1. Functional role of mechanosensitive ion channel Piezol in human periodontal ligament cells.
- Author
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Ying Jin, Juan Li, Yating Wang, Rui Ye, Xiaoxia Feng, Zheng Jing, and Zhihe Zhao
- Subjects
ION channels ,LIGAMENTS ,BIOMECHANICS ,HOMEOSTASIS ,COMPRESSIVE strength ,OSTEOCLASTOGENESIS ,REVERSE transcriptase polymerase chain reaction - Abstract
Objective: To evaluate the function of Piezol, an evolutionarily conserved mechanically activated channel, in periodontal ligament (PDL) tissue homeostasis under compressive loading. Materials and Methods: Primary human PDL cells (hPDLCs) were isolated, cultured, and then subjected to 2.0 g/cm² static compressive loading for 0.5, 3, 6, and 12 hours, respectively. The expressions of Piezol and osteoclastogenesis marker gene were assessed by semiquantitative reverse transcription-polymerase chain reaction. In addition, Piezol inhibitor, GsMTx4, was used to block the function of Piezol, and tumor necrosis factor-a was also used as a positive control. After 12 hours of compressive loading the PDLCs were co-cultured with murine monocytic cell line RAW264.7. Immunofluorescence, western blot, enzyme-linked immunosorbent assay, and tartrate-resistant acid phosphatase staining were also used to test the potency of PDLCs to induce osteoclastogenesis and the activation of nuclear factor (NF)-KB. Results: Piezol, cyclooxygenase-2, receptor activator of NF-κB ligand, and prostaglandin E2 were significantly upregulated under static compressive stimuli. GsMTx4 repressed osteoclastogenesis in the mechanical stress-pretreated PDLCs-RAW264.7 co-culture system. Furthermore, NF-κB signaling pathway was involved in the mechanical stress-induced osteoclastogenesis. Conclusions: Piezol exerts a transduction role in mechanical stress-induced osteoclastogenesis in hPDLCs. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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