The MicroRNA-23a Has Limited Roles in Bone Formation and Homeostasis In Vivo
Open accessAbstract
(miRNAs) inhibit bone formation by inhibiting the translation of specific genes. Several in vitro studies have suggested that miR-23a inhibits osteogenic differentiation by suppressing the translation of Runx2, a transcription factor essential for osteoblastogenesis, and of Satb2, a member of the special AT rich binding protein family. In the present study, we used a gain-of-function approach to determine the roles of miR-23a in bone formation and homeostasis in vivo. The miR-23a transgenic (Tg) mice grew normally and their body size and weight were similar to those of wild-type (WT) littermates. Bone structure and morphology were similar in Tg and WT mice. Furthermore, the numbers of osteoblasts and osteoclasts, as well as their activities in bone were similar between Tg and WT mice. Our results indicate that miR-23 has limited roles in bone formation and maintenance in vivo in mice.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
miR-23a is highly expressed in osteoblasts, chondrocytes, and fibroblast cell lines.
“miR-23a is highly expressed in osteoblasts, chondrocytes, and fibroblast cell lines.”
From Recent advances of miR-23 in human diseases and growth development (2025) · cites this paper as [110]
The Discussion reports induction of miR-23a in MC3T3-E1 cells, an in vitro model of osteogenic differentiation, and the Tissue expression section reports higher expression in bone than in several other tissues. Neither passage establishes high expression specifically in osteoblasts, chondrocytes, and fibroblast cell lines; the copy does not report expression in the latter two cell types. (LLM, conf=0.77)
Experimental — accuracy not yet measuredIn vitro experiments demonstrated that miR-23a can control the progression of osteoblast and chondrocyte lineages and inhibit osteogenic differentiation by targeting Runx2 and Satb2 in mice.
“The experiments in vitro have demonstrated that it can control the progression of osteoblast and chondrocyte lineages and inhibit osteogenic differentiation by targeting the transcription factors Runx2 and Satb2 in mice.”
From Recent advances of miR-23 in human diseases and growth development (2025) · cites this paper as [110]
The Discussion reports that miR-23a overexpression inhibited osteogenic differentiation in cultured MC3T3-E1 cells by suppressing Runx2 and Satb2 translation. Our copy does not establish that miR-23a controls chondrocyte lineage progression. It also reports no comparable effect on osteogenic differentiation in the transgenic mice, so the in vitro finding should not be read as an in vivo result. The supplied passages have section labels but no page numbers. (LLM, conf=0.86)
Experimental — accuracy not yet measuredThere existed no notable variance in the number of osteoblasts and osteoclasts between miR-23 transgenic and wild-type mice, along with their activity in bone.
“there existed no notable variance in the number of osteoblasts and osteoclasts between miR-23 transgenic and wild-type mice, along with their activity in the bone.”
From Recent advances of miR-23 in human diseases and growth development (2025) · cites this paper as [110]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 315,771 · see citing works
MicroRNAs: Target Recognition and Regulatory Functions
Bartel, D. P. (2009) · Cell · doi:10.1016/j.cell.2009.01.002 · Cited by 20,068 · see citing works
MicroRNA genes are transcribed by RNA polymerase II
Lee, Y., Kim, M., Han, J., Yeom, K.-H., Lee, S., Baek, S. H., & Kim, V. N. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600385 · Cited by 4,355 · see citing works
Komori, T., Yagi, H., Nomura, S., Yamaguchi, A., Sasaki, K., Deguchi, K., Shimizu, Y., Bronson, R. T., Gao, Y.-H., Inada, M., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80258-5 · Cited by 4,244 · see citing works
A METHOD FOR THE RAPID DETERMINATION OF ALKALINE PHOSPHATASE WITH FIVE CUBIC MILLIMETERS OF SERUM
Bessey, O. A., Lowry, O. H., & Brock, M. J. (1946) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)43072-4 · Cited by 3,059 · see citing works
Otto, F., Thornell, A., Crompton, T., Denzel, A., Gilmour, K. C., Rosewell, I. R., Stamp, G., Beddington, R. S. P., Mundlos, S., Olsen, B. R., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80259-7 · Cited by 2,813 · see citing works
‘Green mice’ as a source of ubiquitous green cells
Okabe, M., Ikawa, M., Kominami, K., Nakanishi, T., & Nishimune, Y. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)00313-x · Cited by 2,581 · see citing works
Sudo, H., Kodama, H. A., Amagai, Y., Yamamoto, S., & Kasai, S. (1983) · The Journal of Cell Biology · doi:10.1083/jcb.96.1.191 · Cited by 1,673 · see citing works
Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia
Mundlos, S., Otto, F., Mundlos, C., Mulliken, J. B., Aylsworth, A. S., Albright, S. G., Lindhout, D., Cole, W. G., Henn, W., Knoll, J. H. M., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80260-3 · Cited by 1,502 · see citing works
Quantification of Bone Microarchitecture with the Structure Model Index
Hildebrand, T., & Ruegsegger, P. (1997) · Computer Methods in Biomechanics & Biomedical Engineering · doi:10.1080/01495739708936692 · Cited by 1,053 · see citing works
A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic developmentPreprint
Ducy, P. F., Starbuck, M., Priemel, M., Shen, J., Pinero, G. J., Geoffroy, V., Amling, M., & Karsenty, G. (1999) · Genes & Development · doi:10.1101/gad.13.8.1025 · Cited by 772 · see citing works
The RNaseIII enzyme Dicer is required for morphogenesis but not patterning of the vertebrate limb
Harfe, B. D., McManus, M. T., Mansfield, J. H., Hornstein, E., & Tabin, C. J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504834102 · Cited by 648 · see citing works
MicroRNA control of bone formation and homeostasis
Lian, J. B., Stein, G. S., van Wijnen, A. J., Stein, J. L., Hassan, M. Q., Gaur, T., & Zhang, Y. (2012) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2011.234 · Cited by 586 · see citing works
Lee, B., Thirunavukkarasu, K., Zhou, L., Pastore, L., Baldini, A., Hecht, J. T., Geoffrey, V., Ducy, P. F., & Karsenty, G. (1997) · Nature Genetics · doi:10.1038/ng0797-307 · Cited by 567 · see citing works
SATB2 Is a Multifunctional Determinant of Craniofacial Patterning and Osteoblast Differentiation
Dobreva, G. D., Chahrour, M. H., Dautzenberg, M., Chirivella, L., Kanzler, B., Fariñas, I., Karsenty, G., & Grosschedl, R. (2006) · Cell · doi:10.1016/j.cell.2006.05.012 · Cited by 522 · see citing works
Real-time expression profiling of microRNA precursors in human cancer cell lines
Jiang, J. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki863 · Cited by 497 · see citing works
Li, H., Xie, H., Liu, W., Hu, R., Huang, B., Tan, Y., Liao, E.-Y., Xu, K., Sheng, Z., Zhou, H., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci39832 · Cited by 464 · see citing works
Zhang, Y., Xie, R.-L., Croce, C. M., Stein, J. L., Lian, J. B., van Wijnen, A. J., & Stein, G. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018493108 · Cited by 423 · see citing works
Cbfa1 Is a Positive Regulatory Factor in Chondrocyte Maturation
Enomoto, H., Enomoto‐Iwamoto, M., Iwamoto, M., Nomura, S., Himeno, M., Kitamura, Y., Kishimoto, T., & Komori, T. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.12.8695 · Cited by 387 · see citing works
Hassan, M. Q., Gordon, J. A. R., Beloti, M. M., Croce, C. M., van Wijnen, A. J., Stein, J. L., Stein, G. S., & Lian, J. B. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007698107 · Cited by 344 · see citing works
Dicer-dependent pathways regulate chondrocyte proliferation and differentiation
Kobayashi, T., Lü, J., Cobb, B. S., Rodda, S. J., McMahon, A. P., Schipani, E., Merkenschlager, M., & Kronenberg, H. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707900105 · Cited by 333 · see citing works
Geoffroy, V., Kneissel, M., Fournier, B., BOYDE, A., & Matthias, P. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.17.6222-6233.2002 · Cited by 263 · see citing works
SUMO modification of a novel MAR-binding protein, SATB2, modulates immunoglobulin μ gene expressionPreprint
Dobreva, G. D., Dambacher, J., & Grosschedl, R. (2003) · Genes & Development · doi:10.1101/gad.1153003 · Cited by 255 · see citing works
Russell, A. P., Wada, S., Vergani, L., Hock, M. B., Lamon, S., Léger, B., Ushida, T., Cartoni, R., Wadley, G. D., Hespel, P., et al. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.08.015 · Cited by 224 · see citing works
Self-citationWada, S., Kato, Y., Okutsu, M., Miyaki, S., Suzuki, K., Yan, Z., Schiaffino, S., Asahara, H., Ushida, T., & Akimoto, T. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.271270 · Cited by 200 · see citing works
Self-citationSignaling Networks that Control the Lineage Commitment and Differentiation of Bone Cells
Soltanoff, C. S., Yang, S., Chen, W., & Li, Y. (2009) · Critical Reviews in Eukaryotic Gene Expression · doi:10.1615/critreveukargeneexpr.v19.i1.10 · Cited by 196 · see citing works
Lau, K. ‐. W., Onishi, T., Wergedal, J. E., Singer, F. R., & Baylink, D. J. (1987) · Clinical Chemistry · doi:10.1093/clinchem/33.4.458 · Cited by 194 · see citing works
Britanova, O. V., Depew, M. J., Schwark, M., Thomas, B. L., Milétich, I., Sharpe, P. T., & Tarabykin, V. S. (2006) · The American Journal of Human Genetics · doi:10.1086/508214 · Cited by 181 · see citing works
Oskowitz, A., Lü, J., Penfornis, P., Ylöstalo, J., McBride, J., Flemington, E. K., Prockop, D. J., & Pochampally, R. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809807105 · Cited by 176 · see citing works
Gaur, T., Hussain, S., Mudhasani, R., Parulkar, I., Colby, J. L., Frederick, D., Kream, B. E., van Wijnen, A. J., Stein, J. L., Stein, G. S., et al. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.01.008 · Cited by 156 · see citing works
Leoyklang, P., Suphapeetiporn, K., Siriwan, P., Desudchit, T., Chaowanapanja, P., Gahl, W. A., & Shotelersuk, V. (2007) · Human Mutation · doi:10.1002/humu.20515 · Cited by 131 · see citing works
Zhang, Y., Xie, R., Gordon, J., LeBlanc, K., Stein, J. L., Lian, J. B., van Wijnen, A. J., & Stein, G. S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.340398 · Cited by 123 · see citing works
Hiruma, Y., Tsuda, E., Maeda, N., Okada, A., Kabasawa, N., Miyamoto, M., Hattori, H., & Fukuda, C. (2012) · Bone · doi:10.1016/j.bone.2012.11.036 · Cited by 79 · see citing works
Harada, S., Tominari, T., Matsumoto, C., Hirata, M., Takita, M., Inada, M., & Miyaura, C. (2011) · Journal of Pharmacological Sciences · doi:10.1254/jphs.10193sc · Cited by 49 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
(2015) · PubMed Central · Cited by 208 · see citing works
miR-21 deficiency inhibits osteoclast function and prevents bone loss in mice
Hu, C.-H., Sui, B.-D., Du, F.-Y., Shuai, Y., Zheng, C.-X., Zhao, P., Yu, X.-R., & Jin, Y. (2017) · Scientific Reports · doi:10.1038/srep43191 · Cited by 127 · see citing works
Deregulated miRNAs in bone health: Epigenetic roles in osteoporosis
Bellavia, D., Luca, A. D., Carina, V., Costa, V., Raimondi, L., Salamanna, F., Alessandro, R., Fini, M., & Giavaresi, G. (2019) · Bone · doi:10.1016/j.bone.2019.02.013 · Cited by 104 · see citing works
The role of microRNAs in bone remodeling
Jing, D., Hao, J., Shen, Y., Tang, G., Li, M., Huang, S.-H., & Zhao, Z. (2015) · International Journal of Oral Science · doi:10.1038/ijos.2015.22 · Cited by 106 · see citing works
MicroRNAs Modulate Signaling Pathways in Osteogenic Differentiation of Mesenchymal Stem Cells
Mazziotta, C., Lanzillotti, C., Iaquinta, M. R., Taraballi, F., Torreggiani, E., Rotondo, J. C., Oton, L., Mazzoni, E., Frontini, F., Bononi, I., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052362 · Cited by 69 · see citing works
Chen, Y., Yang, Y., Fan, X.-L., Lin, P., Yang, H., Chen, X., & Xu, X. (2019) · Bioscience Reports · doi:10.1042/bsr20181108 · Cited by 46 · see citing works
Mechanosensitive miRNAs and Bone Formation
Chen, Z., Zhang, Y., Liang, C., Chen, L., Zhang, G., & Qian, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081684 · Cited by 45 · see citing works
miR‑10a‑5p inhibits osteogenic differentiation of bone marrow‑derived mesenchymal stem cells
Zhang, Y., Zhou, L., Zhang, Z., Ren, F., Chen, L., & Lan, Z. (2020) · Molecular Medicine Reports · doi:10.3892/mmr.2020.11110 · Cited by 24 · see citing works
Sujitha, S., & Rasool, M. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.105703 · Cited by 22 · see citing works
Potekhina, Y. P., Filatova, A. I., Трегубова, Е. С., & Мохов, Д. Е. (2020) · Современные технологии в медицине · doi:10.17691/stm2020.12.4.10 · Cited by 13 · see citing works
Fujiwara, Y., Ding, C., Sanada, Y., Yimiti, D., Ishikawa, M., Nakasa, T., Kamei, N., Imaizumi, K., Lotz, M., Akimoto, T., et al. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1043259 · Cited by 11 · see citing works
Self-citationMa, T.-L., Zhu, P., Ke, Z.-R., Chen, J.-X., Hu, Y.-H., & Xie, J. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.891313 · Cited by 9 · see citing works
Liu, X., Zhang, K., Wang, L., Geng, B., Liu, Z., Yi, Q., & Xia, Y. (2022) · Physiological Research · doi:10.33549/physiolres.934922 · Cited by 9 · see citing works
Recent advances of miR-23 in human diseases and growth development
Qian, X., Jiang, Y., Yang, Y., Zhang, Y., Xu, N., Xu, B., Pei, K., Yu, Z., & Wu, W. (2025) · Non-coding RNA Research · doi:10.1016/j.ncrna.2024.12.010 · Cited by 5 · see citing works
- Authors
- PARK, J., WADA, S., USHIDA, T., & AKIMOTO, T.
- Affiliations
- Konkuk University (KR)
- Center for Disease Biology and Integrative Medicine, The University of Tokyo (JP)
- The University of Tokyo (JP)
- Venue
- Physiological Research
- Published
- 2015-10-16
- Volume
- 64
- Issue
- 5
- Pages
- 711-719
- ISSN
- 0862-8408 (ISSN-L)
- 1802-9973
- OpenAlex
- W310092238
- Cited by
- 14
- References
- 34
- Citations by year
- 2024: 1 · 2023: 1 · 2022: 2 · 2021: 1 · 2020: 2 · 2019: 3 · 2017: 2 · 2015: 2
- FWCI
- 0.58
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by-nc
- Locations
- Physiological Research (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology (21680049)
- University of Tokyo
- Japan Society for the Promotion of Science (21680049, 22240058, 25282198)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Keywords
- miR-23a, microRNA, bone formation, bone homeostasis, osteoblasts, osteoclasts, Runx2, SATB2, osteogenic differentiation, transgenic mice, gain-of-function
- MeSH terms
- Animals, Homeostasis, Male, Mice, Inbred C57BL, Mice, Transgenic, Osteoblasts, Osteogenesis, MicroRNAs, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review