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The Signaling Pathway of PGE(2) and Its Regulatory Role in T Cell Differentiation
Prostaglandin E2 (PGE(2)) is a lipid mediator derived from the fatty acid arachidonic acid. As an essential inflammatory factor, PGE(2) has a critical impact on immune regulation through the prostanoid E (EP) receptor pathway. T cells, including CD4(+) and CD8(+) T cell subsets, play crucial roles i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641993/ https://www.ncbi.nlm.nih.gov/pubmed/34867083 http://dx.doi.org/10.1155/2021/9087816 |
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author | An, Yang Yao, Jiameng Niu, Xiaoyin |
author_facet | An, Yang Yao, Jiameng Niu, Xiaoyin |
author_sort | An, Yang |
collection | PubMed |
description | Prostaglandin E2 (PGE(2)) is a lipid mediator derived from the fatty acid arachidonic acid. As an essential inflammatory factor, PGE(2) has a critical impact on immune regulation through the prostanoid E (EP) receptor pathway. T cells, including CD4(+) and CD8(+) T cell subsets, play crucial roles in the adaptive immune response. Previous studies have shown that PGE(2) is involved in regulating CD4(+) T cell differentiation and inflammatory cytokine production via the EP receptor pathway, thereby affecting the development of diseases mediated by CD4(+) T cells. In this review, we summarize the signaling pathway of PGE(2) and describe the relationship between PGE(2) and T cell differentiation. Hence, this review may provide important evidence for immune therapies and may even promote the development of biomedicines. |
format | Online Article Text |
id | pubmed-8641993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-86419932021-12-04 The Signaling Pathway of PGE(2) and Its Regulatory Role in T Cell Differentiation An, Yang Yao, Jiameng Niu, Xiaoyin Mediators Inflamm Review Article Prostaglandin E2 (PGE(2)) is a lipid mediator derived from the fatty acid arachidonic acid. As an essential inflammatory factor, PGE(2) has a critical impact on immune regulation through the prostanoid E (EP) receptor pathway. T cells, including CD4(+) and CD8(+) T cell subsets, play crucial roles in the adaptive immune response. Previous studies have shown that PGE(2) is involved in regulating CD4(+) T cell differentiation and inflammatory cytokine production via the EP receptor pathway, thereby affecting the development of diseases mediated by CD4(+) T cells. In this review, we summarize the signaling pathway of PGE(2) and describe the relationship between PGE(2) and T cell differentiation. Hence, this review may provide important evidence for immune therapies and may even promote the development of biomedicines. Hindawi 2021-11-26 /pmc/articles/PMC8641993/ /pubmed/34867083 http://dx.doi.org/10.1155/2021/9087816 Text en Copyright © 2021 Yang An et al. https://creativecommons.org/licenses/by/4.0/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 | Review Article An, Yang Yao, Jiameng Niu, Xiaoyin The Signaling Pathway of PGE(2) and Its Regulatory Role in T Cell Differentiation |
title | The Signaling Pathway of PGE(2) and Its Regulatory Role in T Cell Differentiation |
title_full | The Signaling Pathway of PGE(2) and Its Regulatory Role in T Cell Differentiation |
title_fullStr | The Signaling Pathway of PGE(2) and Its Regulatory Role in T Cell Differentiation |
title_full_unstemmed | The Signaling Pathway of PGE(2) and Its Regulatory Role in T Cell Differentiation |
title_short | The Signaling Pathway of PGE(2) and Its Regulatory Role in T Cell Differentiation |
title_sort | signaling pathway of pge(2) and its regulatory role in t cell differentiation |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8641993/ https://www.ncbi.nlm.nih.gov/pubmed/34867083 http://dx.doi.org/10.1155/2021/9087816 |
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