| Literature DB >> 30370560 |
Chiharu Fujihara1, Yu Kanai1, Risa Masumoto1, Jirouta Kitagaki1, Masahiro Matsumoto1, Satoru Yamada2, Tetsuhiro Kajikawa1, Shinya Murakami1.
Abstract
Fibroblast growth factor-2 (FGF-2) stimulates periodontal regeneration by a broad spectrum of effects on periodontal ligament (PDL) cells, such as proliferation, migration, and production of extracellular matrix. A critical factor in the success of periodontal regeneration is the rapid resolution of inflammatory responses in the tissue. We explored an anti-inflammatory effect of FGF-2 during periodontal regeneration and healing. We found that FGF-2 on mouse periodontal ligament cells (MPDL22) markedly downregulated CD40 expression, a key player of inflammation. In addition, FGF-2 inhibited CD40 signaling by the non-canonical nuclear factor-kappa B2 (NFκB2) pathway, resulting in decreased production of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α), which have the potential to recruit immune cells to inflamed sites. Furthermore, in vivo treatment of FGF-2 enhanced healing of skin wounds by counteracting the CD40-mediated inflammation. These results reveal that FGF-2 has an important function as a negative regulator of inflammation during periodontal regeneration and healing.Entities:
Keywords: CD40; anti-inflammation; fibroblast growth factor-2 (FGF-2); periodontal ligament (PDL) cells; wound healing
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Year: 2018 PMID: 30370560 DOI: 10.1002/jcp.27469
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384