CD206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model

Abstract In endometriosis, M2 MΦs are dominant in endometriotic lesions, but the actual role of M2 MΦ is unclear. CD206 positive (+) MΦ is classified in one of M2 type MΦs and are known to produce cytokines and chemokines. In the present study, we used CD206 diphtheria toxin receptor mice, which ena...

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Autores principales: Yosuke Ono, Osamu Yoshino, Takehiro Hiraoka, Erina Sato, Akiko Furue, Allah Nawaz, Hideki Hatta, Yoshiyuki Fukushi, Shinichiro Wada, Kazuyuki Tobe, Yasushi Hirota, Yutaka Osuga, Nobuya Unno, Shigeru Saito
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/eed1cc98f63d4060a23cb57e168a58b1
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spelling oai:doaj.org-article:eed1cc98f63d4060a23cb57e168a58b12021-12-02T15:23:04ZCD206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model10.1038/s41598-020-79578-32045-2322https://doaj.org/article/eed1cc98f63d4060a23cb57e168a58b12021-01-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-79578-3https://doaj.org/toc/2045-2322Abstract In endometriosis, M2 MΦs are dominant in endometriotic lesions, but the actual role of M2 MΦ is unclear. CD206 positive (+) MΦ is classified in one of M2 type MΦs and are known to produce cytokines and chemokines. In the present study, we used CD206 diphtheria toxin receptor mice, which enable to deplete CD206+ cells with diphtheria toxin (DT) in an endometriosis mouse model. The depletion of CD206+ MΦ decreased the total weight of endometriotic-like lesions significantly (p < 0.05). In the endometriotic-like lesions in the DT group, a lower proliferation of endometriotic cells and the decrease of angiogenesis were observed. In the lesions, the mRNA levels of VEGFA and TGFβ1, angiogenic factors, in the DT group significantly decreased to approximately 50% and 30% of control, respectively. Immunohistochemical study revealed the expressions of VEGFA and an endothelial cell marker CD31 in lesions of the DT group, were dim compared to those in control. Also, the number of TGFβ1 expressing MΦ was significantly reduced compared to control. These data suggest that CD206+ MΦ promotes the formation of endometriotic-like lesions by inducing angiogenesis around the lesions.Yosuke OnoOsamu YoshinoTakehiro HiraokaErina SatoAkiko FurueAllah NawazHideki HattaYoshiyuki FukushiShinichiro WadaKazuyuki TobeYasushi HirotaYutaka OsugaNobuya UnnoShigeru SaitoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yosuke Ono
Osamu Yoshino
Takehiro Hiraoka
Erina Sato
Akiko Furue
Allah Nawaz
Hideki Hatta
Yoshiyuki Fukushi
Shinichiro Wada
Kazuyuki Tobe
Yasushi Hirota
Yutaka Osuga
Nobuya Unno
Shigeru Saito
CD206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model
description Abstract In endometriosis, M2 MΦs are dominant in endometriotic lesions, but the actual role of M2 MΦ is unclear. CD206 positive (+) MΦ is classified in one of M2 type MΦs and are known to produce cytokines and chemokines. In the present study, we used CD206 diphtheria toxin receptor mice, which enable to deplete CD206+ cells with diphtheria toxin (DT) in an endometriosis mouse model. The depletion of CD206+ MΦ decreased the total weight of endometriotic-like lesions significantly (p < 0.05). In the endometriotic-like lesions in the DT group, a lower proliferation of endometriotic cells and the decrease of angiogenesis were observed. In the lesions, the mRNA levels of VEGFA and TGFβ1, angiogenic factors, in the DT group significantly decreased to approximately 50% and 30% of control, respectively. Immunohistochemical study revealed the expressions of VEGFA and an endothelial cell marker CD31 in lesions of the DT group, were dim compared to those in control. Also, the number of TGFβ1 expressing MΦ was significantly reduced compared to control. These data suggest that CD206+ MΦ promotes the formation of endometriotic-like lesions by inducing angiogenesis around the lesions.
format article
author Yosuke Ono
Osamu Yoshino
Takehiro Hiraoka
Erina Sato
Akiko Furue
Allah Nawaz
Hideki Hatta
Yoshiyuki Fukushi
Shinichiro Wada
Kazuyuki Tobe
Yasushi Hirota
Yutaka Osuga
Nobuya Unno
Shigeru Saito
author_facet Yosuke Ono
Osamu Yoshino
Takehiro Hiraoka
Erina Sato
Akiko Furue
Allah Nawaz
Hideki Hatta
Yoshiyuki Fukushi
Shinichiro Wada
Kazuyuki Tobe
Yasushi Hirota
Yutaka Osuga
Nobuya Unno
Shigeru Saito
author_sort Yosuke Ono
title CD206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model
title_short CD206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model
title_full CD206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model
title_fullStr CD206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model
title_full_unstemmed CD206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model
title_sort cd206+ macrophage is an accelerator of endometriotic-like lesion via promoting angiogenesis in the endometriosis mouse model
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/eed1cc98f63d4060a23cb57e168a58b1
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