| First Author | Koumakis E | Year | 2019 |
| Journal | Sci Rep | Volume | 9 |
| Issue | 1 | Pages | 1808 |
| PubMed ID | 30755642 | Mgi Jnum | J:276124 |
| Mgi Id | MGI:6304739 | Doi | 10.1038/s41598-018-37551-1 |
| Citation | Koumakis E, et al. (2019) Novel function of PiT1/SLC20A1 in LPS-related inflammation and wound healing. Sci Rep 9(1):1808 |
| abstractText | PiT1/SLC20A1 is an inorganic phosphate transporter with additional functions including the regulation of TNFalpha-induced apoptosis, erythropoiesis, cell proliferation and insulin signaling. Recent data suggest a relationship between PiT1 and NF-kappaB-dependent inflammation: (i) Pit1 mRNA is up-regulated in the context of NF-kappaB pathway activation; (ii) NF-kappaB target gene transcription is decreased in PiT1-deficient conditions. This led us to investigate the role of PiT1 in lipopolysaccharide (LPS)-induced inflammation. MCP-1 and IL-6 concentrations were impaired in PiT1-deficient bone marrow derived macrophages (BMDMs) upon LPS stimulation. Lower MCP-1 and IL-6 serum levels were observed in Mx1-Cre; Pit1(lox/lox) mice dosed intraperitoneally with LPS. Lower PiT1 expression correlated with decreased in vitro wound healing and lower reactive oxygen species levels. Reduced IkappaB degradation and lower p65 nuclear translocation were observed in PiT1-deficient cells stimulated with LPS. Conversely, PiT1 expression was induced in vitro upon LPS stimulation. Addition of an NF-kappaB inhibitor abolished LPS-induced PiT1 expression. Furthermore, we showed that p65 expression activated Pit1 promoter activity. Finally, ChIP assays demonstrated that p65 directly binds to the mPit1 promoter in response to LPS. These data demonstrate a completely novel function of PiT1 in the response to LPS and provide mechanistic insights into the regulation of PiT1 expression by NF-kappaB. |
