Front. Immunol.Frontiers in ImmunologyFront. Immunol.1664-3224Frontiers Media S.A.10.3389/fimmu.2025.1748838CorrectionCorrection: Promotion of BST2 expression by the transcription factor IRF6 affects the progression of endometriosisLiJixin1†ConceptualizationWriting – original draftHeYanan1†Funding acquisitionWriting – original draftQuYanjun1MethodologySupervisionWriting – review & editingRenChengcheng1InvestigationMethodologyWriting – review & editingWangXiaotong1Formal analysisInvestigationWriting – review & editingChengYan1Project administrationValidationWriting – review & editingSunLiyuan1Data curationMethodologyWriting – review & editingZhangXin2Project administrationWriting – review & editingZhangGuangmei1*ConceptualizationWriting – original draftDepartment of Gynecology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, ChinaCentral Laboratory, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, ChinaCorrespondence: Guangmei Zhang, hydyyguangmeizhang@126.com
These authors have contributed equally to this work
There was a mistake in Figure 3B as published. Two small images (a and b) were placed in the wrong position.
The corrected Figure 3B appears below. The positions of the two images have been swapped and updated.
Also, due to figure compression, the quality of the Western blot images for β-tubulin in Figure 2F and actin in Figure 6A was compromised. To avoid misleading readers, we have uploaded high-quality versions of these two WB images as requested.
Identification of endometrial stromal cells and BST2 expression at the cellular level. (A, B), The identification of endometrial stromal cells on the morphology (A) and Immunofluorescence (B). (C, D), BST2 mRNA (C) and protein (D) expression at the cellular level. (E, F), Identification of the transfection efficiency of Si-BST2 at the mRNA (E) and protein (F) levels. *p < 0.05; **p < 0.01; ****p < 0.0001.
Three black-and-white images show a bright, elongated object against varied backgrounds. The first and last images display the object on a white background, while the middle image features it in a darker context with blurred surroundings. The object appears consistent in each frame.
The effect of BST2 on cell proliferation and apoptosis. (A–C), The proliferation of EESCs was examined by CCK-8 assay (A) and EdU (B, C) after Si-BST2 or Si-NC treatment for 48 h. (D), The proliferation-related protein PCNA was measured by Western blot assay after Si-BST2 or Si-NC treatment for 48 h. (E), The Flow cytometry was performed to detect the apoptosis rates of the EESCs transfected with Si-BST2 or Si-NC. (F), Western blot analysis was used to measure the levels of Bax and Bcl2 in cells transfected with Si-BST2 or Si-NC. *p < 0.05; **p < 0.01.
Fluorescence micrographs showing EdU, DAPI, and merged images. Top row: Si-NC treatment showing green EdU and blue DAPI fluorescence. Bottom row: Si-BST2 treatment with similar fluorescence patterns. Scale bars are included.
BST2 activated the NF-κB signaling pathway. (A), The expressions of key proteins of NF-κB pathway were measured by western blot analysis after transfection with Si-BST2 or Si-NC for 48h. (B), The Representative images of Immunofluorescence showed the cellular localization of NF-κB p65 protein in EESCs after transfection with Si-BST2 or Si-NC for 48h. (C, D), The protein expressions of NF-κB pathway were measured by western blot analysis after treatment with Si-BST2 or Si-NC or/and the NF-κB pathway activator IL-1β. ns, p ≥ 0.05; *p < 0.05; **p < 0.01; ****p < 0.0001.
Three panels display X-ray images. The left and right panels show bright areas on a light background with black bands. The center panel shows a similar bright area on a dark background with two bands.
High-quality raw image of β-tubulin in Figure 2F:
High-quality raw image of actin in Figure 6A:
The original version of this article has been updated.
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Edited and reviewed by: Bernd Rolauffs, University of Freiburg Medical Center, Germany