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Protective role of ABCC drug subfamily resistance transporters (ABCC1-7) in intestinal inflammation.
- Source :
-
Immunologic research [Immunol Res] 2025 Jan 14; Vol. 73 (1), pp. 33. Date of Electronic Publication: 2025 Jan 14. - Publication Year :
- 2025
-
Abstract
- The ABCC subfamily contains thirteen members. Nine of these transporters are called multidrug resistance proteins (MRPs). The MRPs have been associated with developing ulcerative colitis (UC). This study aimed to evaluate the ABCC expression in UC patients and its role in a dextran sulfate sodium (DSS)-induced colitis mice model under 5-aminosalicylates or methylprednisolone treatment and compared with control without inflammation. DSS-induced colitis mice were treated with 5-aminosalicylates (50 mg/kg 24 h) or methylprednisolone (2 mg/kg 24 h). Human rectal biopsies were obtained from UC patients. The abcc-relative mRNA levels and protein expression were determined by RT-PCR and immunohistochemistry. abcc4, abcc5, and abcc6 mRNA levels were significantly increased in DSS-induced colitis compared to the other groups. The 5-aminosalicylate treatment dramatically increased the abcc2 and abcc3 mRNA levels vs. control. Methylprednisolone treatment increased abcc1 vs. DSS-induced colitis and colitis treated with 5-aminosalicylate. Immunohistochemical analysis revealed down-regulation of ABCC1/ABCC2/ABCC5/ABCC7 in mice colitis vs. control. Treatment with 5-aminosalicylate restored ABCC5 levels, while methylprednisolone restored ABCC2/ABCC5/ABCC7 in colitis mice at similar control levels. Relative mRNA levels of mrp1-5 were increased in active UC patients vs. control. ABCC2/ABCC4/ABCC7 were conspicuously expressed in the mucosa of 5-aminosalicylate and/or methylprednisolone-treated UC patients, while ABCC2/ABCC4/ABCC5/ABCC7 in submucosa, ABCC1/ABCC5/ABCC7 in muscular, and ABCC1/ABCC4/ABCC5/ABCC7 in serosa were expressed vs. controls. This is the first report about the differential up-regulation of the ABCC subfamily gene and protein expression in DSS-induced colitis under aminosalicylates or methylprednisolone treatment.<br />Competing Interests: Declarations. Ethics approval: This study was approved by the Ethics Committee of the National Institute of Medical Sciences and Nutrition “Salvador Zubirán” (GAS-2724–18-21–1). It was carried out following the principles of the Helsinki Declaration, and the written informed consent of all participants was obtained before enrollment. The animal study was reviewed and approved by all experimental procedures approved by the Institutional Animal Care and Use Committee (IACUC-GAS-1963–19-20–1). Competing interests: The authors declare no competing interests.<br /> (© 2025. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Subjects :
- Animals
Humans
Mice
Male
Disease Models, Animal
Multidrug Resistance-Associated Protein 2
Female
Mesalamine therapeutic use
Mesalamine pharmacology
Colitis chemically induced
Colitis metabolism
Colitis drug therapy
Colitis genetics
Adult
Middle Aged
RNA, Messenger metabolism
RNA, Messenger genetics
Intestinal Mucosa metabolism
Intestinal Mucosa pathology
Intestinal Mucosa drug effects
Multidrug Resistance-Associated Proteins genetics
Multidrug Resistance-Associated Proteins metabolism
Colitis, Ulcerative drug therapy
Colitis, Ulcerative genetics
Colitis, Ulcerative immunology
Colitis, Ulcerative chemically induced
Colitis, Ulcerative metabolism
Dextran Sulfate
Methylprednisolone therapeutic use
Methylprednisolone pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1559-0755
- Volume :
- 73
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Immunologic research
- Publication Type :
- Academic Journal
- Accession number :
- 39808251
- Full Text :
- https://doi.org/10.1007/s12026-024-09583-5