Critical role of tumor necrosis factor receptor 1, but not 2, in hepatic stellate cell proliferation, extracellular matrix remodeling, and liver fibrogenesis
Open accessAbstract
Tumor necrosis factor (TNF) has been implicated in the progression of many chronic liver diseases leading to fibrosis; however, the role of TNF in fibrogenesis is controversial and the specific contribution of TNF receptors to hepatic stellate cell (HSC) activation remains to be established. Using HSCs from wild-type, TNF-receptor-1 (TNFR1) knockout, TNF-receptor-2 (TNFR2) knockout, or TNFR1/R2 double-knockout (TNFR-DKO) mice, we show that loss of both TNF receptors reduced procollagen-α1(I) expression, slowed down HSC proliferation, and impaired platelet-derived growth factor (PDGF)-induced promitogenic signaling in HSCs. TNFR-DKO HSCs exhibited decreased AKT phosphorylation and in vitro proliferation in response to PDGF. These effects were reproduced in TNFR1 knockout, but not TNFR2 knockout, HSCs. In addition, matrix metalloproteinase 9 (MMP-9) expression was dependent on TNF binding to TNFR1 in primary mouse HSCs. These results were validated in the human HSC cell line, LX2, using neutralizing antibodies against TNFR1 and TNFR2. Moreover, in vivo liver damage and fibrogenesis after bile-duct ligation were reduced in TNFR-DKO and TNFR1 knockout mice, compared to wild-type or TNFR2 knockout mice. Conclusion: TNF regulates HSC biology through its binding to TNFR1, which is required for HSC proliferation and MMP-9 expression. These data indicate a regulatory role for TNF in extracellular matrix remodeling and liver fibrosis, suggesting that targeting TNFR1 may be of benefit to attenuate liver fibrogenesis. (HEPATOLOGY 2011;)
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TNFα and its receptor 1 are key regulators of HSC activation.
“Importantly, TNF signaling has a prominent role in promoting fibrosis, given that TNFα and its receptor 1 are key regulators of HSC activation.( 73 )”
From The Emerging Role of B Cells in the Pathogenesis of NAFLD (2021) · cites this paper as [73]
TNF signaling has a prominent role in promoting fibrosis.
“Importantly, TNF signaling has a prominent role in promoting fibrosis, given that TNFα and its receptor 1 are key regulators of HSC activation.( 73 )”
From The Emerging Role of B Cells in the Pathogenesis of NAFLD (2021) · cites this paper as [73]
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Cites
Bataller, R., & Brenner, D. A. (2005) · Journal of Clinical Investigation · doi:10.1172/jci24282 · Cited by 4,958 · see citing works
Mechanisms of Hepatic Fibrogenesis
Friedman, S. L. (2008) · Gastroenterology · doi:10.1053/j.gastro.2008.03.003 · Cited by 2,640 · see citing works
Yu, Q., & Stamenkovic, I. (2000) · PubMed · Cited by 1,952 · see citing works
Yu, Q., & Stamenkovic, I. (2000) · Genes & Development · doi:10.1101/gad.14.2.163 · Cited by 1,754 · see citing works
Bataller, R. A. (2005) · Journal of Clinical Investigation · doi:10.1172/jci200524282c1 · Cited by 1,480 · see citing works
Grell, M., Douni, E. K., Wajant, H., Löhden, M., Clauss, M. A., Maxeiner, B., Georgopoulos, S., Lesslauer, W., Kollias, G. A., Pfizenmaier, K., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90192-2 · Cited by 1,328 · see citing works
Human hepatic stellate cell lines, LX-1 and LX-2: new tools for analysis of hepatic fibrosis
Xu, L., Hui, A. Y., Albanis, E., Arthur, M. J., O’Byrne, S. M., Blaner, W. S., Mukherjee, P., Friedman, S. L., & Eng, F. J. (2004) · Gut · doi:10.1136/gut.2004.042127 · Cited by 1,020 · see citing works
Mechanisms of Liver Injury. I. TNF-α-induced liver injury: role of IKK, JNK, and ROS pathways
Schwabe, R. F., & Brenner, D. A. (2006) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00422.2005 · Cited by 684 · see citing works
The type 1 receptor (CD120a) is the high-affinity receptor for soluble tumor necrosis factor
Grell, M., Wajant, H., Zimmermann, G., & Scheurich, P. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.2.570 · Cited by 478 · see citing works
Bradham, C. A., Plümpe, J., Manns, M. P., Brenner, D. A., & Trautwein, C. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.275.3.g387 · Cited by 355 · see citing works
Purified Rat Liver Fat-Storing Cells in Culture Divide and Contain Collagen
Leeuw, A. D. M., McCarthy, S. P., Geerts, A. E., & Knook, D. L. (1984) · Hepatology · doi:10.1002/hep.1840040307 · Cited by 325 · see citing works
Friedman, S. L., Rockey, D. C., McGuire, R. F., Maher, J. J., Boyles, J. K., & Yamasaki, G. (1992) · Hepatology · doi:10.1002/hep.1840150211 · Cited by 284 · see citing works
Interleukin-1 participates in the progression from liver injury to fibrosis
Gieling, R. G., Wallace, K., & Han, Y.-P. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90564.2008 · Cited by 279 · see citing works
Yamada, Y., Webber, E. M., Kirillova, I., Peschon, J. J., & Fausto, N. (1998) · Hepatology · doi:10.1002/hep.510280410 · Cited by 260 · see citing works
Solis-Herruzo, J. A., Brenner, D. A., & Chojkier, M. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)60642-8 · Cited by 237 · see citing works
Yamada, Y., & Fausto, N. (1998) · Europe PMC (PubMed Central) · Cited by 208 · see citing works
Mechanisms of crosstalk between TNF-induced NF-κB and JNK activation in hepatocytes
Wullaert, A., Heyninck, K., & Beyaert, R. (2006) · Biochemical Pharmacology · doi:10.1016/j.bcp.2006.07.003 · Cited by 200 · see citing works
Simeonova, P. P., Gallucci, R. M., Hulderman, T., Wilson, R., Kommineni, C., Rao, M., & Luster, M. I. (2001) · Toxicology and Applied Pharmacology · doi:10.1006/taap.2001.9304 · Cited by 186 · see citing works
Redox Regulation of Tumor Necrosis Factor Signaling
Han, D., Ybanez, M. D., Ahmadi, S., Yeh, K., & Kaplowitz, N. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2611 · Cited by 169 · see citing works
Han, Y., Zhou, L., Wang, J., Xiong, S., Garner, W. L., French, S. W., & Tsukamoto, H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m310999200 · Cited by 153 · see citing works
Moles, A., Tarrats, N., Fernández-Checa, J. C., & Marı́, M. (2008) · Hepatology · doi:10.1002/hep.22753 · Cited by 105 · see citing works
Self-citationRadbill, B. D., Gupta, R., Ramirez, M. C. M., DiFeo, A. V., Martignetti, J. A., Alvarez, C. E., Friedman, S. L., Narla, G., Vrabie, R., Bowles, R., et al. (2010) · Digestive Diseases and Sciences · doi:10.1007/s10620-010-1296-0 · Cited by 95 · see citing works
Acidic Sphingomyelinase Controls Hepatic Stellate Cell Activation and in Vivo Liver Fibrogenesis
Moles, A., Tarrats, N., Morales, A., Domínguez, M., Bataller, R. A., Caballería, J., García‐Ruiz, C., Fernández-Checa, J. C., & Marı́, M. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.091257 · Cited by 88 · see citing works
Self-citationSUDO, K., YAMADA, Y., Moriwaki, H., Saito, K., & Seishima, M. (2005) · Cytokine · doi:10.1016/j.cyto.2004.11.001 · Cited by 80 · see citing works
Zhou, L., Yan, C., Gieling, R. G., Kida, Y., Garner, W. L., Li, W., & Han, Y.-P. (2009) · BMC Immunology · doi:10.1186/1471-2172-10-15 · Cited by 79 · see citing works
de Meijer, V. E., Sverdlov, D., Popov, Y. V., Le, H. D., Meisel, J. A., Nosé, V., Schuppan, D., & Puder, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011256 · Cited by 72 · see citing works
Hernández‐Muñoz, I., de la Torre, P., Sánchez-Alcázar, J. A., García‐Ruíz, I., de Santiago, E., Muñoz-Yagüe, M. T., & Solís-Herruzo, J. (1997) · Gastroenterology · doi:10.1053/gast.1997.v113.pm9247485 · Cited by 66 · see citing works
Peppel, K., Zhang, L., Orman, E. S., Hagen, P. O., Amalfitano, A., Brian, L., & Freedman, N. J. (2004) · Cardiovascular Research · doi:10.1016/j.cardiores.2004.10.031 · Cited by 60 · see citing works
Cao, Q., Mak, K. M., & Lieber, C. S. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02672-4 · Cited by 54 · see citing works
Hern, I., de la Torre, P., Rey-Campos, J., García‐Ruíz, I., Sánchez-Alcázar, J. A., Muñoz, R., Rippe, R. A., Muñoz‐Yagüe, T., & Solís-Herruzo, A. (2000) · DNA and Cell Biology · doi:10.1089/10445490050043317 · Cited by 28 · see citing works
TNF-α inhibits liver collagen-α1(I) gene expression through a tissue-specific regulatory region
Houglum, K., Buck, M., Kim, D. J., et al. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.274.5.g840 · Cited by 27 · see citing works
Migita, K., Maeda, Y., Abiru, S., Nakamura, M., Komori, A., Yokoyama, T., Takii, Y., Mori, T., Yatsuhashi, H., Eguchi, K., et al. (2005) · Life Sciences · doi:10.1016/j.lfs.2005.10.003 · Cited by 23 · see citing works
Varela‐Rey, M., Fontán, L., Blanco, P., et al. (2007) · Cytokine · doi:10.1016/j.cyto.2007.03.013 · Cited by 21 · see citing works
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Seki, E., & Schwabe, R. F. (2015) · Hepatology · doi:10.1002/hep.27332 · Cited by 972 · see citing works
Pradere, J.-P., Kluwe, J., De Minicis, S., Jiao, J.-J., Gwak, G.-Y., Dapito, D. H., Jang, M.-K., Guenther, N. D., Mederacke, I., Friedman, R., et al. (2013) · Hepatology · doi:10.1002/hep.26429 · Cited by 613 · see citing works
Chen, P., Stärkel, P., Turner, J. R., Ho, S. B., & Schnabl, B. (2015) · Hepatology · doi:10.1002/hep.27489 · Cited by 312 · see citing works
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- Authors
- Tarrats, N., Moles, A., Morales, A., García-Ruiz, C., Fernández-Checa, J. C., & Marí, M.
- Affiliations
- Hospital Clínic de Barcelona (ES)
- Consejo Superior de Investigaciones Científicas (ES)
- University of Southern California (US)
- Corresponding author
- Fernández-Checa, José C.
- Venue
- Hepatology
- Published
- 2011-07
- Volume
- 54
- Issue
- 1
- Pages
- 319-327
- ISSN
- 0270-9139 (ISSN-L)
- PMC
- PMC3125435
- OpenAlex
- W2023044058
- Cited by
- 128
- References
- 33
- Citations by year
- 2025: 3 · 2024: 8 · 2023: 11 · 2022: 6 · 2021: 11 · 2020: 9 · 2019: 10 · 2018: 8 · 2017: 8 · 2016: 5 · 2015: 13 · 2014: 10 · 2013: 11 · 2012: 12
- FWCI
- 7.30
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Hepatology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
- Funders
- National Institute on Alcohol Abuse and Alcoholism (P50-AA11999, P50AA011999)
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
- Keywords
- TNF-α, TNF receptor 1, TNF receptor 2, hepatic stellate cells, liver fibrosis, extracellular matrix remodeling, stellate cell proliferation, platelet-derived growth factor signaling, Akt phosphorylation, MMP-9, type I procollagen, bile duct ligation, chronic liver disease
- MeSH terms
- Collagen Type I, alpha 1 Chain, Animals, Antibodies, Bile Ducts, Cell Line, Disease Models, Animal, Extracellular Matrix, Humans, Ligation, Liver Cirrhosis, Mice, Inbred C57BL, Phosphorylation, Mice, Knockout, Matrix Metalloproteinase 9, Collagen Type I, Receptors, Tumor Necrosis Factor, Type I, Receptors, Tumor Necrosis Factor, Type II, Cell Proliferation, Proto-Oncogene Proteins c-akt, Mice, Hepatic Stellate Cells
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