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...

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Published inBiomedicines Vol. 9; no. 11; p. 1519
Main Authors 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
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 22.10.2021
MDPI
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Summary: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.
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Y. Ono. and T. Kawakita. contributed equally to the paper.
ISSN:2227-9059
2227-9059
DOI:10.3390/biomedicines9111519