The DOI matches its Crossref record, with a small difference in title or year; 41 of the 41 references it cites were found in a registry or an index.
Mixed lineage kinase 3 mediates release of C‐X‐C motif ligand 10–bearing chemotactic extracellular vesicles from lipotoxic hepatocytes
Open accessAbstract
Mixed lineage kinase 3 (MLK3) deficiency reduces macrophage‐associated inflammation in a murine model of nonalcoholic steatohepatitis (NASH). However, the mechanistic links between MLK3 activation in hepatocytes and macrophage‐driven inflammation in NASH are uncharted. Herein, we report that MLK3 mediates the release of (C‐X‐C motif) ligand 10 (CXCL10)‐laden extracellular vesicles (EVs) from lipotoxic hepatocytes, which induce macrophage chemotaxis. Primary mouse hepatocytes (PMHs) and Huh7 cells were treated with palmitate or lysophosphatidylcholine (LPC). Released EVs were isolated by differential ultracentrifugation. LPC treatment of PMH or Huh7 cells induced release of EVs, which was prevented by either genetic or pharmacological inhibition of MLK3. Mass spectrometry identified the potent chemokine, CXCL10, in the EVs, which was markedly enriched in EVs isolated from LPC‐treated hepatocytes versus untreated cells. Green fluorescent protein (GFP)‐tagged CXCL10 was present in vesicular structures and colocalized with the red fluorescent protein (RFP)‐tagged EV marker, CD63, after LPC treatment of cotransfected Huh‐7 cells. Either genetic deletion or pharmacological inhibition of MLK3 prevented CXCL10 enrichment in EVs. Treatment of mouse bone‐marrow–derived macrophages with lipotoxic hepatocyte‐derived EVs induced macrophage chemotaxis, an effect blocked by incubation with CXCL10‐neutralizing antisera. MLK3‐deficient mice fed a NASH‐inducing diet had reduced concentrations of total plasma EVs and CXCL10 containing EVs compared to wild‐type mice. Conclusions: During hepatocyte lipotoxicity, activated MLK3 induces the release of CXCL10‐bearing vesicles from hepatocytes, which are chemotactic for macrophages. (H epatology 2016;63:731–744)
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“They also secrete inflammatory and fibrogenic cytokines either directly, such as interleukin (IL)-1β and IL-18,35,36 or via extracellular vesicles containing C-X-C motif chemokine ligand (CXCL)10, a ligand for C-X-C motif chemokine receptor (CXCR)3, and mitochondrial DNA, a key TLR9 ligand.37”
From Understanding the cellular interactome of non-alcoholic fatty liver disease (2022) · cites this paper as [37]
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Cites
Tissue-based map of the human proteome
Uhlén, M., Fagerberg, L., Hallström, B. M., Lindskog, C., Oksvold, P., Mardinoglu, A., Sivertsson, Å., Kampf, C., Sjöstedt, E., Asplund, A., et al. (2015) · Science · doi:10.1126/science.1260419 · Cited by 15,286
Extracellular vesicles: Exosomes, microvesicles, and friends
Raposo, G., & Stoorvogel, W. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201211138 · Cited by 8,099
Isolation and Characterization of Exosomes from Cell Culture Supernatants and Biological Fluids
Théry, C., Amigorena, S., Raposo, G., & Clayton, A. (2006) · Current Protocols in Cell Biology · doi:10.1002/0471143030.cb0322s30 · Cited by 5,766
Prevalence of Hepatic Steatosis in An Urban Population in the United States: Impact of Ethnicity
Browning, J. D., Szczepaniak, L. S., Dobbins, R., Nuremberg, P., Horton, J. D., Cohen, J. C., Grundy, S. M., & Hobbs, H. H. (2004) · Hepatology · doi:10.1002/hep.20466 · Cited by 3,664
The Natural History of Nonalcoholic Fatty Liver Disease: A Population-Based Cohort Study
Adams, L. A., Lymp, J. F., St. Sauver, J., Sanderson, S. O., Lindor, K. D., Feldstein, A., & Angulo, P. (2005) · Gastroenterology · doi:10.1053/j.gastro.2005.04.014 · Cited by 2,890
Long-term follow-up of patients with NAFLD and elevated liver enzymes
Ekstedt, M., Franzén, L. E., Mathiesen, U. L., Thorelius, L., Holmqvist, M., Bodemar, G., & Kechagias, S. (2006) · Hepatology · doi:10.1002/hep.21327 · Cited by 2,302
Colombo, M., Moita, C. F., van Niel, G., Kowal, J., Vigneron, J., Benaroch, P., Manel, N., Moita, L. F., Théry, C., & Raposo, G. (2013) · Journal of Cell Science · doi:10.1242/jcs.128868 · Cited by 1,534
Hepatocyte apoptosis and fas expression are prominent features of human nonalcoholic steatohepatitis
Feldstein, A. E., Canbay, A., Angulo, P., Taniai, M., Burgart, L. J., Lindor, K. D., & Gores, G. J. (2003) · Gastroenterology · doi:10.1016/s0016-5085(03)00907-7 · Cited by 1,085
Self-citationNeuschwander‐Tetri, B. A. (2010) · Hepatology · doi:10.1002/hep.23719 · Cited by 1,077
CXCR3 ligands: redundant, collaborative and antagonistic functions
Groom, J. R., & Luster, A. D. (2011) · Immunology and Cell Biology · doi:10.1038/icb.2010.158 · Cited by 1,006
Webber, J., & Clayton, A. (2013) · Journal of Extracellular Vesicles · doi:10.3402/jev.v2i0.19861 · Cited by 817
Complexity of Danger: The Diverse Nature of Damage-associated Molecular Patterns
Schaefer, L. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.r114.619304 · Cited by 649
Activation and Dysregulation of the Unfolded Protein Response in Nonalcoholic Fatty Liver Disease
Puri, P., Mirshahi, F., Cheung, O., Natarajan, R., Maher, J. W., Kellum, J. M., & Sanyal, A. J. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.10.039 · Cited by 615
Tosello-Trampont, A.-C., Landes, S. G., Nguyen, V., Novobrantseva, T. I., & Hahn, Y. S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.417014 · Cited by 415
Goh, K. C., Haque, S. J., & Williams, B. R. G. (1999) · The EMBO Journal · doi:10.1093/emboj/18.20.5601 · Cited by 388
The chemotaxis of M1 and M2 macrophages is regulated by different chemokines
Xuan, W., Qu, Q., Zheng, B., Xiong, S., & Fan, G.-H. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.1a0314-170r · Cited by 357
A real-time view of life within 100 nm of the plasma membrane
Steyer, J. A., & Almers, W. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35067069 · Cited by 349
Protein Targeting to Exosomes/Microvesicles by Plasma Membrane Anchors
Shen, B., Wu, N., Yang, J.-M., & Gould, S. J. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.208660 · Cited by 292
Exosomes in the pathogenesis, diagnostics and therapeutics of liver diseases
Masyuk, A. I., Masyuk, T. V., & LaRusso, N. F. (2013) · Journal of Hepatology · doi:10.1016/j.jhep.2013.03.028 · Cited by 286
Lysophosphatidylcholine as a death effector in the lipoapoptosis of hepatocytes
Han, M. S., Park, S. Y., Shinzawa, K., Kim, S., Chung, K. W., Lee, J., Kwon, C. H. D., Lee, K., Lee, J.-H., Park, C. K., et al. (2007) · Journal of Lipid Research · doi:10.1194/jlr.m700184-jlr200 · Cited by 258
Zhang, X., Shen, J., Man, K., Chu, E. S., Yau, T. O., Sung, J. C. Y., Go, M. Y. Y., Deng, J., Lu, L., Wong, V. W., et al. (2014) · Journal of Hepatology · doi:10.1016/j.jhep.2014.07.006 · Cited by 223
Mechanisms of lysophosphatidylcholine-induced hepatocyte lipoapoptosis
Kakisaka, K., Cazanave, S. C., Fingas, C. D., Guicciardi, M. E., Bronk, S. F., Werneburg, N. W., Mott, J. L., & Gores, G. J. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00301.2011 · Cited by 222
Self-citationMechanisms of Disease: pathogenesis of nonalcoholic fatty liver disease
Sanyal, A. J. (2005) · Nature Clinical Practice Gastroenterology & Hepatology · doi:10.1038/ncpgasthep0084 · Cited by 216
Povero, D., Eguchi, A., Niesman, I. R., Andronikou, N., du Jeu, X. D. M., Mulya, A., Berk, M. P., Lazić, M., Thapaliya, S., Parola, M., et al. (2013) · Science Signaling · doi:10.1126/scisignal.2004512 · Cited by 213
JNK1-dependent PUMA Expression Contributes to Hepatocyte Lipoapoptosis
Cazanave, S. C., Mott, J. L., Elmi, N. A., Bronk, S. F., Werneburg, N. W., Akazawa, Y., Kahraman, A., Garrison, S. P., Zambetti, G. P., Charlton, M., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.022491 · Cited by 197
Self-citationImmature myeloid cells induced by a high-fat diet contribute to liver inflammation #
Deng, Z., Liu, Y., Liu, C., Xiang, X., Wang, J., Cheng, Z., Shah, S. V., Zhang, S., Zhang, L., Zhuang, X., et al. (2009) · Hepatology · doi:10.1002/hep.23148 · Cited by 149
Metabolic Stress Signaling Mediated by Mixed-Lineage Kinases
Jaeschke, A., & Davis, R. J. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.07.008 · Cited by 137
Role of MLK3 in the Regulation of Mitogen-Activated Protein Kinase Signaling Cascades
Brancho, D., Ventura, J., Jaeschke, A., Doran, B., Flavell, R. A., & Davis, R. J. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.9.3670-3681.2005 · Cited by 127
Kim, K.-Y., Kim, B.-C., Xu, Z., & Kim, S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313947200 · Cited by 93
Chmielewski, S., Olejnik, A., Sikorski, K., Pelisek, J., Błaszczyk, K., Aoqui, C., Nowicka, H., Zernecke, A., Heemann, U. W., Wesoły, J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113318 · Cited by 84
Petrovic‐Djergovic, D., Popovic, M., Chittiprol, S., Cortado, H. H., Ransom, R. F., & Partida‐Sánchez, S. (2015) · Clinical & Experimental Immunology · doi:10.1111/cei.12579 · Cited by 78
Molecular pathways: hepatitis C virus, CXCL10, and the inflammatory road to liver cancer
Brownell, J., & Polyak, S. J. (2013) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-12-0928 · Cited by 70
Tacke, F., Zimmermann, H. W., Berres, M., Trautwein, C., & Wasmuth, H. E. (2011) · Liver International · doi:10.1111/j.1478-3231.2011.02504.x · Cited by 67
Khalili, K., Lan, F. P., Hanbidge, A. E., Muradali, D., Oreopoulos, D. G., & Wanless, I. R. (2003) · American Journal of Roentgenology · doi:10.2214/ajr.180.6.1801601 · Cited by 64
Teoh, N., Ajamieh, H., Wong, H. J., Croft, K. D., Mori, T. A., ALLISON, A. C., & Farrell, G. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104376 · Cited by 56
Ibrahim, S. H., Gores, G. J., Hirsova, P., Kirby, M., Miles, L., Jaeschke, A., & Kohli, R. (2013) · Liver International · doi:10.1111/liv.12353 · Cited by 54
Self-citationSikorski, K., Chmielewski, S., Przybył, Ł., Heemann, U. W., Wesoły, J., Baumann, M., & Bluyssen, H. A. R. (2011) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00276.2010 · Cited by 52
Hepatitis C Virus NS5A Inhibits Mixed Lineage Kinase 3 to Block Apoptosis
Amako, Y., Igloi, Z., Mankouri, J., Kazlauskas, A., Saksela, K., Dallas, M. L., Peers, C., & Harris, M. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.491985 · Cited by 43
Humphrey, R. K., Yu, S. M. A., Bellary, A., Gonuguntla, S., Yebra, M., & Jhala, U. S. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.425884 · Cited by 21
Structure of mouse IP-10, a chemokine
Jabeen, T., Leonard, P. M., Jamaluddin, H., & Acharya, K. R. (2008) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444908007026 · Cited by 19
TIRF Microscopy Analysis of the Mechanism of Insulin Exocytosis
Nagamatsu, S. (2006) · Endocrine Journal · doi:10.1507/endocrj.kr-75 · Cited by 16
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Metadata
- Authors
- Ibrahim, S. H., Hirsova, P., Tomita, K., Bronk, S. F., Werneburg, N. W., Harrison, S. A., Goodfellow, V. S., Malhi, H., & Gores, G. J.
- Affiliations
- Mayo Clinic (US)
- Brooke Army Medical Center, Fort Sam Houston,Houston,TX
- Califia Bio (United States) (US)
- Corresponding author
- Gores, Gregory J.
- Venue
- Hepatology
- Published
- 2015-12-11
- Volume
- 63
- Issue
- 3
- Pages
- 731-744
- ISSN
- 0270-9139 (ISSN-L)
- 1527-3350
- PMC
- PMC4764421
- OpenAlex
- W2146229869
- Cited by
- 232
- References
- 41
- Citations by year
- 2026: 7 · 2025: 11 · 2024: 22 · 2023: 24 · 2022: 34 · 2021: 29 · 2020: 37 · 2019: 23 · 2018: 19 · 2017: 14 · 2016: 10 · 2015: 1
- FWCI
- 6.37
- Type
- journal article
- Language
- en
- Update notices
- correction (2016-08-01)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Hepatology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Mayo Clinic
- National Institutes of Health (KL2TR000136, DK97178)
- Center for Cell Signaling in Gastroenterology, Mayo Clinic (P30 DK084567)
- National Institute of Diabetes and Digestive and Kidney Diseases (K08DK097178, DK-41876, R37DK041876, R01DK041876, P30DK084567, DK 97178)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Health Sciences › Medicine › Hepatology › Liver Disease Diagnosis and Treatment
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Keywords
- MLK3, CXCL10, extracellular vesicles, lipotoxicity, hepatocytes, macrophage chemotaxis, nonalcoholic steatohepatitis, lysophosphatidylcholine, palmitate, chemokine secretion, CD63
- MeSH terms
- Extracellular Vesicles, Mitogen-Activated Protein Kinase Kinase Kinase 11, Animals, Chemotaxis, Disease Models, Animal, Humans, Liver, Macrophages, Signal Transduction, MAP Kinase Kinase Kinases, Hepatocytes, Cell Line, Tumor, Mice, Chemokine CXCL10, Non-alcoholic Fatty Liver Disease
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