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Secretion of heat shock ‐60, ‐70 kD protein, IL‐1β and TNFα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development

The extracellular heat shock proteins (eHsp) family act as molecular chaperones regulating folding, transporting protein and are associated with immune modulation in different physiological and pathological processes. They have been localized in different gestational tissues and their concentration...

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Autores principales: Álvarez‐Cabrera, María C., Barrientos‐Galeana, Edgar, Barrera‐García, Asyadette, Osorio‐Caballero, Mauricio, Acevedo, Jesús F., Flores‐Herrera, Oscar, Díaz, Néstor F., Molina‐Hernández, Anayansí, García‐López, Guadalupe, Flores‐Herrera, Héctor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201347/
https://www.ncbi.nlm.nih.gov/pubmed/30133944
http://dx.doi.org/10.1111/jcmm.13824
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author Álvarez‐Cabrera, María C.
Barrientos‐Galeana, Edgar
Barrera‐García, Asyadette
Osorio‐Caballero, Mauricio
Acevedo, Jesús F.
Flores‐Herrera, Oscar
Díaz, Néstor F.
Molina‐Hernández, Anayansí
García‐López, Guadalupe
Flores‐Herrera, Héctor
author_facet Álvarez‐Cabrera, María C.
Barrientos‐Galeana, Edgar
Barrera‐García, Asyadette
Osorio‐Caballero, Mauricio
Acevedo, Jesús F.
Flores‐Herrera, Oscar
Díaz, Néstor F.
Molina‐Hernández, Anayansí
García‐López, Guadalupe
Flores‐Herrera, Héctor
author_sort Álvarez‐Cabrera, María C.
collection PubMed
description The extracellular heat shock proteins (eHsp) family act as molecular chaperones regulating folding, transporting protein and are associated with immune modulation in different physiological and pathological processes. They have been localized in different gestational tissues and their concentration in amniotic fluid and serum has been determined. In the present study, we proposed to determine the concentration of eHsp‐60, ‐70, IL‐1β and TNFα in the serum of pregnant patients with 34 weeks of gestation with and without clinical evidences of preeclampsia (PE). Our results indicate significant increase of these markers in patients with PE with respect to healthy pregnant patients without active labor. Finally, the concentration of eHsp‐60 and ‐70 correlated positively with the hepatic dysfunction markers uric acid, lactate dehydrogenase (LDH), glutamic oxaloacetic transaminase (GOT) glutamic pyruvic transaminase (GPT), and inflammatory IL‐1β and TNFα response. In conclusion, our results demonstrate a strong associated between Hsp and marker of hepatic dysfunction.
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spelling pubmed-62013472018-11-01 Secretion of heat shock ‐60, ‐70 kD protein, IL‐1β and TNFα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development Álvarez‐Cabrera, María C. Barrientos‐Galeana, Edgar Barrera‐García, Asyadette Osorio‐Caballero, Mauricio Acevedo, Jesús F. Flores‐Herrera, Oscar Díaz, Néstor F. Molina‐Hernández, Anayansí García‐López, Guadalupe Flores‐Herrera, Héctor J Cell Mol Med Short Communications The extracellular heat shock proteins (eHsp) family act as molecular chaperones regulating folding, transporting protein and are associated with immune modulation in different physiological and pathological processes. They have been localized in different gestational tissues and their concentration in amniotic fluid and serum has been determined. In the present study, we proposed to determine the concentration of eHsp‐60, ‐70, IL‐1β and TNFα in the serum of pregnant patients with 34 weeks of gestation with and without clinical evidences of preeclampsia (PE). Our results indicate significant increase of these markers in patients with PE with respect to healthy pregnant patients without active labor. Finally, the concentration of eHsp‐60 and ‐70 correlated positively with the hepatic dysfunction markers uric acid, lactate dehydrogenase (LDH), glutamic oxaloacetic transaminase (GOT) glutamic pyruvic transaminase (GPT), and inflammatory IL‐1β and TNFα response. In conclusion, our results demonstrate a strong associated between Hsp and marker of hepatic dysfunction. John Wiley and Sons Inc. 2018-08-22 2018-11 /pmc/articles/PMC6201347/ /pubmed/30133944 http://dx.doi.org/10.1111/jcmm.13824 Text en © 2018 Instituto Nacional de Perinatología. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communications
Álvarez‐Cabrera, María C.
Barrientos‐Galeana, Edgar
Barrera‐García, Asyadette
Osorio‐Caballero, Mauricio
Acevedo, Jesús F.
Flores‐Herrera, Oscar
Díaz, Néstor F.
Molina‐Hernández, Anayansí
García‐López, Guadalupe
Flores‐Herrera, Héctor
Secretion of heat shock ‐60, ‐70 kD protein, IL‐1β and TNFα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development
title Secretion of heat shock ‐60, ‐70 kD protein, IL‐1β and TNFα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development
title_full Secretion of heat shock ‐60, ‐70 kD protein, IL‐1β and TNFα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development
title_fullStr Secretion of heat shock ‐60, ‐70 kD protein, IL‐1β and TNFα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development
title_full_unstemmed Secretion of heat shock ‐60, ‐70 kD protein, IL‐1β and TNFα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development
title_short Secretion of heat shock ‐60, ‐70 kD protein, IL‐1β and TNFα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development
title_sort secretion of heat shock ‐60, ‐70 kd protein, il‐1β and tnfα levels in serum of a term normal pregnancy and patients with pre‐eclampsia development
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201347/
https://www.ncbi.nlm.nih.gov/pubmed/30133944
http://dx.doi.org/10.1111/jcmm.13824
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