Original Article

Expression profiling of microRNAs in RAW264.7 cells treated with a combination of tumor necrosis factor alpha and RANKL during osteoclast differentiation

Corresponding Author

T. Kagiya

Division of Functional Morphology, Department of Anatomy, Iwate Medical University, Iwate, Japan

Tadayoshi Kagiya, DDS, Division of Functional Morphology, Department of Anatomy, Iwate Medical University, 2-1-1 Nishitokuta, Yahaba-cho, Iwate, 028-3694, Japan

Tel: +81 19 651 5111

Fax: +81 19 908 8010

e-mail: [email protected]

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S. Nakamura,

S. Nakamura

Division of Maxillofacial Diagnostic and Surgical Sciences, Department of Oral and Maxillofacial Oncology, Kyushu University Graduate School of Dental Science, Fukuoka, Japan

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T. Kagiya,

Corresponding Author

T. Kagiya

Division of Functional Morphology, Department of Anatomy, Iwate Medical University, Iwate, Japan

Tadayoshi Kagiya, DDS, Division of Functional Morphology, Department of Anatomy, Iwate Medical University, 2-1-1 Nishitokuta, Yahaba-cho, Iwate, 028-3694, Japan

Tel: +81 19 651 5111

Fax: +81 19 908 8010

e-mail: [email protected]

Search for more papers by this author

S. Nakamura,

S. Nakamura

Division of Maxillofacial Diagnostic and Surgical Sciences, Department of Oral and Maxillofacial Oncology, Kyushu University Graduate School of Dental Science, Fukuoka, Japan

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First published: 18 October 2012

https://doi.org/10.1111/jre.12017

Citations: 93

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Abstract

Background and Objective

Tumor necrosis factor alpha (TNF-α), a cytokine involved in the pathogenesis of periodontal disease, induces osteoclast differentiation and indirectly promotes alveolar bone resorption. We investigated TNF-α-regulated osteoclast differentiation, focusing on microRNAs. MicroRNAs are small, noncoding RNAs that are involved in various biological processes, including cellular differentiation, proliferation and apoptosis. Aside from miR-21, miR-155 and miR-223, the identities of the microRNAs that play roles in osteoclast differentiation are unknown. Notably, no previous studies have reported the expression profiling of microRNAs during TNF-α-regulated osteoclast differentiation.

Material and Methods

We used microarrays to screen the levels of expression of mature microRNAs in RAW264.7 cells treated with a combination of TNF-α and RANKL, or RANKL alone for 0, 24 or 82 h during osteoclast formation. We validated the results of the microarray analyses through quantitative RT-PCR analyses of representative microRNAs in RAW264.7 cells and murine bone marrow macrophages.

Results

During osteoclast formation, the expression of 44 mature microRNAs differed by more than twofold between untreated cells and cells treated with a combination of TNF-α and RANKL, and the expression of 52 mature microRNAs differed upon RANKL treatment. According to quantitative RT-PCR analyses, miR-378 was upregulated and miR-223 was downregulated during osteoclast formation. Furthermore, miR-21, miR-29b, miR-146a, miR-155 and miR-210 were highly expressed during osteoclast differentiation in TNF-α/RANKL-treated cells compared with RANKL-treated cells.

Conclusions

These results suggest that miR-223 and miR-378 may play important roles in osteoclastogenesis, and that miR-21, miR-29b, miR-146a, miR-155 and miR-210 are involved in TNF-α-regulated osteoclast differentiation.

Supporting Information

References

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Volume48, Issue3

June 2013

Pages 373-385

Expression profiling of microRNAs in RAW264.7 cells treated with a combination of tumor necrosis factor alpha and RANKL during osteoclast differentiation

Abstract

Background and Objective

Material and Methods

Results

Conclusions

Supporting Information

References

Citing Literature

References

Information

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Expression profiling of microRNAs in RAW264.7 cells treated with a combination of tumor necrosis factor alpha and RANKL during osteoclast differentiation

Abstract

Background and Objective

Material and Methods

Results

Conclusions

Supporting Information

References

Citing Literature

References

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Information