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ERK contributes to B cell receptor-induced cell spreading in the A20 mouse B cell line
B cells provide protective immunity by secreting antibodies. When a B cell encounters its specific antigen, B-cell receptor (BCR) signaling initiates actin remodeling. This allows B cells to spread on antigen-bearing surfaces and find more antigen, which increases BCR signaling and facilitates B cel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Caltech Library
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729986/ https://www.ncbi.nlm.nih.gov/pubmed/36506348 http://dx.doi.org/10.17912/micropub.biology.000665 |
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author | Peters, Victoria Deretic, Nikola Choi, Kate Gold, Michael R |
author_facet | Peters, Victoria Deretic, Nikola Choi, Kate Gold, Michael R |
author_sort | Peters, Victoria |
collection | PubMed |
description | B cells provide protective immunity by secreting antibodies. When a B cell encounters its specific antigen, B-cell receptor (BCR) signaling initiates actin remodeling. This allows B cells to spread on antigen-bearing surfaces and find more antigen, which increases BCR signaling and facilitates B cell activation. The BCR activates multiple signaling pathways that target actin-regulatory proteins. Although the extracellular signal-regulated kinases ERK1 and ERK2 regulate actin-dependent processes in adherent cells, their role in BCR-induced actin remodeling had not been investigated. Here, we show that targeting ERK with chemical inhibitors or siRNA inhibits BCR-induced spreading in a murine B cell line. |
format | Online Article Text |
id | pubmed-9729986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Caltech Library |
record_format | MEDLINE/PubMed |
spelling | pubmed-97299862022-12-09 ERK contributes to B cell receptor-induced cell spreading in the A20 mouse B cell line Peters, Victoria Deretic, Nikola Choi, Kate Gold, Michael R MicroPubl Biol New Finding B cells provide protective immunity by secreting antibodies. When a B cell encounters its specific antigen, B-cell receptor (BCR) signaling initiates actin remodeling. This allows B cells to spread on antigen-bearing surfaces and find more antigen, which increases BCR signaling and facilitates B cell activation. The BCR activates multiple signaling pathways that target actin-regulatory proteins. Although the extracellular signal-regulated kinases ERK1 and ERK2 regulate actin-dependent processes in adherent cells, their role in BCR-induced actin remodeling had not been investigated. Here, we show that targeting ERK with chemical inhibitors or siRNA inhibits BCR-induced spreading in a murine B cell line. Caltech Library 2022-11-23 /pmc/articles/PMC9729986/ /pubmed/36506348 http://dx.doi.org/10.17912/micropub.biology.000665 Text en Copyright: © 2022 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | New Finding Peters, Victoria Deretic, Nikola Choi, Kate Gold, Michael R ERK contributes to B cell receptor-induced cell spreading in the A20 mouse B cell line |
title | ERK contributes to B cell receptor-induced cell spreading in the A20 mouse B cell line |
title_full | ERK contributes to B cell receptor-induced cell spreading in the A20 mouse B cell line |
title_fullStr | ERK contributes to B cell receptor-induced cell spreading in the A20 mouse B cell line |
title_full_unstemmed | ERK contributes to B cell receptor-induced cell spreading in the A20 mouse B cell line |
title_short | ERK contributes to B cell receptor-induced cell spreading in the A20 mouse B cell line |
title_sort | erk contributes to b cell receptor-induced cell spreading in the a20 mouse b cell line |
topic | New Finding |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729986/ https://www.ncbi.nlm.nih.gov/pubmed/36506348 http://dx.doi.org/10.17912/micropub.biology.000665 |
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