Literature DB >> 25982395

Structural, functional, and evolutionary aspects of galectins in aquatic mollusks: From a sweet tooth to the Trojan horse.

G R Vasta1, C Feng2, M A Bianchet3, T R Bachvaroff4, S Tasumi2.   

Abstract

Galectins constitute a conserved and widely distributed lectin family characterized by their binding affinity for β-galactosides and a unique binding site sequence motif in the carbohydrate recognition domain (CRD). In spite of their structural conservation, galectins display a remarkable functional diversity, by participating in developmental processes, cell adhesion and motility, regulation of immune homeostasis, and recognition of glycans on the surface of viruses, bacteria and protozoan parasites. In contrast with mammals, and other vertebrate and invertebrate taxa, the identification and characterization of bona fide galectins in aquatic mollusks has been relatively recent. Most of the studies have focused on the identification and domain organization of galectin-like transcripts or proteins in diverse tissues and cell types, including hemocytes, and their expression upon environmental or infectious challenge. Lectins from the eastern oyster Crassostrea virginica, however, have been characterized in their molecular, structural and functional aspects and some notable features have become apparent in the galectin repertoire of aquatic mollusks. These including less diversified galectin repertoires and different domain organizations relative to those observed in vertebrates, carbohydrate specificity for blood group oligosaccharides, and up regulation of galectin expression by infectious challenge, a feature that supports their proposed role(s) in innate immune responses. Although galectins from some aquatic mollusks have been shown to recognize microbial pathogens and parasites and promote their phagocytosis, they can also selectively bind to phytoplankton components, suggesting that they also participate in uptake and intracellular digestion of microalgae. In addition, the experimental evidence suggests that the protozoan parasite Perkinsus marinus has co-evolved with the oyster host to be selectively recognized by the oyster hemocyte galectins over algal food or bacterial pathogens, thereby subverting the oyster's innate immune/feeding recognition mechanisms to gain entry into the host cells.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Galectin; Glycan ligands; Microbial recognition; Parasite; Phytoplankton

Mesh:

Substances:

Year:  2015        PMID: 25982395      PMCID: PMC4509915          DOI: 10.1016/j.fsi.2015.05.012

Source DB:  PubMed          Journal:  Fish Shellfish Immunol        ISSN: 1050-4648            Impact factor:   4.581


  98 in total

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Authors:  A M Lackie
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Authors:  Gerardo R Vasta; Hafiz Ahmed; Mihai Nita-Lazar; Aditi Banerjee; Marta Pasek; Surekha Shridhar; Prasun Guha; José A Fernández-Robledo
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4.  Serum Galectin-3 level, not Galectin-1, is associated with the clinical feature and outcome in patients with acute ischemic stroke.

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Review 5.  Pregnancy Galectinology: Insights Into a Complex Network of Glycan Binding Proteins.

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Review 6.  Biochemical Characterization of Oyster and Clam Galectins: Selective Recognition of Carbohydrate Ligands on Host Hemocytes and Perkinsus Parasites.

Authors:  Gerardo R Vasta; Chiguang Feng; Satoshi Tasumi; Kelsey Abernathy; Mario A Bianchet; Iain B H Wilson; Katharina Paschinger; Lai-Xi Wang; Muddasar Iqbal; Anita Ghosh; Mohammed N Amin; Brina Smith; Sean Brown; Aren Vista
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7.  First Insights into the Repertoire of Secretory Lectins in Rotifers.

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8.  A qPCR-Based Survey of Haplosporidium nelsoni and Perkinsus spp. in the Eastern Oyster, Crassostrea virginica in Maine, USA.

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Review 9.  The Role of Anti-Viral Effector Molecules in Mollusc Hemolymph.

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