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Indoleamine 2,3-Dioxygenase Is Dispensable for The Immunomodulatory Function of Stem Cells from Human Exfoliated Deciduous Teeth
OBJECTIVE: In this study, we sought to better understand the immunoregulatory function of stem cells derived from human exfoliated deciduous teeth (SHED). We studied the role of the interferon gamma (IFN-γ)-indoleamine 2,3-dioxygenase (IDO)-axis in immunoregulation of SHED compared to bone marrow de...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086338/ https://www.ncbi.nlm.nih.gov/pubmed/28042544 |
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author | Alipour, Razieh Masoumi Karimi, Masoumeh Hashemi-Beni, Batool Adib, Minoo Sereshki, Nasrin Sadeghi, Farzaneh |
author_facet | Alipour, Razieh Masoumi Karimi, Masoumeh Hashemi-Beni, Batool Adib, Minoo Sereshki, Nasrin Sadeghi, Farzaneh |
author_sort | Alipour, Razieh |
collection | PubMed |
description | OBJECTIVE: In this study, we sought to better understand the immunoregulatory function of stem cells derived from human exfoliated deciduous teeth (SHED). We studied the role of the interferon gamma (IFN-γ)-indoleamine 2,3-dioxygenase (IDO)-axis in immunoregulation of SHED compared to bone marrow derived mesenchymal stem cells (BMMSCs) under the same conditions. MATERIALS AND METHODS: In this cross-sectional study, recently isolated human T cells were stimulated either by mitogen or inactivated allogeneic peripheral blood mononuclear cells (PBMCs). These T cells were subsequently co-cultured with, either SHED or BMMSCs in the presence or absence of 1-methyl-tryptophan (1-MT) or neutralizing anti- human-IFN-γ antibodies. In all co-cultures we evaluated lymphocyte activation as well as IDO activity. RESULTS: SHED, similar to conventional BMMSCs, had anti-proliferative effects on stimulated T cells and reduced their cytokine production. This property of SHED and BMMSCs was changed by IFN-γ neutralization. We detected IDO in the immunosuppressive supernatant of all co-cultures. Removal of IDO decreased the immunosuppression of BMMSCs. CONCLUSION: SHED, like BMMSCs, produced the IDO enzyme. Although IFN-γ is one of inducer of IDO production in SHED, these cells were not affected by IFN-γ in the same manner as BMMSCs. Unlike BMMSCs, the IDO enzyme did not contribute to their immunosuppression and might have other cell-type specific roles. |
format | Online Article Text |
id | pubmed-5086338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-50863382017-01-01 Indoleamine 2,3-Dioxygenase Is Dispensable for The Immunomodulatory Function of Stem Cells from Human Exfoliated Deciduous Teeth Alipour, Razieh Masoumi Karimi, Masoumeh Hashemi-Beni, Batool Adib, Minoo Sereshki, Nasrin Sadeghi, Farzaneh Cell J Original Article OBJECTIVE: In this study, we sought to better understand the immunoregulatory function of stem cells derived from human exfoliated deciduous teeth (SHED). We studied the role of the interferon gamma (IFN-γ)-indoleamine 2,3-dioxygenase (IDO)-axis in immunoregulation of SHED compared to bone marrow derived mesenchymal stem cells (BMMSCs) under the same conditions. MATERIALS AND METHODS: In this cross-sectional study, recently isolated human T cells were stimulated either by mitogen or inactivated allogeneic peripheral blood mononuclear cells (PBMCs). These T cells were subsequently co-cultured with, either SHED or BMMSCs in the presence or absence of 1-methyl-tryptophan (1-MT) or neutralizing anti- human-IFN-γ antibodies. In all co-cultures we evaluated lymphocyte activation as well as IDO activity. RESULTS: SHED, similar to conventional BMMSCs, had anti-proliferative effects on stimulated T cells and reduced their cytokine production. This property of SHED and BMMSCs was changed by IFN-γ neutralization. We detected IDO in the immunosuppressive supernatant of all co-cultures. Removal of IDO decreased the immunosuppression of BMMSCs. CONCLUSION: SHED, like BMMSCs, produced the IDO enzyme. Although IFN-γ is one of inducer of IDO production in SHED, these cells were not affected by IFN-γ in the same manner as BMMSCs. Unlike BMMSCs, the IDO enzyme did not contribute to their immunosuppression and might have other cell-type specific roles. Royan Institute 2017 2016-09-26 /pmc/articles/PMC5086338/ /pubmed/28042544 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited 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 work is properly cited. |
spellingShingle | Original Article Alipour, Razieh Masoumi Karimi, Masoumeh Hashemi-Beni, Batool Adib, Minoo Sereshki, Nasrin Sadeghi, Farzaneh Indoleamine 2,3-Dioxygenase Is Dispensable for The Immunomodulatory Function of Stem Cells from Human Exfoliated Deciduous Teeth |
title | Indoleamine 2,3-Dioxygenase Is Dispensable for The
Immunomodulatory Function of Stem Cells from
Human Exfoliated Deciduous Teeth |
title_full | Indoleamine 2,3-Dioxygenase Is Dispensable for The
Immunomodulatory Function of Stem Cells from
Human Exfoliated Deciduous Teeth |
title_fullStr | Indoleamine 2,3-Dioxygenase Is Dispensable for The
Immunomodulatory Function of Stem Cells from
Human Exfoliated Deciduous Teeth |
title_full_unstemmed | Indoleamine 2,3-Dioxygenase Is Dispensable for The
Immunomodulatory Function of Stem Cells from
Human Exfoliated Deciduous Teeth |
title_short | Indoleamine 2,3-Dioxygenase Is Dispensable for The
Immunomodulatory Function of Stem Cells from
Human Exfoliated Deciduous Teeth |
title_sort | indoleamine 2,3-dioxygenase is dispensable for the
immunomodulatory function of stem cells from
human exfoliated deciduous teeth |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086338/ https://www.ncbi.nlm.nih.gov/pubmed/28042544 |
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