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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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