Dynamic Regulation of Cell Volume and Extracellular ATP of Human Erythrocytes.

The peptide mastoparan 7 (MST7) triggered in human erythrocytes (rbcs) the release of ATP and swelling. Since swelling is a well-known inducer of ATP release, and extracellular (ATPe), interacting with P (purinergic) receptors, can affect cell volume (Vr), we explored the dynamic regulation between...

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Main Authors: M Florencia Leal Denis, H Ariel Alvarez, Natalia Lauri, Cora L Alvarez, Osvaldo Chara, Pablo J Schwarzbaum
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4927150?pdf=render
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author M Florencia Leal Denis
H Ariel Alvarez
Natalia Lauri
Cora L Alvarez
Osvaldo Chara
Pablo J Schwarzbaum
author_facet M Florencia Leal Denis
H Ariel Alvarez
Natalia Lauri
Cora L Alvarez
Osvaldo Chara
Pablo J Schwarzbaum
author_sort M Florencia Leal Denis
collection DOAJ
description The peptide mastoparan 7 (MST7) triggered in human erythrocytes (rbcs) the release of ATP and swelling. Since swelling is a well-known inducer of ATP release, and extracellular (ATPe), interacting with P (purinergic) receptors, can affect cell volume (Vr), we explored the dynamic regulation between Vr and ATPe.We made a quantitative assessment of MST7-dependent kinetics of Vr and of [ATPe], both in the absence and presence of blockers of ATP efflux, swelling and P receptors.In rbcs 10 μM MST7 promoted acute, strongly correlated changes in [ATPe] and Vr. Whereas MST7 induced increases of 10% in Vr and 190 nM in [ATPe], blocking swelling in a hyperosmotic medium + MST7 reduced [ATPe] by 40%. Pre-incubation of rbcs with 10 μM of either carbenoxolone or probenecid, two inhibitors of the ATP conduit pannexin 1, reduced [ATPe] by 40-50% and swelling by 40-60%, while in the presence of 80 U/mL apyrase, an ATPe scavenger, cell swelling was prevented. While exposure to 10 μM NF110, a blocker of ATP-P2X receptors mediating sodium influx, reduced [ATPe] by 48%, and swelling by 80%, incubation of cells in sodium free medium reduced swelling by 92%.Results were analyzed by means of a mathematical model where ATPe kinetics and Vr kinetics were mutually regulated. Model dependent fit to experimental data showed that, upon MST7 exposure, ATP efflux required a fast 1960-fold increase of ATP permeability, mediated by two kinetically different conduits, both of which were activated by swelling and inactivated by time. Both experimental and theoretical results suggest that, following MST7 exposure, ATP is released via two conduits, one of which is mediated by pannexin 1. The accumulated ATPe activates P2X receptors, followed by sodium influx, resulting in cell swelling, which in turn further activates ATP release. Thus swelling and P2X receptors constitute essential components of a positive feedback loop underlying ATP-induced ATP release of rbcs.
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spelling doaj.art-36fcd231401f47d9b379babfd6a62c052022-12-22T01:43:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01116e015830510.1371/journal.pone.0158305Dynamic Regulation of Cell Volume and Extracellular ATP of Human Erythrocytes.M Florencia Leal DenisH Ariel AlvarezNatalia LauriCora L AlvarezOsvaldo CharaPablo J SchwarzbaumThe peptide mastoparan 7 (MST7) triggered in human erythrocytes (rbcs) the release of ATP and swelling. Since swelling is a well-known inducer of ATP release, and extracellular (ATPe), interacting with P (purinergic) receptors, can affect cell volume (Vr), we explored the dynamic regulation between Vr and ATPe.We made a quantitative assessment of MST7-dependent kinetics of Vr and of [ATPe], both in the absence and presence of blockers of ATP efflux, swelling and P receptors.In rbcs 10 μM MST7 promoted acute, strongly correlated changes in [ATPe] and Vr. Whereas MST7 induced increases of 10% in Vr and 190 nM in [ATPe], blocking swelling in a hyperosmotic medium + MST7 reduced [ATPe] by 40%. Pre-incubation of rbcs with 10 μM of either carbenoxolone or probenecid, two inhibitors of the ATP conduit pannexin 1, reduced [ATPe] by 40-50% and swelling by 40-60%, while in the presence of 80 U/mL apyrase, an ATPe scavenger, cell swelling was prevented. While exposure to 10 μM NF110, a blocker of ATP-P2X receptors mediating sodium influx, reduced [ATPe] by 48%, and swelling by 80%, incubation of cells in sodium free medium reduced swelling by 92%.Results were analyzed by means of a mathematical model where ATPe kinetics and Vr kinetics were mutually regulated. Model dependent fit to experimental data showed that, upon MST7 exposure, ATP efflux required a fast 1960-fold increase of ATP permeability, mediated by two kinetically different conduits, both of which were activated by swelling and inactivated by time. Both experimental and theoretical results suggest that, following MST7 exposure, ATP is released via two conduits, one of which is mediated by pannexin 1. The accumulated ATPe activates P2X receptors, followed by sodium influx, resulting in cell swelling, which in turn further activates ATP release. Thus swelling and P2X receptors constitute essential components of a positive feedback loop underlying ATP-induced ATP release of rbcs.http://europepmc.org/articles/PMC4927150?pdf=render
spellingShingle M Florencia Leal Denis
H Ariel Alvarez
Natalia Lauri
Cora L Alvarez
Osvaldo Chara
Pablo J Schwarzbaum
Dynamic Regulation of Cell Volume and Extracellular ATP of Human Erythrocytes.
PLoS ONE
title Dynamic Regulation of Cell Volume and Extracellular ATP of Human Erythrocytes.
title_full Dynamic Regulation of Cell Volume and Extracellular ATP of Human Erythrocytes.
title_fullStr Dynamic Regulation of Cell Volume and Extracellular ATP of Human Erythrocytes.
title_full_unstemmed Dynamic Regulation of Cell Volume and Extracellular ATP of Human Erythrocytes.
title_short Dynamic Regulation of Cell Volume and Extracellular ATP of Human Erythrocytes.
title_sort dynamic regulation of cell volume and extracellular atp of human erythrocytes
url http://europepmc.org/articles/PMC4927150?pdf=render
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