CD24 induces changes to the surface receptors of B cell microvesicles with variable effects on their RNA and protein cargo

Abstract The CD24 cell surface receptor promotes apoptosis in developing B cells, and we recently found that it induces B cells to release plasma membrane-derived, CD24-bearing microvesicles (MVs). Here we have performed a systematic characterization of B cell MVs released from WEHI-231 B lymphoma c...

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Autores principales: D. Craig Ayre, Ian C. Chute, Andrew P. Joy, David A. Barnett, Andrew M. Hogan, Marc P. Grüll, Lourdes Peña-Castillo, Andrew S. Lang, Stephen M. Lewis, Sherri L. Christian
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/5fdc4db9bd1d46f7b03db8910ae362c7
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spelling oai:doaj.org-article:5fdc4db9bd1d46f7b03db8910ae362c72021-12-02T15:05:08ZCD24 induces changes to the surface receptors of B cell microvesicles with variable effects on their RNA and protein cargo10.1038/s41598-017-08094-82045-2322https://doaj.org/article/5fdc4db9bd1d46f7b03db8910ae362c72017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08094-8https://doaj.org/toc/2045-2322Abstract The CD24 cell surface receptor promotes apoptosis in developing B cells, and we recently found that it induces B cells to release plasma membrane-derived, CD24-bearing microvesicles (MVs). Here we have performed a systematic characterization of B cell MVs released from WEHI-231 B lymphoma cells in response to CD24 stimulation. We found that B cells constitutively release MVs of approximately 120 nm, and that CD24 induces an increase in phosphatidylserine-positive MV release. RNA cargo is predominantly comprised of 5S rRNA, regardless of stimulation; however, CD24 causes a decrease in the incorporation of protein coding transcripts. The MV proteome is enriched with mitochondrial and metabolism-related proteins after CD24 stimulation; however, these changes were variable and could not be fully validated by Western blotting. CD24-bearing MVs carry Siglec-2, CD63, IgM, and, unexpectedly, Ter119, but not Siglec-G or MHC-II despite their presence on the cell surface. CD24 stimulation also induces changes in CD63 and IgM expression on MVs that is not mirrored by the changes in cell surface expression. Overall, the composition of these MVs suggests that they may be involved in releasing mitochondrial components in response to pro-apoptotic stress with changes to the surface receptors potentially altering the cell type(s) that interact with the MVs.D. Craig AyreIan C. ChuteAndrew P. JoyDavid A. BarnettAndrew M. HoganMarc P. GrüllLourdes Peña-CastilloAndrew S. LangStephen M. LewisSherri L. ChristianNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-16 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
D. Craig Ayre
Ian C. Chute
Andrew P. Joy
David A. Barnett
Andrew M. Hogan
Marc P. Grüll
Lourdes Peña-Castillo
Andrew S. Lang
Stephen M. Lewis
Sherri L. Christian
CD24 induces changes to the surface receptors of B cell microvesicles with variable effects on their RNA and protein cargo
description Abstract The CD24 cell surface receptor promotes apoptosis in developing B cells, and we recently found that it induces B cells to release plasma membrane-derived, CD24-bearing microvesicles (MVs). Here we have performed a systematic characterization of B cell MVs released from WEHI-231 B lymphoma cells in response to CD24 stimulation. We found that B cells constitutively release MVs of approximately 120 nm, and that CD24 induces an increase in phosphatidylserine-positive MV release. RNA cargo is predominantly comprised of 5S rRNA, regardless of stimulation; however, CD24 causes a decrease in the incorporation of protein coding transcripts. The MV proteome is enriched with mitochondrial and metabolism-related proteins after CD24 stimulation; however, these changes were variable and could not be fully validated by Western blotting. CD24-bearing MVs carry Siglec-2, CD63, IgM, and, unexpectedly, Ter119, but not Siglec-G or MHC-II despite their presence on the cell surface. CD24 stimulation also induces changes in CD63 and IgM expression on MVs that is not mirrored by the changes in cell surface expression. Overall, the composition of these MVs suggests that they may be involved in releasing mitochondrial components in response to pro-apoptotic stress with changes to the surface receptors potentially altering the cell type(s) that interact with the MVs.
format article
author D. Craig Ayre
Ian C. Chute
Andrew P. Joy
David A. Barnett
Andrew M. Hogan
Marc P. Grüll
Lourdes Peña-Castillo
Andrew S. Lang
Stephen M. Lewis
Sherri L. Christian
author_facet D. Craig Ayre
Ian C. Chute
Andrew P. Joy
David A. Barnett
Andrew M. Hogan
Marc P. Grüll
Lourdes Peña-Castillo
Andrew S. Lang
Stephen M. Lewis
Sherri L. Christian
author_sort D. Craig Ayre
title CD24 induces changes to the surface receptors of B cell microvesicles with variable effects on their RNA and protein cargo
title_short CD24 induces changes to the surface receptors of B cell microvesicles with variable effects on their RNA and protein cargo
title_full CD24 induces changes to the surface receptors of B cell microvesicles with variable effects on their RNA and protein cargo
title_fullStr CD24 induces changes to the surface receptors of B cell microvesicles with variable effects on their RNA and protein cargo
title_full_unstemmed CD24 induces changes to the surface receptors of B cell microvesicles with variable effects on their RNA and protein cargo
title_sort cd24 induces changes to the surface receptors of b cell microvesicles with variable effects on their rna and protein cargo
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/5fdc4db9bd1d46f7b03db8910ae362c7
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