The DOI matches its Crossref record; 67 of the 68 references it cites were found in a registry or an index.
A self-sustained loop of inflammation-driven inhibition of beige adipogenesis in obesity
Open accessAbstract
In obesity, inflammation of white adipose tissue (AT) is associated with diminished generation of beige adipocytes ('beige adipogenesis'), a thermogenic and energy-dissipating function mediated by beige adipocytes that express the uncoupling protein UCP1. Here we delineated an inflammation-driven inhibitory mechanism of beige adipogenesis in obesity that required direct adhesive interactions between macrophages and adipocytes mediated by the integrin α 4 and its counter-receptor VCAM-1, respectively; expression of the latter was upregulated in obesity. This adhesive interaction reciprocally and concomitantly modulated inflammatory activation of macrophages and downregulation of UCP1 expression dependent on the kinase Erk in adipocytes. Genetic or pharmacological inactivation of the integrin α 4 in mice resulted in elevated expression of UCP1 and beige adipogenesis of subcutaneous AT in obesity. Our findings, established in both mouse systems and human systems, reveal a self-sustained cycle of inflammation-driven impairment of beige adipogenesis in obesity.
Overview
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
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“A similar mechanism was found in human adipocytes as well [278].”
From The Role of Exercise in the Interplay between Myokines, Hepatokines, Osteokines, Adipokines, and Modulation of Inflammation for Energy Substrate Redistribution and Fat Mass Loss: A Review (2020) · cites this paper as [278]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
Livak, K. J., & Schmittgen, T. D. (2001) · Methods · doi:10.1006/meth.2001.1262 · Cited by 180,860
Fiji: an open-source platform for biological-image analysis
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., et al. (2012) · Nature Methods · doi:10.1038/nmeth.2019 · Cited by 66,890
Mizgerd, J. P., Kubo, H., Kutkoski, G. J., Bhagwan, S. D., Scharffetter-Kochanek, K., Beaudet, A. L., & Doerschuk, C. M. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.186.8.1357 · Cited by 7,332
Macrophage activation and polarization: nomenclature and experimental guidelines
Murray, P. J., Allen, J. E., Biswas, S. K., Fisher, E. A., Gilroy, D. W., Goerdt, S., Gordon, S., Hamilton, J. A., Ivashkiv, L. B., Lawrence, T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.008 · Cited by 6,337
Macrophage plasticity and polarization: in vivo veritas
Sica, A., & Mantovani, A. (2012) · Journal of Clinical Investigation · doi:10.1172/jci59643 · Cited by 6,335
Obesity induces a phenotypic switch in adipose tissue macrophage polarization
Lumeng, C. N., Bodzin, J. L., & Saltiel, A. R. (2007) · Journal of Clinical Investigation · doi:10.1172/jci29881 · Cited by 4,664
Identification and Importance of Brown Adipose Tissue in Adult Humans
Cypess, A. M., Lehman, S., Williams, G., Tal, I., Rodman, D., Goldfine, A. B., Kuo, F. C., Palmer, E. L., Tseng, Y.-H., Doria, A., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0810780 · Cited by 4,399
Getting to the site of inflammation: the leukocyte adhesion cascade updated
Ley, K., Laudanna, C., Cybulsky, M. I., & Nourshargh, S. (2007) · Nature Reviews Immunology · doi:10.1038/nri2156 · Cited by 4,354
Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human
Wu, J., Boström, P., Sparks, L. M., Li, Y., Choi, J. H., Giang, A.-H., Khandekar, M. J., Virtanen, K. A., Nuutila, P., Schaart, G., et al. (2012) · Cell · doi:10.1016/j.cell.2012.05.016 · Cited by 3,406
Murray, P. J. (2017) · Annual Review of Physiology · doi:10.1146/annurev-physiol-022516-034339 · Cited by 2,981
Flagged first, then by citations
1 of the 68 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Garrido, C. et al. ELND002 is a potent inhibitor of α4 integrin-mediated human leukocyte adhesion in vitro. J. Neuroimmunol. 228, 92 (2010).
Cited by
Sorted by citations
Items 101–175 of 175
Exercise‐induced β‐hydroxybutyrate promotes Treg cell differentiation to ameliorate colitis in mice
Hao, F., Tian, M., Wang, H., Li, S., Wang, X., Jin, X., Wang, Y., Jiao, Y., & Tian, M. (2024) · The FASEB Journal · doi:10.1096/fj.202301686rr · Cited by 17
Recruitment of Thermogenic Fat: Trigger of Fat Burning
Wang, Z., Yu, X., & Chen, Y. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.696505 · Cited by 16
Importance of temperature on immuno‐metabolic regulation and cancer progression
Wang, H., Çolakoğlu, M., & Trajkovski, M. (2022) · FEBS Journal · doi:10.1111/febs.16632 · Cited by 14
Molecular and cellular regulation of thermogenic fat
Wang, C., Wang, X., & Hu, W. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1215772 · Cited by 14
Zhao, L. Q., Li, W., Zhang, P., Wang, D., Yang, L., & Yuan, G. (2024) · Endocrine · doi:10.1007/s12020-024-03734-2 · Cited by 14
Common traits between the beige fat-inducing stimuli
Stojanović, O., Kieser, S., & Trajkovski, M. (2018) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2018.05.011 · Cited by 13
CHRNA2: a new paradigm in beige thermoregulation and metabolism
Ma, Y., Liu, S., Jun, H., & Wu, J. (2021) · Trends in Cell Biology · doi:10.1016/j.tcb.2021.11.009 · Cited by 15
Wang, Y., Gao, X., Chen, X., Li, Q., Li, X., & Zhao, J. (2022) · Nutrients · doi:10.3390/nu14142903 · Cited by 14
Castoldi, Â., Sanin, D. E., Bakker, N. V. T., de Aguiar, C. F., Monteiro, L. D. B., Rana, N., Grzes, K. M., Kabat, A. M., Curtis, J., Cameron, A. M., et al. (2023) · iScience · doi:10.1016/j.isci.2023.107719 · Cited by 14
miR-345-5p regulates adipogenesis via targeting VEGF-B
Liu, X., He, Y., Feng, Z., Sheng, J., Dong, A., Zhang, M., & Cao, L. (2020) · Aging · doi:10.18632/aging.103649 · Cited by 13
Troullinaki, M., Chen, L., Witt, A., Pyrina, I., Phieler, J., Kourtzelis, I., Chmelař, J., Sprott, D., Gercken, B., Koutsilieris, M., et al. (2020) · The FASEB Journal · doi:10.1096/fj.201900125rr · Cited by 12
Self-citationMacrophages expressing uncoupling protein 1 increase in adipose tissue in response to cold in humans
Finlin, B. S., Memetimin, H., Confides, A. L., Zhu, B., Westgate, P. M., Dupont‐Versteegden, E. E., & Kern, P. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-03014-3 · Cited by 11
Leung, W. K. C., Yu, A. P., Lai, C. W. K., & Siu, P. M. (2018) · Journal of Diabetes Research · doi:10.1155/2018/8956509 · Cited by 13
Nikolakopoulou, P., Chatzigeorgiou, A., Kourtzelis, I., Toutouna, L., Masjkur, J. R., Arps‐Forker, C., Poser, S., Rozman, J., Rathkolb, B., Aguilar‐Pimentel, J. A., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-29434-2 · Cited by 10
Self-citationMyeloid SOCS3 Deficiency Regulates Angiogenesis via Enhanced Apoptotic Endothelial Cell Engulfment
Korovina, I., Neuwirth, A., Sprott, D., Troullinaki, M., Poitz, D. M., Deußen, A., & Ameln, A. K. (2019) · Journal of Innate Immunity · doi:10.1159/000502645 · Cited by 11
Free fatty acids stabilize integrin β1 via S-nitrosylation to promote monocyte–endothelial adhesion
Yao, Q., Cui, Q., Liu, J., Xie, X., Jiang, T., Wang, H., Zhao, Z., Zhao, W., Du, X., Lai, B., et al. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102765 · Cited by 10
Wang, Q., Hartig, S. M., Ballantyne, C. M., & Wu, H. (2024) · Immunological Reviews · doi:10.1111/imr.13338 · Cited by 11
Maurer, S., Dieckmann, S., Lund, J. T., Fromme, T., Hess, A. L., Colson, C., Kjølbæk, L., Astrup, A. V., Gillum, M. P., Larsen, L. H., et al. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000681 · Cited by 10
Heme induces innate immune memoryPreprint
Jentho, E., Novakovic, B., Ruiz-Moreno, C., Kourtzelis, I., Martins, R., Chavakis, T., Soares, M. P., Kalafati, L., Guerra, J., Röstel, F., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2019.12.12.874578 · Cited by 10
Self-citationKeidai, Y., Fujikura, J., & Yabe, D. (2025) · Cell Transplantation · doi:10.1177/09636897251346599 · Cited by 9
Chen, K. Y., Angulo, A. D., Guo, X., More, A., Ochsner, S. A., Lopez, E., Saul, D., Pang, W., Sun, Y., McKenna, N. J., et al. (2022) · Frontiers in Aging · doi:10.3389/fragi.2021.803482 · Cited by 8
Role of Epicardial Adipose Tissue in Triggering and Maintaining Atrial Fibrillation
Wang, W., Tian, Y., Wang, W., Yin, H., Yin, D., & Tian, Y. (2022) · Cardiovascular Innovations and Applications · doi:10.15212/cvia.2022.0012 · Cited by 8
Boulet, N., Luijten, I. H. N., Cannon, B., & Nedergaard, J. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00352.2020 · Cited by 7
The Yin-Yang functions of macrophages in metabolic disorders
Bai, J., & Liu, F. (2022) · Life Medicine · doi:10.1093/lifemedi/lnac035 · Cited by 7
Cell-cell crosstalk between fat cells and immune cells
Liu, J., & Chen, Y. (2024) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00024.2024 · Cited by 7
Analysis of the Role of Stellate Cell VCAM-1 in NASH Models in Mice
Chung, K., Legaki, A., Papadopoulos, G., Gercken, B., Gebler, J., Schwabe, R. F., Chavakis, T., & Chatzigeorgiou, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054813 · Cited by 8
Self-citationNanomaterials for the treatment and monitoring of obesity: Targeting adipose tissue macrophages
Tang, Y., Chen, O., Dong, B., Liu, L., Ying, W., & Liu, H. (2025) · Acta Biomaterialia · doi:10.1016/j.actbio.2025.09.052 · Cited by 10
CD9 regulates macrophage-mediated remodeling of adipose tissue in obesity
Chini, J., DeMarco, N., Mitchell, D. V., McCright, S. J., Shen, K. M., Pandey, D., Clement, R. L., Miller, J., Jain, R., Taylor, D. M., et al. (2026) · JCI Insight · doi:10.1172/jci.insight.193837 · Cited by 7
CD90 Is Dispensable for White and Beige/Brown Adipocyte Differentiation
Dahlhaus, M., Roos, J., Engel, D., Tews, D., Halbgebauer, D., Funcke, J., Kiener, S., Schuler, P. J., Döscher, J., Hoffmann, T. K., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217907 · Cited by 6
Shi, W. (2025) · American Journal of Translational Research · doi:10.62347/aiws5429 · Cited by 7
F AP deficiency enhances thermogenesis and attenuates metabolic inflammation in diet‐induced obesity
Wu, Y., Li, Y., Sun, M., Yu, F., Liu, H., Xu, J., & Tang, X. (2023) · Obesity · doi:10.1002/oby.23955 · Cited by 5
Neutrophil Migration Is Mediated by VLA-6 in the Inflamed Adipose Tissue
Lim, H., Choe, Y. H., Lee, J., Kim, G. E., Hyun, J. W., & Hyun, Y. (2024) · Immune Network · doi:10.4110/in.2024.24.e23 · Cited by 4
M2 Macrophages in the Metabolic Organs and in the Neuroendocrine System
Rőszer, T. (2020) · Progress in inflammation research · doi:10.1007/978-3-030-50480-9_9 · Cited by 7
Foxo in T Cells Regulates Thermogenic Program through Ccr4/Ccl22 Axis
Kikuchi, T., Nakae, J., Kawano, Y., Watanabe, N., Onodera, M., & Itoh, H. (2019) · iScience · doi:10.1016/j.isci.2019.11.006 · Cited by 5
A key role of polyamine metabolism in adipose tissue homeostasis that regulates obesity
Mund, C., Sinha, A. N., Aderhold, A., Mateska, I., Hagag, E., Traikov, S., Gercken, B., Soto, A., Pollock, J., Arndt, L., et al. (2025) · Metabolism · doi:10.1016/j.metabol.2025.156358 · Cited by 5
Self-citationThe role of immune responses and microbiota in adipose tissue homeostasis
Azar, S., & Rehermann, B. (2025) · The Journal of Physiology · doi:10.1113/jp286422 · Cited by 5
Loss of ADAM29 does not affect viability and fertility in mice but improves wound healing
Campos-Iglesias, D., Montero, A. A., Rodríguez, F., López-Otı́n, C., & Freije, J. M. P. (2024) · iScience · doi:10.1016/j.isci.2024.110135 · Cited by 4
Pham, U. N. T., Chou, K.-C., Ngo, T.-L.-H., Pan, W., Ruan, T., & Lin, Y. (2025) · Biomaterials · doi:10.1016/j.biomaterials.2025.123570 · Cited by 4
Tang, R., Sun, W. Y., Zhang, J., Mao, L., Quanquin, N. M., Wu, D., & Sun, Y. (2022) · Current Microbiology · doi:10.1007/s00284-022-02762-3 · Cited by 4
Patel, R. P., Varghese, J. F., & Yadav, U. C. S. (2020) · Springer eBooks · doi:10.1007/978-3-030-53370-0_11 · Cited by 5
Witt, A., Mirtschink, P., Palladini, A., Mateska, I., Abdelmegeed, H., Grzybek, M., Wielockx, B., Peitzsch, M., Coskun, Ü., Chavakis, T., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.04.282905 · Cited by 4
Self-citationPuente-Ruiz, S. C., Ide, L., Schuller, J., Ben-Kraiem, A., Hoffmann, A., Ghosh, A., Noé, F., Wolfrum, C., Krause, K., Gericke, M. T., et al. (2025) · iScience · doi:10.1016/j.isci.2025.112819 · Cited by 3
Self-citationGPCR-mediated regulation of beige adipocyte formation: Implications for obesity and metabolic health
Cui, Y., Auclair, H., He, R., & Zhang, Q. (2024) · Gene · doi:10.1016/j.gene.2024.148421 · Cited by 3
A Fat Lot of Good for Wound Healing
Casano, A. M., & Sixt, M. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.02.009 · Cited by 2
Insights into current models for developing brown adipocytes from induced pluripotent stem cells
Butts, J. C., Martino, J., & Brown, A. C. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823884-4.00004-3 · Cited by 2
Rőszer, T. (2024) · Results and problems in cell differentiation · doi:10.1007/978-3-031-65944-7_6 · Cited by 3
Mund, C., Sinha, A. N., Aderhold, A., Mateska, I., Hagag, E., Traikov, S., Gercken, B., Soto, A., Pollock, J., Arndt, L., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.19.621837 · Cited by 2
Self-citationMetabolic inflammation, obesity, and cancer
Alzaïd, F., Blériot, C., Anagnostopoulos, G., Chakarov, S., Venteclef, N., & Ginhoux, F. (2026) · Immunity · doi:10.1016/j.immuni.2026.07.020 · Cited by 1
Neutrophil serine proteases inhibit thermogenic capacity of visceral white adipose tissue
Yuan, L., Wu, X., Zong, J., Jiang, M., Gao, S., Zhang, Z., Huang, X., Zhu, M., Xiang, M., Wang, L., et al. (2026) · Nature Metabolism · doi:10.1038/s42255-026-01598-6 · Cited by 1
Sasiarini, L., Sujuti, H., Handayani, D., & Rudijanto, A. (2024) · Current Research in Nutrition and Food Science Journal · doi:10.12944/crnfsj.12.3.18 · Cited by 1
Padhye, A. S., Kiriaev, L., Tiong, C. F., Gearing, L. J., Wilson, T., Houweling, P. J., & Tachas, G. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.23.625028 · Cited by 1
Macrophage retention inhibits beige adipogenesis in obesity
Holmes, D. I. R. (2017) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2017.54
Heterogeneity of White Adipose Tissue
Kwok, K. H. M., & Xu, A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811297-7.00021-4 · Cited by 2
Regulation of Brown Adipose Tissue Function via Metabolites Derived from Diet by Gut Microbiota
Goto, T., Kim, M., Kawarasaki, S., Takahashi, H., & Kawada, T. (2019) · Oleoscience · doi:10.5650/oleoscience.19.145
The study on knee osteoarthritis in diabetic patients based on nanometric magnetic bead method
Luo, D., Hou, D., & Luo, S. (2020) · Materials Express · doi:10.1166/mex.2020.1815
Silke, J. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733218432.793575596
Saas, P., & Perruche, S. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734462995.793556078
Desevin, K., Cortez, B. N., Lin, J. Z., Lama, D., Layne, M. D., Farmer, S. R., & Rabhi, N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.26.554950
Rabhi, N., Desevin, K., Cortez, B. N., Lin, J. Z., Lama, D., Layne, M. D., & Farmer, S. R. (2024) · Research Square · doi:10.21203/rs.3.rs-3895059/v1
VEGFB promotes adipose tissue thermogenesis by inhibiting norepinephrine clearance in macrophages
Wang, L., Jin, J., Zhang, N., Dai, Y., Bai, X., Li, J., Yu, Y., Shi, X., Bai, H., Yang, Q., et al. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2024.167536
Okla, M. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1633584
A two-pronged nanomedicine counteracts obesity by remodeling adipose niche
Wang, L., Chen, J., Li, J., Zhang, J., Zou, M., Liu, Q., Jing, X., Jia, Q., Li, J., Zhang, Z., et al. (2025) · Journal of Controlled Release · doi:10.1016/j.jconrel.2025.114387
Adhesion‐Related Macrophages Regulate Metabolic Homeostasis Through CAV‐1 Dependency
Hu, W., Liao, X., Xie, L., Sun, X., Jing, L., Zeng, Q., Jiang, H., Zhang, H., Li, L., Wang, F., et al. (2026) · Advanced Science · doi:10.1002/advs.202520936
Importance de la lipolyse adipocytaire dans le contrôle de l’homéostasie des monocytes
Stunault, M. I. (2020) · theses.fr (ABES) · doi:10.70675/7182b6c6zc8aaz4c67z9badz2f04195f1787
Étude de l’influence de la glutaminolyse des macrophages dans les maladies cardio-métaboliques
Merlin, J. (2020) · theses.fr (ABES) · doi:10.70675/68e10f28zf840z48bfz9bacz5511a3a2b208
Gao, P., Wang, W., Wang, W., Liu, M., Wu, G., Tian, Y., Yin, D., & Tian, Y. (2026) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000001825
Lee, S. H., Kar, A., Gelev, K. Z., Chen, Z. J., Das, S. S., Heinonen, S., Saarinen, T., Vaittinen, M., Kamińska, D., Peltoniemi, H. H., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-72248-4
Li, J., Huang, H., Wang, W., Zhou, R., Liu, F., Yang, Z., Cui, Z., Niu, Z., Shi, S., & Wang, P. (2026) · Journal of Pharmaceutical Analysis · doi:10.1016/j.jpha.2026.101651
NMI Regulates Adipose Adaptive Thermogenesis Through TLR4/IRF3 Signaling to Promote Obesity
Li, T., Zhao, X.-Y., Zhang, M., Weng, Z., Guo, X.-R., Liu, Y., Wang, Q., & Huan-huan, L. (2026) · Advanced Science · doi:10.1002/advs.75921
Zhang, J., Zhang, Y., Wang, M., Tang, C., Yong, H., Chen, D., Kan, J., Xu, J., Chen, X. S., & Liu, J. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.109574
Ortega, M. P. C., Peña-Peña, M., Carbó, R., Medina-Urrutia, A. X., Osorio‐Alonso, H., Jiang, B., Almanza-Pérez, J. C., Blancas‐Flores, G., Villafaña, S., Romero‐Nava, R., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27156693
Li, H., Lu, W., Liu, J., Luo, D., Wang, M., Dong, R., Chu, J., Chen, Q., Wang, H., Huang, J., et al. (2026) · Phytomedicine · doi:10.1016/j.phymed.2026.158702
SVEP1 couples adipose niche remodeling to macrophage activation and impaired metabolism in obesityPreprint
Kislev, N., Kavin, N., Izgilov, R., & Benayahu, D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.19.751140
Single-Cell Insights into Obesity: Cellular Mechanisms across Metabolic Organs
Tang, Y., & Lin, D. (2026) · Journal of Nutrition · doi:10.1016/j.tjnut.2026.101893
CRISPR screens identify ACSL4 as a key regulator in macrophage activation and metabolic inflammation
Lin, Y., Jing, D., Liu, Y., Gao, R., Zhao, Q., Jiang, X., Da, H., Ren, Y., Cao, Q., Jiang, J., et al. (2026) · British Journal of Pharmacology · doi:10.1111/bph.70681
Metadata
- Authors
- Chung, K.-J., Chatzigeorgiou, A., Economopoulou, M., Garcia-Martin, R., Alexaki, V. I., Mitroulis, I., Nati, M., Gebler, J., Ziemssen, T., Goelz, S. E., Phieler, J., Lim, J.-H., Karalis, K. P., Papayannopoulou, T., Blüher, M., Hajishengallis, G., & Chavakis, T.
- Affiliations
- German Center for Diabetes Research (DE)
- Technische Universität Dresden (DE)
- Elan Pharmaceuticals, Inc. (Ireland) (IE)
- Biomedical Research Foundation of the Academy of Athens (GR)
- University of Washington (US)
- Leipzig University (DE)
- University of Pennsylvania (US)
- Corresponding author
- Chung, Kyoung-Jin
- Chavakis, Triantafyllos
- ORCID
- Venue
- Nature Immunology
- Published
- 2017-04-17
- Volume
- 18
- Issue
- 6
- Pages
- 654-664
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC5436941
- OpenAlex
- W2605432571
- Cited by
- 175
- References
- 68
- Citations by year
- 2026: 14 · 2025: 10 · 2024: 18 · 2023: 13 · 2022: 14 · 2021: 19 · 2020: 26 · 2019: 23 · 2018: 30 · 2017: 8
- FWCI
- 17.60
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion, other-oa)
- Site cant be reached (submittedVersion)
- PuSH - Publication Server of Helmholtz Zentrum München (submittedVersion)
- Funders
- National Institute of Dental and Craniofacial Research (R01DE024716, R37DE026152)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
- Keywords
- obesity, beige adipogenesis, white adipose tissue inflammation, CD49d, VCAM-1, ERK kinase, UCP1, thermogenesis, adipose tissue macrophages
- MeSH terms
- Adipocytes, Beige, Uncoupling Protein 1, Adult, Aged, Aged, 80 and over, Animals, Cell Adhesion, Cell Differentiation, Feedback, Female, Humans, Inflammation, Macrophages, Male, Middle Aged, Monocytes, Obesity, RNA, Messenger, T-Lymphocytes, Immunoblotting, Down-Regulation, Adipocytes, Vascular Cell Adhesion Molecule-1, Integrin alpha4, 3T3-L1 Cells, Extracellular Signal-Regulated MAP Kinases, Subcutaneous Fat, Adipogenesis, Mice, Adipose Tissue, White, Gene Knockdown Techniques, Young Adult, Diet, High-Fat, Real-Time Polymerase Chain Reaction
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