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http://dx.doi.org/10.5483/BMBRep.2018.51.9.126

The purinergic receptor P2X5 contributes to bone loss in experimental periodontitis  

Kim, Hyunsoo (Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine)
Kajikawa, Tetsuhiro (Department of Microbiology, Penn Dental Medicine, University of Pennsylvania)
Walsh, Matthew C. (Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine)
Takegahara, Noriko (Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine)
Jeong, Yun Hee (Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine)
Hajishengallis, George (Department of Microbiology, Penn Dental Medicine, University of Pennsylvania)
Choi, Yongwon (Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine)
Publication Information
BMB Reports / v.51, no.9, 2018 , pp. 468-473 More about this Journal
Abstract
Purinergic receptor signaling is increasingly recognized as an important regulator of inflammation. The P2X family purinergic receptors P2X5 and P2X7 have both been implicated in bone biology, and it has been suggested recently that P2X5 may be a significant regulator of inflammatory bone loss. However, a role for P2X5 in periodontitis is unknown. The present study aimed to evaluate the functional role of P2X5 in ligature-induced periodontitis in mice. Five days after placement of ligature, analysis of alveolar bone revealed decreased bone loss in $P2rx5^{-/-}$ mice compared to $P2rx7^{-/-}$ and WT control mice. Gene expression analysis of the gingival tissue of ligated mice showed that IL1b, IL6, IL17a and Tnfsf11 expression levels were significantly reduced in $P2rx5^{-/-}$ compared to WT mice. These results suggest the P2X5 receptor may regulate bone loss related to periodontitis and it may thus be a novel therapeutic target in this oral disease.
Keywords
Bone loss; Inflammation; Osteoclast; Periodontitis; Purinergic receptor;
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