The DOI matches its Crossref record; 407 of the 408 references it cites were found in a registry or an index.
Transforming Growth Factor-β1 to the Bone
Abstract
TGF-β1 is a ubiquitous growth factor that is implicated in the control of proliferation, migration, differentiation, and survival of many different cell types. It influences such diverse processes as embryogenesis, angiogenesis, inflammation, and wound healing. In skeletal tissue, TGF-β1 plays a major role in development and maintenance, affecting both cartilage and bone metabolism, the latter being the subject of this review. Because it affects both cells of the osteoblast and osteoclast lineage, TGF-β1 is one of the most important factors in the bone environment, helping to retain the balance between the dynamic processes of bone resorption and bone formation. Many seemingly contradictory reports have been published on the exact functioning of TGF-β1 in the bone milieu. This review provides an overall picture of the bone-specific actions of TGF-β1 and reconciles experimental discrepancies that have been reported for this multifunctional cytokine.
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“Noted exercise-associated bone-derived factors affecting bone formation include TGFβ1 (REF.162) and sclerostin163.”
From Exerkines in health, resilience and disease (2022) · cites this paper as [162]
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“In general, studies using rodents and primates as experimental models do not report such favourable outcomes concerning the osteopromotive ability of TGF-β1 compared to studies using dogs (Janssens et al., 2005).”
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“Furthermore, TGFβ1 is known to regulate the proliferation and differentiation of osteoprogenitor cells [6].”
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“…regulator of osteoclast/osteoblast coupling is release of bone matrix embedded growth factors such as transforming growth factor beta (TGFb) (Janssens et al., 2005), bone morphogenetic protein 2 (BMP2) (Wan and Cao, 2005), and fibroblast growth factor (FGF) family members (Xiao et al.,…”
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“Whereas TGF-b is produced chiefly by lymphoid cells, it is also present in high concentrations in the bone, thrombocytes, and serum (8).”
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“Depending on the stage of osteoblast differentiation, TGFb either promotes or inhibits osteoblast development and mineralization (Harris et al., 1994; Alliston et al., 2001; Maeda et al., 2004; Janssens et al., 2005).”
BackgroundRole of TGF-β in a Mouse Model of High Turnover Renal Osteodystrophy
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“TGFβ1 functions via binding to its receptor, TGFβ receptor II (TGFBRII), present on the surface of cells [20,41]; therefore, to determine whether TGFβ1 functions through TGFBRII, we evaluated”
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“TGF-b 1 is an important regulatory factor in every stage of bone regeneration [16,56,46].”
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“The importance of TGF-β1 in bone development and homeostasis has been extensively illustrated both in vitro and in vivo (Janssens et al. 2005).”
BackgroundPrimary aldosteronism and impaired natriuresis in mice underexpressing TGFβ1
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“Indeed, the RANKL/OPG ratio varies at different cell maturation stages (Gori et al., 2000; Thomas et al., 2001), and osteoblast differentiation at early stages is only activated by TGFβ; otherwise, the differentiation is repressed (Janssens et al., 2005).”
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Transglutaminase 2 as a biomarker of osteoarthritis: an update
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“TGF- b1 is also able to induce osteophytes similar to those found in osteoarthritis and TGF-b is highly expressed in osteophytes themselves (Janssens et al. 2005; Blaney Davidson et al. 2007).”
BackgroundKim, H., Hong, J. M., Yoon, K., Kim, N., Cho, D., Choi, J., Lee, I. K., & Kim, S. (2012) · Bone · doi:10.1016/j.bone.2012.07.015 · Cited by 33
An Ex Vivo Rodent Mandible Culture Model for Bone Repair
Smith, E. L., Locke, M., Waddington, R., & Sloan, A. (2010) · Tissue Engineering. Part C, Methods · doi:10.1089/ten.tec.2009.0698 · Cited by 34
Alexander, K. A., Tseng, H., Salga, M., Genêt, F., & Lévesque, J.-P. (2020) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00636-w · Cited by 33
Sueyoshi, T., Yamamoto, K., & Akiyama, H. (2012) · Matrix Biology · doi:10.1016/j.matbio.2012.07.002 · Cited by 32
Toom, A., Arend, A., Gunnarsson, D., Ulfsparre, R., Suutre, S., Haviko, T., & Selstam, G. (2007) · Calcified Tissue International · doi:10.1007/s00223-007-9000-x · Cited by 32
“Also, TGF-s3 has been shown to act in a sequential manner with BMP-2 in the regulation of cartilage differentiation in chick limb formation [28] and in fracture healing [ 20 ].”
BackgroundResultInfluentialDetection of Rare Nonsynonymous Variants in TGFB1 in Otosclerosis Patients
Thys, M., Schrauwen, I., Vanderstraeten, K., Dieltjens, N., Fransén, E., Ealy, M., Cremers, C. W. R. J., de Heyning, P. V., Vincent, R., Offeciers, E., et al. (2009) · Annals of Human Genetics · doi:10.1111/j.1469-1809.2009.00505.x · Cited by 31
“The precise role of TGF-β1 in the different stages of these processes is not clear (Janssens et al., 2005).”
BackgroundWinklmayr, M., Kluge, C., Winklmayr, W., Küchenhoff, H., Steiner, M., Ritter, M., & Hartl, A. J. (2014) · Radiation and Environmental Biophysics · doi:10.1007/s00411-014-0568-z · Cited by 32
Chondroitin sulfate and growth factor signaling in the skeleton: Possible links to MPS VI
Alliston, T. N. (2010) · Journal of Pediatric Rehabilitation Medicine · doi:10.3233/prm-2010-0117 · Cited by 31
Differential regulation of osteoadherin (OSAD) by TGF-β1 and BMP-2
Rehn, A. P., Chalk, A. M., & Wendel, M. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.08.133 · Cited by 31
Hu, Z., Peel, S. A. F., Ho, S. K. C., Sándor, G. K. B., & Clokie, C. M. L. (2009) · Growth Factors · doi:10.1080/08977190903137819 · Cited by 30
“Growth factors added to bone graft material can enhance and even accelerate the normal regenerative processes and healing of bone (Caffesse and Quinones 2000; Chen et al. 2004; Janssens et al. 2005).”
BackgroundBioinspired Collagen-Apatite Nanocomposites for Bone Regeneration
Liu, S., Sun, Y., Fu, Y., Chang, D., Fu, C., Wang, G., Liu, Y., Tay, F. R., & Zhou, Y.-H. (2016) · Journal of Endodontics · doi:10.1016/j.joen.2016.04.027 · Cited by 30
“The rationale for examining these molecules is that Osx is expressed in osteoblasts of endochondral and membranous bones (20); VEGFR-1 is a high-affinity receptor for vascular endothelial growth factor produced by endothelial cells during angiogenesis (21); and TGF-b1 influences growth, differentiation, and extracellu…”
BackgroundSaito, A., Nagaishi, K., Iba, K., Mizue, Y., Chikenji, T., Otani, M., Nakano, M. H., Oyama, K., Yamashita, T., & Fujimiya, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-19516-6 · Cited by 30
ZNF521 Represses Osteoblastic Differentiation in Human Adipose-Derived Stem Cells
Chiarella, E., Aloisio, A., Scicchitano, S., Lucchino, V., Montalcini, Y., Galasso, O., Greco, M., Gasparini, G., Mesuraca, M., Bond, H. M., et al. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19124095 · Cited by 30
Verbeke, S., Bertoni, F., Bacchini, P., Oosting, J., Sciot, R., Krenács, T., & Bovée, J. V. M. G. (2013) · Modern Pathology · doi:10.1038/modpathol.2013.56 · Cited by 30
Fibrillin-1 directly regulates osteoclast formation and function by a dual mechanism
Tiedemann, K., Boraschi-Diaz, I., Rajakumar, I., Kaur, J., Roughley, P. J., Reinhardt, D. P., & Komarova, S. V. (2013) · Journal of Cell Science · doi:10.1242/jcs.127571 · Cited by 31
“In turn, TGFb and BMPs are important regulators of bone growth and remodeling (Giannoudis et al., 2007; Guo et al., 2008; Janssens et al., 2005; Quinn et al., 2001).”
BackgroundUejima, S., Okada, K., Kagami, H., Taguchi, A., & Ueda, M. (2008) · Cytotherapy · doi:10.1080/14653240802071616 · Cited by 29
Hu, X., Yin, X., Zhang, H., Guo, C., & Tang, M. (2016) · Molecular Medicine Reports · doi:10.3892/mmr.2016.5729 · Cited by 29
BMP9 is a potential therapeutic agent for use in oral and maxillofacial bone tissue engineering
Liu, L., Chen, Y., Song, D., & Huang, D. (2020) · Biochemical Society Transactions · doi:10.1042/bst20200376 · Cited by 28
The Auxiliary Role of Heparin in Bone Regeneration and its Application in Bone Substitute Materials
Wang, J., Xiao, L., Wang, W., Zhang, D., Ma, Y., Zhang, Y., & Wang, X. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.837172 · Cited by 31
“…osteogenic differentiation, facilitates production of extracellular matrix (ECM) proteins, stimulates type II collagen expression, stimulates chondrocyte precursors proteoglycan synthesis, reduces osteoblast apoptosis, and inhibits hematopoietic precursors (Janssens et al., 2005; Xu et al., 2020).”
BackgroundAnthwal, N., Chai, Y., & Tucker, A. S. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21567 · Cited by 29
Biphasic effects of TGFβ1 on BMP9-induced osteogenic differentiation of mesenchymal stem cells
Li, R., Deng, Z., Hu, N., Liang, X., Liu, B., Luo, J., Chen, L., Yin, L., Luo, X., Shui, W., et al. (2012) · BMB Reports · doi:10.5483/bmbrep.2012.45.9.053 · Cited by 29
Sustained Delivery of Biomolecules From Gelatin Carriers for Applications in Bone Regeneration
Song, J., & Leeuwenburgh, S. C. G. (2014) · Therapeutic Delivery · doi:10.4155/tde.14.42 · Cited by 28
Metadata
- Authors
- Janssens, K., ten Dijke, P., Janssens, S., & Van Hul, W.
- Affiliations
- University of Antwerp (BE)
- Department of Molecular Cell Biology (P.t.D.), Leids Universitair Medisch Centrum, 2333 AL Leiden, The Netherlands;
- University of Lausanne (CH)
- Department of Medical Genetics (K.J., W.V.H.), University of Antwerp, 2610 Antwerp, Belgium;
- Venue
- Endocrine Reviews
- Publisher
- The Endocrine Society
- Published
- 2005-10-01
- Volume
- 26
- Issue
- 6
- Pages
- 743-774
- ISSN
- 0163-769X (ISSN-L)
- 1945-7189
- OpenAlex
- W2144206769
- Cited by
- 710
- References
- 408
- Citations by year
- 2026: 12 · 2025: 26 · 2024: 24 · 2023: 35 · 2022: 30 · 2021: 30 · 2020: 27 · 2019: 22 · 2018: 23 · 2017: 34 · 2016: 37 · 2015: 26 · 2014: 46 · 2013: 57 · 2012: 47
- FWCI
- 2.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrine Reviews (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- Funders
- Fonds Wetenschappelijk Onderzoek
- Universiteit Antwerpen
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Keywords
- TGF-β1, bone metabolism, osteoblasts, osteoclasts, bone remodeling, bone resorption, bone formation, cartilage, skeletal development, cytokine signaling
- MeSH terms
- Animals, Bone and Bones, Bone Development, Bone Resorption, Cells, Cultured, Humans, Osteoblasts, Osteoclasts, Phenotype, Stem Cells, Signal Transduction, Transforming Growth Factor beta, Protein Isoforms, Transforming Growth Factor beta1
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