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Static magnetic field attenuates lipopolysaccharide-induced inflammation in pulp cells by affecting cell membrane stability.
Hsieh, Sung-Chih; Tsao, Jeng-Ting; Lew, Wei-Zhen; Chan, Ya-Hui; Lee, Lin-Wen; Lin, Che-Tong; Huang, Yung-Kai; Huang, Haw-Ming.
Afiliação
  • Hsieh SC; School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 11031, Taiwan ; Department of Dentistry, Wan Fang Hospital, Taipei 11696, Taiwan.
  • Tsao JT; Division of Allergy and Immunology, Department of Internal Medicine, Cathay General Hospital, Taipei 10630, Taiwan.
  • Lew WZ; School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 11031, Taiwan.
  • Chan YH; School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 11031, Taiwan.
  • Lee LW; Department of Microbiology and Immunology, Taipei Medical University, Taipei 11031, Taiwan.
  • Lin CT; School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 11031, Taiwan.
  • Huang YK; School of Oral Hygiene, College of Oral Medicine, Taipei Medical University, 250 Wu-Hsing Street, Taipei 11031, Taiwan.
  • Huang HM; School of Dentistry, College of Oral Medicine, Taipei Medical University, Taipei 11031, Taiwan ; Graduate Institute of Biomedical Materials and Tissue Engineering, College of Dental Medicine, Taipei Medical University, 250 Wu-Hsing Street, Taipei 11031, Taiwan.
ScientificWorldJournal ; 2015: 492683, 2015.
Article em En | MEDLINE | ID: mdl-25884030
ABSTRACT
One of the causes of dental pulpitis is lipopolysaccharide- (LPS-) induced inflammatory response. Following pulp tissue inflammation, odontoblasts, dental pulp cells (DPCs), and dental pulp stem cells (DPSCs) will activate and repair damaged tissue to maintain homeostasis. However, when LPS infection is too serious, dental repair is impossible and disease may progress to irreversible pulpitis. Therefore, the aim of this study was to examine whether static magnetic field (SMF) can attenuate inflammatory response of dental pulp cells challenged with LPS. In methodology, dental pulp cells were isolated from extracted teeth. The population of DPSCs in the cultured DPCs was identified by phenotypes and multilineage differentiation. The effects of 0.4 T SMF on DPCs were observed through MTT assay and fluorescent anisotropy assay. Our results showed that the SMF exposure had no effect on surface markers or multilineage differentiation capability. However, SMF exposure increases cell viability by 15%. In addition, SMF increased cell membrane rigidity which is directly related to higher fluorescent anisotropy. In the LPS-challenged condition, DPCs treated with SMF demonstrated a higher tolerance to LPS-induced inflammatory response when compared to untreated controls. According to these results, we suggest that 0.4 T SMF attenuates LPS-induced inflammatory response to DPCs by changing cell membrane stability.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Membrana Celular / Polpa Dentária / Campos Magnéticos / Inflamação Limite: Humans Idioma: En Revista: ScientificWorldJournal Assunto da revista: MEDICINA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Taiwan

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Membrana Celular / Polpa Dentária / Campos Magnéticos / Inflamação Limite: Humans Idioma: En Revista: ScientificWorldJournal Assunto da revista: MEDICINA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Taiwan