Involvement of nuclear factor-kappaB in macrophage migration inhibitory factor gene transcription up-regulation induced by interleukin- 1 beta in ectopic endometrial cells
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⤵ 19 in-corpus citations
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Interleukin-1β up-regulates macrophage migration inhibitory factor gene transcription in ectopic endometrial cells through the activation of nuclear factor-κB.
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Abstract
OBJECTIVE: To investigate the involvement of the nuclear factor (NF)-kappaB in the interleukin (IL)-1 beta-mediated macrophage migration inhibitory factor (MIF) gene activation.
DESIGN: Prospective study.
SETTING: Human reproduction research laboratory.
PATIENT(S): Nine women with endometriotic lesions.
INTERVENTION(S): Endometriotic lesions were obtained during laparoscopic surgery.
MAIN OUTCOME MEASURE(S): The MIF protein secretion was analyzed by ELISA, MIF mRNA expression by quantitative real-time polymerase chain reaction (PCR), NF-kappaB translocation into the nucleus by electrophoresis mobility shift assay, I kappaB phosphorylation and degradation by Western blot, and human MIF promoter activity by transient cell transfection.
RESULT(S): This study showed a significant dose-dependent increase of MIF protein secretion and mRNA expression, the NF-kappaB translocation into the nucleus, I kappaB phosphorylation, I kappaB degradation, and human MIF promoter activity in endometriotic stromal cells in response to IL-1 beta. Curcumin (NF-kappaB inhibitor) significantly inhibited all these IL-1 beta-mediated effects. Analysis of the activity of deletion constructs of the human MIF promoter and a computer search localized two putative regulatory elements corresponding to NF-kappaB binding sites at positions -2538/-2528 bp and -1389/-1380 bp.
CONCLUSION(S): This study suggests the involvement of the nuclear transcription factor NF-kappaB in MIF gene activation in ectopic endometrial cells in response to IL-1 beta and identifies a possible pathway of endometriosis-associated inflammation and ectopic cell growth.
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Cited by (20)
- Targeting TLR4 Attenuates Endometriosis Progression by Suppressing NF-κB/NLRP3 Inflammasome Activation and Angiogenesis 2026
- The interaction between inflammation and estrogen in adenomyosis : from molecular mechanisms to therapeutic strategies 2026
- Endometriosis as a risk factor for age-related macular degeneration: A nationwide population-based study 2025
- An Update on the Multifaceted Role of NF-kappaB in Endometriosis 2022
- A systematic review of toll-like receptors in endometriosis 2021
- Role of inflammation in benign gynecologic disorders: from pathogenesis to novel therapies† 2021
- Therapeutic potential of curcumin in endometrial disorders: Current status and future perspectives 2021
- Co-morbidity of type 1 diabetes and endometriosis: bringing a new paradigm into focus 2019
- Low-dose SKA Progesterone and Interleukin-10 modulate the inflammatory pathway in endometriotic cell lines 2017
- Kinase signalling pathways in endometriosis: potential targets for non-hormonal therapeutics 2016
- Endometriosis and possible inflammation markers 2015
- An overview of early drug development for endometriosis 2015
- Macrophages in Pathophysiology of Endometriosis 2014
- Physiologic activation of nuclear factor kappa-B in the endometrium during the menstrual cycle is altered in endometriosis patients 2011
- MiR-199a attenuates endometrial stromal cell invasiveness through suppression of the IKKβ/NF-κB pathway and reduced interleukin-8 expression 2011
- Constitutive and tumor necrosis factor-alpha-stimulated activation of nuclear factor-kappaB in immortalized endometriotic cells and their suppression by trichostatin A 2010
- Involvement of the nuclear factor-kB pathway in the pathogenesis of endometriosis 2010
- Involvement of the nuclear factor-κB pathway in the pathogenesis of endometriosis 2010
- Evaluation of erythrocyte band 3 phosphotyrosine level, glutathione content, CA-125, and human epididymal secretory protein E4 as combined parameters in endometriosis 2010
- TAK1 activation for cytokine synthesis and proliferation of endometriotic cells 2009
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- pubmed
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