Ibandronate promotes osteogenic differentiation of periodontal ligament stem cells by regulating the expression of microRNAs
Creators
- 1. Department of General Dentistry and Emergency, College of Stomatology, Fourth Military Medical University, Xi'an, Shaanxi 710032 (China)
- 2. Clinical Laboratory, 451 Hospital of Chinese PLA, Xi'an 710054 (China)
- 3. Department of Special Dentistry, College of Stomatology, Fourth Military Medical University, Xi'an, Shaanxi 710032 (China)
- 4. Department of Orthodontics, College of Stomatology, Fourth Military Medical University, Xi'an, Shaanxi 710032 (China)
- 5. Department of Periodontology, College of Stomatology, Fourth Military Medical University, Xi'an, Shaanxi 710032 (China)
Description
Research highlights: → Ibandronate significantly promote the proliferation of PDLSC cells. → Ibandronate enhanced the expression of ALP, COL-1, OPG, OCN, Runx2. → The expression of a class of miRNAs, e.g., miR-18a, miR-133a, miR-141 and miR-19a, was significantly modified in PDLSC cells cultured with ibandronate. → Ibandronate regulates the expression of diverse bone formation-related genes via miRNAs in PDLSCs. → Ibandronate can suppress the activity of osteoclast while promoting the proliferation of osteoblast by regulating the expression of microRNAs. -- Abstract: Bisphosphonates (BPs) have a profound effect on bone resorption and are widely used to treat osteoclast-mediated bone diseases. They suppress bone resorption by inhibiting the activity of mature osteoclasts and/or the formation of new osteoclasts. Osteoblasts may be an alternative target for BPs. Periodontal ligament stem cells (PDLSCs) exhibit osteoblast-like features and are capable of differentiating into osteoblasts or cementoblasts. This study aimed to determine the effects of ibandronate, a nitrogen-containing BP, on the proliferation and the differentiation of PDLSCs and to identify the microRNAs (miRNAs) that mediate these effects. The PDLSCs were treated with ibandronate, and cell proliferation was measured using the MTT (3-dimethylthiazol-2,5-diphenyltetrazolium bromide) assay. The expression of genes and miRNAs involved in osteoblastic differentiation was assayed using quantitative real-time reverse-transcription polymerase chain reaction (qRT-PCR). Ibandronate promoted the proliferation of PDLSCs and enhanced the expression of alkaline phosphatase (ALP), type I collagen (COL-1), osteoprotegerin (OPG), osteocalcin (OCN), and Runx2. The expression of miRNAs, including miR-18a, miR-133a, miR-141 and miR-19a, was significantly altered in the PDLSCs cultured with ibandronate. In PDLSCs, ibandronate regulates the expression of diverse bone formation-related genes via miRNAs. The exact mechanism underlying the role of ibandronate in osteoblasts has not been completely understood. Ibandronate may suppress the activity of osteoclasts while promoting the proliferation of osteoblasts by regulating the expression of miRNAs.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2010.11.079Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2010.11.079;
- PII
- S0006-291X(10)02145-5;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 404
- Journal Issue
- 1
- Journal Page Range
- p. 127-132
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45025640
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ALKALINE PHOSPHATASE; BROMIDES; CELL CULTURES; CELL PROLIFERATION; COLLAGEN; CONNECTIVE TISSUE CELLS; GENES; LIGAMENTS; NITROGEN; POLYMERASE CHAIN REACTION; SKELETAL DISEASES; SKELETON; STEM CELLS; TRANSCRIPTION
- Descriptors DEC
- ANIMAL CELLS; ANIMAL TISSUES; BODY; BROMINE COMPOUNDS; CONNECTIVE TISSUE; DISEASES; ELEMENTS; ENZYMES; ESTERASES; GENE AMPLIFICATION; HALIDES; HALOGEN COMPOUNDS; HYDROLASES; NONMETALS; ORGANIC COMPOUNDS; ORGANS; PHOSPHATASES; PROTEINS; SCLEROPROTEINS; SOMATIC CELLS
Optional Information
- Copyright
- Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.