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FXYD5 Protein Has a Pro-inflammatory Role in Epithelial Cells.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2016 May 20; Vol. 291 (21), pp. 11072-82. Date of Electronic Publication: 2016 Mar 22. - Publication Year :
- 2016
-
Abstract
- The FXYD proteins are a family of small membrane proteins that share an invariant four amino acid signature motif F-X-Y-D and act as tissue-specific regulatory subunits of the Na,K-ATPase. FXYD5 (also termed dysadherin or RIC) is a structurally and functionally unique member of the FXYD family. As other FXYD proteins, FXYD5 specifically interacts with the Na,K-ATPase and alters its kinetics by increasing Vmax However, unlike other family members FXYD5 appears to have additional functions, which cannot be readily explained by modulation of transport kinetics. Knockdown of FXYD5 in MDA-MB-231 breast cancer cells largely decreases expression and secretion of the chemokine CCL2 (MCP-1). A related effect has also been observed in renal cell carcinoma cells. The current study aims to further characterize the relationship between the expression of FXYD5 and CCL2 secretion. We demonstrate that transfection of M1 epithelial cell line with FXYD5 largely increases lipopolysaccharide (LPS) stimulated CCL2 mRNA and secretion of the translated protein. We have completed a detailed analysis of the molecular events leading to the above response. Our key findings indicate that FXYD5 generates a late response by increasing the surface expression of the TNFα receptor, without affecting its total protein level, or mRNA transcription. LPS administration to mice demonstrates induced secretion of CCL2 and TNFα in FXYD5-expressing lung peripheral tissue, which suggests a possible role for FXYD5 in normal epithelia during inflammation.<br /> (© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.)
- Subjects :
- Animals
Cell Line
Cell Line, Tumor
Chemokine CCL2 genetics
Chemokine CCL2 metabolism
Epithelial Cells metabolism
Gene Expression drug effects
Gene Knockdown Techniques
Humans
Inflammation Mediators metabolism
Ion Channels
Kinetics
Lipopolysaccharides pharmacology
Membrane Glycoproteins antagonists & inhibitors
Membrane Glycoproteins genetics
Membrane Proteins genetics
Mice
Microfilament Proteins
Neoplasm Proteins antagonists & inhibitors
Neoplasm Proteins genetics
RNA, Messenger genetics
RNA, Messenger metabolism
Receptors, Tumor Necrosis Factor genetics
Receptors, Tumor Necrosis Factor metabolism
Recombinant Proteins genetics
Recombinant Proteins metabolism
Signal Transduction drug effects
Membrane Glycoproteins metabolism
Membrane Proteins metabolism
Neoplasm Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1083-351X
- Volume :
- 291
- Issue :
- 21
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 27006401
- Full Text :
- https://doi.org/10.1074/jbc.M115.699041