IRX3 and IRX5 Inhibit Adipogenic Differentiation of Hypertrophic Chondrocytes and Promote Osteogenesis
Open accessAbstract
Maintaining the correct proportions of different cell types in the bone marrow is critical for bone function. Hypertrophic chondrocytes (HCs) and osteoblasts are a lineage continuum with a minor contribution to adipocytes, but the regulatory network is unclear. Mutations in transcription factors, IRX3 and IRX5, result in skeletal patterning defects in humans and mice. We found coexpression of Irx3 and Irx5 in late-stage HCs and osteoblasts in cortical and trabecular bone. Irx3 and Irx5 null mutants display severe bone deficiency in newborn and adult stages. Quantitative analyses of bone with different combinations of functional alleles of Irx3 and Irx5 suggest these two factors function in a dosage-dependent manner. In Irx3 and Irx5 nulls, the amount of bone marrow adipocytes was increased. In Irx5 nulls, lineage tracing revealed that removal of Irx3 specifically in HCs exacerbated reduction of HC-derived osteoblasts and increased the frequency of HC-derived marrow adipocytes. β-catenin loss of function and gain of function specifically in HCs affects the expression of Irx3 and Irx5, suggesting IRX3 and IRX5 function downstream of WNT signaling. Our study shows that IRX3 and IRX5 regulate fate decisions in the transition of HCs to osteoblasts and to marrow adipocytes, implicating their potential roles in human skeletal homeostasis and disorders. Abstract Fate decision of hypertrophic chondrocyte is controlled by Irx3 and Irx5. With normal expression of Irx3 and Irx5, hypertrophic chondrocytes preferentially differentiate into Col1a1+ osteoblasts, and few are differentiated into Perilipin+ adipocytes. Upon deletion of Irx3 and Irx5, osteogenesis of hypertrophic chondrocyte is inhibited and adipogenesis is promoted, which causes repaired bone formation and increased bone marrow adipose tissue amount. © 2020 American Society for Bone and Mineral Research.
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Global Msx2 knockout impairs osteoclast formation, whereas loss of Irx3 has no effect on osteoclasts.
“According to previous studies, global Msx2 knockout impairs osteoclast formation, whereas loss of Irx3 has no effect on osteoclasts26,27.”
From Targeting Msx2 as a brake in the fusion fate of osteoclasts and an anabolic therapy in pre-clinical models of osteoporosis (2025) · cites this paper as [27]
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HTSeq—a Python framework to work with high-throughput sequencing data
Anders, S., Pyl, P. T., & Huber, W. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btu638 · Cited by 21,464 · see citing works
Trapnell, C., Roberts, A., Goff, L. A., Pertea, G. M., Kim, D., Kelley, D. R., Pimentel, H., Salzberg, S. L., Rinn, J. L., & Pachter, L. S. (2012) · Nature Protocols · doi:10.1038/nprot.2012.016 · Cited by 11,930 · see citing works
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907 · see citing works
Frayling, T. M., Timpson, N. J., Weedon, M. N., Zeggini, E., Freathy, R. M., Lindgren, C. M., Perry, J. R. B., Elliott, K. S., Lango, H., Rayner, N. W., et al. (2007) · Science · doi:10.1126/science.1141634 · Cited by 4,531 · see citing works
Full-length RNA-seq from single cells using Smart-seq2
Picelli, S., Faridani, O. R., Björklund, Å. K., Winberg, G., Sagasser, S., & Sandberg, R. (2014) · Nature Protocols · doi:10.1038/nprot.2014.006 · Cited by 4,137 · see citing works
Adipocytokines: mediators linking adipose tissue, inflammation and immunity
Tilg, H., & Moschen, A. R. (2006) · Nature reviews. Immunology · doi:10.1038/nri1937 · Cited by 3,195 · see citing works
Developmental regulation of the growth plate
Kronenberg, H. M. (2003) · Nature · doi:10.1038/nature01657 · Cited by 2,859 · see citing works
Leptin Inhibits Bone Formation through a Hypothalamic Relay
Ducy, P., Amling, M., Takeda, S., Priemel, M., Schilling, A. F., Beil, F. T., Shen, J., Vinson, C., Rueger, J. M., & Karsenty, G. (2000) · Cell · doi:10.1016/s0092-8674(00)81558-5 · Cited by 2,077 · see citing works
Inhibition of Adipogenesis by Wnt Signaling
Ross, S. E., Hemati, N., Longo, K. A., Bennett, C. N., Lucas, P. C., Erickson, R. L., & MacDougald, O. A. (2000) · Science · doi:10.1126/science.289.5481.950 · Cited by 1,876 · see citing works
Variation in FTO contributes to childhood obesity and severe adult obesity
Christian Dina, C., Meyre, D., Gallina, S., Durand, E., Körner, A., Jacobson, P., Carlsson, L. M. S., Kieß, W., Vatin, V., Lecœur, C., et al. (2007) · Nature Genetics · doi:10.1038/ng2048 · Cited by 1,620 · see citing works
Day, T. F., Guo, X., Garrett-Beal, L., & Yang, Y. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.03.016 · Cited by 1,616 · see citing works
Forming functional fat: a growing understanding of adipocyte differentiation
Cristancho, A. G., & Lazar, M. A. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3198 · Cited by 1,382 · see citing works
Zhou, B. O., Yue, R., Murphy, M. M., Peyer, J. G., & Morrison, S. J. (2014) · Cell Stem Cell · doi:10.1016/j.stem.2014.06.008 · Cited by 1,381 · see citing works
<i>FTO</i> Obesity Variant Circuitry and Adipocyte Browning in Humans
Claussnitzer, M., Dankel, S. N., Kim, K.-H., Quon, G., Meuleman, W., Haugen, C., Glunk, V., Sousa, I. S., Beaudry, J. L., Puviindran, V., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1502214 · Cited by 1,332 · see citing works
Self-citationObesity-associated variants within FTO form long-range functional connections with IRX3
Smemo, S., Tena, J. J., Kim, K.-H., Gamazon, E. R., Sakabe, N. J., Gómez-Marín, C., Aneas, I., Credidio, F. L., Sobreira, D. R., Wasserman, N. F., et al. (2014) · Nature · doi:10.1038/nature13138 · Cited by 1,219 · see citing works
Self-citationIntestinal polyposis in mice with a dominant stable mutation of the β‐catenin gene
Harada, N., Tamai, Y., Ishikawa, T., Sauer, B., Takaku, K., Oshima, M., & Taketo, M. M. (1999) · The EMBO Journal · doi:10.1093/emboj/18.21.5931 · Cited by 1,198 · see citing works
Canonical Wnt/β-Catenin Signaling Prevents Osteoblasts from Differentiating into Chondrocytes
Hill, T. P., Später, D., Taketo, M. M., Birchmeier, W., & Hartmann, C. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.02.013 · Cited by 1,086 · see citing works
Self-citationRodda, S. J., & McMahon, A. P. (2006) · Development · doi:10.1242/dev.02480 · Cited by 1,011 · see citing works
Adipocyte tissue volume in bone marrow is increased with aging and in patients with osteoporosis
Justesen, J., Stenderup, K., Ebbesen, E., Mosekilde, L., Steiniche, T., & Kassem, M. (2004) · Biogerontology (Dordrecht) · doi:10.1023/a:1011513223894 · Cited by 847 · see citing works
Hypertrophic chondrocytes can become osteoblasts and osteocytes in endochondral bone formation
Yang, L., Tsang, K. Y., Tang, H. C., Chan, D. T.-M., & Cheah, K. S. E. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302703111 · Cited by 755 · see citing works
Self-citationTCF/LEFs and Wnt Signaling in the NucleusPreprint
Cadigan, K. M., & Waterman, M. L. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a007906 · Cited by 750 · see citing works
Genetic Control of Bone Formation
Karsenty, G., Kronenberg, H. M., & Settembre, C. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.042308.113308 · Cited by 667 · see citing works
Gremlin 1 Identifies a Skeletal Stem Cell with Bone, Cartilage, and Reticular Stromal Potential
Worthley, D. L., Churchill, M., Compton, J. T., Tailor, Y. H., Rao, M., Si, Y., Levin, D. E., Schwartz, M. G., Uygur, A., Hayakawa, Y., et al. (2015) · Cell · doi:10.1016/j.cell.2014.11.042 · Cited by 635 · see citing works
Altered endochondral bone development in matrix metalloproteinase 13-deficient mice
Stickens, D., Behonick, D. J., Ortéga, N., Heyer, B. S., Hartenstein, B., Yu, Y., Fosang, A., Schorpp‐Kistner, M., Angel, P. E., & Werb, Z. (2004) · Development · doi:10.1242/dev.01461 · Cited by 608 · see citing works
Osteo-chondroprogenitor cells are derived from Sox9 expressing precursors
Akiyama, H., Kim, J., Nakashima, K., Balmes, G. C., Iwai, N., Deng, J. M., Zhang, Z., Martin, J. F., Behringer, R. R., Nakamura, T., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504750102 · Cited by 607 · see citing works
Identification of the Human Skeletal Stem Cell
Chan, C. K. F., Gulati, G. S., Sinha, R., Vincent-Tompkins, J., Lopez, M., Carter, A. C., Ransom, R. C., Reinisch, A., Wearda, T. L., Murphy, M. P., et al. (2018) · Cell · doi:10.1016/j.cell.2018.07.029 · Cited by 602 · see citing works
Zhou, X., von der Mark, K., Henry, S. P., Norton, W., Adams, H. P., & Crombrugghe, B. D. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004820 · Cited by 585 · see citing works
Cawthorn, W., Scheller, E., Learman, B. S., Parlee, S., Simon, B., Mori, H., Ning, X.-M., Bree, A. J., Schell, B. A., Broome, D. T., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.06.003 · Cited by 506 · see citing works
Scheller, E. L., Doucette, C. R., Learman, B. S., Cawthorn, W. P., Khandaker, S., Schell, B., Wu, B., Ding, S.-Y., Bredella, M. A., Fazeli, P. K., et al. (2015) · Nature Communications · doi:10.1038/ncomms8808 · Cited by 433 · cited 1× · see citing works
“This finding is consistent with the reported variation in adipocyte development between proximal and distal tibias.((50)) To investigate whether specific ablation of Irx3 and Irx5 would affect the fate determination of HC-derived cells, we double-labeled cells with HC lineage marker and adipocyte marker Perilipin at t…”
ResultEndochondral ossification is required for haematopoietic stem-cell niche formation
Chan, C. K. F., Chen, C., Luppen, C. A., Kim, J., DeBoer, A., Wei, K., Helms, J. A., Kuo, C. J., Kraft, D. L., & Weissman, I. L. (2008) · Nature · doi:10.1038/nature07547 · Cited by 430 · see citing works
A subset of chondrogenic cells provides early mesenchymal progenitors in growing bones
Ono, N., Ono, W., Nagasawa, T., & Kronenberg, H. M. (2014) · Nature Cell Biology · doi:10.1038/ncb3067 · Cited by 418 · see citing works
Resting zone of the growth plate houses a unique class of skeletal stem cells
Mizuhashi, K., Ono, W., Matsushita, Y., Sakagami, N., Takahashi, A., Saunders, T. L., Nagasawa, T., Kronenberg, H. M., & Ono, N. (2018) · Nature · doi:10.1038/s41586-018-0662-5 · Cited by 418 · see citing works
Osteoblasts and Osteoclasts in Bone Remodeling and Inflammation
Tanaka, Y., Nakayamada, S., & Okada, Y. (2005) · Current Drug Targets - Inflammation & Allergy · doi:10.2174/1568010054022015 · Cited by 382 · see citing works
Dominance of SOX9 function over RUNX2 during skeletogenesis
Zhou, G. D., Zheng, Q., Engin, F., Munivez, E. M., Chen, Y., Sebald, E. T., Krakow, D., & Lee, B. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605170103 · Cited by 367 · see citing works
Gli1 identifies osteogenic progenitors for bone formation and fracture repair
Shi, Y., He, G., Lee, W., McKenzie, J. A., Silva, M. J., & Long, F. (2017) · Nature Communications · doi:10.1038/s41467-017-02171-2 · Cited by 345 · see citing works
Shukunami, C., Ishizeki, K., Atsumi, T., Ohta, Y., Suzuki, F., & Hiraki, Y. (1997) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.1997.12.8.1174 · Cited by 306 · see citing works
Aghajanian, P., & Mohan, S. (2018) · Bone Research · doi:10.1038/s41413-018-0021-z · Cited by 288 · see citing works
Song, L., Liu, M., Ono, N., Bringhurst, F. R., Kronenberg, H. M., & Guo, J. (2012) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1694 · Cited by 234 · see citing works
Hu, D. P., Ferro, F., Yang, F. F., Taylor, A., Chang, W., Miclau, T., Marcucio, R., & Bahney, C. S. (2017) · Development · doi:10.1242/dev.130807 · Cited by 221 · see citing works
Osteogenic fate of hypertrophic chondrocytes
Yang, G., Zhu, L., Hou, N., Lan, Y., Wu, X., Zhou, B., Teng, Y., & Yang, X. Y. (2014) · Cell Research · doi:10.1038/cr.2014.111 · Cited by 208 · see citing works
Tsang, K. Y., Chan, D. T.-M., Cheslett, D., Chan, W. C. W., So, C. L., Melhado, I. G., Chan, T. W. Y., Kwan, K. M., Hunziker, E. B., Yamada, Y., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050044 · Cited by 188 · see citing works
Self-citationPark, J., Gebhardt, M., Golovchenko, S., Pérez‐Brangulí, F., Hattori, T., Hartmann, C., Zhou, X., deCrombrugghe, B., Stock, M., Schneider, H., et al. (2015) · Biology Open · doi:10.1242/bio.201411031 · Cited by 179 · see citing works
Self-citationScheller, E., Troiano, N., Vanhoutan, J. N., Bouxsein, M., Fretz, J. A., Xi, Y., Nelson, T., Katz, G., Berry, R., Church, C., et al. (2014) · Methods in Enzymology · doi:10.1016/b978-0-12-411619-1.00007-0 · Cited by 173 · see citing works
Mediation of the Acute Stress Response by the Skeleton
Berger, J. M., Singh, P. P., Khrimian, L., Morgan, D. A., Chowdhury, S., Arteaga‐Solis, E., Horváth, T. L., Domingos, A. I., Marsland, A. L., Yadav, V. K., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.08.012 · Cited by 166 · see citing works
Marrow Fat and Bone: Review of Clinical Findings
Schwartz, A. V. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00040 · Cited by 158 · see citing works
Cawthorn, W. P., Scheller, E. L., Parlee, S. D., Pham, H. A., Learman, B. S., Redshaw, C., Sulston, R. J., Burr, A. A., Das, A. K., Simon, B. R., et al. (2015) · Endocrinology · doi:10.1210/en.2015-1477 · Cited by 141 · see citing works
Iroquois homeobox gene 3 establishes fast conduction in the cardiac His–Purkinje network
Zhang, S., Kim, K.-H., Rosen, A., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106911108 · Cited by 137 · see citing works
Bagi, C. M., Hanson, N., Andresen, C. J., Pero, R. W., Lariviere, R., Turner, C. H., & Laib, A. (2005) · Bone · doi:10.1016/j.bone.2005.07.028 · Cited by 135 · see citing works
Morphologic stages of the terminal hypertrophic chondrocyte of growth plate cartilage
Farnum, C. E., & Wilsman, N. J. (1987) · The Anatomical Record · doi:10.1002/ar.1092190303 · Cited by 131 · see citing works
Roles of Chondrocytes in Endochondral Bone Formation and Fracture Repair
Hinton, R. J., Jing, Y., Jing, J., & Feng, J. Q. (2016) · Journal of Dental Research · doi:10.1177/0022034516668321 · Cited by 130 · see citing works
Nakamura, Y., Alves, E. D. P., Veenstra, G. J. C., & Hoppler, S. (2016) · Development · doi:10.1242/dev.131664 · Cited by 126 · see citing works
Li, D., Sakuma, R., Vakili, N. A., Mo, R., Puviindran, V., Deimling, S. J., Zhang, X., Hopyan, S., & Hui, C. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.03.001 · Cited by 111 · see citing works
Self-citationIdentification and characterization of an injury-induced skeletal progenitor
Marecic, O., Tevlin, R., McArdle, A., Seo, E. Y., Wearda, T. L., Duldulao, C. R., Walmsley, G. G., Nguyen, A., Weissman, I. L., Chan, C. K. F., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1513066112 · Cited by 108 · see citing works
Consanguinity and genetic disorders. Profile from Jordan
Hamamy, H., Masri, A. T., Al-Hadidy, A. M., et al. (2007) · Saudi Medical Journal · doi:10.15537/1658-3175.3967 · Cited by 98 · see citing works
Gaborit, N., Sakuma, R., Wylie, J. N., Kim, K.-H., Zhang, S., Hui, C., & Bruneau, B. G. (2012) · Development · doi:10.1242/dev.081703 · Cited by 93 · see citing works
Self-citationThe Unique Metabolic Characteristics of Bone Marrow Adipose Tissue
Li, Y.-J., Meng, Y., & Yu, X.-J. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00069 · Cited by 92 · see citing works
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1
Bonnard, C., Strobl, A. C., Shboul, M., et al. (2012) · Nature Genetics · doi:10.1038/ng.2259 · Cited by 87 · see citing works
Houben, A., Kostanova‐Poliakova, D., Weißenböck, M., Graf, J., Teufel, S., von der Mark, K., & Hartmann, C. (2016) · Development · doi:10.1242/dev.137489 · Cited by 81 · see citing works
Self-citationBone marrow adipose tissue as an endocrine organ: close to the bone?
Sulston, R. J., & Cawthorn, W. P. (2016) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2016-0012 · Cited by 67 · see citing works
Giovannone, D., Paul, S., Schindler, S., Arata, C., Farmer, D. T., Patel, P., Smeeton, J., & Crump, J. G. (2019) · eLife · doi:10.7554/elife.42736 · Cited by 65 · see citing works
Tan, Z., Niu, B., Tsang, K. Y., Melhado, I. G., Ohba, S., He, X., Huang, Y., Wang, C., McMahon, A. P., Jauch, R., et al. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007346 · Cited by 60 · see citing works
Self-citationDeletion of beta catenin in hypertrophic growth plate chondrocytes impairs trabecular bone formation
Golovchenko, S., Hattori, T., Hartmann, C., Gebhardt, M., Gebhard, S., Heß, A., Pausch, F., Schlund, B., & von der Mark, K. (2013) · Bone · doi:10.1016/j.bone.2013.03.019 · Cited by 58 · see citing works
Self-citationSunters, A., McCluskey, J. T., & Grigoriadis, A. E. (1998) · Developmental Genetics · doi:10.1002/(sici)1520-6408(1998)22:4 · Cited by 55 · see citing works
A Second Career for Chondrocytes—Transformation into Osteoblasts
Wolff, L. I., & Hartmann, C. (2019) · Current Osteoporosis Reports · doi:10.1007/s11914-019-00511-3 · Cited by 43 · see citing works
Self-citationIRX5 regulates adipocyte amyloid precursor protein and mitochondrial respiration in obesity
Bjune, J.-I., Haugen, C., Gudbrandsen, O. A., Nordbø, O. P., Nielsen, H. J., Våge, V., Njølstad, P. R., Sagen, J. V., Dankel, S. N., & Mellgren, G. (2018) · International Journal of Obesity · doi:10.1038/s41366-018-0275-y · Cited by 40 · see citing works
Bone Marrow Adipocyte Developmental Origin and Biology
Bukowska, J., Frazier, T. P., Smith, S., Brown, T. A., Bender, R., McCarthy, M., Wu, X.-Y., Bunnell, B., & Gimble, J. (2018) · Current Osteoporosis Reports · doi:10.1007/s11914-018-0442-z · Cited by 37 · see citing works
Cain, C. J., Gaborit, N., Lwin, W. W., et al. (2016) · Bone Reports · doi:10.1016/j.bonr.2016.02.005 · Cited by 35 · see citing works
The extended chondrocyte lineage: implications for skeletal homeostasis and disorders
Tsang, K. Y., & Cheah, K. S. E. (2019) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2019.07.011 · Cited by 29 · see citing works
Self-citationHamamy, H., Teebi, A. S., Oudjhane, K., et al. (2007) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.31594 · Cited by 28 · see citing works
Increased Bone Marrow Adiposity in a Context of Energy Deficit: The Tip of the Iceberg?
Ghali, O., Rassy, N. A., Hardouin, P., & Chauveau, C. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00125 · Cited by 27 · see citing works
Mechanistic insights into skeletal development gained from genetic disorders
Yip, R. K. H., Chan, D. T.-M., & Cheah, K. S. E. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.02.002 · Cited by 26 · see citing works
Self-citationJanssens, S., Denayer, T., Deroo, T., Roy, F. M. V., & Vleminckx, K. (2010) · The International Journal of Developmental Biology · doi:10.1387/ijdb.092985sj · Cited by 23 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Wai AW, Ng LJ, Watanabe H, Yamada Y, Tam PP, Cheah KS. Disrupted expression of matrix genes in the growth plate of the mouse carti- lage matrix deficiency (cmd) mutant. Dev Genet. 1998;22(4):349-58.
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Ma, Q., Wang, S., Xue, H., Ni, L., Yuan, P., Shen, Y., Zheng, B., Wang, Q., Zhang, J., Wang, H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-61938-0 · Cited by 15 · see citing works
“According to previous studies, global Msx2 knockout impairs osteoclast formation, whereas loss of Irx3 has no effect on osteoclasts 26,27 .”
- Authors
- Tan, Z., Kong, M., Wen, S., Tsang, K. Y., Niu, B., Hartmann, C., Chan, D., Hui, C.-C., & Cheah, K. S. E.
- Affiliations
- University of Hong Kong (HK)
- University of Münster (DE)
- University of Toronto (CA)
- Corresponding author
- Cheah, Kathryn S.E.
- ORCID
- Venue
- Journal of Bone and Mineral Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2020-07-14
- Volume
- 35
- Issue
- 12
- Pages
- 2444-2457
- ISSN
- 0884-0431 (ISSN-L)
- 1523-4681
- OpenAlex
- W3043357509
- Cited by
- 52
- References
- 72
- Citations by year
- 2026: 2 · 2025: 9 · 2024: 14 · 2023: 9 · 2022: 10 · 2021: 7 · 2020: 1
- FWCI
- 2.19
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Bone and Mineral Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Jimmy & Emily Tang Endowed Professorship
- Research Grants Council, University Grants Committee (AoE/M-04/04, GRF 17129017, T12-708/12-N, AoE/M‐04/04, T12‐708/12‐N)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
- Health Sciences › Medicine › Rheumatology › Bone Tumor Diagnosis and Treatments
- Keywords
- IRX3, IRX5, hypertrophic chondrocytes, bone formation, adipogenesis, bone marrow adipocytes, Wnt signaling, β-catenin, dosage-dependent regulation, skeletal homeostasis, COL1A1, perilipin, lineage tracing
- MeSH terms
- Animals, Cell Differentiation, Osteoblasts, Osteogenesis, Transcription Factors, Homeodomain Proteins, Chondrocytes, Adipogenesis, Mice
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