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Insulin restores glucose inhibition of adenosine transport by increasing the expression and activity of the equilibrative nucleoside transporter 2 in human umbilical vein endothelium

Identifieur interne : 002E21 ( Main/Exploration ); précédent : 002E20; suivant : 002E22

Insulin restores glucose inhibition of adenosine transport by increasing the expression and activity of the equilibrative nucleoside transporter 2 in human umbilical vein endothelium

Auteurs : Gonzalo Mu Oz [Chili] ; Rody San Martín [Chili] ; Marcelo Farías [Chili] ; Luis Cea [Chili] ; Andrea Vecchiola [Chili] ; Paola Casanello [Chili] ; Luis Sobrevia [Chili]

Source :

RBID : ISTEX:06ABCF2A336D782B37EC4B3BA33F9D9932DF985E

English descriptors

Abstract

L‐Arginine transport and nitric oxide (NO) synthesis (L‐arginine/NO pathway) are stimulated by insulin, adenosine or elevated extracellular D‐glucose in human umbilical vein endothelial cells (HUVEC). Adenosine uptake via the human equilibrative nucleoside transporters 1 (hENT1) and 2 (hENT2) has been proposed as a mechanism regulating adenosine plasma concentration, and therefore its vascular effects in human umbilical veins. Thus, altered expression and/or activity of hENT1 or hENT2 could lead to abnormal physiological plasma adenosine level. We have characterized insulin effect on adenosine transport in HUVEC cultured in normal (5 mM) or high (25 mM) D‐glucose. Insulin (1 nM) increased overall adenosine transport associated with higher hENT2‐, but lower hENT1‐mediated transport in normal D‐glucose. Insulin increased hENT2 protein abundance in normal or high D‐glucose, but reduced hENT1 protein abundance in normal D‐glucose. Insulin did not alter the reduced hENT1 protein abundance, but blocked the reduced hENT1 and hENT2 mRNA expression induced by high D‐glucose. Insulin effect on hENT1 mRNA expression in normal D‐glucose was blocked by NG‐nitro‐L‐arginine methyl ester (L‐NAME, NO synthase inhibitor) and mimicked by S‐nitroso‐N‐acetyl‐L,D‐penicillamine (SNAP, NO donor). L‐NAME did not block insulin effect on hENT2 expression. In conclusion, insulin stimulation of overall adenosine transport results from increased hENT2 expression and activity via a NO‐independent mechanism. These findings could be important in hyperglycemia‐associated pathological pregnancies, such as gestational diabetes, where plasma adenosine removal by the endothelium is reduced, a condition that could alter the blood flow from the placenta to the fetus affecting fetus growth and development. J. Cell. Physiol. 209: 826–835, 2006. © 2006 Wiley‐Liss, Inc.

Url:
DOI: 10.1002/jcp.20769


Affiliations:


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<term>Adenosine</term>
<term>Adenosine transport</term>
<term>Aguayo</term>
<term>Casanello</term>
<term>Cell type</term>
<term>Cellular physiology</term>
<term>Chile</term>
<term>Control insulin insulin</term>
<term>Crucial mechanism</term>
<term>Culture medium</term>
<term>Dglucose</term>
<term>Diabetic rats</term>
<term>Endothelial</term>
<term>Endothelial cells</term>
<term>Endothelium</term>
<term>Enos</term>
<term>Enos activity</term>
<term>Ent1</term>
<term>Equilibrative</term>
<term>Equilibrative nucleoside transporter</term>
<term>Ester</term>
<term>Experimental condition</term>
<term>Extracellular</term>
<term>Extracellular adenosine</term>
<term>Gestational</term>
<term>Gestational diabetes</term>
<term>Hent1</term>
<term>Hent1 mrna expression</term>
<term>Hent1 protein abundance</term>
<term>Hent2</term>
<term>Hent2 activity</term>
<term>Hent2 expression</term>
<term>Hent2 mrna expression</term>
<term>Hent2 protein abundance</term>
<term>High dglucose</term>
<term>Human umbilical vein</term>
<term>Human umbilical vein endothelium</term>
<term>Huvec</term>
<term>Hypoxanthine</term>
<term>Incubation period</term>
<term>Inhibitory effect</term>
<term>Insulin</term>
<term>Insulin effect</term>
<term>Lymphocyte</term>
<term>Mammalian cells</term>
<term>Methyl ester</term>
<term>Mrna</term>
<term>Mrna expression</term>
<term>Nbmpr</term>
<term>Nitric</term>
<term>Nitric oxide</term>
<term>Nitric oxide synthesis</term>
<term>Normal insulin</term>
<term>Nucleoside</term>
<term>Nucleoside membrane transporters</term>
<term>Nucleoside transporters</term>
<term>Overall adenosine transport</term>
<term>Oxide</term>
<term>Pathway</term>
<term>Pawelczyk</term>
<term>Pharmacol</term>
<term>Physiol</term>
<term>Plasma adenosine</term>
<term>Protein abundance</term>
<term>Results show</term>
<term>Sakowicz</term>
<term>Similar results</term>
<term>Sobrevia</term>
<term>Stimulatory effect</term>
<term>Total enos</term>
<term>Transport</term>
<term>Transport activity</term>
<term>Transporter</term>
<term>Umbilical</term>
<term>Umbilical vein</term>
<term>Unaltered</term>
<term>Universidad catolica</term>
<term>Vasquez</term>
<term>Vmax</term>
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<div type="abstract" xml:lang="en">L‐Arginine transport and nitric oxide (NO) synthesis (L‐arginine/NO pathway) are stimulated by insulin, adenosine or elevated extracellular D‐glucose in human umbilical vein endothelial cells (HUVEC). Adenosine uptake via the human equilibrative nucleoside transporters 1 (hENT1) and 2 (hENT2) has been proposed as a mechanism regulating adenosine plasma concentration, and therefore its vascular effects in human umbilical veins. Thus, altered expression and/or activity of hENT1 or hENT2 could lead to abnormal physiological plasma adenosine level. We have characterized insulin effect on adenosine transport in HUVEC cultured in normal (5 mM) or high (25 mM) D‐glucose. Insulin (1 nM) increased overall adenosine transport associated with higher hENT2‐, but lower hENT1‐mediated transport in normal D‐glucose. Insulin increased hENT2 protein abundance in normal or high D‐glucose, but reduced hENT1 protein abundance in normal D‐glucose. Insulin did not alter the reduced hENT1 protein abundance, but blocked the reduced hENT1 and hENT2 mRNA expression induced by high D‐glucose. Insulin effect on hENT1 mRNA expression in normal D‐glucose was blocked by NG‐nitro‐L‐arginine methyl ester (L‐NAME, NO synthase inhibitor) and mimicked by S‐nitroso‐N‐acetyl‐L,D‐penicillamine (SNAP, NO donor). L‐NAME did not block insulin effect on hENT2 expression. In conclusion, insulin stimulation of overall adenosine transport results from increased hENT2 expression and activity via a NO‐independent mechanism. These findings could be important in hyperglycemia‐associated pathological pregnancies, such as gestational diabetes, where plasma adenosine removal by the endothelium is reduced, a condition that could alter the blood flow from the placenta to the fetus affecting fetus growth and development. J. Cell. Physiol. 209: 826–835, 2006. © 2006 Wiley‐Liss, Inc.</div>
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