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1.
Cells ; 10(6)2021 05 24.
Article in English | MEDLINE | ID: mdl-34073755

ABSTRACT

Interleukin-4 (IL-4) and IL-13 are the major T helper 2 (Th2) cytokines, and they are involved in the regulation of metabolism in the adipose tissue. The liver contains diverse innate and adaptive immune cells, but it remains to be determined whether Th2 cytokines modulate energy metabolism in the liver. Here, using gene expression data from the Gene Expression Omnibus (GEO) and the BXD mouse reference population, we determined that the Th2 cytokines IL-4 and IL-13 increase the secretion of fibroblast growth factor 21 (FGF21) in the liver. In vitro experiments confirmed that FGF21 was highly expressed in response to IL-4 and IL-13, and this response was abolished by the Janus kinase (JAK)-signal transducer and activator of transcription 6 (STAT6) blockade. Moreover, FGF21 expression in response to Th2 cytokines was augmented by selective peroxisome proliferator-activated receptor α (PPARα) inhibition. In vivo administration of IL-4 increased FGF21 protein levels in the liver in a STAT6-dependent manner, but FGF21 secretion in response to IL-4 was not observed in the epididymal white adipose tissue (eWAT) despite the activation of STAT6. Intraperitoneal administration of IL-33, an activator of type 2 immune responses, significantly increased the level of FGF21 in the serum and liver after 24 h, but repeated administration of IL-33 attenuated this effect. Taken together, these data demonstrate that the IL-4/IL-13-STAT6 axis regulates metabolic homeostasis through the induction of FGF21 in the liver.


Subject(s)
Adipose Tissue/metabolism , Fibroblast Growth Factors/metabolism , Interleukin-33/metabolism , Animals , Gene Expression/physiology , Interleukin-4/metabolism , Liver/metabolism , Liver/pathology , Mice , PPAR alpha/metabolism , STAT6 Transcription Factor/metabolism
2.
IEEE Trans Image Process ; 22(3): 1186-98, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23192553

ABSTRACT

In this paper, we propose a chromatic aberration (CA) correction algorithm based on a false color filtering technique. In general, CA produces color distortions called color fringes near the contrasting edges of captured images, and these distortions cause false color artifacts. In the proposed method, a false color filtering technique is used to filter out the false color components from the chroma-signals of the input image. The filtering process is performed with the adaptive weights obtained from both the gradient and color differences, and the weights are designed to reduce the various types of color fringes regardless of the colors of the artifacts. Moreover, as preprocessors of the filtering process, a transient improvement (TI) technique is applied to enhance the slow transitions of the red and blue channels that are blurred by the CA. The TI process improves the filtering performance by narrowing the false color regions before the filtering process when severe color fringes (typically purple fringes) occur widely. Last, the CA-corrected chroma-signal is combined with the TI chroma-signal to avoid incorrect color adjustment. The experimental results show that the proposed method substantially reduces the CA artifacts and provides natural-looking replacement colors, while it avoids incorrect color adjustment.


Subject(s)
Algorithms , Artifacts , Colorimetry/methods , Image Enhancement/methods , Image Interpretation, Computer-Assisted/methods , Photography/methods , Signal Processing, Computer-Assisted , Color , Reproducibility of Results , Sensitivity and Specificity
3.
Adv Mater ; 24(31): 4271-7, 2012 Aug 16.
Article in English | MEDLINE | ID: mdl-22740066

ABSTRACT

Alginate microribbons with longitudinally grooved microstructures are continuously fabricated by means of a microfluidic system. The number and dimensions of the microgroovesare successfully controlled by regulation of the slit-shaped channel (yellow in figure). This method opens up the possibility of mass production of scaffolds for tissue engineering purposes, as it is proved that the grooved flat fibers can be used to align other types of cells in culture.


Subject(s)
Alginates/chemistry , Tissue Engineering , Animals , Cells, Cultured , Dimethylpolysiloxanes/chemistry , Glucuronic Acid/chemistry , Hexuronic Acids/chemistry , Microfluidic Analytical Techniques , Microscopy, Fluorescence , Neurons/cytology , Rats , Rats, Sprague-Dawley
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