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- Models of Investigation
-
1. Antifungal innate immunity in C. elegans
- Dr. Jonathan Ewbank
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2. The anti-microbial defense of Drosophila: a paradigm for innate immunity
- Prof. Jules Hoffmann
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3. Phagocytosis in the fruit fly, Drosophila melanogaster
- Dr. Lynda Stuart
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4. Innate immune sensing and response
- Prof. Bruce Beutler
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5. Macrophages and systems biology
- Prof. David Hume
- Cell Types and Recruitment
-
6. Leukocyte recruitment in vivo
- Prof. Paul Kubes
-
8. Eosinophils
- Prof. Tim Williams
-
9. Dendritic cells: linking innate to different forms of adaptive immunity
- Prof. Ralph Steinman
-
11. Innate-like lymphocytes 1
- Prof. Adrian Hayday
-
12. Innate-like lymphocytes 2
- Prof. Adrian Hayday
- Recognition and Signaling
-
13. Colony stimulating factor-1 regulation of macrophages in development and disease
- Prof. E. Richard Stanley
-
14. Fc receptors: linking innate and acquired immunity
- Prof. Ken G C Smith
-
15. Phagocytosis
- Prof. Joel Swanson
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16. Clearance of apoptotic cells and the control of inflammation
- Prof. Sir John Savill
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17. Signaling by innate immune receptors
- Prof. Michael Karin
-
18. Nuclear receptors at the crossroads of inflammation and atherosclerosis
- Prof. Christopher Glass
- Modulation of Effector Responses
-
19. Humoral innate immunity and the acute phase response 1
- Prof. Alberto Mantovani
-
20. Humoral innate immunity and the acute phase response 2
- Prof. Alberto Mantovani
-
21. Cytokines regulating the innate response
- Prof. Anne O’Garra
-
22. Arginase and nitric oxide
- Dr. Peter Murray
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23. Novel lipid mediators in resolution of inflammation
- Prof. Charles Serhan
-
25. Cationic peptides in innate immunity
- Dr. Dawn Bowdish
-
26. Iron metabolism and innate immunity
- Prof. Tomas Ganz
- Pathogen-Host Interactions
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27. Innate recognition of viruses
- Prof. Caetano Reis e Sousa
-
28. Type I interferons in innate immunity to viral infections
- Prof. Christine Biron
-
29. HIV-1 and immunopathogenesis: innate immunity
- Prof. Luis Montaner
-
30. Understanding and combating tuberculosis
- Prof. David Russell
-
32. Innate immunity and malaria
- Prof. Douglas Golenbock
- Health and Disease
-
33. Innate immunity in children
- Prof. David Speert
-
34. From bench to bedside: evolution of anti-TNFalpha therapy in rheumatoid arthritis
- Prof. Sir Ravinder Maini
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35. NOD-like receptors in innate immunity and inflammatory disease
- Prof. Gabriel Nunez
-
36. Paneth cells in innate immunity and inflammatory bowel disease
- Prof. Satish Keshav
-
37. Innate immunity in the brain in health and disease
- Prof. V. Hugh Perry
-
38. The fate of monocytes in atherosclerosis
- Prof. Gwendolyn Randolph
-
39. Macrophages, a cellular toolbox used by tumors to promote progression and metastasis
- Prof. Jeffrey Pollard
- Archived Lectures *These may not cover the latest advances in the field
-
40. Monocyte/macrophages in innate immunity
- Prof. Emeritus Siamon Gordon
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41. Innate immunity in C. elegans
- Dr. Jonathan Ewbank
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43. NLR genes: infection, inflammation and vaccines
- Prof. Jenny Ting
-
44. Manipulation of innate immune response: lessons from shigella
- Prof. Philippe Sansonetti
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45. Innate immunity of the lung and adaptation to air breathing at birth
- Prof. Jeffrey Whitsett
Printable Handouts
Navigable Slide Index
- Introduction
- Iron is an essential trace metal
- Microbe mechanisms for iron uptake
- Iron sequestration
- Hepcidin causes hypoferremia
- Hypoferremia of infection: N.meningitidis in mice
- The effect of injection of iron transferrin
- Iron supplementations effects in humans
- Normal iron economy and iron in inflammation
- Properties of hepcidin
- Hepcidin mediates extracellular iron homeostasis
- Ferroportin
- Iron regulation by hepcidin
- Hepcidin binding to ferroportin
- Ferroportin regulation by hepcidin
- Hepcidin-ferroportin interaction
- The effect of low and high amounts of hepcidin
- Hepcidin regulation
- Regulation of hepcidin by inflammation
- Human response to IL-6
- Anemia of inflammation
- Hepcidin and anemia of inflammation
- mHepcidin and iron response - acute inflammation
- mHepcidin-1 response to chronic inflammation
- A model of "anemia of chronic disease" in cancer
- The tumor causes microangiopathy
- The effect of hepcidin in the mouse model
- Anemia of inflammation (1)
- Anemia of inflammation (2)
- Targeting anemia of inflammation
- Hepcidin and disease
- Hereditary hemochromatosis
- Hereditary hemochromatosis simplified
- Summary
- Acknowledgements
Topics Covered
- Iron is an essential element for nearly all infectious microorganisms as well as for their plant and animal hosts
- Within hours of infection, animals sequester iron within macrophages as well as in specialized extracellular proteins
- The cellular component of this response causes a marked decrease in extracellular iron concentration
- Hepcidin is a recently characterized peptide that functions as the homeostatic iron-regulatory hormone and as the mediator of inflammatory iron sequestration
- It acts by binding to the sole known cellular iron exporter, ferroportin, and inducing its internalization and degradation
- Pathological regulation or dysregulation of the hepcidin-ferroportin axis is responsible for a number of common iron-related disorders including anemia of inflammation, hereditary hemochromatosis and iron-loading anemias
- Update interview: Structural basis of the hepcidin-ferroportin interaction
- Update interview: Changes in iron status transcriptionally regulate hepcidin through the bone morphogenetic protein receptor (BMPR) pathway
- Update interview: BMP2 and BMP6 as the key ligands
- Update interview: Hepcidin synthesis is prominently modulated by erythropoiesis through erythroferrone
- Update interview: Iron is essential for clonal expansion of lymphocytes
- Update interview: Severe restriction of iron availability can be immunosuppressive
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Ganz, T. (2020, July 8). Iron metabolism and innate immunity [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/FSAE2408.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Tomas Ganz has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Update Available
The speaker addresses developments since the publication of the original talk. We recommend listening to the associated update as well as the lecture.
- Full lecture Duration: 26:48 min
- Update Interview Duration: 14:56 min
A selection of talks on Immunology
Transcript
Please wait while the transcript is being prepared...
0:00
I am Professor Tomas Ganz from the
Department of Medicine at the University
of California, Los Angeles.
I will speak to you today about "Iron
Metabolism and Innate Immunity".
0:12
Iron is an essential trace metal.
It is a component of oxygen carriers as
well as redox enzymes involved in energy
metabolism, nucleotide synthesis,
and other intermediary metabolism.
Iron is also essential for microbes and
it can be limiting for microbial growth.
0:30
During infection, microbes depend
on host derived iron to supply
themselves with this
essential trace element.
They use at least three different
mechanisms to obtain the iron
that they need.
They secrete small organic
molecules called siderophores,
which are potent iron chelators.
Once loaded with iron, the siderophores
are taken back up by the microbes and
the iron is utilized.
Microbes also have pumps that are capable
of transporting inorganic iron.
And finally, some microbes are also
capable of transporting host derived
ferroproteins and reutilizing their
iron for their own metabolic needs.
Taking advantage of the extreme
dependence of the invading
1:10
microorganisms on iron,
the host responds by sequestering iron,
making it more difficult for
the microbes to obtain it.
Intracellular microbes reside
within the phagocytic vacuole.
And this environment is subject to the
activity of Nramp1, an iron transporter,
which pumps iron from the phagocytic
vacuole to the cytoplasm.
This action is thought to decrease the
concentration of iron in the phagocytic
vacuole and makes it more difficult for
the microbes to get this
essential trace element.
Humans and animals with mutated
versions of Nramp1 are more susceptible
to intracellular microbes.
Extracellular microbes are subject
to the activity of host defense cell
derived lactoferrin and siderocalin,
two proteins which bind iron.
Lactoferrin binds ferric iron, and
siderocalin binds iron
within certain siderophores.
Regardless of which of these
two proteins acts, it deprives
the extracellular microbes of an essential
portion of their supply of iron.
The iron regulatory hormone hepcidin,
which is the main subject
of today's lecture,
acts on the transport mechanisms which
supply iron to the extracellular fluid.
Under the influence of hepcidin,
iron becomes depleted in the extracellular
fluid, making it again more difficult for
the microbes to obtain it.
This figure illustrates the effect
of hepcidin in a mouse.