Cargando…

CSF-1-induced DC-SIGN(+) macrophages are present in the ovarian endometriosis

BACKGROUND: Researchers have found that macrophages are the predominant cells in the peritoneal fluid (PF) of endometriosis patients. CSF-1 has been found to accumulate in the lesions and PF of endometriosis patients, and CSF-1 induces THP-1-derived macrophages to polarize toward a CD169(+) DC-SIGN(...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiaocui, Li, Wei, Hong, Yunlang, Cai, Zhenzhen, Zheng, Min, An
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903642/
https://www.ncbi.nlm.nih.gov/pubmed/35260161
http://dx.doi.org/10.1186/s12958-022-00901-w
_version_ 1784664784085450752
author Xiaocui, Li
Wei, Hong
Yunlang, Cai
Zhenzhen, Zheng
Min, An
author_facet Xiaocui, Li
Wei, Hong
Yunlang, Cai
Zhenzhen, Zheng
Min, An
author_sort Xiaocui, Li
collection PubMed
description BACKGROUND: Researchers have found that macrophages are the predominant cells in the peritoneal fluid (PF) of endometriosis patients. CSF-1 has been found to accumulate in the lesions and PF of endometriosis patients, and CSF-1 induces THP-1-derived macrophages to polarize toward a CD169(+) DC-SIGN(+) phenotype. Does the cytokine CSF-1 induce monocytes to differentiate into macrophages with a DC-SIGN(+) phenotype in endometriosis? METHODS: The level of CSF-1 in the endometrium of control subjects, and the eutopic, and ectopic endometrium of endometriosis patients was evaluated by real-time polymerase chain reaction (qRT–PCR) and was determined by enzyme-linked immunosorbent assay (ELISA) in the PF of control and endometriosis patients. CSF-1 expression was examined with a MILLIPLEX MAP Mouse Cytokine/Chemokine Magnetic Bead Panel. DC-SIGN(+) macrophages were detected by immunohistochemical staining of tissues and flow cytometric analysis of the PF of control subjects (N = 25) and endometriosis (N = 35) patients. The phenotypes and biological activities of CSF-1 -induced macrophages were compared in an in vitro coculture system with peripheral blood lymphocytes from control subjects. RESULTS: In this study, we found that the proportion of DC-SIGN(+) CD169(+) macrophages was higher in the abdominal immune microenvironment of endometriosis patients. CSF-1 was primarily secreted from ectopic lesions and peritoneum in mice with endometriosis. In addition, CSF-1 induced the polarization of macrophages toward a DC-SIGN(+) CD169(+) phenotype; this effect was abolished by the addition of an anti-CSF-1R antibody. CSF-1 induced the generation of DC-SIGN(+) macrophages, leading to a depressed status of peripheral blood lymphocytes, including a high percentage of Treg cells and a low percentage of CD8(+) T cells. Similarly, blockade with the anti-CSF-1R antibody abrogated this biological effect. CONCLUSIONS: This is the first study on the role of DC-SIGN(+) macrophages in the immune microenvironment of endometriosis. Further study of the mechanism and biological activities of CSF-1-induced DC-SIGN(+) macrophages will enhance our understanding of the physiology of endometriosis. GRAPHICAL ABSTRACT: [Image: see text]
format Online
Article
Text
id pubmed-8903642
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-89036422022-03-18 CSF-1-induced DC-SIGN(+) macrophages are present in the ovarian endometriosis Xiaocui, Li Wei, Hong Yunlang, Cai Zhenzhen, Zheng Min, An Reprod Biol Endocrinol Research BACKGROUND: Researchers have found that macrophages are the predominant cells in the peritoneal fluid (PF) of endometriosis patients. CSF-1 has been found to accumulate in the lesions and PF of endometriosis patients, and CSF-1 induces THP-1-derived macrophages to polarize toward a CD169(+) DC-SIGN(+) phenotype. Does the cytokine CSF-1 induce monocytes to differentiate into macrophages with a DC-SIGN(+) phenotype in endometriosis? METHODS: The level of CSF-1 in the endometrium of control subjects, and the eutopic, and ectopic endometrium of endometriosis patients was evaluated by real-time polymerase chain reaction (qRT–PCR) and was determined by enzyme-linked immunosorbent assay (ELISA) in the PF of control and endometriosis patients. CSF-1 expression was examined with a MILLIPLEX MAP Mouse Cytokine/Chemokine Magnetic Bead Panel. DC-SIGN(+) macrophages were detected by immunohistochemical staining of tissues and flow cytometric analysis of the PF of control subjects (N = 25) and endometriosis (N = 35) patients. The phenotypes and biological activities of CSF-1 -induced macrophages were compared in an in vitro coculture system with peripheral blood lymphocytes from control subjects. RESULTS: In this study, we found that the proportion of DC-SIGN(+) CD169(+) macrophages was higher in the abdominal immune microenvironment of endometriosis patients. CSF-1 was primarily secreted from ectopic lesions and peritoneum in mice with endometriosis. In addition, CSF-1 induced the polarization of macrophages toward a DC-SIGN(+) CD169(+) phenotype; this effect was abolished by the addition of an anti-CSF-1R antibody. CSF-1 induced the generation of DC-SIGN(+) macrophages, leading to a depressed status of peripheral blood lymphocytes, including a high percentage of Treg cells and a low percentage of CD8(+) T cells. Similarly, blockade with the anti-CSF-1R antibody abrogated this biological effect. CONCLUSIONS: This is the first study on the role of DC-SIGN(+) macrophages in the immune microenvironment of endometriosis. Further study of the mechanism and biological activities of CSF-1-induced DC-SIGN(+) macrophages will enhance our understanding of the physiology of endometriosis. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2022-03-08 /pmc/articles/PMC8903642/ /pubmed/35260161 http://dx.doi.org/10.1186/s12958-022-00901-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xiaocui, Li
Wei, Hong
Yunlang, Cai
Zhenzhen, Zheng
Min, An
CSF-1-induced DC-SIGN(+) macrophages are present in the ovarian endometriosis
title CSF-1-induced DC-SIGN(+) macrophages are present in the ovarian endometriosis
title_full CSF-1-induced DC-SIGN(+) macrophages are present in the ovarian endometriosis
title_fullStr CSF-1-induced DC-SIGN(+) macrophages are present in the ovarian endometriosis
title_full_unstemmed CSF-1-induced DC-SIGN(+) macrophages are present in the ovarian endometriosis
title_short CSF-1-induced DC-SIGN(+) macrophages are present in the ovarian endometriosis
title_sort csf-1-induced dc-sign(+) macrophages are present in the ovarian endometriosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903642/
https://www.ncbi.nlm.nih.gov/pubmed/35260161
http://dx.doi.org/10.1186/s12958-022-00901-w
work_keys_str_mv AT xiaocuili csf1induceddcsignmacrophagesarepresentintheovarianendometriosis
AT weihong csf1induceddcsignmacrophagesarepresentintheovarianendometriosis
AT yunlangcai csf1induceddcsignmacrophagesarepresentintheovarianendometriosis
AT zhenzhenzheng csf1induceddcsignmacrophagesarepresentintheovarianendometriosis
AT minan csf1induceddcsignmacrophagesarepresentintheovarianendometriosis