Journal
PURINERGIC SIGNALLING
Volume 16, Issue 2, Pages 187-211Publisher
SPRINGER
DOI: 10.1007/s11302-020-09699-x
Keywords
N-6-etheno-ATP; Ecto-nucleotidases; Purine nucleoside phosphorylase; 8-Aminoguanine
Categories
Funding
- NIH [NS087978, DK091190, HL109002, HL069846, DK068575, DK079307]
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The goal of this study was to determine the validity of using N-6-etheno-bridged adenine nucleotides to evaluate ecto-nucleotidase activity. We observed that the metabolism of N-6-etheno-ATP versus ATP was quantitatively similar when incubated with recombinant CD39, ENTPD2, ENTPD3, or ENPP-1, and the quantitative metabolism of N-6-etheno-AMP versus AMP was similar when incubated with recombinant CD73. This suggests that ecto-nucleotidases process N-6-etheno-bridged adenine nucleotides similarly to endogenous adenine nucleotides. Four cell types rapidly (t(1/2), 0.21 to 0.66 h) metabolized N-6-etheno-ATP. Applied N-6-etheno-ATP was recovered in the medium as N-6-etheno-ADP, N-6-etheno-AMP, N-6-etheno-adenosine, and surprisingly N-6-etheno-adenine; intracellular N-6-etheno compounds were undetectable. This suggests minimal cellular uptake, intracellular metabolism, or deamination of these compounds. N-6-etheno-ATP, N-6-etheno-ADP, N-6-etheno-AMP, N-6-etheno-adenosine, and N-6-etheno-adenine had little affinity for recombinant A(1), A(2A), or A(2B) receptors, for a subset of P2X receptors (H-3-alpha,beta-methylene-ATP binding to rat bladder membranes), or for a subset of P2Y receptors (S-35-ATP-alpha S binding to rat brain membranes), suggesting minimal pharmacological activity. N-6-etheno-adenosine was partially converted to N-6-etheno-adenine in four different cell types; this was blocked by purine nucleoside phosphorylase (PNPase) inhibition. Intravenous N-6-etheno-ATP was quickly metabolized, with N-6-etheno-adenine being the main product in naive rats, but not in rats pretreated with a PNPase inhibitor. PNPase inhibition reduced the urinary excretion of endogenous adenine and attenuated the conversion of exogenous adenosine to adenine in the renal cortex. The N-6-etheno-bridge method is a valid technique to assess extracellular metabolism of adenine nucleotides by ecto-nucleotidases. Also, rats express an enzyme with PNPase-like activity that metabolizes N-6-etheno-adenosine to N-6-etheno-adenine.
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