Abstract |
Scaffold proteins such as radixin help to modulate the plasma membrane localization and transport activity of the multidrug resistance-associated protein 2 (MRP2/ABCC2) and P-glycoprotein (P-gp/ABCB1) efflux transporters in the liver. We examined changes in radixin expression and interaction with efflux transporters in adjuvant-induced arthritic (AA) rats, an animal model of rheumatoid arthritis, as well as in human liver cancer (HepG2) cells because inflammation affects drug pharmacokinetics via the efflux transporters. The expression levels of radixin and phosphorylated radixin (p- radixin) were measured 24 h after treatment with inflammatory cytokines comprising tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6 or sodium nitroprusside (SNP; a nitric oxide donor). The protein levels of radixin, MRP2, and P-gp in the rat liver were next examined. We also investigated whether inflammation affected the formation of complexes between radixin and MRP2 or P-gp. The mRNA and protein levels of radixin in HepG2 cells were significantly decreased by TNF-α treatment, while minimal changes were observed after treatment with IL-1β, IL-6 or SNP. TNF-α also significantly decreased the protein levels of p- radixin, suggesting that TNF-α inhibited the activation of radixin and thereby reduced the activity of the efflux transporters. Complex formation of radixin with MRP2 and P-gp was significantly decreased in AA rats but this was reversed by prednisolone and dexamethasone treatment, indicating that decreased interactions of radixin with MRP2 and P-gp likely occur during liver inflammation. These data suggest that liver inflammation reduces radixin function by decreasing its interactions with MRP2 and P-gp.
|
Authors | Atsushi Kawase, Misaki Nakasaka, Hatsune Bando, Saori Yasuda, Hiroaki Shimada, Masahiro Iwaki |
Journal | Inflammation
(Inflammation)
Vol. 43
Issue 1
Pg. 85-94
(Feb 2020)
ISSN: 1573-2576 [Electronic] United States |
PMID | 31654296
(Publication Type: Journal Article)
|
Chemical References |
- ABCC2 protein, human
- ATP Binding Cassette Transporter, Subfamily B, Member 1
- ATP-Binding Cassette Transporters
- Abcc2 protein, rat
- Anti-Inflammatory Agents
- Cytokines
- Cytoskeletal Proteins
- Membrane Proteins
- Multidrug Resistance-Associated Protein 2
- Nitric Oxide Donors
- radixin
|
Topics |
- ATP Binding Cassette Transporter, Subfamily B, Member 1
(metabolism)
- ATP-Binding Cassette Transporters
(metabolism)
- Animals
- Anti-Inflammatory Agents
(pharmacology)
- Arthritis, Experimental
(genetics, metabolism, microbiology)
- Cytokines
(pharmacology)
- Cytoskeletal Proteins
(genetics, metabolism)
- Female
- Hep G2 Cells
- Humans
- Liver
(drug effects, metabolism)
- Membrane Proteins
(genetics, metabolism)
- Multidrug Resistance-Associated Protein 2
- Mycobacterium
- Nitric Oxide Donors
(pharmacology)
- Phosphorylation
- Protein Binding
- Rats, Sprague-Dawley
|