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Overexpression of Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in Jurkat cells

Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains (CBP/PAG) is a membrane-bound adaptor protein that downregulates the activation of Src family kinases present in lipid rafts. To elucidate the role of CBP/PAG in human T cell activation, a cell line overexpres...

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Autores principales: Cong, Bei-Bei, Gao, Mei-Hua, Li, Bing, Wang, Bing, Zhang, Bei, Wang, Li-Na, Zhang, Shu-Chao, Li, Hua-Qiao, Wang, Zhong, Han, Shu-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920370/
https://www.ncbi.nlm.nih.gov/pubmed/29725363
http://dx.doi.org/10.3892/etm.2018.5940
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author Cong, Bei-Bei
Gao, Mei-Hua
Li, Bing
Wang, Bing
Zhang, Bei
Wang, Li-Na
Zhang, Shu-Chao
Li, Hua-Qiao
Wang, Zhong
Han, Shu-Yi
author_facet Cong, Bei-Bei
Gao, Mei-Hua
Li, Bing
Wang, Bing
Zhang, Bei
Wang, Li-Na
Zhang, Shu-Chao
Li, Hua-Qiao
Wang, Zhong
Han, Shu-Yi
author_sort Cong, Bei-Bei
collection PubMed
description Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains (CBP/PAG) is a membrane-bound adaptor protein that downregulates the activation of Src family kinases present in lipid rafts. To elucidate the role of CBP/PAG in human T cell activation, a cell line overexpressing CBP/PAG was constructed and the function of CBP/PAG in Jurkat cells was examined. The present study revealed that increased CBP/PAG expression in T cells significantly enhanced their apoptosis and reduced cellular activation and proliferation. Overexpression of CBP/PAG suppressed the growth of Jurkat cells by recruiting c-Src and its negative regulator, C-terminal Src kinase (CSK), to lipid rafts. The negative regulation of CBP/PAG was enhanced in the presence of anti-cluster of differentiation (CD)59 monoclonal antibodies. In addition, a significant association was revealed between the location of CBP/PAG and CD59, which were co-expressed in the same region of the cell membrane, implicating a potential overlap of the elicited signaling pathways. These results indicate that CBP/PAG functions as a negative regulator of cell signal transduction and suggest that CD59 may strengthen the role of negative feedback regulation.
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spelling pubmed-59203702018-05-03 Overexpression of Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in Jurkat cells Cong, Bei-Bei Gao, Mei-Hua Li, Bing Wang, Bing Zhang, Bei Wang, Li-Na Zhang, Shu-Chao Li, Hua-Qiao Wang, Zhong Han, Shu-Yi Exp Ther Med Articles Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains (CBP/PAG) is a membrane-bound adaptor protein that downregulates the activation of Src family kinases present in lipid rafts. To elucidate the role of CBP/PAG in human T cell activation, a cell line overexpressing CBP/PAG was constructed and the function of CBP/PAG in Jurkat cells was examined. The present study revealed that increased CBP/PAG expression in T cells significantly enhanced their apoptosis and reduced cellular activation and proliferation. Overexpression of CBP/PAG suppressed the growth of Jurkat cells by recruiting c-Src and its negative regulator, C-terminal Src kinase (CSK), to lipid rafts. The negative regulation of CBP/PAG was enhanced in the presence of anti-cluster of differentiation (CD)59 monoclonal antibodies. In addition, a significant association was revealed between the location of CBP/PAG and CD59, which were co-expressed in the same region of the cell membrane, implicating a potential overlap of the elicited signaling pathways. These results indicate that CBP/PAG functions as a negative regulator of cell signal transduction and suggest that CD59 may strengthen the role of negative feedback regulation. D.A. Spandidos 2018-05 2018-03-09 /pmc/articles/PMC5920370/ /pubmed/29725363 http://dx.doi.org/10.3892/etm.2018.5940 Text en Copyright: © Cong et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Cong, Bei-Bei
Gao, Mei-Hua
Li, Bing
Wang, Bing
Zhang, Bei
Wang, Li-Na
Zhang, Shu-Chao
Li, Hua-Qiao
Wang, Zhong
Han, Shu-Yi
Overexpression of Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in Jurkat cells
title Overexpression of Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in Jurkat cells
title_full Overexpression of Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in Jurkat cells
title_fullStr Overexpression of Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in Jurkat cells
title_full_unstemmed Overexpression of Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in Jurkat cells
title_short Overexpression of Csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in Jurkat cells
title_sort overexpression of csk-binding protein/phosphoprotein associated with glycosphingolipid-enriched microdomains induces cluster of differentiation 59-mediated apoptosis in jurkat cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920370/
https://www.ncbi.nlm.nih.gov/pubmed/29725363
http://dx.doi.org/10.3892/etm.2018.5940
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