Cargando…
Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence
Amniotic epithelial cells (AECs) are a class of fetal stem cells that derives from the epiblast and resides in the amnion until birth. AECs are suitable candidates for regenerative medicine because of the ease of collection, their low immunogenicity and inability to form tumors after transplantation...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129913/ https://www.ncbi.nlm.nih.gov/pubmed/27259996 http://dx.doi.org/10.18632/oncotarget.9694 |
_version_ | 1782470642991366144 |
---|---|
author | Germanio, Clara Di Bernier, Michel Petr, Michael Mattioli, Mauro Barboni, Barbara de Cabo, Rafael |
author_facet | Germanio, Clara Di Bernier, Michel Petr, Michael Mattioli, Mauro Barboni, Barbara de Cabo, Rafael |
author_sort | Germanio, Clara Di |
collection | PubMed |
description | Amniotic epithelial cells (AECs) are a class of fetal stem cells that derives from the epiblast and resides in the amnion until birth. AECs are suitable candidates for regenerative medicine because of the ease of collection, their low immunogenicity and inability to form tumors after transplantation. Even though human AECs have been widely investigated, the fact remains that very little is known about AECs isolated from rat, one of the most common animal models in medical testing. In this study, we showed that rat AECs retained stemness properties and plasticity, expressed the pluripotency markers Sox2, Nanog, and Oct4 and were able to differentiate toward the osteogenic lineage. The addition of conditioned medium collected from rat AECs to lipopolysaccharide-activated macrophages elicited anti-inflammatory properties through a decrease of Tnfa expression and slowed tumor cell proliferation in vitro and in vivo. The senescence-associated secretory phenotype was also significantly lower upon incubation of senescent human IMR-90 fibroblast cells with conditioned medium from rat AECs. These results confirm the potential of AECs in the modulation of inflammatory mechanisms and open new therapeutic possibilities for regenerative medicine and anti-aging therapies as well. |
format | Online Article Text |
id | pubmed-5129913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-51299132016-12-11 Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence Germanio, Clara Di Bernier, Michel Petr, Michael Mattioli, Mauro Barboni, Barbara de Cabo, Rafael Oncotarget Research Paper: Gerotarget (Focus on Aging) Amniotic epithelial cells (AECs) are a class of fetal stem cells that derives from the epiblast and resides in the amnion until birth. AECs are suitable candidates for regenerative medicine because of the ease of collection, their low immunogenicity and inability to form tumors after transplantation. Even though human AECs have been widely investigated, the fact remains that very little is known about AECs isolated from rat, one of the most common animal models in medical testing. In this study, we showed that rat AECs retained stemness properties and plasticity, expressed the pluripotency markers Sox2, Nanog, and Oct4 and were able to differentiate toward the osteogenic lineage. The addition of conditioned medium collected from rat AECs to lipopolysaccharide-activated macrophages elicited anti-inflammatory properties through a decrease of Tnfa expression and slowed tumor cell proliferation in vitro and in vivo. The senescence-associated secretory phenotype was also significantly lower upon incubation of senescent human IMR-90 fibroblast cells with conditioned medium from rat AECs. These results confirm the potential of AECs in the modulation of inflammatory mechanisms and open new therapeutic possibilities for regenerative medicine and anti-aging therapies as well. Impact Journals LLC 2016-05-29 /pmc/articles/PMC5129913/ /pubmed/27259996 http://dx.doi.org/10.18632/oncotarget.9694 Text en Copyright: © 2016 Germanio et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Gerotarget (Focus on Aging) Germanio, Clara Di Bernier, Michel Petr, Michael Mattioli, Mauro Barboni, Barbara de Cabo, Rafael Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence |
title | Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence |
title_full | Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence |
title_fullStr | Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence |
title_full_unstemmed | Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence |
title_short | Conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence |
title_sort | conditioned medium derived from rat amniotic epithelial cells confers protection against inflammation, cancer, and senescence |
topic | Research Paper: Gerotarget (Focus on Aging) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129913/ https://www.ncbi.nlm.nih.gov/pubmed/27259996 http://dx.doi.org/10.18632/oncotarget.9694 |
work_keys_str_mv | AT germanioclaradi conditionedmediumderivedfromratamnioticepithelialcellsconfersprotectionagainstinflammationcancerandsenescence AT berniermichel conditionedmediumderivedfromratamnioticepithelialcellsconfersprotectionagainstinflammationcancerandsenescence AT petrmichael conditionedmediumderivedfromratamnioticepithelialcellsconfersprotectionagainstinflammationcancerandsenescence AT mattiolimauro conditionedmediumderivedfromratamnioticepithelialcellsconfersprotectionagainstinflammationcancerandsenescence AT barbonibarbara conditionedmediumderivedfromratamnioticepithelialcellsconfersprotectionagainstinflammationcancerandsenescence AT decaborafael conditionedmediumderivedfromratamnioticepithelialcellsconfersprotectionagainstinflammationcancerandsenescence |