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Osteocytes Regulate Primary Lymphoid Organs and Fat Metabolism
Open accessAbstract
Osteocytes act as mechanosensors to control local bone volume. However, their roles in the homeostasis of remote organs are largely unknown. We show that ablation of osteocytes in mice (osteocyte-less [OL] mice) leads to severe lymphopenia, due to lack of lymphoid-supporting stroma in both the bone marrow and thymus, and complete loss of white adipose tissues. These effects were reversed when osteocytes were replenished within the bone. In contrast, neither in vivo supply of T cell progenitors and humoral factors via shared circulation with a normal parabiotic partner nor ablation of specific hypothalamic nuclei rescued thymic atrophy and fat loss in OL mice. Furthermore, ablation of the hypothalamus in OL mice led to hepatic steatosis, which was rescued by parabiosis with normal mice. Our results define a role for osteocytes as critical regulators of lymphopoiesis and fat metabolism and suggest that bone acts as a central regulator of multiple organs.
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“Osteocytes also act on the immune system by modifying the microenvironment in primary lymphoid organs and thereby influencing lymphopoiesis [210].”
From Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells (2015) · cites this paper as [210]
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Cites
SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver
Horton, J. D., Goldstein, J. L., & Brown, M. S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci15593 · Cited by 4,794
SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver
Horton, J. D., Goldstein, J. L., & Brown, M. S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215593 · Cited by 4,092
Bonewald, L. F. (2011) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.320 · Cited by 2,287
Leptin Regulates Bone Formation via the Sympathetic Nervous System
Takeda, S., Elefteriou, F., Levasseur, R., Liu, X., Zhao, L., Parker, K. L., Armstrong, D., Ducy, P., & Karsenty, G. (2002) · Cell · doi:10.1016/s0092-8674(02)01049-8 · Cited by 1,735
Resolution and characterization of pro-B and pre-pro-B cell stages in normal mouse bone marrow.
Hardy, R. R., Carmack, C. E., Shinton, S. A., Kemp, J. D., & Hayakawa, K. (1991) · The Journal of Experimental Medicine · doi:10.1084/jem.173.5.1213 · Cited by 1,604
Signals from the Sympathetic Nervous System Regulate Hematopoietic Stem Cell Egress from Bone Marrow
Katayama, Y., Battista, M., Kao, W.-M., Hidalgo, A., Peired, A. J., Thomas, S. A., & Frenette, P. S. (2006) · Cell · doi:10.1016/j.cell.2005.10.041 · Cited by 1,412
Self-citationLeptin regulation of bone resorption by the sympathetic nervous system and CART
Elefteriou, F., Ahn, J. D., Takeda, S., Starbuck, M., Yang, X., Liu, X., Kondo, H., Richards, W. G., Bannon, T. W., Noda, M., et al. (2005) · Nature · doi:10.1038/nature03398 · Cited by 1,311 · cited 1×
“It is recognized that certain areas of the brain, such as the ventromedial hypothalamic nucleus (VMH) and arcuate nucleus (ARC), also control bone metabolism via the sympathetic nervous system in response to leptin signaling (Elefteriou et al., 2005; Takeda et al., 2002).”
BackgroundInsulin signaling in osteoblasts integrates bone remodeling and energy metabolism
Ferron, M., Wei, J., Yoshizawa, T., Del Fattore, A., DePinho, R. A., Teti, A., Ducy, P., & Karsenty, G. (2010) · Cell · doi:10.1016/j.cell.2010.06.003 · Cited by 1,123
Acquired and Inherited Lipodystrophies
Garg, A. (2004) · New England Journal of Medicine · doi:10.1056/nejmra025261 · Cited by 940
Targeted ablation of osteocytes induces osteoporosis with defective mechanotransduction.
Tatsumi, S., Ishii, K., Amizuka, N., Li, M., Kobayashi, T., Kohno, K., Ito, M., Takeshita, S., & Ikeda, K. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.05.001 · Cited by 848
Self-citationCortical and Trabecular Bone Mineral Loss From the Spine and Hip in Long-Duration Spaceflight
Lang, T., LeBlanc, A., Evans, H., Lu, Y., Genant, H., & Yu, A. (2004) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.040307 · Cited by 828
Hematopoiesis is severely altered in mice with an induced osteoblast deficiency
Višnjić, D., Kalajzić, Ž., Rowe, D. W., Katavić, V., Lorenzo, J., & Aguila, H. L. (2004) · Blood · doi:10.1182/blood-2003-11-4011 · Cited by 804
O’Brien, C. A., Jia, D., Plotkin, L. I., Bellido, T., Powers, C. C., Stewart, S. A., Manolagas, S. C., & Weinstein, R. S. (2003) · Endocrinology · doi:10.1210/en.2003-0990 · Cited by 771
Insulin Receptor Signaling in Osteoblasts Regulates Postnatal Bone Acquisition and Body Composition
Fulzele, K. S., Riddle, R. C., DiGirolamo, D. J., Cao, X., Wan, C., Chen, D., Monier‐Faugere, M., Aja, S. M., Hussain, M. A., Brüning, J. C., et al. (2010) · Cell · doi:10.1016/j.cell.2010.06.002 · Cited by 768
The contribution of bone to whole-organism physiology
Karsenty, G., & Ferron, M. (2012) · Nature · doi:10.1038/nature10763 · Cited by 537
Mechanosensation and transduction in osteocytes
Klein-Nulend, J., Bakker, A. D., Bacabac, R. G., Vatsa, A., & Weinbaum, S. (2013) · Bone · doi:10.1016/j.bone.2012.10.013 · Cited by 528
Histologic evidence for osteopenia and increased bone turnover in ovariectomized rats
Wronski, T. J., Walsh, C. C., & Ignaszewski, L. A. (1986) · Bone · doi:10.1016/8756-3282(86)90683-6 · Cited by 316
Guéguinou, N., Huin-Schohn, C., Bascove, M., Bueb, J.-L., Tschirhart, E., Legrand-Frossi, C., & Frippiat, J.-P. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.0309167 · Cited by 280
Egawa, T., Kawabata, K., Kawamoto, H., Amada, K., Okamoto, R., Fujii, N., Kishimoto, T., Katsura, Y., & Nagasawa, T. (2001) · Immunity · doi:10.1016/s1074-7613(01)00185-6 · Cited by 220
Lipodystrophy: metabolic insights from a rare disorder
Huang-Doran, I., Sleigh, A., Rochford, J. J., O'Rahilly, S., & Savage, D. B. (2010) · Journal of Endocrinology · doi:10.1677/joe-10-0272 · Cited by 215
Lettéron, P., Sutton, A., Mansouri, A., Fromenty, B., & Pessayre, D. (2003) · Hepatology · doi:10.1053/jhep.2003.50309 · Cited by 189
Myelopoiesis is regulated by osteocytes through Gsα-dependent signaling
Fulzele, K. S., Krause, D. S., Panaroni, C., Saini, V., Barry, K. J., Liu, X., Lotinun, S., Baron, R., Bonewald, L. F., Feng, J. Q., et al. (2012) · Blood · doi:10.1182/blood-2012-06-437160 · Cited by 152
Genetic evidence points to an osteocalcin-independent influence of osteoblasts on energy metabolism
Yoshikawa, Y., Kode, A., Xu, L., Mosialou, I., Silva, B. C. C., Ferron, M., Clemens, T. L., Economides, A. N., & Kousteni, S. (2011) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.417 · Cited by 142
Effects of Simulated Weightlessness on Bone Mineral Metabolism
Globus, R. K., Bikle, D. D., & Morey, E. R. (1984) · Endocrinology · doi:10.1210/endo-114-6-2264 · Cited by 126
Fbxw7 regulates lipid metabolism and cell fate decisions in the mouse liver
Onoyama, I., Suzuki, A., Matsumoto, A., Tomita, K., Katagiri, H., Oike, Y., Nakayama, K., & Nakayama, K. (2010) · Journal of Clinical Investigation · doi:10.1172/jci40725 · Cited by 118
Lipodystrophy: lessons in lipid and energy metabolism
Simha, V., & Garg, A. (2006) · Current Opinion in Lipidology · doi:10.1097/01.mol.0000217898.52197.18 · Cited by 115
Increased weight gain after ovariectomy is not a consequence of leptin resistance
Chen, Y., & Heiman, M. L. (2001) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2001.280.2.e315 · Cited by 115
Immune system dysregulation during spaceflight: clinical risk for exploration-class missions
Crucian, B., & Sams, C. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.0709500 · Cited by 108
Belavý, D. L., Beller, G., Armbrecht, G., Perschel, F. H., Fitzner, R., Bock, O., Börst, H., Degner, C., Gast, U., & Felsenberg, D. (2010) · Osteoporosis International · doi:10.1007/s00198-010-1371-6 · Cited by 96
Ciani, C., Doty, S. B., & Fritton, S. P. (2009) · Bone · doi:10.1016/j.bone.2009.01.376 · Cited by 65
Shindo, N., Fujisawa, T., Sugimoto, K., Nojima, K., Fukai, A., Yoshikawa, Y., Wang, X., Yasuda, O., Ikegami, H., & Rakugi, H. (2010) · Journal of Hepatology · doi:10.1016/j.jhep.2009.12.033 · Cited by 65
Erben, R. G., Raith, S., Eberle, J., & Stangassinger, M. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.274.3.e476 · Cited by 63
Galactocerebrosides Are Required Postnatally for Stromal-Dependent Bone Marrow Lymphopoiesis
Katayama, Y., & Frenette, P. S. (2003) · Immunity · doi:10.1016/s1074-7613(03)00150-x · Cited by 29
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Osteoimmunology: evolving concepts in bone–immune interactions in health and disease
Tsukasaki, M., & Takayanagi, H. (2019) · Nature reviews. Immunology · doi:10.1038/s41577-019-0178-8 · Cited by 812
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Okamoto, K., Nakashima, T., Shinohara, M., Negishi-Koga, T., Komatsu, N., Terashima, A., Sawa, S., Nitta, T., & Takayanagi, H. (2017) · Physiological Reviews · doi:10.1152/physrev.00036.2016 · Cited by 534
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Fornetti, J., Welm, A. L., & Stewart, S. A. (2018) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3618 · Cited by 540
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Capulli, M., Paone, R., & Rucci, N. (2014) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2014.05.003 · Cited by 413
Metadata
- Authors
- Sato, M., Asada, N., Kawano, Y., Wakahashi, K., Minagawa, K., Kawano, H., Sada, A., Ikeda, K., Matsui, T., & Katayama, Y.
- Affiliations
- Hokkaido University (JP)
- Kobe University (JP)
- National Center for Geriatrics and Gerontology (JP)
- Japan Science and Technology Agency (JP)
- Corresponding author
- Katayama, Yoshio
- ORCID
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2013-11
- Volume
- 18
- Issue
- 5
- Pages
- 749-758
- ISSN
- 1550-4131 (ISSN-L)
- OpenAlex
- W2062462056
- Cited by
- 126
- References
- 33
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 6 · 2023: 6 · 2022: 10 · 2021: 14 · 2020: 14 · 2019: 12 · 2018: 8 · 2017: 13 · 2016: 10 · 2015: 12 · 2014: 10
- FWCI
- 4.77
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Institutional Repositories DataBase (IRDB) (submittedVersion)
- Hokkaido University Collection of Scholarly and Academic Papers (Hokkaido University) (submittedVersion)
- Funders
- Japan Society for the Promotion of Science
- Ministry of Education, Culture, Sports, Science and Technology (23118517)
- Takeda Science Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Keywords
- osteocytes, lymphopenia, lymphoid stroma, bone marrow, thymus, thymic atrophy, fat metabolism, parabiosis, hypothalamus, hepatic steatosis, lymphocyte development, mechanosensing
- MeSH terms
- Animals, Atrophy, Bone Marrow, Lymphoid Tissue, Lymphopenia, Mice, Inbred C57BL, Osteocytes, Stromal Cells, Lymphopoiesis, Lipid Metabolism, Mice, Thymocytes, Cellular Microenvironment
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