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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

Alternative (M2) activation of Kupffer cells by PPARδ ameliorates obesity-induced insulin resistance

TL;DR: It is shown that in response to the Th2 cytokine interleukin-4 (IL-4), peroxisome proliferator-activated receptor delta (PPARdelta) directs expression of the alternative phenotype in Kupffer cells and adipose tissue macrophages of lean mice, suggesting an unexpected beneficial role for alternatively activated K upffer cells in metabolic syndrome and type 2 diabetes.
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Diabetes and advanced glycation endproducts.

TL;DR: This data indicates that glycation endproducts are a viable source of disease progression in elderly people with diabetes and the use of these products should not be considered a substitute for medical treatment.
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Intracellular functions of galectins

TL;DR: This review summarizes the intracellular activities displayed by several galectins and discusses the possible underlying mechanisms.
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Pro-Inflammatory CD11c+CD206+ Adipose Tissue Macrophages Are Associated With Insulin Resistance in Human Obesity

TL;DR: These findings identify proinflammatory CD11c+ ATMs as markers of insulin resistance in human obesity and indicates they metabolize lipid and may initiate adaptive immune responses.
Journal Article

Mac-2, a novel 32,000 Mr mouse macrophage subpopulation-specific antigen defined by monoclonal antibodies.

TL;DR: Two monoclonal antibodies obtained by fusion of mouse myeloma cells with rat spleen cells immunized to immunoadsorbent-purified macrophage glycoproteins show that antigenic determinants recognized by these two antibodies reside on the same molecular species, termed Mac-2, which is induced in macrophages only in response to specific differentiative signals.
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