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Blood Cell Membrane Fluidity and Intracellular Ca(2+) Changes in Antiretroviral-Naïve and -Treated HIV-1–Infected Patients

We previously showed that lymphocytes and erythrocytes of HIV-1–infected patients, prior to antiretroviral therapy, presented significant changes in intracellular calcium concentration ([Ca(2+)](int)) and membrane fluidity. The present study evaluates the same parameters after response to highly act...

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Autores principales: Santos, Nuno C., Martins e Silva, J., Freitas, Teresa, Doroana, M., Duarte, N., Tavares, L., Antunes, F., Saldanha, Carlota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763957/
https://www.ncbi.nlm.nih.gov/pubmed/20191248
http://dx.doi.org/10.1100/tsw.2010.34
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author Santos, Nuno C.
Martins e Silva, J.
Freitas, Teresa
Doroana, M.
Duarte, N.
Tavares, L.
Antunes, F.
Saldanha, Carlota
author_facet Santos, Nuno C.
Martins e Silva, J.
Freitas, Teresa
Doroana, M.
Duarte, N.
Tavares, L.
Antunes, F.
Saldanha, Carlota
author_sort Santos, Nuno C.
collection PubMed
description We previously showed that lymphocytes and erythrocytes of HIV-1–infected patients, prior to antiretroviral therapy, presented significant changes in intracellular calcium concentration ([Ca(2+)](int)) and membrane fluidity. The present study evaluates the same parameters after response to highly active antiretroviral therapy (HAART). Blood samples were collected from patients prior to and after antiretroviral therapy, and from control subjects. Membrane fluidity and [Ca(2+)](int) were assessed by fluorescence spectroscopy measurements, using three different probes: TMA-DPH and DPH for membrane fluidity, and fura-2 for Ca(2+). When compared with the control group, both untreated and treated patients presented increased lymphocyte [Ca(2+)](int) and decreased lymphocyte membrane fluidity, without significant differences between the two groups of patients. On the contrary, the therapy reversed the membrane fluidity variations observed in erythrocytes. The decreased erythrocyte [Ca(2+)](int) of untreated patients was not reversed by HAART. AIDS patients present changes in lymphocyte (mostly noninfected) and erythrocyte properties, partially reversed by HAART, consistent with a process of facilitated propagation of the infection to new cells, stimulation of virion production, and maintenance of a reservoir of erythrocyte-bound infectious virus. These observations can be related with the action of the HIV Nef protein in the cell's proteins and lipid composition, as well as with the recently observed cell infection by HIV-1 via endocytosis.
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spelling pubmed-57639572018-06-03 Blood Cell Membrane Fluidity and Intracellular Ca(2+) Changes in Antiretroviral-Naïve and -Treated HIV-1–Infected Patients Santos, Nuno C. Martins e Silva, J. Freitas, Teresa Doroana, M. Duarte, N. Tavares, L. Antunes, F. Saldanha, Carlota ScientificWorldJournal Original Research We previously showed that lymphocytes and erythrocytes of HIV-1–infected patients, prior to antiretroviral therapy, presented significant changes in intracellular calcium concentration ([Ca(2+)](int)) and membrane fluidity. The present study evaluates the same parameters after response to highly active antiretroviral therapy (HAART). Blood samples were collected from patients prior to and after antiretroviral therapy, and from control subjects. Membrane fluidity and [Ca(2+)](int) were assessed by fluorescence spectroscopy measurements, using three different probes: TMA-DPH and DPH for membrane fluidity, and fura-2 for Ca(2+). When compared with the control group, both untreated and treated patients presented increased lymphocyte [Ca(2+)](int) and decreased lymphocyte membrane fluidity, without significant differences between the two groups of patients. On the contrary, the therapy reversed the membrane fluidity variations observed in erythrocytes. The decreased erythrocyte [Ca(2+)](int) of untreated patients was not reversed by HAART. AIDS patients present changes in lymphocyte (mostly noninfected) and erythrocyte properties, partially reversed by HAART, consistent with a process of facilitated propagation of the infection to new cells, stimulation of virion production, and maintenance of a reservoir of erythrocyte-bound infectious virus. These observations can be related with the action of the HIV Nef protein in the cell's proteins and lipid composition, as well as with the recently observed cell infection by HIV-1 via endocytosis. TheScientificWorldJOURNAL 2010-02-19 /pmc/articles/PMC5763957/ /pubmed/20191248 http://dx.doi.org/10.1100/tsw.2010.34 Text en Copyright © 2010 Nuno C. Santos et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Santos, Nuno C.
Martins e Silva, J.
Freitas, Teresa
Doroana, M.
Duarte, N.
Tavares, L.
Antunes, F.
Saldanha, Carlota
Blood Cell Membrane Fluidity and Intracellular Ca(2+) Changes in Antiretroviral-Naïve and -Treated HIV-1–Infected Patients
title Blood Cell Membrane Fluidity and Intracellular Ca(2+) Changes in Antiretroviral-Naïve and -Treated HIV-1–Infected Patients
title_full Blood Cell Membrane Fluidity and Intracellular Ca(2+) Changes in Antiretroviral-Naïve and -Treated HIV-1–Infected Patients
title_fullStr Blood Cell Membrane Fluidity and Intracellular Ca(2+) Changes in Antiretroviral-Naïve and -Treated HIV-1–Infected Patients
title_full_unstemmed Blood Cell Membrane Fluidity and Intracellular Ca(2+) Changes in Antiretroviral-Naïve and -Treated HIV-1–Infected Patients
title_short Blood Cell Membrane Fluidity and Intracellular Ca(2+) Changes in Antiretroviral-Naïve and -Treated HIV-1–Infected Patients
title_sort blood cell membrane fluidity and intracellular ca(2+) changes in antiretroviral-naïve and -treated hiv-1–infected patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763957/
https://www.ncbi.nlm.nih.gov/pubmed/20191248
http://dx.doi.org/10.1100/tsw.2010.34
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