Title of article :
Signaling Pathway in the Osmotic Resistance Induced by Angiotensin II AT2 Receptor Activation in Human Erythrocytes
Author/Authors :
Guimarães-Nobre, Camila Cristina Grupo de Pesquisa em Fisiologia Eritróide - GPFisEri - Universidade Federal do Rio de Janeiro - Campus Macaé, Brazil , Mendonça-Reis, Evelyn Programa de Pós-graduação em Endocrinologia - Faculdade de Medicina - Universidade Federal do Rio de Janeiro, Brazil , Passin hoda- Costa, Luana Faculdade de Farmácia - Universidade Federal do Rio de Janeiro - Campus Macaé, Brazil , Miranda-Alves, Leandro Programa de Pós-graduação em Farmacologia e Química Medicinal - Instituto de Ciências Biomédicas - Universidade Federal do Rio de Janeiro, Brazil , Berto-Junior, Clemilson Faculdade de Farmácia - Universidade Federal do Rio de Janeiro - Campus Macaé, Brazil
Abstract :
Background: Angiotensin II regulates blood volume via AT1 (AT1R) and AT2 (AT2R) receptors. As cell
integrity is an important feature of mature erythrocyte, we sought to evaluate, in vitro, whether angiotensin II modulates resistance to hemolysis and the signaling pathway involved.
Methods: Human blood samples were collected and hemolysis assay and angiotensin II signaling pathway
profiling in erythrocytes were done.
Results: Hemolysis assay created a hemolysis curve in presence of Ang II in several concentrations (10-6 M,
10-8 M, 10-10 M, 10-12 M). Angiotensin II demonstrated protective effect, both in osmotic stressed and
physiological situations, by reducing hemolysis in NaCl 0.4% and 0.9%. By adding receptors antagonists
(losartan, AT1R antagonist and PD 123319, AT2R antagonist) and/or signaling modulators for AMPK,
Akt/PI3K, p38 and PKC we showed the protective effect was enhanced with losartan and abolished with PD
123319. Also, we showed activation of p38 as well as PI3K/Akt pathways in this system.
Conclusions: Ang II protects human erythrocytes from hypo-osmotic conditions-induced hemolysis by
activating AT2 receptors and triggering intracellular pathways.
Keywords :
Angiotensin II , Erythrocyte , Osmotic fragility , Signaling pathway
Journal title :
Reports of Biochemistry and Molecular Biology (RBMB)