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'); Reports of Biochemistry and Molecular Biology rbmb.net Basic Sciences http://rbmb.net 1 admin 2322-3480 2322-3480 10.61882/rbmb en jalali 1400 5 1 gregorian 2021 8 1 10 2 online 1 fulltext
en Signaling Pathway in the Osmotic Resistance Induced by Angiotensin II AT2 Receptor Activation in Human Erythrocytes زیست شناسی سلولی Cell Biology مقالات اصلی Original Article <div style="text-align: justify;"><strong><em>Background:</em></strong> Angiotensin&nbsp;II regulates&nbsp;blood&nbsp;volume&nbsp;via&nbsp;AT1 (AT1R)&nbsp;and&nbsp;AT2 (AT2R)&nbsp;receptors.&nbsp;As cell integrity is an important feature of mature erythrocyte, we sought to evaluate,<em> in vitro</em>, whether Angiotensin II modulates resistance to hemolysis and the signaling pathway&nbsp;involved.<br> <br> <strong><em>Methods: </em></strong>Human blood samples were collected and hemolysis assay and angiotensin II signaling pathway profiling in erythrocytes were done.<br> <br> <strong><em>Results:</em></strong> Hemolysis assay created a hemolysis curve in presence of Ang II in several concentrations (10<sup>-6 </sup>M, 10<sup>-8 </sup>M, 10<sup>-10 </sup>M, 10<sup>-12 </sup>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 PKC as well as PI3K/Akt pathways in this system.<br> <br> <strong><em>Conclusions:</em></strong> Briefly, Ang II protects human erythrocytes from hypo-osmotic conditions-induced hemolysis by activating AT2 receptors and triggering both the intracellular pathways.</div> Angiotensin II, Erythrocyte, Osmotic fragility, Signaling pathway. 314 326 http://rbmb.net/browse.php?a_code=A-10-713-1&slc_lang=en&sid=1 Camila Cristina Guimarães-Nobre 100319475328460012682 100319475328460012682 No Grupo de Pesquisa em Fisiologia Eritróide - GPFisEri, Universidade Federal do Rio de Janeiro, Campus Macaé, Brazil & Programa de Pós-graduação em Endocrinologia, Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Brazil. Evelyn Mendonça-Reis 100319475328460012683 100319475328460012683 No Grupo de Pesquisa em Fisiologia Eritróide - GPFisEri, Universidade Federal do Rio de Janeiro, Campus Macaé, Brazil & Programa de Pós-graduação em Endocrinologia, Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Brazil. Luana Passinho-da-Costa 100319475328460012684 100319475328460012684 No Grupo de Pesquisa em Fisiologia Eritróide - GPFisEri, Universidade Federal do Rio de Janeiro, Campus Macaé, Brazil & Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Campus Macaé, Brazil. Leandro Miranda-Alves 100319475328460012685 100319475328460012685 No Laboratório de Endocrinologia Experimental- LEEx, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Brazil & Programa de Pós-graduação em Endocrinologia, Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Brazil & Programa de Pós-graduação em Farmacologia e Química Medicinal, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Brazil. Clemilson Berto-Junior 100319475328460012686 100319475328460012686 Yes Grupo de Pesquisa em Fisiologia Eritróide - GPFisEri, Universidade Federal do Rio de Janeiro, Campus Macaé, Brazil & Laboratório de Endocrinologia Experimental- LEEx, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Brazil & Programa de Pós-graduação em Endocrinologia, Faculdade de Medicina, Universidade Federal do Rio de Janeiro, Brazil & Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Campus Macaé, Brazil.