Revisiting the role of interleukin-8 in chronic lymphocytic leukemia
The proliferation and survival of malignant B cells in chronic lymphocytic leukemia (CLL) depend on signals from the microenvironment in lymphoid tissues. Among a plethora of soluble factors, IL-8 has been considered one of the most relevant to support CLL B cell progression in an autocrine fashion,...
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_20452322_v7_n1_p_Risnik http://hdl.handle.net/20.500.12110/paper_20452322_v7_n1_p_Risnik |
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paper:paper_20452322_v7_n1_p_Risnik2023-06-08T16:33:31Z Revisiting the role of interleukin-8 in chronic lymphocytic leukemia The proliferation and survival of malignant B cells in chronic lymphocytic leukemia (CLL) depend on signals from the microenvironment in lymphoid tissues. Among a plethora of soluble factors, IL-8 has been considered one of the most relevant to support CLL B cell progression in an autocrine fashion, even though the expression of IL-8 receptors, CXCR1 and CXCR2, on leukemic B cells has not been reported. Here we show that circulating CLL B cells neither express CXCR1 or CXCR2 nor they respond to exogenous IL-8 when cultured in vitro alone or in the presence of monocytes/nurse-like cells. By intracellular staining and ELISA we show that highly purified CLL B cells do not produce IL-8 spontaneously or upon activation through the B cell receptor. By contrast, we found that a minor proportion (<0.5%) of contaminating monocytes in enriched suspensions of leukemic cells might be the actual source of IL-8 due to their strong capacity to release this cytokine. Altogether our results indicate that CLL B cells are not able to secrete or respond to IL-8 and highlight the importance of methodological details in in vitro experiments. © 2017 The Author(s). 2017 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_20452322_v7_n1_p_Risnik http://hdl.handle.net/20.500.12110/paper_20452322_v7_n1_p_Risnik |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
description |
The proliferation and survival of malignant B cells in chronic lymphocytic leukemia (CLL) depend on signals from the microenvironment in lymphoid tissues. Among a plethora of soluble factors, IL-8 has been considered one of the most relevant to support CLL B cell progression in an autocrine fashion, even though the expression of IL-8 receptors, CXCR1 and CXCR2, on leukemic B cells has not been reported. Here we show that circulating CLL B cells neither express CXCR1 or CXCR2 nor they respond to exogenous IL-8 when cultured in vitro alone or in the presence of monocytes/nurse-like cells. By intracellular staining and ELISA we show that highly purified CLL B cells do not produce IL-8 spontaneously or upon activation through the B cell receptor. By contrast, we found that a minor proportion (<0.5%) of contaminating monocytes in enriched suspensions of leukemic cells might be the actual source of IL-8 due to their strong capacity to release this cytokine. Altogether our results indicate that CLL B cells are not able to secrete or respond to IL-8 and highlight the importance of methodological details in in vitro experiments. © 2017 The Author(s). |
title |
Revisiting the role of interleukin-8 in chronic lymphocytic leukemia |
spellingShingle |
Revisiting the role of interleukin-8 in chronic lymphocytic leukemia |
title_short |
Revisiting the role of interleukin-8 in chronic lymphocytic leukemia |
title_full |
Revisiting the role of interleukin-8 in chronic lymphocytic leukemia |
title_fullStr |
Revisiting the role of interleukin-8 in chronic lymphocytic leukemia |
title_full_unstemmed |
Revisiting the role of interleukin-8 in chronic lymphocytic leukemia |
title_sort |
revisiting the role of interleukin-8 in chronic lymphocytic leukemia |
publishDate |
2017 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_20452322_v7_n1_p_Risnik http://hdl.handle.net/20.500.12110/paper_20452322_v7_n1_p_Risnik |
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1768545439914655744 |