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. 2021 Apr 23;4:499. doi: 10.1038/s42003-021-02018-z

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© The Author(s) 2021

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — a ELISA for FGL2 concentrations in cell culture supernatant. b FGL2 mRNA expression levels in different kinds of cells. (a, b) The individual immune cell populations were isolated from PBMC. EECs and ESCs from endometrium were primary cultured. c ELISA for FGL2 concentrations in cell culture supernatant. The individual immune cell populations were isolated from the peritoneal fluid of women with or without endometriosis (PF: peritoneal fluid). d CD32B expression on cell surfaces was measured by FCM. e Confocal microscopic analysis of nucleus (blue), CD32B (green), CD68 (red), expression in normal endometrium, eutopic endometrium, and ectopic lesions. Data represent the mean value ± SEM.