Artículo

Galectin-8: a matricellular lectin with key roles in angiogenesis

Troncoso, María Fernanda Icon; Ferragut, Fátima Icon; Bacigalupo, Maria Lorena Icon; Cardenas Delgado, Victor Manuel Icon; Nugnes, Lorena Gisela Icon; Gentilini, Lucas Daniel Icon; Laderach, Diego Jose Icon; Wolfenstein, Carlota Elisa Icon; Compagno, Daniel Georges Icon; Rabinovich, Gabriel Adrián Icon; Elola, Maria Teresa Icon

Otros responsables

Fecha

10/2014

Editorial

Oxford University Press

Revista

Glycobiology

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

0959-6658

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

Galectin-8 (gal-8) is a “tandem-repeat”-type galectin, containing two carbohydrate recognition domains connected by a linker peptide. gal-8 is expressed both in the cytoplasm and nucleus in vascular endothelial cells (ECs) from normal and tumor-associated blood vessels, and in lymphatic endothelial cells. Herein, we describe a novel role for gal-8 in the regulation of vascular and lymphatic angiogenesis and provide evidence of its critical implications in tumor biology. Functional assays revealed central roles for gal-8 in the control of capillary-tube formation, EC migration and in vivo angiogenesis. So far, two endothelial ligands have been described for gal-8, namely podoplanin in lymphatic vessels and CD166 (ALCAM, activated leukocyte cell adhesion molecule) in vascular ECs. Other related gal-8 functions are also summarized here, including cell adhesion and migration, which collectively demonstrate the multi-functionality of this complex lectin. Thus, gal-8 is an important component of the angiogenesis network, and an essential molecule in the extracellular matrix by providing molecular anchoring to this surrounding matrix. The implications of gal-8 in tumor angiogenesis remain to be further explored, but it is exciting to speculate that modulating gal-8-glycan interactions could be used to block lymphatic-vascular connections vital for metastasis.

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