Int Immunopharmacol. 2020;86:106695.
Soluble Siglec-9 alleviates intestinal inflammation through inhibition of the NF-κB pathway.
제1저자 강은애 · 교신저자 김주성
소속 (4)
- Department of Internal Medicine and Institute of Gastroenterology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
- Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
- Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul 03080, Republic of Korea; Department of Gastroenterology, Mediplex Sejong Hospital, Incheon 21080, Republic of Korea.
- Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul 03080, Republic of Korea. Electronic address: jooskim@snu.ac.kr.
Abstract
BACKGROUND Sialic acid-binding immunoglobulin-like lectins (Siglecs) are a superfamily of immunoreceptors recognizing sialic acid. Siglec-9 has been shown to mediate inhibitory immune responses. The aim of this study was to evaluate the effect of a soluble form of Siglec-9 (sSiglec-9) on inflamed intestinal epithelial cells (IECs), murine macrophages, and experimental murine colitis models.
METHODS COLO 205 human IECs and RAW 264.7 murine macrophages were pretreated with sSiglec-9 and then stimulated with TNF-α or lipopolysaccharides, respectively. The expression of proinflammatory cytokines such as IL-8 and TNF-α was measured using real-time RT-PCR and ELISA. To demonstrate the inhibitory effects of sSiglec-9 on the NF-κB pathway, IκBα phosphorylation/degradation was determined using western blotting and the DNA binding activity of NF-κB was evaluated using an electrophoretic mobility shift assay. Further, mouse models with dextran sulfate sodium-induced acute colitis and piroxicam-induced IL-10-/- chronic colitis were generated. Intraperitoneal injections of sSiglec-9 were performed, and body weight, colon length, and histopathologic findings were examined.
RESULTS sSiglec-9 suppressed IL-8 and TNF-α gene expression in stimulated COLO 205 and RAW 264.7 cells. sSiglec-9 inhibited IκBα phosphorylation/degradation and the DNA binding activity of NF-κB. sSiglec-9 injections significantly ameliorated weight loss, colon shortening, and the severity of intestinal inflammation in acute and chronic colitis mouse models.
CONCLUSION sSiglec-9 may inhibit NF-κB activation in IECs and macrophages and alleviate experimental colitis in mice, suggesting that sSiglec-9 is a potential therapeutic agent for the treatment of inflammatory bowel disease.
Copyright © 2020 Elsevier B.V. All rights reserved.
Keywords
Experimental colitisInflammatory bowel diseasesNF–κBSiglec–9
Conflict of interest statement
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
그 밖의 정보
- 출판 형태
- Journal Article
- 저널
- International immunopharmacology · eISSN 1878-1705
- 전자 출판
- 2020-06-20
- MeSH
- Animals · Antigens, CD / pharmacology / therapeutic use · Cell Line · Colitis / chemically induced / drug therapy · Dextran Sulfate / toxicity · Disease Models, Animal · Epithelial Cells / drug effects · Humans · Inflammation / chemically induced / drug therapy / metabolism · Interleukin-8 / metabolism · Intestines / drug effects / pathology · Lipopolysaccharides / toxicity · Macrophages / drug effects · Mice · Mice, Inbred C57BL · NF-KappaB Inhibitor alpha / metabolism · NF-kappa B / antagonists & inhibitors · Piroxicam / toxicity · Recombinant Proteins / pharmacology / therapeutic use · Sialic Acid Binding Immunoglobulin-like Lectins / pharmacology / therapeutic use · Signal Transduction / drug effects · Tumor Necrosis Factor-alpha / metabolism / toxicity
- Substances
- Antigens, CD · CXCL8 protein, human · Interleukin-8 · Lipopolysaccharides · NF-kappa B · Recombinant Proteins · SIGLEC9 protein, human · Sialic Acid Binding Immunoglobulin-like Lectins · Tnf protein, mouse · Tumor Necrosis Factor-alpha · NF-KappaB Inhibitor alpha · Piroxicam · Dextran Sulfate