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PLoS One
2017 Nov 10;1211:e0187333. doi: 10.1371/journal.pone.0187333.
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The axis IL-10/claudin-10 is implicated in the modulation of aggressiveness of melanoma cells by B-1 lymphocytes.
Perez EC
,
Xander P
,
Laurindo MFL
,
Novaes E Brito RR
,
Vivanco BC
,
Mortara RA
,
Mariano M
,
Lopes JD
,
Keller AC
.
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B-1 lymphocytes are known to increase the metastatic potential of B16F10 melanoma cells via the extracellular signal-regulated kinase (ERK) pathway. Since IL-10 is associated with B-1 cells performance, we hypothesized that IL-10 could be implicated in the progression of melanoma. In the present work, we found that the C57BL/6 mice, inoculated with B16F10 cells that were co-cultivated with B-1 lymphocytes from IL-10 knockout mice, developed fewer metastatic nodules than the ones which were injected with the melanoma cells that were cultivated in the presence of wild-type B-1 cells. The impairment of metastatic potential of the B16F10 cells was correlated with low activation of the ERK signaling pathway, supporting the idea that the production of IL-10 by B-1 cells influences the behavior of the tumor. A microarray analysis of the B-1 lymphocytes revealed that IL-10 deficiency is associated with down-regulation of the genes that code for claudin-10, a protein that is involved in cell-to-cell contact and that has been linked to lung adenocarcinoma. In order to determine the impact of claudin-10 in the cross-talk between B-1 lymphocytes and the B16F10 tumor cells, we took advantage of small interfering RNA. The silencing of claudin-10 gene in B-1 lymphocytes inhibited activation of the ERK pathway and abrogated the B-1-induced aggressive behavior of the B16F10 cells. Thus, our findings suggest that the axis IL-10/claudin-10 is a promising target for the development of therapeutic agents against aggressive melanoma.
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29145406
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Fig 3. IL-10 deficiency is associated with impaired expression of claudin-10 in B-1 lymphocytes.Total RNA of B-1 lymphocytes enriched culture from wild-type (B-1WT) or IL-10-/- knockout (B-1IL-10-/-) mice was submitted to microarray analysis. A) Heatmap showing differential expression of eleven transcripts between B-1WT and B-1IL-10-/- lymphocytes, and the down-regulation of claudin-10 (cldn-10) in B-1IL-10-/- samples. B) Western blot analysis of cldn-10 protein in whole-cell extracts from B-1WT and B-1IL-10-/-. β-actin protein was used as internal control.
Aziz,
The role of B-1 cells in inflammation.
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Aziz,
The role of B-1 cells in inflammation.
2015,
Pubmed
Baumgarth,
The double life of a B-1 cell: self-reactivity selects for protective effector functions.
2011,
Pubmed
Bolstad,
A comparison of normalization methods for high density oligonucleotide array data based on variance and bias.
2003,
Pubmed
Choi,
Baicalein Inhibits the Migration and Invasion of B16F10 Mouse Melanoma Cells through Inactivation of the PI3K/Akt Signaling Pathway.
2017,
Pubmed
Eljaszewicz,
Collaborating with the enemy: function of macrophages in the development of neoplastic disease.
2013,
Pubmed
Fujimura,
Tumor-associated macrophages in skin: How to treat their heterogeneity and plasticity.
2016,
Pubmed
Gonzaga,
Evaluation of Experimental Infection with L. ( L.) Amazonensis in X-Linked Immunodeficient Mice.
2017,
Pubmed
González-Mariscal,
Crosstalk of tight junction components with signaling pathways.
2008,
Pubmed
Günzel,
Claudin-10 exists in six alternatively spliced isoforms that exhibit distinct localization and function.
2009,
Pubmed
Irizarry,
Exploration, normalization, and summaries of high density oligonucleotide array probe level data.
2003,
Pubmed
Lopes,
B-1 cell: the precursor of a novel mononuclear phagocyte with immuno-regulatory properties.
2009,
Pubmed
Neesse,
Claudin-4 as therapeutic target in cancer.
2012,
Pubmed
Neesse,
Claudin-4-targeted optical imaging detects pancreatic cancer and its precursor lesions.
2013,
Pubmed
Popi,
B-1 cells facilitate Paracoccidioides brasiliensis infection in mice via IL-10 secretion.
2008,
Pubmed
Popi,
An Overview of B-1 Cells as Antigen-Presenting Cells.
2016,
Pubmed
Pérez,
B-1 lymphocytes increase metastatic behavior of melanoma cells through the extracellular signal-regulated kinase pathway.
2008,
Pubmed
Sindhava,
Multiple regulatory mechanisms control B-1 B cell activation.
2012,
Pubmed
Singh,
Claudin proteins, outside-in signaling, and carcinogenesis.
2017,
Pubmed
Soini,
Tight junctions in lung cancer and lung metastasis: a review.
2012,
Pubmed
Staquicini,
A subset of host B lymphocytes controls melanoma metastasis through a melanoma cell adhesion molecule/MUC18-dependent interaction: evidence from mice and humans.
2008,
Pubmed
Vigna,
Granuloma formation in vitro requires B-1 cells and is modulated by Paracoccidioides brasiliensis gp43 antigen.
2006,
Pubmed
Xander,
Crosstalk between B16 melanoma cells and B-1 lymphocytes induces global changes in tumor cell gene expression.
2013,
Pubmed
,
Echinobase
Zhang,
Expression of CLDN1 and CLDN10 in lung adenocarcinoma in situ and invasive lepidic predominant adenocarcinoma.
2013,
Pubmed