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PI3K Signaling in Normal B Cells and Chronic Lymphocytic Leukemia (CLL)
B cells provide immunity to extracellular pathogens by secreting a diverse repertoire of antibodies with high affinity and specificity for exposed antigens. The B cell receptor (B cell receptor (BCR)) is a transmembrane antibody, which facilitates the clonal selection of B cells producing secreted a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704136/ https://www.ncbi.nlm.nih.gov/pubmed/26350103 http://dx.doi.org/10.1007/82_2015_484 |
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author | Okkenhaug, Klaus Burger, Jan A. |
author_facet | Okkenhaug, Klaus Burger, Jan A. |
author_sort | Okkenhaug, Klaus |
collection | PubMed |
description | B cells provide immunity to extracellular pathogens by secreting a diverse repertoire of antibodies with high affinity and specificity for exposed antigens. The B cell receptor (B cell receptor (BCR)) is a transmembrane antibody, which facilitates the clonal selection of B cells producing secreted antibodies of the same specificity. The diverse antibody repertoire is generated by V(D)J recombination of heavy and light chain genes, whereas affinity maturation is mediated by activation-induced cytidine deaminase (AID)-mediated mutagenesis. These processes, which are essential for the generation of adaptive humoral immunity, also render B cells susceptible to chromosomal rearrangements and point mutations that in some cases lead to cancer. In this chapter, we will review the central role of PI3Ks in mediating signals from the B cell receptor that not only facilitate the development of functional B cell repertoire, but also support the growth and survival of neoplastic B cells, focusing on chronic lymphocytic leukemia (chronic lymphocytic leukemia (CLL)) B cells. Perhaps because of the central role played by PI3K in BCR signaling, B cell Leukemia and Lymphomas are the first diseases for which a PI3K inhibitor has been approved for clinical use. |
format | Online Article Text |
id | pubmed-4704136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-47041362016-01-07 PI3K Signaling in Normal B Cells and Chronic Lymphocytic Leukemia (CLL) Okkenhaug, Klaus Burger, Jan A. Curr Top Microbiol Immunol Article B cells provide immunity to extracellular pathogens by secreting a diverse repertoire of antibodies with high affinity and specificity for exposed antigens. The B cell receptor (B cell receptor (BCR)) is a transmembrane antibody, which facilitates the clonal selection of B cells producing secreted antibodies of the same specificity. The diverse antibody repertoire is generated by V(D)J recombination of heavy and light chain genes, whereas affinity maturation is mediated by activation-induced cytidine deaminase (AID)-mediated mutagenesis. These processes, which are essential for the generation of adaptive humoral immunity, also render B cells susceptible to chromosomal rearrangements and point mutations that in some cases lead to cancer. In this chapter, we will review the central role of PI3Ks in mediating signals from the B cell receptor that not only facilitate the development of functional B cell repertoire, but also support the growth and survival of neoplastic B cells, focusing on chronic lymphocytic leukemia (chronic lymphocytic leukemia (CLL)) B cells. Perhaps because of the central role played by PI3K in BCR signaling, B cell Leukemia and Lymphomas are the first diseases for which a PI3K inhibitor has been approved for clinical use. Springer International Publishing 2015-09-09 /pmc/articles/PMC4704136/ /pubmed/26350103 http://dx.doi.org/10.1007/82_2015_484 Text en © The Author(s) 2015 Open Access This chapter is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, 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. |
spellingShingle | Article Okkenhaug, Klaus Burger, Jan A. PI3K Signaling in Normal B Cells and Chronic Lymphocytic Leukemia (CLL) |
title | PI3K Signaling in Normal B Cells and Chronic Lymphocytic
Leukemia (CLL) |
title_full | PI3K Signaling in Normal B Cells and Chronic Lymphocytic
Leukemia (CLL) |
title_fullStr | PI3K Signaling in Normal B Cells and Chronic Lymphocytic
Leukemia (CLL) |
title_full_unstemmed | PI3K Signaling in Normal B Cells and Chronic Lymphocytic
Leukemia (CLL) |
title_short | PI3K Signaling in Normal B Cells and Chronic Lymphocytic
Leukemia (CLL) |
title_sort | pi3k signaling in normal b cells and chronic lymphocytic
leukemia (cll) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704136/ https://www.ncbi.nlm.nih.gov/pubmed/26350103 http://dx.doi.org/10.1007/82_2015_484 |
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