Arch Med Sci. 2015 Jun 19;11(3):628-37. doi: 10.5114/aoms.2015.52369.
Angiotensin II suppresses osteoblastic differentiation and mineralized nodule formation via AT1 receptor in ROS17/2.8 cells.
Archives of medical science : AMS
Kumiko Nakai, Takayuki Kawato, Toyoko Morita, Yoji Yamazaki, Hideki Tanaka, Morio Tonogi, Hidero Oki, Masao Maeno
Affiliations
Affiliations
- Division of Oral Health Sciences, Nihon University Graduate School of Dentistry, Tokyo, Japan.
- Department of Oral Health Sciences, Nihon University School of Dentistry, Tokyo, Japan ; Division of Functional Morphology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
- Department of Oral Health Sciences, Nihon University School of Dentistry, Tokyo, Japan ; The Lion Foundation for Dental Health, Tokyo, Japan.
- The Lion Foundation for Dental Health, Tokyo, Japan.
- Department of Oral and Maxillofacial Surgery, Nihon University School of Dentistry, Tokyo, Japan.
- Department of Oral and Maxillofacial Surgery, Nihon University School of Dentistry, Tokyo, Japan ; Division of Immunology and Pathobiology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.
PMID: 26170858
PMCID: PMC4495158 DOI: 10.5114/aoms.2015.52369
Abstract
INTRODUCTION: Angiotensin II (Ang II) not only regulates systemic blood pressure through a vasoconstrictive effect, but also promotes bone resorption. We recently reported that Ang II (10(-6) M) stimulated the production of matrix metalloproteinases via the AT1 receptor in osteoblastic ROS17/2.8 cells, but suppressed alkaline phosphatase activity. However, the roles of Ang II in osteoblastic differentiation and the function of osteogenesis in osteoblasts are unclear. Therefore, we examined the effect of Ang II on the expression of osteogenesis-related transcription factors and extracellular matrix (ECM) proteins, as well as mineralized nodule formation in ROS17/2.8 cells.
MATERIAL AND METHODS: ROS17/2.8 cells were cultured with 0 (control) or 10(-6) M Ang II in the presence or absence of the AT1 receptor blocker losartan. Mineralized nodule formation was detected by Alizarin Red staining. Gene and protein expression levels of transcription factors and ECM proteins were determined using real-time PCR and Western blotting, respectively.
RESULTS: Runx2, Msx2, and osteocalcin expression significantly decreased with Ang II compared to the control, whereas AJ18 expression significantly increased. Osterix, Dlx5, type I collagen, bone sialoprotein, and osteopontin expression was unaffected. Mineralized nodule formation and calcium content in mineralized nodules decreased with Ang II. Losartan blocked suppressive or stimulatory effects of Ang II on Runx2, Msx2, osteocalcin, and AJ18 expression.
CONCLUSIONS: These results suggest that Ang II suppresses osteoblastic differentiation by altering the expression of osteogenesis-related transcription factors via the AT1 receptor and the function of osteogenesis in ROS17/2.8 cells.
Keywords: angiotensin; extracellular matrix proteins; osteoblast; transcription factors
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