Low-power laser irradiation promotes the proliferation and osteogenic differentiation of human periodontal ligament cells via cyclic adenosine monophosphate.
- Author:
Jyun-Yi WU
1
;
Chia-Hsin CHEN
;
Li-Yin YEH
;
Ming-Long YEH
;
Chun-Chan TING
;
Yan-Hsiung WANG
Author Information
- Publication Type:Journal Article
- MeSH: Adenine; analogs & derivatives; pharmacology; Adenylyl Cyclase Inhibitors; Alkaline Phosphatase; analysis; genetics; radiation effects; Anthraquinones; Bone Morphogenetic Protein 2; genetics; Calcium; metabolism; radiation effects; Cell Culture Techniques; Cell Differentiation; radiation effects; Cell Line; Cell Proliferation; radiation effects; Coloring Agents; Core Binding Factor Alpha 1 Subunit; genetics; Cyclic AMP; antagonists & inhibitors; radiation effects; Gene Expression; radiation effects; Humans; L-Lactate Dehydrogenase; analysis; Lasers, Semiconductor; Low-Level Light Therapy; instrumentation; Osteocalcin; genetics; Osteogenesis; genetics; radiation effects; Periodontal Ligament; cytology; radiation effects; Radiation Dosage; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; Tetrazolium Salts; Thiazoles
- From: International Journal of Oral Science 2013;5(2):85-91
- CountryChina
- Language:English
- Abstract: Retaining or improving periodontal ligament (PDL) function is crucial for restoring periodontal defects. The aim of this study was to evaluate the physiological effects of low-power laser irradiation (LPLI) on the proliferation and osteogenic differentiation of human PDL (hPDL) cells. Cultured hPDL cells were irradiated (660 nm) daily with doses of 0, 1, 2 or 4 J⋅cm(-2). Cell proliferation was evaluated by the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay, and the effect of LPLI on osteogenic differentiation was assessed by Alizarin Red S staining and alkaline phosphatase (ALP) activity. Additionally, osteogenic marker gene expression was confirmed by real-time reverse transcription-polymerase chain reaction (RT-PCR). Our data showed that LPLI at a dose of 2 J⋅cm(-2) significantly promoted hPDL cell proliferation at days 3 and 5. In addition, LPLI at energy doses of 2 and 4 J⋅cm(-2) showed potential osteogenic capacity, as it stimulated ALP activity, calcium deposition, and osteogenic gene expression. We also showed that cyclic adenosine monophosphate (cAMP) is a critical regulator of the LPLI-mediated effects on hPDL cells. This study shows that LPLI can promote the proliferation and osteogenic differentiation of hPDL cells. These results suggest the potential use of LPLI in clinical applications for periodontal tissue regeneration.
