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Factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion
Human antibody-secreting cells (ASC) in peripheral blood are found after vaccination or infection but rapidly apoptose unless they migrate to the bone marrow (BM). Yet, elements of the BM microenvironment required to sustain long-lived plasma cells (LLPC) remain elusive. Here, we identify BM factors...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135805/ https://www.ncbi.nlm.nih.gov/pubmed/30209264 http://dx.doi.org/10.1038/s41467-018-05853-7 |
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author | Nguyen, Doan C. Garimalla, Swetha Xiao, Haopeng Kyu, Shuya Albizua, Igor Galipeau, Jacques Chiang, Kuang-Yueh Waller, Edmund K. Wu, Ronghu Gibson, Greg Roberson, James Lund, Frances E. Randall, Troy D. Sanz, Iñaki Lee, F. Eun-Hyung |
author_facet | Nguyen, Doan C. Garimalla, Swetha Xiao, Haopeng Kyu, Shuya Albizua, Igor Galipeau, Jacques Chiang, Kuang-Yueh Waller, Edmund K. Wu, Ronghu Gibson, Greg Roberson, James Lund, Frances E. Randall, Troy D. Sanz, Iñaki Lee, F. Eun-Hyung |
author_sort | Nguyen, Doan C. |
collection | PubMed |
description | Human antibody-secreting cells (ASC) in peripheral blood are found after vaccination or infection but rapidly apoptose unless they migrate to the bone marrow (BM). Yet, elements of the BM microenvironment required to sustain long-lived plasma cells (LLPC) remain elusive. Here, we identify BM factors that maintain human ASC > 50 days in vitro. The critical components of the cell-free in vitro BM mimic consist of products from primary BM mesenchymal stromal cells (MSC), a proliferation-inducing ligand (APRIL), and hypoxic conditions. Comparative analysis of protein–protein interactions between BM-MSC proteomics with differential RNA transcriptomics of blood ASC and BM LLPC identify two major survival factors, fibronectin and YWHAZ. The MSC secretome proteins and hypoxic conditions play a role in LLPC survival utilizing mechanisms that downregulate mTORC1 signaling and upregulate hypoxia signatures. In summary, we identify elements of the BM survival niche critical for maturation of blood ASC to BM LLPC. |
format | Online Article Text |
id | pubmed-6135805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61358052018-09-14 Factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion Nguyen, Doan C. Garimalla, Swetha Xiao, Haopeng Kyu, Shuya Albizua, Igor Galipeau, Jacques Chiang, Kuang-Yueh Waller, Edmund K. Wu, Ronghu Gibson, Greg Roberson, James Lund, Frances E. Randall, Troy D. Sanz, Iñaki Lee, F. Eun-Hyung Nat Commun Article Human antibody-secreting cells (ASC) in peripheral blood are found after vaccination or infection but rapidly apoptose unless they migrate to the bone marrow (BM). Yet, elements of the BM microenvironment required to sustain long-lived plasma cells (LLPC) remain elusive. Here, we identify BM factors that maintain human ASC > 50 days in vitro. The critical components of the cell-free in vitro BM mimic consist of products from primary BM mesenchymal stromal cells (MSC), a proliferation-inducing ligand (APRIL), and hypoxic conditions. Comparative analysis of protein–protein interactions between BM-MSC proteomics with differential RNA transcriptomics of blood ASC and BM LLPC identify two major survival factors, fibronectin and YWHAZ. The MSC secretome proteins and hypoxic conditions play a role in LLPC survival utilizing mechanisms that downregulate mTORC1 signaling and upregulate hypoxia signatures. In summary, we identify elements of the BM survival niche critical for maturation of blood ASC to BM LLPC. Nature Publishing Group UK 2018-09-12 /pmc/articles/PMC6135805/ /pubmed/30209264 http://dx.doi.org/10.1038/s41467-018-05853-7 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Nguyen, Doan C. Garimalla, Swetha Xiao, Haopeng Kyu, Shuya Albizua, Igor Galipeau, Jacques Chiang, Kuang-Yueh Waller, Edmund K. Wu, Ronghu Gibson, Greg Roberson, James Lund, Frances E. Randall, Troy D. Sanz, Iñaki Lee, F. Eun-Hyung Factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion |
title | Factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion |
title_full | Factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion |
title_fullStr | Factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion |
title_full_unstemmed | Factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion |
title_short | Factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion |
title_sort | factors of the bone marrow microniche that support human plasma cell survival and immunoglobulin secretion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135805/ https://www.ncbi.nlm.nih.gov/pubmed/30209264 http://dx.doi.org/10.1038/s41467-018-05853-7 |
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