining. The villus length and crypt depth were measured using the Image-Pro Plus version 5.1 morphometric analysis software (100× field; Media Cybernetics, Inc., Silver Spring, MD, USA). Data are expressed as the mean ± standard error of 27-1 samples per group pooled from six independent experiments. * p < 0.05 compared to the VH group [vehicle-treated (distilled water; 0.1 mL/mouse)]. NS = nonsensitized; OVA = ovalbumin.
Article Snippet: The villus length and crypt depth on H&E stained slides were measured using the
Techniques: Derivative Assay, Staining, Software
Journal: Journal of Food and Drug Analysis
Article Title: Pacific oyster-derived polysaccharides attenuate allergen-induced intestinal inflammation in a murine model of food allergy
doi: 10.1016/j.jfda.2015.08.006
Figure Lengend Snippet: Effect of oyster-derived polysaccharides (OPS) on the infiltration of interleukin-4 (IL-4) + cells in duodenum. Mice were treated as described in . Immunohistochemical (IHC) staining was performed to detect IL-4 + cells in the duodenum. The image was analyzed and the positive signal (the red color) was quantified using the Image-Pro Plus version 5.1 morphometric analysis software (200× field; Media Cybernetics, Inc., Silver Spring, MD, USA). Data are expressed as the mean ± standard error of 20–22 samples per group pooled from four independent experiments. * p < 0.05 compared to the VH group [vehicle-treated (distilled water; 0.1 mL/mouse)]. NS = nonsensitized; OVA = ovalbumin; VH = vehicle.
Article Snippet: The villus length and crypt depth on H&E stained slides were measured using the
Techniques: Derivative Assay, Immunohistochemical staining, Immunohistochemistry, Software