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Professor David Hume
Professor

David Hume

Email: 
Phone: 
+61 7 3443 7315

Overview

Background

The research interests of the Hume Laboratory centre on the biology of macrophages and osteoclasts. These are cells of haematopoietic origin that are closely related to each other but have distinctly different activities.

David Hume was a group leader at the Institute for Molecular Bioscience (1988-2007) and subsequently Director of the Roslin Institute at the University of Edinburgh in Scotland from 2007-2017. He is currently a Professorial Research Fellow at the Mater Research Institute-UQ, located at the Translational Research Institute

Availability

Professor David Hume is:
Available for supervision

Qualifications

  • Bachelor (Honours) of Science (Advanced), Australian National University
  • Doctor of Philosophy, Australian National University

Research interests

  • Macrophages Biology

    Professor David Hume is a Professorial Research Fellow at the Mater Research Institute-UQ located at the Translational Research Institute. He was previously Director of The Roslin Institute at the University of Edinburgh (2007-2017). From 1988-2007, he was at the Institute for Molecular Bioscience at the University of Queensland, serving as Deputy Director of the CRC for Chronic Inflammatory Diseases, and Director of the ARC Special Centre for Functional and Applied Genomics. At Mater, David co-leads the Macrophage Biology Research Group with Dr Kate Irvine. He has authored over 450 scientific publications and has supervised more than 55 PhD graduates. He is an international authority in genome sciences, with a particular focus on the function of macrophages—specialised cells of the immune system involved in innate immunity against infections, inflammatory disease and cancer. David’s research focusses on macrophages in normal growth, development and physiology, infectious disease resistance and progression and complications of inflammation. His lab investigates mechanisms that regulate the biological functions of macrophages and explores avenues to boost their normal function and/or limit the damage they cause in inflammatory and infectious diseases. He is also interested in the genetic variations in macrophage function between individuals that contribute to susceptibility to inflammatory and infectious diseases. David has been elected to Fellowships in the Royal Society of Edinburgh, the UK Academy of Medical Sciences and the Royal Society of Biology. Since 2000, he has been a leading member of the FANTOM Consortium, which has made extensive contributions to mammalian genome and transcriptome annotation. David has a 35 year track record of attracting major strategic funding (CRC for Chronic Inflammatory Disease, ARC Special Research Centre in Australia; BBSRC Institute Strategic Programmes, Wellcome Trust Centres, UK Agritech Centre and Bill and Melinda Gates Centre Foundation in the UK) as well as continuous research project funding from NHMRC, ARC, BBSRC, MRC and the Wellcome Trust. "I trained as a metabolic biochemist at the Australian National University, and was very fortunate to have a great mentor in Dr Maurie Weidemann. Throughout my career, I have tried to mentor others with the same level of enthusiasm and support given to me. Being a biological scientist in the early 21st century is very much like being a physical scientist in the early 20th century. Each day brings new technologies and completely unexpected discoveries. I believe that the most novel breakthroughs and advances in human medicine and biotechnology come from basic discovery science, and fundamental understanding of macrophage biology has been my research focus for the whole of my career. That said, the applications of that understanding to human disease are clear, especially in the areas of tissue repair and regenerative medicine, and I am committed to pursuing those applications to benefit patients."

Works

Search Professor David Hume’s works on UQ eSpace

627 works between 1976 and 2025

601 - 620 of 627 works

1984

Journal Article

Different colon-stimulating factors are detected by the interleukin-3 dependent cell-lines Fdc-Pl and 32D Cl-23

Hapel, A. J., Warren, H. S. and Hume, D. A. (1984). Different colon-stimulating factors are detected by the interleukin-3 dependent cell-lines Fdc-Pl and 32D Cl-23. Blood, 64 (4), 786-790.

Different colon-stimulating factors are detected by the interleukin-3 dependent cell-lines Fdc-Pl and 32D Cl-23

1984

Conference Publication

Assays for Interleukin-3 (Multi-Csf) Are Not Specific

Hapel, AJ, Warren, HS, Hume, DA, Allan, W and Osborne, JM (1984). Assays for Interleukin-3 (Multi-Csf) Are Not Specific. MARY ANN LIEBERT INC PUBL.

Assays for Interleukin-3 (Multi-Csf) Are Not Specific

1984

Journal Article

The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: Macrophages of endocrine organs

Hume, D. A., Halpin, D., Charlton, H. and Gordon, S. (1984). The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: Macrophages of endocrine organs. Proceedings of the National Academy of Sciences of the United States of America, 81 (13 I), 4174-4177. doi: 10.1073/pnas.81.13.4174

The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: Macrophages of endocrine organs

1984

Journal Article

The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: Macrophages of bone and associated connective tissue

Hume, D. A., Loutit, J. F. and Gordon, S. (1984). The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: Macrophages of bone and associated connective tissue. Journal of Cell Science, VOL. 66 (MAR), 189-194.

The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: Macrophages of bone and associated connective tissue

1983

Journal Article

Optimal conditions for proliferation of bone marrow‐derived mouse macrophages in culture: the roles of CSF‐1, serum, Ca2+, and adherence

Hume, David A. and Gordon, Siamon (1983). Optimal conditions for proliferation of bone marrow‐derived mouse macrophages in culture: the roles of CSF‐1, serum, Ca2+, and adherence. Journal of Cellular Physiology, 117 (2), 189-194. doi: 10.1002/jcp.1041170209

Optimal conditions for proliferation of bone marrow‐derived mouse macrophages in culture: the roles of CSF‐1, serum, Ca2+, and adherence

1983

Journal Article

The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: relationship between macrophages, langerhans cells, reticular cells, and dendritic cells in lymphoid and hematopoietic organs

Hume, David A., Robinson, Anne P., Macpherson, Gordon G. and Gordon, Siamon (1983). The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: relationship between macrophages, langerhans cells, reticular cells, and dendritic cells in lymphoid and hematopoietic organs. Journal of Experimental Medicine, 158 (5), 1522-1536. doi: 10.1084/jem.158.5.1522

The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: relationship between macrophages, langerhans cells, reticular cells, and dendritic cells in lymphoid and hematopoietic organs

1983

Journal Article

The production of oxygen-centered radicals by Bacillus-Calmette-Guerin-activated macrophages: an electron paramagnetic resonance study of the response to phorbol myristate acetate

Hume, David A., Gordon, Siamon, Thornalley, Paul J. and Bannister, Joe V. (1983). The production of oxygen-centered radicals by Bacillus-Calmette-Guerin-activated macrophages: an electron paramagnetic resonance study of the response to phorbol myristate acetate. Biochimica Et Biophysica Acta, 763 (3), 245-250. doi: 10.1016/0167-4889(83)90131-3

The production of oxygen-centered radicals by Bacillus-Calmette-Guerin-activated macrophages: an electron paramagnetic resonance study of the response to phorbol myristate acetate

1983

Journal Article

Immunohistochemical localization of a macrophage-specific antigen in developing mouse retina: phagocytosis of dying neurons and differentiation of microglial cells to form a regular array in the plexiform layers

Hume, D. A., Perry, V. H. and Gordon, S. (1983). Immunohistochemical localization of a macrophage-specific antigen in developing mouse retina: phagocytosis of dying neurons and differentiation of microglial cells to form a regular array in the plexiform layers. Journal of Cell Biology, 97 (1), 253-257. doi: 10.1083/jcb.97.1.253

Immunohistochemical localization of a macrophage-specific antigen in developing mouse retina: phagocytosis of dying neurons and differentiation of microglial cells to form a regular array in the plexiform layers

1983

Journal Article

Mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: identification of resident macrophages in renal medullary and cortical interstitium and the juxtaglomerular complex

Hume, David A. and Gordon, Siamon (1983). Mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: identification of resident macrophages in renal medullary and cortical interstitium and the juxtaglomerular complex. Journal of Experimental Medicine, 157 (5), 1704-1709. doi: 10.1084/jem.157.5.1704

Mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: identification of resident macrophages in renal medullary and cortical interstitium and the juxtaglomerular complex

1983

Journal Article

Urinary hormone levels: a population study of associations between steroid and catecholamine excretion rates

Summers, K. M., Harrison, G. A., Hume, D. A. and Palmer, C. D. (1983). Urinary hormone levels: a population study of associations between steroid and catecholamine excretion rates. Annals of Human Biology, 10 (2), 99-110. doi: 10.1080/03014468300006241

Urinary hormone levels: a population study of associations between steroid and catecholamine excretion rates

1983

Conference Publication

Immunohistochemical Localization of a Macrophage-Specific Antigen in Mouse-Tissues

Hume, DA and Gordon, S (1983). Immunohistochemical Localization of a Macrophage-Specific Antigen in Mouse-Tissues. PROC AUST BIOCHEMICAL SOC.

Immunohistochemical Localization of a Macrophage-Specific Antigen in Mouse-Tissues

1982

Journal Article

Regulation of Bone-Marrow Macrophage Proliferation

Hume, DA and Gordon, S (1982). Regulation of Bone-Marrow Macrophage Proliferation. Advances in Experimental Medicine and Biology, 155, 261-266.

Regulation of Bone-Marrow Macrophage Proliferation

1981

Journal Article

Concanavalin A-induced chemiluminescence in rat thymus lymphocytes. Its origin and role in mitogenesis

Hume, D. A., Wrogemann, K., Ferber, E., Kolbuchbraddon, M. E., Taylor, R. M., Fischer, H. and Weidemann, M. J. (1981). Concanavalin A-induced chemiluminescence in rat thymus lymphocytes. Its origin and role in mitogenesis. Biochemical Journal, 198 (3), 661-667. doi: 10.1042/bj1980661

Concanavalin A-induced chemiluminescence in rat thymus lymphocytes. Its origin and role in mitogenesis

1979

Journal Article

Rapid alterations in cellular morphology and plasma membrane structure induced in rat thymocytes by mitogenic stimuli

Hume, David A., Thornton, Mary R., Weidemann, Maurice J. and Speth, Volker (1979). Rapid alterations in cellular morphology and plasma membrane structure induced in rat thymocytes by mitogenic stimuli. Journal of Cellular Physiology, 101 (3), 523-528. doi: 10.1002/jcp.1041010318

Rapid alterations in cellular morphology and plasma membrane structure induced in rat thymocytes by mitogenic stimuli

1979

Journal Article

Role and Regulation of Glucose-Metabolism in Proliferating Cells

Hume, DA and Weidemann, MJ (1979). Role and Regulation of Glucose-Metabolism in Proliferating Cells. Journal of the National Cancer Institute, 62 (1), 3-3.

Role and Regulation of Glucose-Metabolism in Proliferating Cells

1979

Journal Article

Preferential inhibition by quercetin of mitogen-stimulated thymocyte glucose transport

Hume, D. A., Weidemann, M. J. and Ferber, E. (1979). Preferential inhibition by quercetin of mitogen-stimulated thymocyte glucose transport. Journal of the National Cancer Institute, 62 (5), 1243-1249. doi: 10.1093/jnci/62.5.1243

Preferential inhibition by quercetin of mitogen-stimulated thymocyte glucose transport

1979

Journal Article

Role and regulation of glucose metabolism in proliferating cells

Hume, D. A. and Weidemann, M. J. (1979). Role and regulation of glucose metabolism in proliferating cells. Journal of the National Cancer Institute, 62 (1), 3-8. doi: 10.1093/jnci/62.1.3

Role and regulation of glucose metabolism in proliferating cells

1979

Journal Article

Preferential Inhibition by Quercetin of Mitogen-Stimulated Thymocyte Glucose-Transport

Hume, DA, Weidemann, MJ and Ferber, E (1979). Preferential Inhibition by Quercetin of Mitogen-Stimulated Thymocyte Glucose-Transport. Journal of the National Cancer Institute, 62 (5), 1243-1246.

Preferential Inhibition by Quercetin of Mitogen-Stimulated Thymocyte Glucose-Transport

1978

Journal Article

Aerobic glycolysis and lymphocyte transformation

Hume, David A., Radik, Judith L., Ferber, Ernst and Weidemann, Maurice J. (1978). Aerobic glycolysis and lymphocyte transformation. Biochemical Journal, 174 (3), 703-709. doi: 10.1042/bj1740703

Aerobic glycolysis and lymphocyte transformation

1978

Journal Article

On the stimulation of rat thymocyte 3‐0‐methyl‐glucose transport by mitogenic stimuli

Hume, David A. and Weidemann, Maurice J. (1978). On the stimulation of rat thymocyte 3‐0‐methyl‐glucose transport by mitogenic stimuli. Journal of Cellular Physiology, 96 (3), 303-308. doi: 10.1002/jcp.1040960305

On the stimulation of rat thymocyte 3‐0‐methyl‐glucose transport by mitogenic stimuli

Funding

Current funding

  • 2024 - 2027
    A macrophage-centric holistic view of postnatal development
    ARC Discovery Projects
    Open grant
  • 2022 - 2026
    Macrophage Biology in Health and Disease
    NHMRC Investigator Grants
    Open grant

Past funding

  • 2021 - 2024
    Macrophage control of mammalian growth and development
    ARC Discovery Projects
    Open grant
  • 2019 - 2021
    Macrophage biology, inflammatory pathophysiology, transcriptional regulation, genetic analytics and clinical genetics
    Mater Foundation
    Open grant
  • 2019 - 2022
    CSF1 Therapy for Chronic Liver Disease
    NHMRC Project Grant
    Open grant
  • 2019 - 2021
    CSF1R and the control of microglial function
    NHMRC Project Grant
    Open grant
  • 2018 - 2020
    Osteal macrophages as therapeutic targets for fracture repair
    NHMRC Project Grant
    Open grant
  • 2008 - 2009
    Profiling the pro- and anti-inflammatory functions of histone deacetylases in macrophages
    Cancer Council Queensland
    Open grant
  • 2007 - 2010
    Cellular Activation and Apoptosis in Response to Foreign Cytoplasmic DNA
    NHMRC Project Grant
    Open grant
  • 2007 - 2008
    Regulation of human fibrillin genes in cardiovascular disease
    National Heart Foundation of Australia
    Open grant
  • 2007 - 2009
    Role of bone-associated macrophages in bone remodelling and bone disease
    NHMRC Project Grant
    Open grant
  • 2007 - 2009
    The c-type lectin, Mincle, is a macrophage receptor for Candida albicans.
    NHMRC Project Grant
    Open grant
  • 2006 - 2008
    Molecular genetics of the host response defect in cystic fibrosis
    NHMRC Project Grant
    Open grant
  • 2006 - 2007
    The role of DEP-1 as a tumour suppressor in breast cancer
    Queensland Cancer Fund
    Open grant
  • 2005 - 2008
    Human macrophage transcriptional network
    Riken Genomic Sciences Center
    Open grant
  • 2005
    Developmental Imaging Facility
    ARC Linkage Infrastructure, Equipment and Facilities
    Open grant
  • 2005 - 2007
    Transcription control of the c-fms gene
    NHMRC Project Grant
    Open grant
  • 2004 - 2011
    Dynamic Imaging Facility for Cancer Biology
    Australian Cancer Research Foundation
    Open grant
  • 2004 - 2007
    The development of tyrosine kinase inhibitors for the treatment of inflammation and malignant disease.
    ARC Linkage Projects
    Open grant
  • 2004
    ARC Research Network in Microarray Technology
    ARC Seed Funding for Research Networks
    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
  • 2003
    Agilent Microarray Scanner
    NHMRC Equipment Grant
    Open grant
  • 2003
    Alternative Splicing in the Mouse Transcriptome
    ARC Discovery Projects
    Open grant
  • 2003 - 2004
    Migration And Differentiation Of Dendritic Cells And Monocytes In Inflammatory Arthritis
    NHMRC Project Grant
    Open grant
  • 2003 - 2005
    Molecular genetics of cystic fibrosis
    NHMRC Project Grant
    Open grant
  • 2003 - 2005
    Molecular Genetics Of Macrophage Activation
    NHMRC Project Grant
    Open grant
  • 2003 - 2005
    Molecular genetics of macrophage activation
    NHMRC Project Grant - Standard
    Open grant
  • 2003
    Molecular Regulators of Cytokine Secretion
    University of Queensland Research Development Grants Scheme
    Open grant
  • 2003
    Targeted Structural Genomics of Macrophage Proteins
    University of Queensland Research Development Grants Scheme
    Open grant
  • 2002 - 2006
    Towards Renal Regeneration
    United States National Institutes of Health
    Open grant
  • 2002 - 2008
    Education and training program
    CRC for Chronic Inflammatory Diseases
    Open grant
  • 2002 - 2008
    Office
    CRC for Chronic Inflammatory Diseases
    Open grant
  • 2002 - 2008
    Research Program 1
    CRC for Chronic Inflammatory Diseases
    Open grant
  • 2002 - 2008
    Research Program 2
    CRC for Chronic Inflammatory Diseases
    Open grant
  • 2002 - 2008
    Research Program 3
    CRC for Chronic Inflammatory Diseases
    Open grant
  • 2002 - 2008
    Research Program 4
    CRC for Chronic Inflammatory Diseases
    Open grant
  • 2002 - 2008
    Research Program 5
    CRC for Chronic Inflammatory Diseases
    Open grant
  • 2002
    Defining the human and mammalian methylomes and implications for medical research
    University of Queensland Research Development Grants Scheme
    Open grant
  • 2002 - 2004
    Osteoclast-specific gene regulation
    NHMRC Project Grant
    Open grant
  • 2002 - 2004
    Transciptional regulation of the c-fms (CFS-1R) gene in macrophages
    NHMRC Project Grant
    Open grant
  • 2001 - 2002
    Transgenic animal studies of the function of artificial zinc finger transcription factors
    Sangamo Biosciences Inc.
    Open grant
  • 2001 - 2002
    Approaches to manipulating the expression of the c-fms gene
    Sangamo Biosciences Inc.
    Open grant
  • 2001
    MJ Research Tetrad - 4 x 96well block thermocycler
    Ramaciotti Foundation
    Open grant
  • 2000
    Control of osteociast differentiation
    Mayne Bequest Fund
    Open grant
  • 2000 - 2002
    Genes controlling the development of lung disease in cystic fibrosis mutant mice
    NHMRC Project Grant
    Open grant
  • 2000 - 2002
    Mechanisms of macrophage activation by immunostimulatory DNA
    NHMRC Project Grant
    Open grant
  • 2000
    Regulation of the Tartrate-Resistant Acid Phosphatase Gene.
    ARC Australian Research Council (Small grants)
    Open grant
  • 2000 - 2002
    The role of the microphthalmia transcription factor family in macrophage differentiation
    NHMRC Project Grant
    Open grant
  • 1999 - 2001
    Genetic interactions that regulate the response of macrophages to bacterial lipopolysaccharide
    Merck Genome Research Institute
    Open grant
  • 1999
    Function and regulation of the tartrate resistant acid phosphatase gene
    Mayne Bequest Fund
    Open grant
  • 1999 - 2001
    Human tartrate-resistant purple acid phosphatase: structure and function
    NHMRC Project Grant
    Open grant
  • 1999
    Mechanisms of action of CpG DNA as an activator of macrophage function
    Mayne Bequest Fund
    Open grant
  • 1999 - 2000
    Signal transduction from the macrophage colony-stimulating factor receptor
    Queensland Cancer Fund
    Open grant
  • 1999 - 2000
    Transcriptional regulation of the macrophage colony stimulating factor receptor (c-fms) gene
    NHMRC Project Grant
    Open grant
  • 1998 - 2000
    Transcriptional Regulation of the Macrophage Colony Stimulating Factor Receptor (c-fms) Gene
    NHMRC Project Grant
    Open grant
  • 1997 - 1998
    Crystallisation of tartrate resistant acid phosphatase
    Johnson & Johnson Research Pty Ltd
    Open grant
  • 1997
    Regulation of the HIV-1-LTR in macrophages
    NHMRC Extended Epidemiology Project Grant
    Open grant
  • 1997
    Development of candidate drugs for the treatment of osteoporosis
    Merck Sharp & Dohme Australia
    Open grant
  • 1997 - 1999
    Genes controlling the development of lung disease in normal and cystic fibrosis mice
    NHMRC Project Grant
    Open grant
  • 1997
    Microplate counting system
    NHMRC Equipment Grant
    Open grant
  • 1997
    Microplate counting system.
    Ramaciotti Foundation
    Open grant
  • 1996
    Macrophage DNA recepter project.
    CRC for Vaccine Technology
    Open grant
  • 1996 - 1998
    Function and regulation of the tartrate-resistant acid phosphatase gene
    NHMRC Project Grant
    Open grant
  • 1996 - 1998
    Protein tyrosine phosphatases in macrophages
    Queensland Cancer Fund
    Open grant
  • 1996 - 1998
    Regulation of the urokinase plasminogen activator gene by macrophaghe colony-stimulating factor
    NHMRC Project Grant
    Open grant
  • 1996
    Zeiss axiophot microscope
    NHMRC Equipment Grant
    Open grant
  • 1995 - 1997
    Regulation of HIV-1-LTR in macrophages
    NHMRC Project Grant - HIV/AIDS (CARG)
    Open grant
  • 1995 - 1997
    The role of c-fms and macrophage colony stimulating factor (CSF-1) in tumor progression
    Queensland Cancer Fund
    Open grant

Supervision

Availability

Professor David Hume is:
Available for supervision

Before you email them, read our advice on how to contact a supervisor.

Available projects

  • The role of macrophages in postnatal development

    This project is associated with a successful ARC Discovery Grant and builds upon the discovery that mutation in the CSF1R gene, which controls the deveelopment of macrophages, has severe impacts on postnatal growth and organ development (See paper below). The phenotype can be reversed by transfer of wild-type bone marrow. The PhD project will focus on analysing the precose mechanisms that enable transplanted macrophages to restore normal development. It will develop a wide range of skills in the braod areas of cell and developmental biology, genomics and bioinformatics.

    Enquiries to david.hume@uq.edu.au or Katharine.Irvine@uq.edu.au

    Keshvari S, Caruso M, Teakle N, Batoon L, Sehgal A, Patkar OL, Ferrari-Cestari M, Snell CE, Chen C, Stevenson A, Davis FM, Bush SJ, Pridans C, Summers KM, Pettit AR, Irvine KM, Hume DA.

    CSF1R-dependent macrophages control postnatal somatic growth and organ maturation. PLoS Genet. 2021 Jun 3;17(6):e1009605. doi: 10.1371/journal.pgen.1009605. Online ahead of print.PMID: 34081701

Supervision history

Current supervision

Completed supervision

Media

Enquiries

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