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Sphingosine 1-Phosphate (S1P) in the Peritoneal Fluid Skews M2 Macrophage and Contributes to the Development of Endometriosis
Sphingosine 1-phosphate (S1P), an inflammatory mediator, is abundantly contained in red blood cells and platelets. We hypothesized that the S1P concentration in the peritoneal cavity would increase especially during the menstrual phase due to the reflux of menstrual blood, and investigated the S1P c...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614877/ https://www.ncbi.nlm.nih.gov/pubmed/34829748 http://dx.doi.org/10.3390/biomedicines9111519 |
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author | Ono, Yosuke Kawakita, Takako Yoshino, Osamu Sato, Erina Kano, Kuniyuki Ohba, Mai Okuno, Toshiaki Ito, Masami Koga, Kaori Honda, Masako Furue, Akiko Hiraoka, Takehiro Wada, Shinichiro Iwasa, Takeshi Yokomizo, Takehiko Aoki, Junken Maeda, Nagamasa Unno, Nobuya Osuga, Yutaka Hirata, Shuji |
author_facet | Ono, Yosuke Kawakita, Takako Yoshino, Osamu Sato, Erina Kano, Kuniyuki Ohba, Mai Okuno, Toshiaki Ito, Masami Koga, Kaori Honda, Masako Furue, Akiko Hiraoka, Takehiro Wada, Shinichiro Iwasa, Takeshi Yokomizo, Takehiko Aoki, Junken Maeda, Nagamasa Unno, Nobuya Osuga, Yutaka Hirata, Shuji |
author_sort | Ono, Yosuke |
collection | PubMed |
description | Sphingosine 1-phosphate (S1P), an inflammatory mediator, is abundantly contained in red blood cells and platelets. We hypothesized that the S1P concentration in the peritoneal cavity would increase especially during the menstrual phase due to the reflux of menstrual blood, and investigated the S1P concentration in the human peritoneal fluid (PF) from 14 non-endometriosis and 19 endometriosis patients. Although the relatively small number of samples requires caution in interpreting the results, S1P concentration in the PF during the menstrual phase was predominantly increased compared to the non-menstrual phase, regardless of the presence or absence of endometriosis. During the non-menstrual phase, patients with endometriosis showed a significant increase in S1P concentration compared to controls. In vitro experiments using human intra-peritoneal macrophages (MΦ) showed that S1P stimulation biased them toward an M2MΦ-dominant condition and increased the expression of IL-6 and COX-2. An in vivo study showed that administration of S1P increased the size of the endometriotic-like lesion in a mouse model of endometriosis. |
format | Online Article Text |
id | pubmed-8614877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86148772021-11-26 Sphingosine 1-Phosphate (S1P) in the Peritoneal Fluid Skews M2 Macrophage and Contributes to the Development of Endometriosis Ono, Yosuke Kawakita, Takako Yoshino, Osamu Sato, Erina Kano, Kuniyuki Ohba, Mai Okuno, Toshiaki Ito, Masami Koga, Kaori Honda, Masako Furue, Akiko Hiraoka, Takehiro Wada, Shinichiro Iwasa, Takeshi Yokomizo, Takehiko Aoki, Junken Maeda, Nagamasa Unno, Nobuya Osuga, Yutaka Hirata, Shuji Biomedicines Article Sphingosine 1-phosphate (S1P), an inflammatory mediator, is abundantly contained in red blood cells and platelets. We hypothesized that the S1P concentration in the peritoneal cavity would increase especially during the menstrual phase due to the reflux of menstrual blood, and investigated the S1P concentration in the human peritoneal fluid (PF) from 14 non-endometriosis and 19 endometriosis patients. Although the relatively small number of samples requires caution in interpreting the results, S1P concentration in the PF during the menstrual phase was predominantly increased compared to the non-menstrual phase, regardless of the presence or absence of endometriosis. During the non-menstrual phase, patients with endometriosis showed a significant increase in S1P concentration compared to controls. In vitro experiments using human intra-peritoneal macrophages (MΦ) showed that S1P stimulation biased them toward an M2MΦ-dominant condition and increased the expression of IL-6 and COX-2. An in vivo study showed that administration of S1P increased the size of the endometriotic-like lesion in a mouse model of endometriosis. MDPI 2021-10-22 /pmc/articles/PMC8614877/ /pubmed/34829748 http://dx.doi.org/10.3390/biomedicines9111519 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ono, Yosuke Kawakita, Takako Yoshino, Osamu Sato, Erina Kano, Kuniyuki Ohba, Mai Okuno, Toshiaki Ito, Masami Koga, Kaori Honda, Masako Furue, Akiko Hiraoka, Takehiro Wada, Shinichiro Iwasa, Takeshi Yokomizo, Takehiko Aoki, Junken Maeda, Nagamasa Unno, Nobuya Osuga, Yutaka Hirata, Shuji Sphingosine 1-Phosphate (S1P) in the Peritoneal Fluid Skews M2 Macrophage and Contributes to the Development of Endometriosis |
title | Sphingosine 1-Phosphate (S1P) in the Peritoneal Fluid Skews M2 Macrophage and Contributes to the Development of Endometriosis |
title_full | Sphingosine 1-Phosphate (S1P) in the Peritoneal Fluid Skews M2 Macrophage and Contributes to the Development of Endometriosis |
title_fullStr | Sphingosine 1-Phosphate (S1P) in the Peritoneal Fluid Skews M2 Macrophage and Contributes to the Development of Endometriosis |
title_full_unstemmed | Sphingosine 1-Phosphate (S1P) in the Peritoneal Fluid Skews M2 Macrophage and Contributes to the Development of Endometriosis |
title_short | Sphingosine 1-Phosphate (S1P) in the Peritoneal Fluid Skews M2 Macrophage and Contributes to the Development of Endometriosis |
title_sort | sphingosine 1-phosphate (s1p) in the peritoneal fluid skews m2 macrophage and contributes to the development of endometriosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8614877/ https://www.ncbi.nlm.nih.gov/pubmed/34829748 http://dx.doi.org/10.3390/biomedicines9111519 |
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