Cargando…
Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells
Breast cancer remains as a challenging disease with high mortality in women. Increasing evidence points the importance of understanding a crosstalk between breast cancers and immune cells, but little is known about the effect of breast cancer-derived factors on the migratory properties of dendritic...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958978/ https://www.ncbi.nlm.nih.gov/pubmed/27451948 http://dx.doi.org/10.1038/srep30207 |
_version_ | 1782444350718869504 |
---|---|
author | Hwang, Hyundoo Shin, Changsik Park, Juhee Kang, Enoch Choi, Bongseo Han, Jae-A Do, Yoonkyung Ryu, Seongho Cho, Yoon-Kyoung |
author_facet | Hwang, Hyundoo Shin, Changsik Park, Juhee Kang, Enoch Choi, Bongseo Han, Jae-A Do, Yoonkyung Ryu, Seongho Cho, Yoon-Kyoung |
author_sort | Hwang, Hyundoo |
collection | PubMed |
description | Breast cancer remains as a challenging disease with high mortality in women. Increasing evidence points the importance of understanding a crosstalk between breast cancers and immune cells, but little is known about the effect of breast cancer-derived factors on the migratory properties of dendritic cells (DCs) and their consequent capability in inducing T cell immune responses. Utilizing a unique 3D microfluidic device, we here showed that breast cancers (MCF-7, MDA-MB-231, MDA-MB-436 and SK-BR-3)-derived soluble factors increase the migration of DCs toward CCL19. The enhanced migration of DCs was mainly mediated via the highly activated JNK/c-Jun signaling pathway, increasing their directional persistence, while the velocity of DCs was not influenced, particularly when they were co-cultured with triple negative breast cancer cells (TNBCs or MDA-MB-231 and MDA-MB-436). The DCs up-regulated inflammatory cytokines IL-1β and IL-6 and induced T cells more proliferative and resistant against activation-induced cell death (AICD), which secret high levels of inflammatory cytokines IL-1β, IL-6 and IFN-γ. This study demonstrated new possible evasion strategy of TNBCs utilizing their soluble factors that exploit the directionality of DCs toward chemokine responses, leading to the building of inflammatory milieu which may support their own growth. |
format | Online Article Text |
id | pubmed-4958978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49589782016-08-04 Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells Hwang, Hyundoo Shin, Changsik Park, Juhee Kang, Enoch Choi, Bongseo Han, Jae-A Do, Yoonkyung Ryu, Seongho Cho, Yoon-Kyoung Sci Rep Article Breast cancer remains as a challenging disease with high mortality in women. Increasing evidence points the importance of understanding a crosstalk between breast cancers and immune cells, but little is known about the effect of breast cancer-derived factors on the migratory properties of dendritic cells (DCs) and their consequent capability in inducing T cell immune responses. Utilizing a unique 3D microfluidic device, we here showed that breast cancers (MCF-7, MDA-MB-231, MDA-MB-436 and SK-BR-3)-derived soluble factors increase the migration of DCs toward CCL19. The enhanced migration of DCs was mainly mediated via the highly activated JNK/c-Jun signaling pathway, increasing their directional persistence, while the velocity of DCs was not influenced, particularly when they were co-cultured with triple negative breast cancer cells (TNBCs or MDA-MB-231 and MDA-MB-436). The DCs up-regulated inflammatory cytokines IL-1β and IL-6 and induced T cells more proliferative and resistant against activation-induced cell death (AICD), which secret high levels of inflammatory cytokines IL-1β, IL-6 and IFN-γ. This study demonstrated new possible evasion strategy of TNBCs utilizing their soluble factors that exploit the directionality of DCs toward chemokine responses, leading to the building of inflammatory milieu which may support their own growth. Nature Publishing Group 2016-07-25 /pmc/articles/PMC4958978/ /pubmed/27451948 http://dx.doi.org/10.1038/srep30207 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hwang, Hyundoo Shin, Changsik Park, Juhee Kang, Enoch Choi, Bongseo Han, Jae-A Do, Yoonkyung Ryu, Seongho Cho, Yoon-Kyoung Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells |
title | Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells |
title_full | Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells |
title_fullStr | Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells |
title_full_unstemmed | Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells |
title_short | Human breast cancer-derived soluble factors facilitate CCL19-induced chemotaxis of human dendritic cells |
title_sort | human breast cancer-derived soluble factors facilitate ccl19-induced chemotaxis of human dendritic cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958978/ https://www.ncbi.nlm.nih.gov/pubmed/27451948 http://dx.doi.org/10.1038/srep30207 |
work_keys_str_mv | AT hwanghyundoo humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells AT shinchangsik humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells AT parkjuhee humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells AT kangenoch humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells AT choibongseo humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells AT hanjaea humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells AT doyoonkyung humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells AT ryuseongho humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells AT choyoonkyoung humanbreastcancerderivedsolublefactorsfacilitateccl19inducedchemotaxisofhumandendriticcells |