Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells

During decidualization, endometrial stromal cells undergo reticular stress (RS) and unfolded protein response (UPR), allowing the endoplasmic reticulum-expansion and immunomodulators production. Physiological RS generates the activation of sensing proteins, inflammasome activation and mature-IL-1β s...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Grasso, E., Gori, S., Soczewski, E., Fernández, L., Gallino, L., Vota, D., Martínez, G., Irigoyen, M., Ruhlmann, C., Lobo, T.F., Salamone, G., Mattar, R., Daher, S., Leirós, C.P., Ramhorst, R.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_20452322_v8_n1_p_Grasso
Aporte de:
id todo:paper_20452322_v8_n1_p_Grasso
record_format dspace
spelling todo:paper_20452322_v8_n1_p_Grasso2023-10-03T16:38:24Z Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells Grasso, E. Gori, S. Soczewski, E. Fernández, L. Gallino, L. Vota, D. Martínez, G. Irigoyen, M. Ruhlmann, C. Lobo, T.F. Salamone, G. Mattar, R. Daher, S. Leirós, C.P. Ramhorst, R. During decidualization, endometrial stromal cells undergo reticular stress (RS) and unfolded protein response (UPR), allowing the endoplasmic reticulum-expansion and immunomodulators production. Physiological RS generates the activation of sensing proteins, inflammasome activation and mature-IL-1β secretion, associated with pro-implantatory effects. We focus on the impact of RS and UPR on decidualized cells and whether they induce a physiological sterile inflammatory response through IL-1β production. Human endometrial stromal cell line (HESC) after decidualization treatment with MPA + dibutyryl-cAMP (Dec) increased the expression of RS-sensors (ATF6, PERK and IRE1α) and UPR markers (sXBP1 and CHOP) in comparison with Non-dec cells. Then we found increased NLRP3 expression in Dec cells compared with Non-dec cells. In fact STF-083010 (an IRE1α inhibitor) prevented this increase. Downstream, increased levels of active caspase-1 on Dec cells were detected by FAM-Flica Caspase-1 associated with an increase in IL-1β production. Moreover, the treatment with STF-083010 decreased the invasion index observed in Dec cells, evaluated by an in vitro model of implantation. In endometrial biopsies from recurrent spontaneous abortion patients an increased expression of IRE1α was found in comparison with fertile women; while recurrent implantation failure samples showed a lower expression of sXBP1, TXNIP and NLRP3 than fertile women, suggesting that RS/UPR tenors might condition endometrial receptivity. © 2018, The Author(s). JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_20452322_v8_n1_p_Grasso
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description During decidualization, endometrial stromal cells undergo reticular stress (RS) and unfolded protein response (UPR), allowing the endoplasmic reticulum-expansion and immunomodulators production. Physiological RS generates the activation of sensing proteins, inflammasome activation and mature-IL-1β secretion, associated with pro-implantatory effects. We focus on the impact of RS and UPR on decidualized cells and whether they induce a physiological sterile inflammatory response through IL-1β production. Human endometrial stromal cell line (HESC) after decidualization treatment with MPA + dibutyryl-cAMP (Dec) increased the expression of RS-sensors (ATF6, PERK and IRE1α) and UPR markers (sXBP1 and CHOP) in comparison with Non-dec cells. Then we found increased NLRP3 expression in Dec cells compared with Non-dec cells. In fact STF-083010 (an IRE1α inhibitor) prevented this increase. Downstream, increased levels of active caspase-1 on Dec cells were detected by FAM-Flica Caspase-1 associated with an increase in IL-1β production. Moreover, the treatment with STF-083010 decreased the invasion index observed in Dec cells, evaluated by an in vitro model of implantation. In endometrial biopsies from recurrent spontaneous abortion patients an increased expression of IRE1α was found in comparison with fertile women; while recurrent implantation failure samples showed a lower expression of sXBP1, TXNIP and NLRP3 than fertile women, suggesting that RS/UPR tenors might condition endometrial receptivity. © 2018, The Author(s).
format JOUR
author Grasso, E.
Gori, S.
Soczewski, E.
Fernández, L.
Gallino, L.
Vota, D.
Martínez, G.
Irigoyen, M.
Ruhlmann, C.
Lobo, T.F.
Salamone, G.
Mattar, R.
Daher, S.
Leirós, C.P.
Ramhorst, R.
spellingShingle Grasso, E.
Gori, S.
Soczewski, E.
Fernández, L.
Gallino, L.
Vota, D.
Martínez, G.
Irigoyen, M.
Ruhlmann, C.
Lobo, T.F.
Salamone, G.
Mattar, R.
Daher, S.
Leirós, C.P.
Ramhorst, R.
Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells
author_facet Grasso, E.
Gori, S.
Soczewski, E.
Fernández, L.
Gallino, L.
Vota, D.
Martínez, G.
Irigoyen, M.
Ruhlmann, C.
Lobo, T.F.
Salamone, G.
Mattar, R.
Daher, S.
Leirós, C.P.
Ramhorst, R.
author_sort Grasso, E.
title Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells
title_short Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells
title_full Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells
title_fullStr Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells
title_full_unstemmed Impact of the Reticular Stress and Unfolded Protein Response on the inflammatory response in endometrial stromal cells
title_sort impact of the reticular stress and unfolded protein response on the inflammatory response in endometrial stromal cells
url http://hdl.handle.net/20.500.12110/paper_20452322_v8_n1_p_Grasso
work_keys_str_mv AT grassoe impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT goris impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT soczewskie impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT fernandezl impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT gallinol impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT votad impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT martinezg impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT irigoyenm impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT ruhlmannc impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT lobotf impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT salamoneg impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT mattarr impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT dahers impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT leiroscp impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
AT ramhorstr impactofthereticularstressandunfoldedproteinresponseontheinflammatoryresponseinendometrialstromalcells
_version_ 1807316231826440192