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Open AccessJournal ArticleDOI

The Role of Galectins as Modulators of Metabolism and Inflammation.

TLDR
Information on galectin-1, -2, -3, -4, -7, -8, -9, and -12 can all induce T-cell apoptosis and modulate inflammation and the potential to target galectins for therapeutic purposes is presented.
Abstract
Galectins are β-galcotosid-binding lectins. The function of galectins varies with their tissue-specific and subcellular location, and their binding to carbohydrates makes them key players in several intra- and extracellular processes where they bind to glycosylated proteins and lipids. In humans, there are 12 identified galectins, some with tissue-specific distribution. Galectins are found inside cells and in the nucleus, cytosol, and organelles, as well as extracellularly. Galectin-1, -2, -3, -4, -7, -8, -9, and -12 can all induce T-cell apoptosis and modulate inflammation. In the context of metabolic control and loss of the same in, for example, diabetes, galectin-1, -2, -3, -9, and -12 are especially interesting. This review presents information on galectins relevant to the control of inflammation and metabolism and the potential to target galectins for therapeutic purposes.

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Intracellular Neutrophil Oxidants: From Laboratory Curiosity to Clinical Reality.

TL;DR: Experimental data and description of a novel chronic granulomatous disease subtype imply that ROS generated in intracellular compartments are key for NETosis and for controlling inflammatory signaling.
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Gene expression profiling of the early pathogenesis of wooden breast disease in commercial broiler chickens using RNA-sequencing.

TL;DR: It is revealed that presence of molecular perturbations involving the vasculature, extracellular matrix and metabolism are pertinent to the onset and early pathogenesis of WBD in commercial meat-type chickens.
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Extracellular Vesicles as Mediators of Cellular Crosstalk Between Immune System and Kidney Graft.

TL;DR: In conclusion, EVs sustain an intricate crosstalk between graft tissue and innate/adaptive immune systems and are promising as biomarkers and therapeutic tools in KT.
References
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Journal ArticleDOI

Galectin-7 in the Control of Epidermal Homeostasis after Injury

TL;DR: The generation of galectin-7-deficient mice that are viable and do not display phenotypical abnormalities in skin structure or expression of epidermal markers are reported, providing the first genetic evidence showing that galectins can modulate keratinocyte apoptosis, proliferation, and migration during skin repair.
Journal ArticleDOI

Phosphorylation of the β-Galactoside-binding Protein Galectin-3 Modulates Binding to Its Ligands

TL;DR: The process by which phosphorylation modulates protein-carbohydrate interactions has important implications for understanding the biological functions of this protein, and may serve as an “on/off” switch for its sugar binding capabilities.
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Ultrastructural localization of the Charcot-Leyden crystal protein (lysophospholipase) to a distinct crystalloid-free granule population in mature human eosinophils

TL;DR: The ultrastructural immunogold localization of CLC protein (lysophospholipase) to a large, crystalloid-free granule in mature circulating eosinophils supports the persistence of a distinct "primary" granule population that serves as a major intracytoplasmic repository for this enzyme.
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Galectin-12, an Adipose-expressed Galectin-like Molecule Possessing Apoptosis-inducing Activity.

TL;DR: Induction of galectin-12 expression by the thiazolidinedione, troglitazone, was paralleled by an increase in the number of apoptotic cells in adipose tissue and results suggest that galectIn-12, an adipose-expressed galECTin-like molecule, may participate in the apoptosis of adipocytes.
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