, 2006; Sansom et al, 2008) The ecto-nucleoside triphosphate di

, 2006; Sansom et al., 2008). The ecto-nucleoside triphosphate diphosphohydrolase family (ecto-NTPDases) is constituted by eight members (NTPDase1–8) that hydrolyze nucleoside di- and triphosphates to the monophosphate form. Nucleoside monophosphates may then be catalyzed to nucleosides such as adenosine by the action of ecto-5′-nucleotidase. Purine salvage and the regulation of blood clotting, inflammatory processes and immune reactions are among the major roles played by these enzymes to date (Sansom et al., 2008; Burnstock & Verkhratsky, 2009). The adenosinergic 5-Fluoracil signalling can be controlled by adenosine uptake via bidirectional

transporters, followed by intracellular phosphorylation to AMP by adenosine kinase or deamination to inosine by adenosine deaminase (ADA; EC ADA participates in the purine metabolism, where it degrades either adenosine or 2′-deoxyadenosine, producing inosine or 2′-deoxyinosine, respectively

(Franco et al., 1997). A phylogenetic study demonstrated the existence of different ADA-related members, which include ADA1, ADA2 and a similar deduced amino acid sequence named adenosine deaminase like (ADAL) (Maier et al., 2005). Despite its intracellular location, ADA1 may occur on cell surface, anchored to two proteins, CD26 and A1 receptors, acting BGB324 chemical structure as an ecto-ADA cleaving extracellular adenosine (Franco et al., 1997). ADA has been described in mammalian cells and tissues, blood-feeding insects, mollusks and parasites, Plasmodium lophurae, Trichinella spiralis, Fasciola gigantica and Hyalomma dromedarii (Franco et al., 1997; Gounaris, 2002; Mohamed, 2006; Ali, 2008). The characterization and expression of S-adenosylhomocysteinase

were described in T. vaginalis, which catalyzes the reversible hydrolysis of S-adenosylhomocysteine to homocysteine and adenosine (Minotto et al., 1998). Those authors have previously reported the absence or the poor activity of ADA. It is important to mention that T. vaginalis is dependent Cediranib (AZD2171) on salvage pathways to generate de novo nucleotides (Heyworth et al., 1982, 1984). Munagala & Wang (2003) demonstrated that adenosine is the primary precursor of the entire pool of purine nucleotides in T. vaginalis, and activities of ADA, IMP dehydrogenase and GMP synthetase were identified in trichomonads, suggesting a metabolic pathway able to convert adenine to GMP via adenosine. Our group has investigated the purinergic system in T. vaginalis throughout the extracellular nucleotide hydrolysis, and NTPDase and ecto-5′-nucleotidase activities were described (Matos et al., 2001; Tasca et al., 2003, 2005). Considering that (1) extracellular nucleotides and nucleosides, such as adenosine and inosine, act as DAMPs playing a role in cell signalling that contribute to inflammation and immune responses (Bours et al., 2006; Sansom et al.

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