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Innate Immune Cell Trafficking and Function During Sterile Inflammation of the Liver
Abstract
The sterile inflammatory response (inflammation in the absence of infection) to tissue injury and cell death is required for normal wound healing. However, dysregulated sterile inflammation leads to various acute and chronic inflammatory diseases, including those of the liver and gastrointestinal tract. It is therefore important to increase our understanding of the mechanisms that control physiological versus pathological sterile inflammation. We have begun to clarify the cellular and molecular mechanisms that coordinate the innate immune response to tissue damage and cell death in the liver. In this review, we summarize the mechanisms that alert the immune system to the presence of tissue damage and highlight recent advances in our understanding of innate immune cell trafficking to sites of hepatic sterile inflammation. We explore the functions of various innate immune cells in the coordination of tissue repair, including previously underappreciated roles of peritoneal macrophages and platelets. We propose that dysregulation of immune cell trafficking or function at sites of tissue injury contributes to the misdirection of sterile inflammation to promote chronic inflammatory disease.
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“Indeed, the role of DAMPs released from damaged hepatocytes in initiating or amplifying an inflammatory response, analogous to pathogen-associated molecular patterns of infectious pathogens in sterile liver injury, is now well recognized28.”
From Hepatocyte mitochondria-derived danger signals directly activate hepatic stellate cells and drive progression of liver fibrosis (2020) · cites this paper as [28]
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Cites
Neutrophil recruitment and function in health and inflammation
Kolaczkowska, E., & Kubes, P. (2013) · Nature Reviews Immunology · doi:10.1038/nri3399 · Cited by 5,472
Self-citationCirculating mitochondrial DAMPs cause inflammatory responses to injury
Zhang, Q., Raoof, M., Chen, Y., Sumi, Y., Sursal, T., Junger, W., Brohi, K., Itagaki, K., & Hauser, C. J. (2010) · Nature · doi:10.1038/nature08780 · Cited by 3,812
Development of Monocytes, Macrophages, and Dendritic Cells
Geissmann, F., Manz, M. G., Jung, S., Sieweke, M. H., Merad, M., & Ley, K. (2010) · Science · doi:10.1126/science.1178331 · Cited by 3,049
Pro-resolving lipid mediators are leads for resolution physiology
Serhan, C. N. (2014) · Nature · doi:10.1038/nature13479 · Cited by 3,041
Mixed Lineage Kinase Domain-like Protein Mediates Necrosis Signaling Downstream of RIP3 Kinase
Sun, L., Wang, H., Wang, Z., He, S., Chen, S., Liao, D., Wang, L., Yan, J., Liu, W., Lei, X., et al. (2012) · Cell · doi:10.1016/j.cell.2011.11.031 · Cited by 2,698
Cho, Y., Challa, S., Moquin, D., Genga, R., Ray, T. D., Guildford, M., & Chan, F. K.-M. (2009) · Cell · doi:10.1016/j.cell.2009.05.037 · Cited by 2,435
Tissue-resident macrophages originate from yolk-sac-derived erythro-myeloid progenitors
Gomez Perdiguero, E., Klapproth, K., Schulz, C., Busch, K., Azzoni, E., Crozet, L., Garner, H., Trouillet, C., de Bruijn, M. F., Geissmann, F., et al. (2015) · Nature · doi:10.1038/nature13989 · Cited by 2,339
Nahrendorf, M., Swirski, F. K., Aikawa, E., Stangenberg, L., Wurdinger, T., Figueiredo, J.-L., Libby, P., Weissleder, R., & Pittet, M. J. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070885 · Cited by 2,300
Receptor Interacting Protein Kinase-3 Determines Cellular Necrotic Response to TNF-α
He, S., Wang, L., Miao, L., Wang, T., Du, F., Zhao, L., & Wang, X. (2009) · Cell · doi:10.1016/j.cell.2009.05.021 · Cited by 2,214
Monitoring of Blood Vessels and Tissues by a Population of Monocytes with Patrolling Behavior
Auffray, C., Fogg, D., Garfa, M., Elain, G., Join-Lambert, O., Kayal, S., Sarnacki, S., Cumano, A., Lauvau, G., & Geissmann, F. (2007) · Science · doi:10.1126/science.1142883 · Cited by 1,973
AIM2 activates the inflammasome and cell death in response to cytoplasmic DNA
Fernandes-Alnemri, T., Yu, J.-W., Datta, P., Wu, J., & Alnemri, E. S. (2009) · Nature · doi:10.1038/nature07710 · Cited by 1,831
How dying cells alert the immune system to danger
Kono, H., & Rock, K. L. (2008) · Nature Reviews Immunology · doi:10.1038/nri2215 · Cited by 1,737
Regulation of lung injury and repair by Toll-like receptors and hyaluronan
Jiang, D., Liang, J., Fan, J., Yu, S., Chen, S., Luo, Y., Prestwich, G. D., Mascarenhas, M. M., Garg, H. G., Quinn, D. A., et al. (2005) · Nature Medicine · doi:10.1038/nm1315 · Cited by 1,401
Li, J., McQuade, T., Siemer, A. B., Napetschnig, J., Moriwaki, K., Hsiao, Y.-S., Damko, E., Moquin, D., Walz, T., McDermott, A., et al. (2012) · Cell · doi:10.1016/j.cell.2012.06.019 · Cited by 1,222
Intravascular Danger Signals Guide Neutrophils to Sites of Sterile Inflammation
McDonald, B., Pittman, K., Menezes, G. B., Hirota, S. A., Slaba, I., Waterhouse, C. C. M., Beck, P. L., Muruve, D. A., & Kubes, P. (2010) · Science · doi:10.1126/science.1195491 · Cited by 1,210
Self-citationCarcinoma-produced factors activate myeloid cells through TLR2 to stimulate metastasis
Kim, S., Takahashi, H., Lin, W.-W., Descargues, P., Grivennikov, S., Kim, Y., Luo, J.-L., & Karin, M. (2009) · Nature · doi:10.1038/nature07623 · Cited by 1,100
Phagocyte partnership during the onset and resolution of inflammation
Soehnlein, O., & Lindbom, L. (2010) · Nature Reviews Immunology · doi:10.1038/nri2779 · Cited by 1,054
Crispe, I. N. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132629 · Cited by 986
Phagocytosis of apoptotic cells in homeostasis
Arandjelovic, S., & Ravichandran, K. S. (2015) · Nature Immunology · doi:10.1038/ni.3253 · Cited by 959
Neutrophil swarms require LTB4 and integrins at sites of cell death in vivo
Lämmermann, T., Afonso, P. V., Angermann, B., Wang, J. M., Kastenmüller, W., Parent, C. A., & Germain, R. N. (2013) · Nature · doi:10.1038/nature12175 · Cited by 939
Zhao, J., Jitkaew, S., Cai, Z., Choksi, S., Li, Q., Luo, J., & Liu, Z.-G. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1200012109 · Cited by 925
The Sterile Inflammatory Response
Rock, K. L., Latz, E., Ontiveros, F., & Kono, H. (2010) · Annual Review of Immunology · doi:10.1146/annurev-immunol-030409-101311 · Cited by 865
Schaefer, L., Babelova, A., Kiss, E., Hausser, H.-J., Baliova, M., Krzyzankova, M., Marsche, G., Young, M. F., Mihalik, D., Götte, M., et al. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23755 · Cited by 850
In Vivo Imaging Reveals an Essential Role for Neutrophils in Leishmaniasis Transmitted by Sand Flies
Peters, N. C., Egen, J. G., Secundino, N. F. C., Debrabant, A., Kimblin, N., Kamhawi, S., Lawyer, P. G., Fay, M. P., Germain, R. N., & Sacks, D. L. (2008) · Science · doi:10.1126/science.1159194 · Cited by 837
Nr4a1-Dependent Ly6Clow Monocytes Monitor Endothelial Cells and Orchestrate Their Disposal
Carlin, L. M., Stamatiades, E. G., Auffray, C., Hanna, R. N., Glover, L., Vizcay‐Barrena, G., Hedrick, C. C., Cook, H. T., Diebold, S. S., & Geissmann, F. (2013) · Cell · doi:10.1016/j.cell.2013.03.010 · Cited by 827
Monocytes: Protagonists of Infarct Inflammation and Repair After Myocardial Infarction
Nahrendorf, M., Pittet, M. J., & Świrski, F. K. (2010) · Circulation · doi:10.1161/circulationaha.109.916346 · Cited by 818
Hyaluronan Fragments Act as an Endogenous Danger Signal by Engaging TLR2
Scheibner, K. A., Lutz, M. A., Boodoo, S., Fenton, M. J., Powell, J. D., & Horton, M. R. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.2.1272 · Cited by 708
Sterile inflammation in the liver
Kubes, P., & Mehal, W. Z. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.09.008 · Cited by 666
Self-citationNeutrophils scan for activated platelets to initiate inflammation
Sreeramkumar, V., Adrover, J. M., Ballesteros, I., Cuartero, M. I., Rossaint, J., Bilbao, I., Nácher, M., Pitaval, C., Radovanovic, I., Fukui, Y., et al. (2014) · Science · doi:10.1126/science.1256478 · Cited by 663
Complete reversal of acid-induced acute lung injury by blocking of platelet-neutrophil aggregation
Zarbock, A., Singbartl, K., & Ley, K. F. (2006) · Journal of Clinical Investigation · doi:10.1172/jci29499 · Cited by 608
Woodfin, A., Voisin, M.-B., Beyrau, M., Colom, B., Caille, D., Diapouli, F.-M., Nash, G. B., Chavakis, T., Albelda, S. Μ., Rainger, G. E., et al. (2011) · Nature Immunology · doi:10.1038/ni.2062 · Cited by 607
Find-me and eat-me signals in apoptotic cell clearance: progress and conundrums
Ravichandran, K. S. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20101157 · Cited by 572
Huang, H., Tohme, S. T., Al‐Khafaji, A. B., Tai, S., Loughran, P., Chen, L., Wang, S., Kim, J., Billiar, T. R., Wang, Y., et al. (2015) · Hepatology · doi:10.1002/hep.27841 · Cited by 551
Wang, J., & Kubes, P. (2016) · Cell · doi:10.1016/j.cell.2016.03.009 · Cited by 537
Self-citationMultistep Navigation and the Combinatorial Control of Leukocyte Chemotaxis
Foxman, E. F., Campbell, J. J., & Butcher, E. C. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.139.5.1349 · Cited by 534
Platelets express functional Toll-like receptor-4
Andonegui, G., Kerfoot, S. M., McNagny, K. M., Ebbert, K., Patel, K. D., & Kubes, P. (2005) · Blood · doi:10.1182/blood-2005-03-0916 · Cited by 493
Self-citationHeit, B., Tavener, S. A., Raharjo, E., & Kubes, P. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200202114 · Cited by 487
Self-citationDal-Secco, D., Wang, J., Zeng, Z., Kołaczkowska, E., Wong, C. H. Y., Petri, B., Ransohoff, R. M., Charo, I. F., Jenne, C. N., & Kubes, P. (2015) · The Journal of Experimental Medicine · doi:10.1084/jem.20141539 · Cited by 464
Self-citationMlkl knockout mice demonstrate the indispensable role of Mlkl in necroptosis
Wu, J., Huang, Z., Ren, J., Zhang, Z., He, P., Li, Y., Ma, J., Chen, W., Zhang, Y., Zhou, X., et al. (2013) · Cell Research · doi:10.1038/cr.2013.91 · Cited by 462
Dynamics of Neutrophil Migration in Lymph Nodes during Infection
Chtanova, T., Schaeffer, M., Han, S., van Dooren, G. G., Nöllmann, M., Herzmark, P., Chan, S. W., Satija, H., Camfield, K. A., Aaron, H. L., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.07.012 · Cited by 389
Programmed Necrosis in the Cross Talk of Cell Death and Inflammation
Chan, F. K.-M., Luz, N. F., & Moriwaki, K. (2014) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032414-112248 · Cited by 359
Macrophage and T Cell Dynamics during the Development and Disintegration of Mycobacterial Granulomas
Egen, J. G., Rothfuchs, A. G., Feng, C. G., Winter, N., Sher, A., & Germain, R. N. (2008) · Immunity · doi:10.1016/j.immuni.2007.12.010 · Cited by 351
Mossanen, J. C., Krenkel, O., Ergen, C., Govaere, O., Liepelt, A., Puengel, T., Heymann, F., Kalthoff, S., Lefebvre, E., Eulberg, D., et al. (2016) · Hepatology · doi:10.1002/hep.28682 · Cited by 325
Tilg, H., Moschen, A. R., & Szabó, G. (2016) · Hepatology · doi:10.1002/hep.28456 · Cited by 319
Freire-de-Lima, C. G., Xiao, Y. Q., Gardai, S. J., Bratton, D. L., Schiemann, W. P., & Henson, P. M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605146200 · Cited by 310
Absence of receptor interacting protein kinase 3 prevents ethanol-induced liver injury
Roychowdhury, S., McMullen, M. R., Pisano, S. G., Liu, X., & Nagy, L. E. (2013) · Hepatology · doi:10.1002/hep.26200 · Cited by 304
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Self-citationRamachandran, A., McGill, M. R., Xie, Y., Ni, H., Ding, W., & Jaeschke, H. (2013) · Hepatology · doi:10.1002/hep.26547 · Cited by 258
PTEN functions to 'prioritize' chemotactic cues and prevent 'distraction' in migrating neutrophils
Heit, B., Robbins, S. M., Downey, C. M., Guan, Z., Colarusso, P., Miller, B. J., Jirik, F. R., & Kubes, P. (2008) · Nature Immunology · doi:10.1038/ni.1623 · Cited by 254
Self-citationGrommes, J., Alard, J.-É., Drechsler, M. D., Wantha, S., Mörgelin, M., Kuebler, W. M., Jacobs, M. J. H. M., von Hundelshausen, P., Markart, P., Wygrecka, M., et al. (2012) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201108-1533oc · Cited by 237
Tavares, J. C., Hickey, M. J., Hutchison, J. S., Michaud, J., Sutcliffe, I. T., & Kubes, P. (2000) · Circulation Research · doi:10.1161/01.res.87.12.1141 · Cited by 236
Self-citationPlatelets in inflammation and immunity
Herter, J. M., Rossaint, J., & Zarbock, A. (2014) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.12730 · Cited by 235
Apoptotic human cells inhibit migration of granulocytes via release of lactoferrin
Bournazou, I., Pound, J. D., Duffin, R., Bournazos, S., Melville, L. A., Brown, S. B., Rossi, A. G., & Gregory, C. D. (2008) · Journal of Clinical Investigation · doi:10.1172/jci36226 · Cited by 221
Donnelly, D. J., Longbrake, E. E., Shawler, T. M., Kigerl, K. A., Lai, W., Tovar, C. A., Ransohoff, R. M., & Popovich, P. G. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2114-11.2011 · Cited by 219
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Crane, M. J., Daley, J. M., van Houtte, O., Brancato, S. K., Henry, W. L., & Albina, J. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086660 · Cited by 188
Hepatic DNA deposition drives drug‐induced liver injury and inflammation in mice
Marques, P. E., de Oliveira, A. G., Pereira, R. V. S., David, B. A., Gomides, L. F., Saraiva, A. M., Pires, D. A., Novaes, J. T., Patricio, D. D. O., Cisalpino, D., et al. (2014) · Hepatology · doi:10.1002/hep.27216 · Cited by 170
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Christoffersson, G., Henriksnäs, J., Johansson, L., Rolny, C., Ahlström, H., Caballero-Corbalan, J., Segersvärd, R., Permert, J., Korsgren, O., Carlsson, P.-O., et al. (2010) · Diabetes · doi:10.2337/db10-0205 · Cited by 167
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Slaba, I., Wang, J., Kołaczkowska, E., McDonald, B., Lee, W., & Kubes, P. (2015) · Hepatology · doi:10.1002/hep.28003 · Cited by 134
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Rossaint, J., & Zarbock, A. (2015) · Cardiovascular Research · doi:10.1093/cvr/cvv048 · Cited by 93
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Metadata
- Authors
- McDonald, B., & Kubes, P.
- Affiliations
- University of Calgary (CA)
- Corresponding author
- Kubes, Paul
- Venue
- Gastroenterology
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 151
- Issue
- 6
- Pages
- 1087-1095
- ISSN
- 0016-5085 (ISSN-L)
- OpenAlex
- W2531302392
- Cited by
- 123
- References
- 63
- Citations by year
- 2026: 3 · 2025: 9 · 2024: 11 · 2023: 10 · 2022: 20 · 2021: 19 · 2020: 13 · 2019: 16 · 2018: 16 · 2017: 6
- FWCI
- 1.59
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- sterile inflammation, innate immunity, immune cell trafficking, liver, tissue damage, cell death, peritoneal macrophages, platelets, tissue repair, wound healing, chronic inflammatory diseases
- MeSH terms
- Animals, Blood Platelets, Chemotaxis, Hepatitis, Humans, Immunity, Innate, Macrophages, Monocytes, Neutrophils, Cell Death
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