The DOI matches its Crossref record; 44 of the 45 references it cites were found in a registry or an index.
A Paracrine Loop Between Adipocytes and Macrophages Aggravates Inflammatory Changes: Role of Free Fatty Acids and Tumor Necrosis Factor α
Abstract
Objective— Weight gain is associated with infiltration of fat by macrophages, suggesting that they are an important source of inflammation in obese adipose tissue. Here we developed an in vitro coculture system composed of adipocytes and macrophages and examined the molecular mechanism whereby these cells communicate. Methods and Results— Coculture of differentiated 3T3-L1 adipocytes and macrophage cell line RAW264 results in the marked upregulation of proinflammatory cytokines, such as tumor necrosis factor α (TNF-α), and the downregulation of the antiinflammatory cytokine adiponectin. Such inflammatory changes are induced by the coculture without direct contact, suggesting the role of soluble factors. A neutralizing antibody to TNF-α, which occurs mostly in macrophages, inhibits the inflammatory changes in 3T3-L1, suggesting that TNF-α is a major macrophage-derived mediator of inflammation in adipocytes. Conversely, free fatty acids (FFAs) may be important adipocyte-derived mediators of inflammation in macrophages, because the production of TNF-α in RAW264 is markedly increased by palmitate, a major FFA released from 3T3-L1. The inflammatory changes in the coculture are augmented by use of either hypertrophied 3T3-L1 or adipose stromal vascular fraction obtained from obese ob/ob mice. Conclusions— We postulate that a paracrine loop involving FFAs and TNF-α between adipocytes and macrophages establishes a vicious cycle that aggravates inflammatory changes in the adipose tissue.
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?
In the citing paper
“However, FFAs can also serve as ligands for the TLR4 complex (33), thereby activating the classical inflammatory response in the context of increased local extracellular lipid concentrations, which ultimately drives ATMΦ accumulation (34,35).”
From Adipose tissue remodeling and obesity (2011) · cites this paper as [34]
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
Plum, F. (1960) · Archives of Neurology · doi:10.1001/archneur.1960.03840090124020 · Cited by 10,388
Obesity is associated with macrophage accumulation in adipose tissue
Weisberg, S. P., McCann, D., Desai, M., Rosenbaum, M., Leibel, R. L., & Ferrante, A. W. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319246 · Cited by 10,041
Adipose Expression of Tumor Necrosis Factor-α: Direct Role in Obesity-Linked Insulin Resistance
Hotamisligil, G. S., Shargill, N. S., & Spiegelman, B. M. (1993) · Science · doi:10.1126/science.7678183 · Cited by 7,518
Xu, H., Barnes, G. T., Yang, Q., Tan, G., Yang, D., Chou, C. J., Sole, J., Nichols, A., Ross, J. S., Tartaglia, L. A., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200319451 · Cited by 6,760
Ford, E. S., Giles, W. H., & Dietz, W. H. (2002) · JAMA · doi:10.1001/jama.287.3.356 · Cited by 6,698
Grundy, S. M., Brewer, H. B., Cleeman, J. I., Smith, S. C., & Lenfant, C. (2004) · Circulation · doi:10.1161/01.cir.0000111245.75752.c6 · Cited by 5,982
Hotamisligil, G. S., Arner, P., Caro, J. F., Atkinson, R. L., & Spiegelman, B. M. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117936 · Cited by 3,543
Hotamisligil, G. S., Peraldi, P., Budavari, A., Ellis, R., White, M. F., & Spiegelman, B. M. (1996) · Science · doi:10.1126/science.271.5249.665 · Cited by 2,630
‘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
Protection from obesity-induced insulin resistance in mice lacking TNF-α function
Uysal, K. T., Wiesbrock, S. M., Marino, M. W., & Hotamisligil, G. S. (1997) · Nature · doi:10.1038/39335 · Cited by 2,234
Cited by
Sorted by citations
Items 201–300 of 999
Ichioka, M., Suganami, T., Tsuda, N., Shirakawa, I., Hirata, Y., Satoh‐Asahara, N., Shimoda, Y., Tanaka, M., Kim-Saijo, M., Miyamoto, Y., et al. (2011) · Diabetes · doi:10.2337/db10-0864 · Cited by 104
Self-citationEffects of Statins on Adipose Tissue Inflammation
Abe, M., Matsuda, M., Kobayashi, H., Miyata, Y., Nakayama, Y., Komuro, R., Fukuhara, A., & Shimomura, I. (2008) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.160663 · Cited by 106
Emerging Role of Mast Cells and Macrophages in Cardiovascular and Metabolic Diseases
Xu, J., & Shi, G. (2012) · Endocrine Reviews · doi:10.1210/er.2011-0013 · Cited by 105
Rebollo‐Hernanz, M., Zhang, Q., Aguilera, Y., Martin-Cabrejas, M. A., & de Mejı́a, E. G. (2019) · Food and Chemical Toxicology · doi:10.1016/j.fct.2019.110672 · Cited by 108
Role of gut microbiota in the modulation of atherosclerosis-associated immune response
Chistiakov, D. A., Bobryshev, Y. V., Kozarov, E. V., Sobenin, I. A., & Orekhov, A. N. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00671 · Cited by 103
“Frontiers in Microbiology | www.frontiersin.org 4 June 2015 | Volume 6 | Article 671 A paracrine loop involving fatty acids and TNF-α mediates reciprocal proinflammatory changes in adipocytes and infiltrating macrophages during the adipose-associated inflammation (Suganami et al., 2005).”
BackgroundYang, Z., Matsuzaki, K., Takamatsu, S., & Kitanaka, S. (2011) · Molecules · doi:10.3390/molecules16076010 · Cited by 101
“In a coculture system of 3T3-L1 adipocytes and RAW264 macrophages, marked increases in secretion levels of inflammatory mediators such as TNF-α, MCP-1, and NO were observed [6,7].”
BackgroundAdipose Tissue Remodeling as Homeostatic Inflammation
Itoh, M., Suganami, T., Hachiya, R., & Ogawa, Y. (2011) · International Journal of Inflammation · doi:10.4061/2011/720926 · Cited by 107
“However, obesity induces insulin-resistant state and inflammation in the adipose tissue, both of which lead to increased fatty acid release from the adipose tissue [1, 23, 29].”
BackgroundSelf-citationInteractions between adipose tissue and the immune system in health and malnutrition
Wensveen, F. M., Marinović, S., Šestan, M., Wensveen, T. T., & Polić, B. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.10.006 · Cited by 103
Alam, I., Ng, T. P., & Larbi, A. (2012) · Mediators of Inflammation · doi:10.1155/2012/456456 · Cited by 102
“Therefore, a continuous cycle of crosstalk between adipocytes and monocytes [52] may stimulate and perpetuate the proinflammatory status associated with obesity.”
BackgroundSakamoto, Y. S., Kanatsu, J., Toh, M., Naka, A., Kondo, K., & Iida, K. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149676 · Cited by 98
“The expression of inflammatory genes (Ccl2, Il6 and Tnf; encoding CCL-2, IL-6, and TNF-α, respectively) was enhanced by co-culture as previously reported [7].”
BackgroundMethodResultInfluentialIto, A., Suganami, T., Miyamoto, Y., Yoshimasa, Y., Takeya, M., Kamei, Y., & Ogawa, Y. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m701549200 · Cited by 96
Self-citationSaben, J. L., Zhong, Y., Gómez-Acevedo, H., Thakali, K. M., Borengasser, S. J., Andres, A., & Shankar, K. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00076.2013 · Cited by 98
Obesity: An Immunometabolic Perspective
Ray, I., Mahata, S. K., & De, R. K. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00157 · Cited by 107
An update on immune dysregulation in obesity‐related insulin resistance
Daryabor, G., Kabelitz, D., & Kalantar, K. (2018) · Scandinavian Journal of Immunology · doi:10.1111/sji.12747 · Cited by 99
“70 In response to CX3CL1 secreted by adipocytes, CD16+ monocytes produce CCL2 and IL‐6 which recruit CD16− and T cells at the sites of inflammation.71 Fibroblasts and endothelial cells residing in the SVF in response to the inflammatory cytokines produce high levels of MCP1 to allow monocyte migration from the blood i…”
BackgroundCastaneda, O. A., Lee, S.-C., Ho, C., & Huang, T. (2016) · Journal of Food and Drug Analysis · doi:10.1016/j.jfda.2016.11.006 · Cited by 96
Gögebakan, Ö., Osterhoff, M. A., Schüler, R., Pivovarova, O., Kruse, M., Seltmann, A.-C., Mosig, A. S., Rudovich, N., Nauck, M., & Pfeiffer, A. F. H. (2015) · Diabetologia · doi:10.1007/s00125-015-3618-4 · Cited by 95
“The crosstalk between adipocytes and macrophages was shown to be a crucial mechanism aggravating inflammatory changes in adipose tissue [6].”
BackgroundConsequences of Weight Cycling: An Increase in Disease Risk?
Strohacker, K. A., Carpenter, K. C., & McFarlin, B. K. (2009) · International journal of exercise science · doi:10.70252/asaq8961 · Cited by 98
“Free fatty acids and TNF- α act in concert to exacerbate systemic inflammation (54).”
BackgroundCalcitriol and calcium regulate cytokine production and adipocyte–macrophage cross-talk
Sun, X., & Zemel, M. B. (2007) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2007.05.013 · Cited by 95
“This hypothesis is supported by the observation that co-culture of rodent adipocytes and macrophages results in marked elevation of a pro-inflammatory cytokine (TNFα) and down-regulation of an anti-inflammatory factor (adiponectin) in adipocytes [10].”
BackgroundTamura, Y., Sugimoto, M., Murayama, T., Minami, M., Nishikaze, Y., Ariyasu, H., Akamizu, T., Kita, T., Yokode, M., & Arai, H. (2010) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.3368 · Cited by 93
Chazenbalk, G. D., Bertolotto, C., Heneidi, S. G., Jumabay, M., Trivax, B., Aronowitz, J. A., Yoshimura, K., Simmons, C. F., Dumesic, D. A., & Azziz, R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017834 · Cited by 97
Kang, M., Hirai, S., Goto, T., Kuroyanagi, K., Lee, J., Uemura, T., Ezaki, Y., Takahashi, N., & Kawada, T. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.02.002 · Cited by 93
Lipotoxicity-driven metabolic dysfunction-associated steatotic liver disease (MASLD)
Iturbe-Rey, S., Maccali, C., Arrese, M. A., Aspichueta, P., de Oliveira, C. P. M. S., Castro, R. E., Lapitz, A., Izquierdo‐Sánchez, L., Bujanda, L., Perugorria, M. J., et al. (2024) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2024.119053 · Cited by 102
Citrus flavonoid naringenin inhibits TLR2 expression in adipocytes
Yoshida, H., Watanabe, W., Oomagari, H., Tsuruta, E., Shida, M., & Kurokawa, M. (2013) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2012.10.003 · Cited by 99
“Because the paracrine loop involving adipocyte-derived FFA and macrophage-derived TNF-α establishes a cycle that augments the inflammatory changes in adipose tissue [24,44], we next clarified which factor affects the regulation of TLR2 expression in adipose tissue.”
BackgroundMethodKamei, Y., Suganami, T., Ehara, T., Kanai, S., Hayashi, K., Yamamoto, Y., Miura, S., Ezaki, O., Okano, M., & Ogawa, Y. (2009) · Obesity · doi:10.1038/oby.2009.246 · Cited by 92
“Primers used for tumor necrosis factor-α (TNF-α), monocyte chemoattractant protein-1 (MCP-1) and adiponectin were as described (9,10).”
BackgroundMethodSelf-citationFree fatty acids sensitize dendritic cells to amplify TH1/TH17‐immune responses
Stelzner, K., Herbert, D., Popkova, Y., Lorz, A., Schiller, J., Gericke, M. T., Klöting, N., Blüher, M., Franz, S., Simon, J. C., et al. (2016) · European Journal of Immunology · doi:10.1002/eji.201546263 · Cited by 95
Effects of LPS and dietary free fatty acids on MCP-1 in 3T3-L1 adipocytes and macrophages in vitro
Cullberg, K. B., Larsen, J. Ø., Pedersen, S. B., & Richelsen, B. (2014) · Nutrition and Diabetes · doi:10.1038/nutd.2014.10 · Cited by 92
Declèves, A., & Sharma, K. (2014) · Current Opinion in Nephrology & Hypertension · doi:10.1097/mnh.0000000000000087 · Cited by 96
“[53] postulated a paracrine loop involving FFAs and TNF-a between macrophages and adipocytes, generating a vicious cycle that maintains or even increases the chronic inflammatory state.”
BackgroundStress Augments Insulin Resistance and Prothrombotic State
Uchida, Y., Takeshita, K., Yamamoto, K., Kikuchi, R., Nakayama, T., Nomura, M., Cheng, X. W., Egashira, K., Matsushita, T., Nakamura, H., et al. (2012) · Diabetes · doi:10.2337/db11-0828 · Cited by 90
“As previously described, MCP-1 expression in adipose tissue increases macrophage infiltration and induces TNF-a secretion by interactions between macrophages and adipocytes (38).”
The ambiguous role of obesity in oncology by promoting cancer but boosting antitumor immunotherapy
Assumpção, J. A. F., Pasquarelli-do-Nascimento, G., Viegas, M. S., Bonamino, M., & Magalhães, K. G. (2022) · Journal of Biomedical Science · doi:10.1186/s12929-022-00796-0 · Cited by 97
Yamauchi, R., Kobayashi, M., Matsuda, Y., Ojika, M., Shigeoka, S., Yamamoto, Y., Tou, Y., Inoue, T., Katagiri, T., Murai, A., et al. (2010) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf904062c · Cited by 92
Leucine in Obesity: Therapeutic Prospects
Yao, K., Duan, Y., Li, F., Tan, B., Hou, Y., Wu, G., & Yin, Y. (2016) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2016.05.004 · Cited by 90
“Upon activation, macrophages secrete large amounts of cytokines and chemokines, such as TNF-/, IL-6, and MCP-1, which cause insulin resistance in adipocytes (Figure 2) [29].”
BackgroundInfluentialWatanabe, Y., Nagai, Y., Honda, H., Okamoto, N., Yamamoto, S., Hamashima, T., Ishii, Y., Tanaka, M., Suganami, T., Sasahara, M., et al. (2016) · Scientific Reports · doi:10.1038/srep23097 · Cited by 89
Self-citationMetabolic Syndrome, Chronic Kidney, and Cardiovascular Diseases: Role of Adipokines
Tesauro, M., Canale, M. P., Rodia, G., Daniele, N. D., Lauro, D., Scuteri, A., & Cardillo, C. (2011) · Cardiology Research and Practice · doi:10.4061/2011/653182 · Cited by 92
“6 which in turn decrease insulin action on adipocytes, determine hypoadiponectin, and increase leptin production [98, 106].”
BackgroundWatanabe, Y., Nagai, Y., & Takatsu, K. (2013) · Nutrients · doi:10.3390/nu5093757 · Cited by 92
“FFAs derived from adipocytes would activate macrophages through direct or indirect interaction of the TLR4/MD-2 complex and induce TNF-α production [50,58].”
BackgroundSilva, N. D., Samblas, M., Martínez, J. A., & Milagro, F. I. (2018) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-018-0622-4 · Cited by 89
“ry cytokines and decreases anti-inflammatory molecules [36].”
BackgroundSearching for the link between inflammaging and sarcopenia
Wang, T. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101611 · Cited by 90
Gangi, I. M. D., Mazza, T., Fontana, A., Copetti, M., Fusilli, C., Ippolito, A. M., Mattivi, F., Latiano, A., Andriulli, A., Vrhovšek, U., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.6808 · Cited by 88
“In addition, animal models have shown that saturated free fatty acids preferentially upregulate the production of proinflammatory cytokines (including TNF-α and IL-6) via mechanisms mediated in part through the Toll-like receptor 4/nuclear factorkB pathway [32, 33].”
BackgroundTanaka, M., Sato, A., Kishimoto, Y., Mabashi‐Asazuma, H., Kondo, K. N., & Iida, K. (2020) · Nutrients · doi:10.3390/nu12051479 · Cited by 93
“In the co-culture of adipocytes and macrophages, PA, which is a major FFA released from adipocytes, activates MAPK and NF-κB, which mediate inflammatory gene expression in these cells [12,49].”
BackgroundFucoxanthinol, Metabolite of Fucoxanthin, Improves Obesity-Induced Inflammation in Adipocyte Cells
Maeda, H., Kanno, S., Kodate, M., Hosokawa, M., & Miyashita, K. (2015) · Marine Drugs · doi:10.3390/md13084799 · Cited by 89
“Especially, MCP-1 induces a vicious cycle that increases inflammatory responses in obesity by causing monocyte/macrophage accumulation and activation in adipose tissues [6].”
BackgroundGoto, H., Hozumi, A., Osaki, M., Fukushima, T., Sakamoto, K., Yonekura, A., Tomita, M., Furukawa, K., Shindo, H., & Baba, H. (2011) · Cytokine · doi:10.1016/j.cyto.2011.09.005 · Cited by 88
Adipose tissue biology and HIV-infection
Giralt, M., Domingo, P., & Villarroya, F. (2011) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2010.12.001 · Cited by 90
Description of a local cardiac adiponectin system and its deregulation in dilated cardiomyopathy
Skurk, C., Wittchen, F., Suckau, L., Witt, H., Noutsias, M., Fechner, H., Schultheiss, H.-P., & Poller, W. C. (2008) · European Heart Journal · doi:10.1093/eurheartj/ehn136 · Cited by 86
Vitamin D modulates adipose tissue biology: possible consequences for obesity?
Landrier, J., Karkeni, E., Marcotorchino, J., Bonnet, L., & Tourniaire, F. (2015) · Proceedings of The Nutrition Society · doi:10.1017/s0029665115004164 · Cited by 86
Bidirectional crosstalk between neutrophils and adipocytes promotes adipose tissue inflammation
Watanabe, Y., Nagai, Y., Honda, H., Okamoto, N., Yanagibashi, T., Ogasawara, M., Yamamoto, S., Imamura, R., Takasaki, I., Hara, H., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201900477rr · Cited by 89
Lesná, I. K., Králová, A., Čejková, S., Froněk, J., Petráš, M., Sekerková, A., Thieme, F., Janoušek, L., & Poledne, R. (2016) · Journal of Translational Medicine · doi:10.1186/s12967-016-0962-1 · Cited by 83
“Once recruited, the macrophages themselves secrete additional chemokines, which initiate a feed-forward loop that potentiates the inflammatory response [9].”
Kováčiková, M., Sengenès, C., Kováčová, Z., Šiklová, M., Klimčáková, E., Polak, J., Rossmeislová, L., Bajzová, M., Hejnová, J., Hnevkovska, Z., et al. (2010) · International Journal of Obesity · doi:10.1038/ijo.2010.112 · Cited by 81
Diosgenin attenuates inflammatory changes in the interaction between adipocytes and macrophages
Hirai, S., Uemura, T., Mizoguchi, N., Lee, J., Taketani, K., Nakano, Y., Hoshino, S., Tsuge, N., Narukami, T., Yu, R., et al. (2009) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.200900208 · Cited by 83
Correlation of trans fatty acids with the severity of coronary artery disease lesions
Ahmed, S. H., Kharroubi, W., Kaoubaa, N., Zarrouk, A., Batbout, F., Gamra, H., Najjar, M. F., Lizard, G., Hininger‐Favier, I., & Hammami, M. (2018) · Lipids in Health and Disease · doi:10.1186/s12944-018-0699-3 · Cited by 82
“Inflammatory response induction might be due to the effect of Trans FA as an agonist of the toll-like receptor 4 (TLR4) complex [49], which activates pro-inflammatory pathways and induces cytokine expression in different cell types, promotes macrophage accumulation and then inflammation [50].”
Mráz, M., Lacinová, Z., Drápalová, J., Haluzíková, D., Hořínek, A., Matoulek, M., Trachta, P., Kaválková, P., Svacina, S., & Haluzı́k, M. (2011) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2010-1858 · Cited by 85
“This cross-talk between ATMs and adipocytes generates a vicious circle of increased adipose tissue inflammation that contributes to the lowgrade systemic inflammation (13, 14).”
BackgroundVick, M. M., Murphy, B. A., Sessions, D. R., Reedy, S. E., Kennedy, E. L., Horohov, D. W., Cook, R. F., & Fitzgerald, B. P. (2008) · American Journal of Veterinary Research · doi:10.2460/ajvr.69.1.130 · Cited by 82
Chen, S., Okahara, F., Osaki, N., & Shimotoyodome, A. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00418.2014 · Cited by 83
Loss of Stearoyl-CoA Desaturase-1 Attenuates Adipocyte Inflammation
Liu, X., Miyazaki, M., Flowers, M. T., Sampath, H., Zhao, M., Chu, K., Paton, C. M., Joo, D. S., & Ntambi, J. M. (2009) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.109.195636 · Cited by 81
Yu, M., Zhou, H., Zhao, J., Xiao, N., Roychowdhury, S., Schmitt, D. C., Hu, B., Ransohoff, R. M., Harding, C. V., Hise, A. G., et al. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20131314 · Cited by 81
“ATMs are exposed to high local concentrations of FFAs released from adipocytes in obesity, and these serve as important activating ligands for TLR4 and TLR2 signaling in macrophages (Tsujita et al., 1995; Suganami et al., 2005, 2007; Nguyen et al., 2007; Miyazaki et al., 2011; Prieur et al., 2011).”
BackgroundCardiolipotoxicity, Inflammation, and Arrhythmias: Role for Interleukin-6 Molecular Mechanisms
Alì, A., Boutjdir, M., & Aromolaran, A. S. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2018.01866 · Cited by 86
“Given that FFAs are important adipocyte-derived mediators of macrophage related inflammation (Suganami et al., 2005) and macrophages can infiltrate and/or directly couple with Frontiers in Physiology | www.frontiersin.org 3 January 2019 | Volume 9 | Article 1866 FIGURE 1 | Functional crosstalk…”
BackgroundAndo, C., Takahashi, N., Hirai, S., Nishimura, K., Lin, S., Uemura, T., Goto, T., Yu, R., Nakagami, J., Murakami, S., et al. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.10.045 · Cited by 80
“In obese adipose tissues, both pathways are involved in the production of inflammatory mediators from the activated macrophages and/or adipocytes [8,9].”
BackgroundInfluentialSerum amyloid A3 does not contribute to circulating SAA levels
Chiba, T., Han, C. Y., Vaisar, T., Shimokado, K., Kargi, A. Y., Chen, M., Wang, S., McDonald, T. O., O’Brien, K. D., Heinecke, J. W., et al. (2009) · Journal of Lipid Research · doi:10.1194/jlr.m900089-jlr200 · Cited by 78
Maury, E., Noël, L., Detry, R. J., & Brichard, S. M. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-2196 · Cited by 83
Long-term consequences of obesity on female fertility and the health of the offspring
Chandrasekaran, S., & Neal-Perry, G. S. (2017) · Current Opinion in Obstetrics & Gynecology · doi:10.1097/gco.0000000000000364 · Cited by 80
“This in turn creates a chronic low-grade metabolic inflammatory state [13,14], and endocrine dysfunction that affect age of menarche and the development of polycystic ovarian syndrome and subfertility.”
Galiero, R., Caturano, A., Vetrano, E., Cesaro, A., Rinaldi, L., Salvatore, T., Marfella, R., Sardu, C., Moscarella, E., Gragnano, F., et al. (2021) · Reviews in Cardiovascular Medicine · doi:10.31083/j.rcm2203082 · Cited by 86
Reappraisal of Adipose Tissue Inflammation in Obesity
Engin, A. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-63657-8_10 · Cited by 86
Macrophage‐Adipocyte Interaction: Marked Interleukin‐6 Production by Lipopolysaccharide
Yamashita, A., Soga, Y., Iwamoto, Y., Yoshizawa, S., Iwata, H., Kokeguchi, S., Takashiba, S., & Nishimura, F. (2007) · Obesity · doi:10.1038/oby.2007.305 · Cited by 78
Interactive Changes between Macrophages and Adipocytes
Xie, L., Ortega, M. T., Mora, S., & Chapes, S. K. (2010) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00494-09 · Cited by 78
Causes and consequences of low grade endotoxemia and inflammatory diseases
Glaros, T. (2012) · Frontiers in Bioscience-Scholar · doi:10.2741/s405 · Cited by 78
Saturated Fatty Acids and Inflammation: Who Pays the Toll?
Chait, A., & Kim, F. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.110.203984 · Cited by 80
Extracellular Matrix (ECM) and Fibrosis in Adipose Tissue: Overview and Perspectives
Sun, K., Li, X., & Scherer, P. E. (2023) · Comprehensive physiology · doi:10.1002/cphy.c220020 · Cited by 162
“Macrophage crosstalk with adipocytes via secreting TNF-α and FFAs which aggravate local inflammation in obese adipose tissue (53, 132, 240).”
Téo, F. H., de Oliveira, R. T. D., Mamoni, R. L., Ferreira, M. C. S., Nadruz, W., Coelho, O. R., Fernandes, J. L., & Blotta, M. H. S. L. (2013) · Cellular Immunology · doi:10.1016/j.cellimm.2013.01.007 · Cited by 77
Takahashi, K., Yamaguchi, S., Shimoyama, T., Seki, H., Miyokawa, K., Katsuta, H., Tanaka, T., Yoshimoto, K., Ohno, H., Nagamatsu, S., et al. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00131.2007 · Cited by 79
Regulation of adipose tissue lipolysis revisited
Bézaire, V., & Langin, D. (2009) · Proceedings of The Nutrition Society · doi:10.1017/s0029665109990279 · Cited by 84
Insights into the role of macrophage migration inhibitory factor in obesity and insulin resistance
Finucane, O. M., Reynolds, C. M., McGillicuddy, F. C., & Roche, H. M. (2012) · Proceedings of The Nutrition Society · doi:10.1017/s0029665112000730 · Cited by 81
“HFD-induced adipose tissue expansion leads to an increase in pro-inflammatory cytokine secretion and a decrease in anti-inflammatory cytokine production (26,30) .”
Vascular lipases, inflammation and atherosclerosis
Hasham, S. N., & Pillarisetti, S. (2006) · Clinica Chimica Acta · doi:10.1016/j.cca.2006.04.020 · Cited by 76
Flavonoids in adipose tissue inflammation and atherosclerosis: one arrow, two targets
Fardoun, M., Maaliki, D. S., Halabi, N., Iratni, R., Bitto, A., Baydoun, E., & Eid, A. H. (2020) · Clinical Science · doi:10.1042/cs20200356 · Cited by 76
Acedo, S. C., Gambero, S., Cunha, F. G. P., Lorand-Metze, I. G. H., & Gambero, A. (2013) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-013-9629-x · Cited by 76
Impaired Lipid and Glucose Homeostasis in Hexabromocyclododecane-Exposed Mice Fed a High-Fat Diet
Yanagisawa, R., Koike, E., Win‐Shwe, T., Yamamoto, M., & Takano, H. (2014) · Environmental Health Perspectives · doi:10.1289/ehp.1307421 · Cited by 75
Joffe, Y. T., Collins, M., & Goedecke, J. H. (2013) · Nutrients · doi:10.3390/nu5051672 · Cited by 75
Zielińska-Wasielica, J., Olejnik, A. M., Kowalska, K., Olkowicz, M., & Dembczyński, R. (2019) · Foods · doi:10.3390/foods8080326 · Cited by 74
“TNF-α has, thus, been believed to be the crucial mediator in the detrimental paracrine loop between adipocytes and macrophages [40].”
BackgroundAdipocytokines in Atherothrombosis: Focus on Platelets and Vascular Smooth Muscle Cells
Anfossi, G., Russo, I., Doronzo, G., Pomero, A., & Trovati, M. (2010) · Mediators of Inflammation · doi:10.1155/2010/174341 · Cited by 76
“[8, 13–16].”
BackgroundLipodystrophy in HIV 1-infected patients: lessons for obesity research
Villarroya, F., Domingo, P., & Giralt, M. (2007) · International Journal of Obesity · doi:10.1038/sj.ijo.0803698 · Cited by 76
Eggs modulate the inflammatory response to carbohydrate restricted diets in overweight men
Ratliff, J. C., Mutungi, G., Puglisi, M. J., Volek, J. S., & Fernández, M. L. (2008) · Nutrition & Metabolism · doi:10.1186/1743-7075-5-6 · Cited by 79
“An anti-atherogenic adipokine, adiponectin decreases adhesion molecule expression that occurs after inflammation [24] and also decreases TNF-α production by macrophages [25].”
BackgroundProtein targets of inflammatory serine proteases and cardiovascular disease
Sharony, R., Yu, P., Park, J., Galloway, A. C., Mignatti, P., & Pintucci, G. (2010) · Journal of Inflammation · doi:10.1186/1476-9255-7-45 · Cited by 72
“bolic syndrome [2]; furthermore, polymorphonuclear”
Rebollo‐Hernanz, M., Zhang, Q., Aguilera, Y., Martin-Cabrejas, M. A., & de Mejı́a, E. G. (2019) · Antioxidants · doi:10.3390/antiox8080279 · Cited by 78
Sorisky, A., Molgat, A. S. D., & Gagnon, A. (2013) · Advances in Nutrition · doi:10.3945/an.112.003020 · Cited by 75
Zhang, T., Fang, Z.-J., Linghu, K., Liu, J., Gan, L., & Lin, L. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15215 · Cited by 74
Adipose stress-sensing kinases: linking obesity to malfunction
Rudich, A., Kanety, H., & Bashan, N. (2007) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2007.08.006 · Cited by 76
Odaka, Y., Nakano, M., Tanaka, T., Kaburagi, T., Yoshino, H., Sato‐Mito, N., & Sato, K. (2010) · Obesity · doi:10.1038/oby.2009.513 · Cited by 73
Visceral fat and insulin resistance - what we know?
Janochova, K., Haluzik, M., & Bužga, M. (2018) · Biomedical Papers · doi:10.5507/bp.2018.062 · Cited by 81
Kawakubo, M., Tanaka, M., Ochi, K., Watanabe, A., Saka-Tanaka, M., Kanamori, Y., Yoshioka, N., Yamashita, S., Goto, M., Itoh, M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-57935-6 · Cited by 74
Self-citationTesařík, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26062797 · Cited by 72
“The pro-inflammatory cytokines, mainly interleukin 1 β (IL1 β ) and interleukin 6 (IL6), as well as acute-phase proteins and chemokines, mainly C-C motif chemokine ligand-2 (CCL2) and monocyte chemoattractant protein-1 (MCP-1), attract more monocytes/macrophages within the adipose tissue [20].”
Sakamoto, Y. S., Naka, A., Ohara, N., Kondo, K. N., & Iida, K. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201300482 · Cited by 74
Macrophage lipoprotein lipase modulates the development of atherosclerosis but not adiposity
Takahashi, M., Yagyu, H., Tazoe, F., Nagashima, S., Ohshiro, T., Okada, K., Osuga, J.-I., Goldberg, I. J., & Ishibashi, S. (2013) · Journal of Lipid Research · doi:10.1194/jlr.m035568 · Cited by 79
Gut microbiota: a potential manipulator for host adipose tissue and energy metabolism
Rong, B., Tianyu, X., Tiantian, Z., Feng, R., Huang, H., Wu, Q., & Sun, C. (2018) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2018.10.020 · Cited by 73
Nankam, P. A. N., Cornely, M. E., Klöting, N., & Blüher, M. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1000094 · Cited by 71
“This is characterized among others by impaired adipogenesis (21, 22) and angiogenesis (23, 24), fibrosis (20, 25) and hypoxia (26, 27), dysregulated adipokine secretion (27–29), AT inflammation (26, 28, 30) as well as oxidative stress (27, 31).”
BackgroundNguyen, A., Tao, H., Metrione, M., & Hajri, T. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.515320 · Cited by 65
“Investigations using in vitro co-culture systems have demonstrated reciprocal impacts of adipocytes and macrophages and also highlighted the contributions of these cells in inflammation (3, 36).”
BackgroundMiRNA-194 Regulates Palmitic Acid-Induced Toll-Like Receptor 4 Inflammatory Responses in THP-1 Cells
Tian, H., Liu, C., Zou, X., Wu, W., Zhang, C., & Yuan, D. (2015) · Nutrients · doi:10.3390/nu7053483 · Cited by 71
“Pathological concentrations of PA always result in necrotic cell death and inflammatory response, which is crucial for the pathogenesis of metabolic syndrome [27,28].”
BackgroundBarzilay, J. I., Forsberg, C. W., Heckbert, S. R., Cushman, M., & Newman, A. B. (2006) · International Journal of Obesity · doi:10.1038/sj.ijo.0803306 · Cited by 70
Study of the proinflammatory role of human differentiated omental adipocytes
Bassols, J., Ortega, F. J., Moreno‐Navarrete, J. M., Peral, B., Ricart, W., & Fernández‐Real, J. M. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22208 · Cited by 70
“…that encode proteins with diverse proinflammatory functions (TNF-a MCP-1, MIP-1a, MIP-1b, ICAM-1, E-selectin, IL-1b, IL-6, and IL-8) and the down-regulation of the anti-inflammatory adipokine adiponectin [Suganami et al., 2005; Permana et al., MACROPHAGE SECRETION AND HUMAN ADIPOCYTES 1113 Fig.”
BackgroundInfluentialPellegrinelli, V., Rouault, C., Veyrie, N., Clément, K., & Lacasa, D. (2013) · Diabetes · doi:10.2337/db13-0537 · Cited by 70
“increased basal lipolysis in inflammatory 3T3-L1 adipocytes (3,22), suggesting different mechanisms in unilocular human adipocytes.”
BackgroundKiecolt‐Glaser, J. K., Jaremka, L. M., Andridge, R., Peng, J., Habash, D., Fagundes, C. P., Glaser, R., Malarkey, W. B., & Belury, M. A. (2014) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2014.11.018 · Cited by 75
CXCL3 positively regulates adipogenic differentiation
Kusuyama, J., Komorizono, A., Bandow, K., Ohnishi, T., & Matsuguchi, T. (2016) · Journal of Lipid Research · doi:10.1194/jlr.m067207 · Cited by 71
Rahmani, J., Kord‐Varkaneh, H., Hekmatdoost, A., Thompson, J., Clark, C. C. T., Salehi‐Sahlabadi, A., Day, A. S., & Jacobson, K. (2019) · Obesity Reviews · doi:10.1111/obr.12875 · Cited by 71
Association of Adipose Tissue and Adipokines with Development of Obesity-Induced Liver Cancer
Rajesh, Y., & Sarkar, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042163 · Cited by 75
“Additionally, FFAs modulate the inflammation of AT contributing to obesity-related metabolic complications by serving as ligands for the TLR4 complex [60] and stimulating cytokine production by macrophages [61].”
Background
Metadata
- Authors
- Suganami, T., Nishida, J., & Ogawa, Y.
- Affiliations
- Tokyo Medical and Dental University (JP)
- Venue
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Published
- 2005-10
- Volume
- 25
- Issue
- 10
- Pages
- 2062-2068
- ISSN
- 1079-5642 (ISSN-L)
- 1524-4636
- OpenAlex
- W2105448220
- Cited by
- 1,056
- References
- 45
- Citations by year
- 2026: 25 · 2025: 27 · 2024: 27 · 2023: 36 · 2022: 38 · 2021: 57 · 2020: 51 · 2019: 47 · 2018: 34 · 2017: 66 · 2016: 62 · 2015: 66 · 2014: 57 · 2013: 91 · 2012: 54
- FWCI
- 30.26
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Arteriosclerosis Thrombosis and Vascular Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Research Foundation for Clinical Pharmacology
- Ministry of Education, Culture, Sports, Science and Technology
- Novo Nordisk
- Smoking Research Foundation
- Kanae Foundation for the Promotion of Medical Science
- Mishima Kaiun Memorial Foundation
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Disease and Adiposity
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Keywords
- adipocytes, macrophages, paracrine signaling, adipose tissue inflammation, obesity, TNF-α, adiponectin, free fatty acids, palmitate, 3T3-L1 adipocytes, RAW264 macrophages, co-culture, ob/ob mice, adipose stromal vascular fraction, adipocyte hypertrophy
- MeSH terms
- Adipose Tissue, Animals, Cell Communication, Fatty Acids, Nonesterified, Gene Expression Regulation, Hypertrophy, Inflammation, Macrophages, Obesity, Tumor Necrosis Factor-alpha, Adipocytes, Coculture Techniques, Chemokine CCL2, Paracrine Communication, Metabolic Syndrome, 3T3-L1 Cells, Atherosclerosis, 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