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Primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced HLA-DR
The earliest macrophages are generated during embryonic development from erythro-myeloid progenitors (EMPs) via primitive haematopoiesis. Although this process is thought to be spatially restricted to the yolk sac in the mouse, in humans, it remains poorly understood. Human foetal placental macropha...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063560/ https://www.ncbi.nlm.nih.gov/pubmed/36997537 http://dx.doi.org/10.1038/s41467-023-37383-2 |
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author | Thomas, Jake R. Appios, Anna Calderbank, Emily F. Yoshida, Nagisa Zhao, Xiaohui Hamilton, Russell S. Moffett, Ashley Sharkey, Andrew Laurenti, Elisa Hanna, Courtney W. McGovern, Naomi |
author_facet | Thomas, Jake R. Appios, Anna Calderbank, Emily F. Yoshida, Nagisa Zhao, Xiaohui Hamilton, Russell S. Moffett, Ashley Sharkey, Andrew Laurenti, Elisa Hanna, Courtney W. McGovern, Naomi |
author_sort | Thomas, Jake R. |
collection | PubMed |
description | The earliest macrophages are generated during embryonic development from erythro-myeloid progenitors (EMPs) via primitive haematopoiesis. Although this process is thought to be spatially restricted to the yolk sac in the mouse, in humans, it remains poorly understood. Human foetal placental macrophages, or Hofbauer cells (HBC), arise during the primitive haematopoietic wave ~18 days post conception and lack expression of human leukocyte antigen (HLA) class II. Here, we identify a population of placental erythro-myeloid progenitors (PEMPs) in the early human placenta that have conserved features of primitive yolk sac EMPs, including the lack of HLF expression. Using in vitro culture experiments we demonstrate that PEMP generate HBC-like cells lacking HLA-DR expression. We find the absence of HLA-DR in primitive macrophages is mediated via epigenetic silencing of class II transactivator, CIITA, the master regulator of HLA class II gene expression. These findings establish the human placenta as an additional site of primitive haematopoiesis. |
format | Online Article Text |
id | pubmed-10063560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100635602023-04-01 Primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced HLA-DR Thomas, Jake R. Appios, Anna Calderbank, Emily F. Yoshida, Nagisa Zhao, Xiaohui Hamilton, Russell S. Moffett, Ashley Sharkey, Andrew Laurenti, Elisa Hanna, Courtney W. McGovern, Naomi Nat Commun Article The earliest macrophages are generated during embryonic development from erythro-myeloid progenitors (EMPs) via primitive haematopoiesis. Although this process is thought to be spatially restricted to the yolk sac in the mouse, in humans, it remains poorly understood. Human foetal placental macrophages, or Hofbauer cells (HBC), arise during the primitive haematopoietic wave ~18 days post conception and lack expression of human leukocyte antigen (HLA) class II. Here, we identify a population of placental erythro-myeloid progenitors (PEMPs) in the early human placenta that have conserved features of primitive yolk sac EMPs, including the lack of HLF expression. Using in vitro culture experiments we demonstrate that PEMP generate HBC-like cells lacking HLA-DR expression. We find the absence of HLA-DR in primitive macrophages is mediated via epigenetic silencing of class II transactivator, CIITA, the master regulator of HLA class II gene expression. These findings establish the human placenta as an additional site of primitive haematopoiesis. Nature Publishing Group UK 2023-03-30 /pmc/articles/PMC10063560/ /pubmed/36997537 http://dx.doi.org/10.1038/s41467-023-37383-2 Text en © Crown 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Thomas, Jake R. Appios, Anna Calderbank, Emily F. Yoshida, Nagisa Zhao, Xiaohui Hamilton, Russell S. Moffett, Ashley Sharkey, Andrew Laurenti, Elisa Hanna, Courtney W. McGovern, Naomi Primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced HLA-DR |
title | Primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced HLA-DR |
title_full | Primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced HLA-DR |
title_fullStr | Primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced HLA-DR |
title_full_unstemmed | Primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced HLA-DR |
title_short | Primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced HLA-DR |
title_sort | primitive haematopoiesis in the human placenta gives rise to macrophages with epigenetically silenced hla-dr |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063560/ https://www.ncbi.nlm.nih.gov/pubmed/36997537 http://dx.doi.org/10.1038/s41467-023-37383-2 |
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