Skip to menu Skip to content Skip to footer
Professor Matt Sweet
Professor

Matt Sweet

Email: 
Phone: 
+61 7 334 62082

Overview

Background

Matt Sweet is an NHMRC Leadership Fellow and Group Leader at the Institute for Molecular Bioscience (IMB) at The University of Queensland, Brisbane, Australia. Matt studies innate immunity, the body’s danger sensing system that responds to infection, injury and dysregulated homeostasis, and the role of this system in health and disease. Matt’s research team focuses on manipulating the innate immune system for the development of anti-infective and anti-inflammatory strategies. To do so, his lab characterizes the roles of specific innate immune pattern recognition receptors and their downstream signalling pathways/gene products in inflammatory and infectious disease processes, with a particular focus on immunometabolism. He has authored >180 journal articles and book chapters, including in Science (2), Science Translational Medicine, Science Immunology, Nature Immunology, Nature Reviews Immunology, Nature Genetics, Nature Communications(4), PNAS USA (6), Cell Metabolism, Developmental Cell and Journal of Experimental Medicine (2), and his career publications have accrued ~22,000 citations. Matt has held several leadership roles at the IMB, including IMB Director of Higher Degree Research (DHDR, 2021-2025), member of the IMB Senior Executive Committee (2023-2025), founding Director of the IMB Centre for Inflammation and Disease Research (2014-2018), and Deputy Head of the IMB Division of Cell Biology and Molecular Medicine (2014-2018).

Biography

I was awarded a PhD (The University of Queensland) in 1996 for my research under the supervision of Prof David Hume into gene regulation in macrophages, immune cells with important roles in health and disease. I subsequently undertook a short postdoctoral position in the same laboratory, focusing on the activation of macrophages by pathogen products. I then embarked on a CJ Martin post-doctoral training fellowship with Prof Eddy Liew, FRS at the University of Glasgow in Scotland. Returning to The University of Queensland, I had a prominent role within the Cooperative Research Centre for Chronic Inflammatory Diseases (including as UQ node head from 2007-2008) and was appointed as a Group Leader at the IMB in 2007. Since that time, I have held several fellowships, including an ARC Future Fellowship, two NHMRC Senior Research Fellowships, an NHMRC Leadership Fellowship, and a Le Studium Visiting Researcher Award.

Key discoveries

CpG-containing DNA as an activator of innate immunity, and characterization of the receptor (TLR9) detecting this microbial component.

The IL-1 receptor family member ST2 as a critical regulator of innate immunity and inflammation.

Inflammatory and antimicrobial functions of histone deacetylase enzymes (HDACs) in macrophages.

Effects of the growth factor CSF-1 on inflammatory responses in macrophages.

Mechanisms responsible for divergence in TLR responses between human and mouse macrophages, as well as the functional consequences of such divergence.

The first description of the p19/EBI3 heterodimer, subsequently renamed by others as the cytokine IL-39.

TLR-inducible zinc toxicity as an antimicrobial weapon of macrophages, as well as its deficiency in Cystic Fibrosis.

Host evasion strategies used by the bacterial pathogens Salmonella enterica serovar Typhimurium and uropathogenic E. coli.

SCIMP as a novel TLR adaptor that mediates TLR tyrosine phosphorylation and selective cytokine outputs.

Genes and pathways associated with the severity of chronic liver disease.

Molecular mechanisms controlling macrophage immunometabolism, as well as associated inflammatory and antimicrobial responses.

Anti-inflammatory and antibacterial activities of the metabolite ribulose-5-phosphate.

Research training

I have supervised or co-supervised 34 completed PhD students and 26 completed honours students, and have mentored many post-doctoral researchers over the course of my career. Many of my former staff and students continue to have active research careers around the world (USA, UK, Europe, Australia), including as independent laboratory heads. Others have key roles in and industry and government. I currently supervise 4 PhD students in my laboratory, co-supervise 3 PhD students in other laboratories, and oversee the research activities of 3 post-doctoral researchers in my group. Current and former staff/students have received numerous fellowships and awards during their research careers (e.g. ARC DECRA, NHMRC CJ Martin fellowship, UQ post-doctoral fellowship, Smart State scholarship). I have also examined 32 PhD theses and 3 MPhil theses, primarily in the fields of innate immunity, inflammation and host defence.

Professional activities

I have served as an editorial board member for several international journals including Journal of Leukocyte Biology (current), Seminars in Cell & Developmental Biology (current), and Immunology and Cell Biology (past). I have served on NHMRC project grant review panels in 2007, 2008, 2009, 2012 (as panel chair) and 2014, NHMRC Ideas panels in 2020 and 2024, NHMRC Investigator panels in 2021 and 2022, as well as a member of the NHMRC RGMS user reference group committee from 2010-2012. I acted as national representative for the Australasian Society of Immunology (ASI) Infection and Immunity special interest group from 2012-2017 and currently serve as a board member for the International Society for Zinc Biology. At UQ, I served as chair of an animal ethics committee from 2013-2014 and co-organized the UQ Host-Pathogen interaction network from 2007-2010 (prior to the establishment of the Australian Infectious Diseases Research Centre). Other leadership roles have included IMB Director of Higher Degree Research (DHDR, 2021-2025), member of the IMB Senior Executive Committee (2023-2025), founding Director of the IMB Centre for Inflammation and Disease Research (2014-2018), and Deputy Head of the IMB Division of Cell Biology and Molecular Medicine (2014-2018).

I have made extensive contributions to conference organization in my discipline. I co-organized the national TLROZ2009 and TLROZ2012 conferences, I organized the first ever Australasian Society for Immunology (ASI) Infection and Immunity workshop (2009), was chair of the ASI Program Committee and co-organizer of the Infection and Immunity workshop for ASI2017, and I co-organized the annual IMB Inflammation Symposium (2014-2018). I also co-chaired the 2019 World Conference of Inflammation (Sydney, September 2019). In addition, I have been a member of the organizing committee for ASI2009, the 2014 International Cytokine and Interferon Society conference, the Lorne Infection and Immunity conference (2014-2020), the Queensland Immunology Networking Symposium (2020-2024), the Brisbane Immunology Group annual meeting (2008-2024), and the International Society for Zinc Biology Conference (2026).

Availability

Professor Matt Sweet is:
Available for supervision
Media expert

Fields of research

Qualifications

  • Bachelor (Honours) of Science (Advanced), The University of Queensland
  • Doctor of Philosophy, The University of Queensland

Research interests

  • INNATE IMMUNE INFLAMMATORY PATHWAYS

    Cells of the innate immune system such as macrophages play essential roles in detecting and responding to danger, which can be sensed as a result of infection, injury and/or dysregulated homeostasis. These cells use several families of pattern recognition receptors (PRRs), such as the toll-like receptors (TLRs) and nod-like receptors (NLRs), to recognize specific danger signals. Inappropriate or prolonged PRR activation drives dysregulated inflammation, which is central to the pathology of many acute and chronic diseases. Current research is focused on developing approaches to target PRR signaling pathways and other innate immune pathways for potential applications in inflammatory diseases such as chronic liver disease, sepsis and inflammatory bowel diseases. Areas of specific interest including (1) characterizing mechanisms by which novel TLR complex components provide specificity to inflammatory responses; (2) control of inflammatory outputs by immune cell metabolism and (3) the roles of individual histone deacetylase enzymes, particularly HDAC7, in macrophage inflammatory pathways and inflammatory disease processes.

  • INNATE IMMUNE ANTIMICROBIAL PATHWAYS

    Innate immunity plays a pivotal role in protecting against invading microorganisms. Successful pathogens must overcome this system to colonize the host and cause disease. Many important pathogens actively target macrophages, residing in these cells or destroying them to avoid immune defence. We study TLR-inducible macrophage antimicrobial responses, and how the Gram-negative bacterial pathogens Salmonella enterica serovar Typhimurium (S. Typhimurium) and uropathogenic E. coli (UPEC) are able to overcome such responses. Our focus is on developing novel anti-infective strategies, through the manipulation of innate immune antimicrobial responses. Areas of specific interest include (1) characterizing TLR-inducible antimicrobial responses (zinc poisoning, mitochondrial fission) in macrophages, as well as host subversion strategies; (2) defining mechanisms by which specific HDAC enzymes (HDAC6, HDAC7) regulate macrophage host defence pathways; and (3) unravelling the contributions of UPEC-triggered macrophage cell death to immune defence versus host subversion.

  • SPECIES DIFFERENCES IN INNATE IMMUNITY

    Whilst conservation of a gene or pathway across species is an obvious indicator of its importance, the fact that a gene or a pathway is not conserved does not mean that it isn’t important for one particular species. In fact, in the context of co-evolution of host and pathogen, species-specific responses are likely to be critical for host defence. We have characterized differences in TLR responses between human and mouse, and the mechanisms responsible. Our current focus is on characterizing the roles of individual TLR target genes that are differentially regulated between human and mouse in host defence against bacterial pathogens and in inflammatory responses.

Research impacts

Every organism and every cell employ some form of innate defence for protection against agents with the ability to cause harm. In complex multicellular organisms, these innate defence systems also have the capacity to cause damage to the organism itself. As such, innate immunity lies at the heart of almost all disease processes. Our fundamental research in this field has the potential to lead to new anti-infective and/or anti-inflammatory agents that may have applications in the health, livestock and/or veterinary sectors.

Specific indicators of impact

· More than 180 career publications, which have collectively accrued ~22,000 citations (average cites/article: ~120; most cited article: ~1,100 citations. My publications include 42 invited review articles, editorials and book chapters, and of these, 8 reviews have received more than 200 citations, another 4 have received more than 100 citations, and 1 received the Dolph Adams award from the Journal of Leukocyte Biology. I have also been invited to guest edit review series for Seminars in Cell and Developmental Biology, Immunology and Cell Biology and Journal of Leukocyte Biology.

· Contribution to the development and/or validation of several novel small molecule inhibitors of inflammation-relevant proteins, and numerous interactions with the Pharmaceutical/Biotechnology industry.

· Identification of a gene signature associated with severity of chronic liver disease, with these findings currently being pursued for discovery of biomarkers and therapeutic targets.

· Demonstration that antibacterial zinc toxicity is defective in cystic fibrosis, likely contributing to the susceptibility of people with cystic fibrosis to bacterial infections, PCT patent filed.

· First demonstration of antimicrobial and anti-inflammatory effects of the metabolite ribulose-5-phosphate, PCT patent filed.

· >130 invitations to speak nationally and internationally at conferences, institute/departmental seminars, and other forums. I have also chaired ~50 sessions at national and international conferences.

Works

Search Professor Matt Sweet’s works on UQ eSpace

205 works between 1993 and 2025

1 - 20 of 205 works

Featured

2025

Journal Article

Inducible antibacterial responses in macrophages

Sweet, Matthew J., Ramnath, Divya, Singhal, Amit and Kapetanovic, Ronan (2025). Inducible antibacterial responses in macrophages. Nature Reviews Immunology, 25 (2) e12771, 92-107. doi: 10.1038/s41577-024-01080-y

Inducible antibacterial responses in macrophages

Featured

2024

Journal Article

CFTR is required for zinc-mediated antibacterial defense in human macrophages

Das Gupta, Kaustav, Curson, James E. B., Tarique, Abdullah A., Kapetanovic, Ronan, Schembri, Mark A., Fantino, Emmanuelle, Sly, Peter D. and Sweet, Matthew J. (2024). CFTR is required for zinc-mediated antibacterial defense in human macrophages. Proceedings of the National Academy of Sciences, 121 (8) e2315190121, 1-11. doi: 10.1073/pnas.2315190121

CFTR is required for zinc-mediated antibacterial defense in human macrophages

Featured

2023

Journal Article

HDAC7 is an immunometabolic switch triaging danger signals for engagement of antimicrobial versus inflammatory responses in macrophages

Das Gupta, Kaustav, Ramnath, Divya, von Pein, Jessica B., Curson, James E. B., Wang, Yizhuo, Abrol, Rishika, Kakkanat, Asha, Moradi, Shayli Varasteh, Gunther, Kimberley S., Murthy, Ambika M. V., Stocks, Claudia J., Kapetanovic, Ronan, Reid, Robert C., Iyer, Abishek, Ilka, Zoe C., Nauseef, William M., Plan, Manuel, Luo, Lin, Stow, Jennifer L., Schroder, Kate, Karunakaran, Denuja, Alexandrov, Kirill, Shakespear, Melanie R., Schembri, Mark A., Fairlie, David P. and Sweet, Matthew J. (2023). HDAC7 is an immunometabolic switch triaging danger signals for engagement of antimicrobial versus inflammatory responses in macrophages. Proceedings of the National Academy of Sciences, 120 (4) e2212813120, 1-12. doi: 10.1073/pnas.2212813120

HDAC7 is an immunometabolic switch triaging danger signals for engagement of antimicrobial versus inflammatory responses in macrophages

Featured

2020

Journal Article

Mammalian lipid droplets are innate immune hubs integrating cell metabolism and host defense

Bosch, Marta, Sánchez-Álvarez, Miguel, Fajardo, Alba, Kapetanovic, Ronan, Steiner, Bernhard, Dutra, Filipe, Moreira, Luciana, López, Juan Antonio, Campo, Rocío, Marí, Montserrat, Morales-Paytuví, Frederic, Tort, Olivia, Gubern, Albert, Templin, Rachel M., Curson, James E. B., Martel, Nick, Català, Cristina, Lozano, Francisco, Tebar, Francesc, Enrich, Carlos, Vázquez, Jesús, Del Pozo, Miguel A., Sweet, Matthew J., Bozza, Patricia T., Gross, Steven P., Parton, Robert G. and Pol, Albert (2020). Mammalian lipid droplets are innate immune hubs integrating cell metabolism and host defense. Science, 370 (6514) 8085, 309-+. doi: 10.1126/science.aay8085

Mammalian lipid droplets are innate immune hubs integrating cell metabolism and host defense

2020

Journal Article

Class IIa histone deacetylases drive toll-like receptor-inducible glycolysis and macrophage inflammatory responses via pyruvate kinase M2

Das Gupta, Kaustav, Shakespear, Melanie R., Curson, James E.B., Murthy, Ambika M.V., Iyer, Abishek, Hodson, Mark P., Ramnath, Divya, Tillu, Vikas A., von Pein, Jessica B., Reid, Robert C., Tunny, Kathryn, Hohenhaus, Daniel M., Moradi, Shayli Varasteh, Kelly, Gregory M., Kobayashi, Takumi, Gunter, Jennifer H., Stevenson, Alexander J., Xu, Weijun, Luo, Lin, Jones, Alun, Johnston, Wayne A., Blumenthal, Antje, Alexandrov, Kirill, Collins, Brett M., Stow, Jennifer L., Fairlie, David P. and Sweet, Matthew J. (2020). Class IIa histone deacetylases drive toll-like receptor-inducible glycolysis and macrophage inflammatory responses via pyruvate kinase M2. Cell Reports, 30 (8), 2712-2728.e8. doi: 10.1016/j.celrep.2020.02.007

Class IIa histone deacetylases drive toll-like receptor-inducible glycolysis and macrophage inflammatory responses via pyruvate kinase M2

Featured

2019

Journal Article

Uropathogenic Escherichia coli employs both evasion and resistance to subvert innate immune-mediated zinc toxicity for dissemination

Stocks, Claudia J., Phan, Minh-Duy, Achard, Maud E. S., Nhu, Nguyen Thi Khanh, Condon, Nicholas D., Gawthorne, Jayde A., Lo, Alvin W., Peters, Kate M., McEwan, Alastair G., Kapetanovic, Ronan, Schembri, Mark A. and Sweet, Matthew J. (2019). Uropathogenic Escherichia coli employs both evasion and resistance to subvert innate immune-mediated zinc toxicity for dissemination. Proceedings of the National Academy of Sciences, 116 (13), 6341-6350. doi: 10.1073/pnas.1820870116

Uropathogenic Escherichia coli employs both evasion and resistance to subvert innate immune-mediated zinc toxicity for dissemination

Featured

2018

Journal Article

Hepatic expression profiling identifies steatosis-independent and steatosis-driven advanced fibrosis genes

Ramnath, Divya, Irvine, Katharine M., Lukowski, Samuel W., Horsfall, Leigh U., Loh, Zhixuan, Clouston, Andrew D., Patel, Preya J., Fagan, Kevin J., Iyer, Abishek, Lampe, Guy, Stow, Jennifer L., Schroder, Kate, Fairlie, David P., Powell, Joseph E., Powell, Elizabeth E. and Sweet, Matthew J. (2018). Hepatic expression profiling identifies steatosis-independent and steatosis-driven advanced fibrosis genes. JCI Insight, 3 (14) e120274. doi: 10.1172/jci.insight.120274

Hepatic expression profiling identifies steatosis-independent and steatosis-driven advanced fibrosis genes

Featured

2017

Journal Article

SCIMP is a transmembrane non-TIR TLR adaptor that promotes proinflammatory cytokine production from macrophages

Luo, Lin, Bokil, Nilesh J., Wall, Adam A., Kapetanovic, Ronan, Lansdaal, Natalie M., Marceline, Faustine, Burgess, Belinda J., Tong, Samuel J., Guo, Zhong, Alexandrov, Kirill, Ross, Ian L., Hibbs, Margaret L., Stow, Jennifer L. and Sweet, Matthew J. (2017). SCIMP is a transmembrane non-TIR TLR adaptor that promotes proinflammatory cytokine production from macrophages. Nature Communications, 8 (1) 14133, 14133. doi: 10.1038/ncomms14133

SCIMP is a transmembrane non-TIR TLR adaptor that promotes proinflammatory cytokine production from macrophages

2025

Journal Article

Histone deacetylase 7 mediates lipopolysaccharide-inducible mitochondrial fission in macrophages

Abrol, Rishika, Afroz, Syeda Farhana, Curson, James E. B., Raven, Karoline D., Das Gupta, Kaustav, Gunther, Kimberley S., Jones, Alun, Reid, Robert C., Xiong, Zherui, Gunter, Jennifer H., Engel, Jessica A., Engwerda, Christian R., Blumenthal, Antje, Fairlie, David P., Parton, Robert G., Zuryn, Steven, Kapetanovic, Ronan, Ramnath, Divya and Sweet, Matthew J. (2025). Histone deacetylase 7 mediates lipopolysaccharide-inducible mitochondrial fission in macrophages. Journal of Cell Science, 138 (19) jcs.264376, 1-14. doi: 10.1242/jcs.264376

Histone deacetylase 7 mediates lipopolysaccharide-inducible mitochondrial fission in macrophages

2025

Journal Article

Emergence of a carbapenem-resistant atypical uropathogenic Escherichia coli clone as an increasing cause of urinary tract infection

Walker, Lachlan L., Phan, Minh-Duy, Permana, Budi, Lian, Zheng Jie, Nhu, Nguyen Thi Khanh, Cuddihy, Thom, Peters, Kate M., Ramsay, Kay A., Stewart, Chelsea, Pfennigwerth, Niels, Kidd, Timothy J., Harris, Patrick N. A., Paterson, David L., Sweet, Matthew J., Forde, Brian M. and Schembri, Mark A. (2025). Emergence of a carbapenem-resistant atypical uropathogenic Escherichia coli clone as an increasing cause of urinary tract infection. Nature Communications, 16 (1) 8200, 1-10. doi: 10.1038/s41467-025-63477-0

Emergence of a carbapenem-resistant atypical uropathogenic Escherichia coli clone as an increasing cause of urinary tract infection

2025

Journal Article

TLR4 endocytosis and endosomal TLR4 signaling are distinct and independent outcomes of TLR4 activation

Schultz, Thomas E., Mathmann, Carmen D., Domínguez Cadena, Leslie C., Muusse, Timothy W., Kim, Hyoyoung, Wells, James W., Ulett, Glen C., Hamerman, Jessica A., Brooks, Andrew J., Kobe, Bostjan, Sweet, Matthew J., Stacey, Katryn J. and Blumenthal, Antje (2025). TLR4 endocytosis and endosomal TLR4 signaling are distinct and independent outcomes of TLR4 activation. EMBO Reports, 26 (10) 2250056, 2740-2766. doi: 10.1038/s44319-025-00444-2

TLR4 endocytosis and endosomal TLR4 signaling are distinct and independent outcomes of TLR4 activation

2025

Journal Article

Rational design of advanced gene delivery carriers: Macrophage phenotype matters

Wang, Yue, Yao, Yining, Zhang, Yue, Yu, Yingjie, Luo, Jiangqi, Sweet, Matthew J. and Yu, Chengzhong (2025). Rational design of advanced gene delivery carriers: Macrophage phenotype matters. Advanced Materials, 37 (3) e2401504, 1-13. doi: 10.1002/adma.202401504

Rational design of advanced gene delivery carriers: Macrophage phenotype matters

2024

Journal Article

A novel inhibitor of class IIa histone deacetylases attenuates collagen‐induced arthritis

Poon, Eunice K., Liu, Ligong, Wu, Kai‐Chen, Lim, Junxian, Sweet, Matthew J., Lohman, Rink‐Jan, Iyer, Abishek and Fairlie, David P. (2024). A novel inhibitor of class IIa histone deacetylases attenuates collagen‐induced arthritis. British Journal of Pharmacology, 181 (23), 4804-4821. doi: 10.1111/bph.17306

A novel inhibitor of class IIa histone deacetylases attenuates collagen‐induced arthritis

2024

Journal Article

Histone deacetylase 7 activates 6-phosphogluconate dehydrogenase via an enzyme-independent mechanism that involves the N-terminal protein-protein interaction domain

Wang, Yizhuo, Curson, James E.B., Ramnath, Divya, Das Gupta, Kaustav, Reid, Robert C., Karunakaran, Denuja, Fairlie, David P. and Sweet, Matthew J. (2024). Histone deacetylase 7 activates 6-phosphogluconate dehydrogenase via an enzyme-independent mechanism that involves the N-terminal protein-protein interaction domain. Biochemical Journal, 481 (21), 1569-1584. doi: 10.1042/bcj20240380

Histone deacetylase 7 activates 6-phosphogluconate dehydrogenase via an enzyme-independent mechanism that involves the N-terminal protein-protein interaction domain

2024

Journal Article

The activity of early-life gene regulatory elements is hijacked in aging through pervasive AP-1-linked chromatin opening

Patrick, Ralph, Naval-Sanchez, Marina, Deshpande, Nikita, Huang, Yifei, Zhang, Jingyu, Chen, Xiaoli, Yang, Ying, Tiwari, Kanupriya, Esmaeili, Mohammadhossein, Tran, Minh, Mohamed, Amin R., Wang, Binxu, Xia, Di, Ma, Jun, Bayliss, Jacqueline, Wong, Kahlia, Hun, Michael L., Sun, Xuan, Cao, Benjamin, Cottle, Denny L., Catterall, Tara, Barzilai-Tutsch, Hila, Troskie, Robin-Lee, Chen, Zhian, Wise, Andrea F., Saini, Sheetal, Soe, Ye Mon, Kumari, Snehlata, Sweet, Matthew J. ... Nefzger, Christian M. (2024). The activity of early-life gene regulatory elements is hijacked in aging through pervasive AP-1-linked chromatin opening. Cell Metabolism, 36 (8), 1858-1881.e23. doi: 10.1016/j.cmet.2024.06.006

The activity of early-life gene regulatory elements is hijacked in aging through pervasive AP-1-linked chromatin opening

2024

Journal Article

A convergent evolutionary pathway attenuating cellulose production drives enhanced virulence of some bacteria

Nhu, Nguyen Thi Khanh, Rahman, M. Arifur, Goh, Kelvin G. K., Kim, Seung Jae, Phan, Minh-Duy, Peters, Kate M., Alvarez-Fraga, Laura, Hancock, Steven J., Ravi, Chitra, Kidd, Timothy J., Sullivan, Matthew J., Irvine, Katharine M., Beatson, Scott A., Sweet, Matthew J., Irwin, Adam D., Vukovic, Jana, Ulett, Glen C., Hasnain, Sumaira Z. and Schembri, Mark A. (2024). A convergent evolutionary pathway attenuating cellulose production drives enhanced virulence of some bacteria. Nature Communications, 15 (1) 1441, 1441. doi: 10.1038/s41467-024-45176-4

A convergent evolutionary pathway attenuating cellulose production drives enhanced virulence of some bacteria

2023

Journal Article

Apical extrusion prevents apoptosis from activating an acute inflammatory program in epithelia

Duszyc, Kinga, von Pein, Jessica B., Ramnath, Divya, Currin-Ross, Denni, Verma, Suzie, Lim, Fayth, Sweet, Matthew J., Schroder, Kate and Yap, Alpha S. (2023). Apical extrusion prevents apoptosis from activating an acute inflammatory program in epithelia. Developmental Cell, 58 (21), 2235-2248.e6. doi: 10.1016/j.devcel.2023.08.009

Apical extrusion prevents apoptosis from activating an acute inflammatory program in epithelia

2023

Journal Article

TLR4 phosphorylation at tyrosine 672 activates the ERK/c‐FOS signaling module for LPS‐induced cytokine responses in macrophages

Curson, James E. B., Liu, Liping, Luo, Lin, Muusse, Timothy W., Lucas, Richard M., Gunther, Kimberley S., Vajjhala, Parimala R., Abrol, Rishika, Jones, Alun, Kapetanovic, Ronan, Stacey, Katryn J., Stow, Jennifer L. and Sweet, Matthew J. (2023). TLR4 phosphorylation at tyrosine 672 activates the ERK/c‐FOS signaling module for LPS‐induced cytokine responses in macrophages. European Journal of Immunology, 53 (7) e2250056, e2250056. doi: 10.1002/eji.202250056

TLR4 phosphorylation at tyrosine 672 activates the ERK/c‐FOS signaling module for LPS‐induced cytokine responses in macrophages

2023

Journal Article

Histone deacetylase 7: a signalling hub controlling development, inflammation, metabolism and disease

Wang, Yizhuo, Abrol, Rishika, Mak, Jeffrey Y. W., Das Gupta, Kaustav, Ramnath, Divya, Karunakaran, Denuja, Fairlie, David P. and Sweet, Matthew J. (2023). Histone deacetylase 7: a signalling hub controlling development, inflammation, metabolism and disease. The FEBS Journal, 290 (11), 2805-2832. doi: 10.1111/febs.16437

Histone deacetylase 7: a signalling hub controlling development, inflammation, metabolism and disease

2023

Journal Article

Macrophage Nrf 2 the rescue

Stow, Jennifer L. and Sweet, Matthew J. (2023). Macrophage Nrf 2 the rescue. Journal of Cell Biology, 222 (6) e202305036. doi: 10.1083/jcb.202305036

Macrophage Nrf 2 the rescue

Funding

Current funding

  • 2026 - 2028
    How immune cells use zinc to combat infections
    ARC Discovery Projects
    Open grant
  • 2025 - 2026
    Think ZINC: Zinc immune-related Needs in Cystic fibrosis
    Cure4CF Foundation Research Grants
    Open grant
  • 2025 - 2027
    How immune cells use metabolism to respond to different threats
    ARC Discovery Projects
    Open grant
  • 2021 - 2026
    Reprogramming innate immunity to combat inflammatory and infectious diseases
    NHMRC Investigator Grants
    Open grant

Past funding

  • 2023 - 2025
    A novel, portable, low-cost oxygen therapy to improve wound healing using photosynthetic light (2023 RBWH Translational Research Grant administered by RBWH)
    Metro North Hospital and Health Service
    Open grant
  • 2023 - 2026
    Mitochondria as sensors of environmental threats
    ARC Discovery Projects
    Open grant
  • 2020 - 2022
    Improving the ability of CF macrophages to handle mycobacterium abscessus (MABS)
    Vertex Innovation Awards
    Open grant
  • 2020 - 2023
    Defining molecular links between immune cell metabolism and inflammation
    NHMRC IDEAS Grants
    Open grant
  • 2019
    In vivo imaging system for tracking inflammation, infection, cancer, pain and bioactive molecules
    UQ Major Equipment and Infrastructure
    Open grant
  • 2018
    Epifluorescent and live-cell imaging microscopes for the investigation of host-pathogen interactions and for molecular and cellular biology
    UQ Major Equipment and Infrastructure
    Open grant
  • 2018 - 2020
    The dual-edged sword of zinc as an innate immune antimicrobial weapon against uropathogenic E. coli
    NHMRC Project Grant
    Open grant
  • 2017 - 2024
    Drug targets for liver inflammation and fibrosis
    UniQuest Pty Ltd
    Open grant
  • 2017 - 2019
    Combating infectious diseases by harnessing macrophage functions
    NHMRC Project Grant
    Open grant
  • 2017 - 2019
    Demystifying histone deacetylase functions in immune cells
    ARC Discovery Projects
    Open grant
  • 2017 - 2021
    Understanding Uropathogenic E. coli-mediated subversion of innate immunity
    NHMRC Project Grant
    Open grant
  • 2016 - 2019
    A new master adaptor protein for Toll-like Receptor signalling
    NHMRC Project Grant
    Open grant
  • 2016
    Instrumentation for the analysis of cellular and metabolic phenotypes
    UQ Major Equipment and Infrastructure
    Open grant
  • 2016 - 2020
    Pattern Recognition Receptors in Inflammation and Infection
    NHMRC Research Fellowship
    Open grant
  • 2014
    Go8 European Fellowships - Dr Michaela Kindlova -
    Group of Eight European Fellowship
    Open grant
  • 2014 - 2016
    A matter of life and death: defining novel interactions between uropathogenic E. coli and macrophages that influence UTI pathology
    NHMRC Project Grant
    Open grant
  • 2014 - 2017
    Defining the role of zinc in human macrophage responses to Salmonella
    NHMRC Project Grant
    Open grant
  • 2014
    Leica TCS SP8 microscope
    UQ Major Equipment and Infrastructure
    Open grant
  • 2013 - 2015
    Defining the role of MMP-9-expressing macrophages in liver injury in chronic liver disease
    NHMRC Project Grant
    Open grant
  • 2013
    High throughput electrophysiology platform
    UQ Major Equipment and Infrastructure
    Open grant
  • 2013 - 2015
    How filopodia connect macrophages to the outside world
    ARC Discovery Projects
    Open grant
  • 2013 - 2015
    Inhibitors Of Class II HDACs In Inflammatory And Metabolic Disease
    NHMRC Project Grant
    Open grant
  • 2012 - 2013
    Overcoming membrane protein research roadblocks: A Queensland facility for membrane protein production and crystallisation
    ARC Linkage Infrastructure, Equipment and Facilities
    Open grant
  • 2012
    Analytical flow cytometer for cell and developmental biology and drug discovery applications
    UQ Major Equipment and Infrastructure
    Open grant
  • 2012 - 2014
    Profiling global inflammatory signatures for GPCRs in human macrophages
    NHMRC Project Grant
    Open grant
  • 2012
    Quantitave real-time PCR instrumentation for rapid, high-throughput gene expression studies.
    UQ Major Equipment and Infrastructure
    Open grant
  • 2011 - 2015
    NHMRC Research Fellowship (SRF A): Toll-like receptors and innate immunity: genes and pathways regulating infectious and inflammatory diseases
    NHMRC Research Fellowship
    Open grant
  • 2011 - 2015
    Toll-like Receptors in infectious and inflammatory diseases: the double-edged sword of innate immunity
    ARC Future Fellowships
    Open grant
  • 2011
    Real time cell analysis for biological and drug discovery applications
    UQ Major Equipment and Infrastructure
    Open grant
  • 2011 - 2014
    Role of macrophages in uropathogenic E. coli infections
    NHMRC Project Grant
    Open grant
  • 2010 - 2012
    Characterisation of human-specific anti-microbial pathways.
    NHMRC Project Grant
    Open grant
  • 2010
    Combinatorial chemistry (high throughput synthesizer and purification system)
    UQ Major Equipment and Infrastructure
    Open grant
  • 2010 - 2012
    Cytoplasmic DNA as a danger signal for mammalian cells.
    NHMRC Project Grant
    Open grant
  • 2010
    Establishment of a centralised live animal imaging fluorescence/bio-luminescence suite
    UQ Major Equipment and Infrastructure
    Open grant
  • 2010 - 2013
    Regulation of Bone Dynamics by Osteal Tissue Macrophages (Osteomacs)
    NHMRC Project Grant
    Open grant
  • 2010 - 2013
    The role of subgenomic non-coding viral RNA in flavivirus pathogenicity
    NHMRC Project Grant
    Open grant
  • 2009
    Analytical flow cytometer for high throughput cell biology and drug discovery applications
    UQ Major Equipment and Infrastructure
    Open grant
  • 2009 - 2011
    Towards selective targeting of HDACs for anti-inflammatory applications
    NHMRC Project Grant
    Open grant
  • 2008 - 2009
    Profiling the pro- and anti-inflammatory functions of histone deacetylases in macrophages
    Cancer Council Queensland
    Open grant
  • 2008 - 2010
    West Nile virus replication and host response
    NHMRC Project Grant
    Open grant
  • 2007 - 2009
    Design and use of human hematopoietic prostaglandin D2 synthase inhibitors in allergic asthma and bone diseases
    NHMRC Project Grant
    Open grant
  • 2007 - 2009
    Regulation and Function of TLR9
    NHMRC Project Grant
    Open grant
  • 2007 - 2011
    UQ Mid-Career Research Fellowship: Pathogen Surveillance and Immunity
    UQ Mid-Career Research Fellowship
    Open grant
  • 2005 - 2008
    Human macrophage transcriptional network
    Riken Genomic Sciences Center
    Open grant
  • 2004 - 2007
    The development of tyrosine kinase inhibitors for the treatment of inflammation and malignant disease.
    ARC Linkage Projects
    Open grant
  • 2004 - 2006
    Regulation Of Macrophage Function And Gene Expression By The Th2-Promoting Stimulus, ES-62
    NHMRC Project Grant
    Open grant
  • 2004 - 2006
    TLR9 And The Response To Foreign DNA
    NHMRC Project Grant
    Open grant
  • 2003 - 2006
    Gene expression profiling and de novo transcriptome sequencing using geneballs
    ARC Linkage Projects
    Open grant
  • 2001
    Mechanisms of action of the anti-inflammatory molecule ST2/T1 on macrophages.
    UQ Early Career Researcher
    Open grant
  • 1998 - 2002
    Bacterial DNA and DNA vaccines as regulators of macrophage function and as a therapeutic approach to Leishmania
    NHMRC C J Martin Fellowship
    Open grant

Supervision

Availability

Professor Matt Sweet is:
Available for supervision

Looking for a supervisor? Read our advice on how to choose a supervisor.

Available projects

  • TARGETING MAMMALIAN HDACs AS AN ANTI-INFECTIVE STRATEGY

    We have found that specific HDAC enzymes constrain macrophage antimicrobial responses, particularly TLR-inducible mitochondrial fission. This project will explore the specific molecular mechanisms by which HDACs constrain macrophage antimicrobial pathways and will investigate novel anti-infective approaches that target HDAC enzymes.

  • TARGETING TLR SIGNALLING PATHWAYS AS AN ANTI-INFLAMMATORY STRATEGY

    Projects are available to investigate different aspects of TLR-inducible inflammatory pathways in macrophages, for example the role of a novel TLR adaptor in macrophage inflammatory responses and HDAC-mediated control of metabolic pathways in macrophage-mediated inflammation.

  • CHARACTERIZING ZINC POISONING AS AN ANTIMICROBIAL WEAPON

    Innate immune cells deliver toxic levels of zinc to invading microorganisms as an antimicrobial strategy, with zinc-sensitive mutants of a number of pathogens compromised for defence against innate immune cells. This project will focus on the cellular and molecular mechanisms involved in initiation of this host defence pathway.

  • ORGANELLE-MEDIATED CONTROL OF INNATE IMMUNITY

    In addition to controlling energy production, mitochondria are key regulators of macrophage inflammatory and antimicrobial responses. Lipid droplets, which interact with and regulate mitochondria, have also been linked to specific innate immune functions. This project will explore the control of macrophage inflammatory and antimicrobial responses by mitochondria and lipid droplets.

  • CIRCADIAN CONTROL OF INNATE IMMUNITY

    The circadian clock is a conserved gene regulatory network that synchronizes physiological processes with daily fluctuations in sleep/wake cycles. The circadian clock is also an important regulator of immune responses to infection, and this project would explore the mechanisms by which circadian rhythm influences innate immune inflammatory and antimicrobial responses.

Supervision history

Current supervision

Completed supervision

Media

Enquiries

Contact Professor Matt Sweet directly for media enquiries about:

  • anti-infectives
  • anti-inflammatories
  • chronic liver disease
  • histone deacetylases
  • immune system
  • infectious diseases
  • inflammasomes
  • inflammation
  • Inflammatory diseases
  • macrophages
  • Salmonellosis
  • sepsis
  • toll-like receptors
  • urinary tract infections

Need help?

For help with finding experts, story ideas and media enquiries, contact our Media team:

communications@uq.edu.au