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Open AccessJournal ArticleDOI

Ah, sweet mystery of death! Galectins and control of cell fate.

TLDR
Understanding how galectins regulate cell viability and function will broaden the knowledge of the roles of galectin in basic biological processes and facilitate development of therapeutic applications for galECTins in autoimmunity, transplant-related disease, and cancer.
Abstract
Control of cell death is critical in eukaryotic development, immune system homeostasis, and control of tumorigenesis. The galectin family of lectins is implicated in all of these processes. Other families of molecules function as death receptors or death effectors, but galectins are uniquely capable of acting both extracellularly and intracellularly to control cell death. Extracellularly, galectins cross-link glycan ligands to transduce signals that lead directly to death or that influence other signals regulating cell fate. Intracellular expression of galectins can modulate other signals controlling cell viability. Individual galectins can act on multiple cell types, and multiple galectins can act on the same cell. Understanding how galectins regulate cell viability and function will broaden our knowledge of the roles of galectins in basic biological processes and facilitate development of therapeutic applications for galectins in autoimmunity, transplant-related disease, and cancer.

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Journal ArticleDOI

The Tim-3 ligand galectin-9 negatively regulates T helper type 1 immunity

TL;DR: The data suggest that the Tim-3–galectin-9 pathway may have evolved to ensure effective termination of effector TH1 cells.
Journal ArticleDOI

Galectins: structure, function and therapeutic potential.

TL;DR: Current research indicates that galectins play important roles in diverse physiological and pathological processes, including immune and inflammatory responses, tumour development and progression, neural degeneration, atherosclerosis, diabetes, and wound repair, and may be a therapeutic target or employed as therapeutic agents for inflammatory diseases, cancers and several other diseases.
Journal ArticleDOI

Mammalian glycosylation in immunity

TL;DR: This Review focuses on the emerging immunological roles of the mammalian glycome, which is one of the four fundamental macromolecular components of all cells, and is highly regulated in the immune system.
Journal ArticleDOI

Galectin-1: a key effector of regulation mediated by CD4+CD25+ T cells

TL;DR: It is reported that a member of the family of beta-galactoside-binding proteins, galectin-1, is overexpressed in regulatory T cells, and that expression is increased after activation, and it is suggested that galectIn-1 is a key effector of the regulation mediated by these cells.
Journal ArticleDOI

Galectin-3 and galectin-1 bind distinct cell surface glycoprotein receptors to induce T cell death.

TL;DR: It is demonstrated that extracellular galectin-3 directly induces death of human thymocytes and T cells through distinct cell surface events and that the two death pathways may converge inside the cell.
References
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Journal ArticleDOI

The biochemistry of apoptosis

TL;DR: The basic components of the death machinery are reviewed, how they interact to regulate apoptosis in a coordinated manner is described, and the main pathways that are used to activate cell death are discussed.
Journal ArticleDOI

Apoptosis in the pathogenesis and treatment of disease

TL;DR: In multicellular organisms, homeostasis is maintained through a balance between cell proliferation and cell death, and recent evidence suggests that alterations in cell survival contribute to the pathogenesis of a number of human diseases.
Journal ArticleDOI

A model for p53-induced apoptosis

TL;DR: Examination of transcripts induced by p53 expression before the onset of apoptosis stimulated additional biochemical and pharmacological experiments suggesting that p53 results in apoptosis through a three-step process: the transcriptional induction of redox-related genes; the formation of reactive oxygen species; and the oxidative degradation of mitochondrial components, culminating in cell death.
Journal ArticleDOI

Apoptosis of T cells mediated by galectin-1

TL;DR: Galectin-1 induced apoptosis of activated human T cells and human T leukaemia cell lines and represents a new mechanism for regulating the immune response.
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