Molecular Medicine Partnership Unit

 

Iron homeostasis in health and disease

Matthias Hentze and Martina Muckenthaler
Matthias Hentze and Martina Muckenthaler


Martina Muckenthaler and Matthias W. Hentze

Project Summary

As an essential nutrient and a potential toxin, iron poses an exquisite regulatory problem in biology and medicine. Disturbances of the delicate balancing systems for systemic and/or local iron homeostasis are emerging as underlying causes of common hematological, metabolic and neurodegenerative diseases. Our research aims to understand the physiological control of cellular and systemic iron metabolism and its disturbances in human disease

 

Background

Iron is essential for fundamental metabolic processes in cells and organisms. Regulation of systemic iron homeostasis evolved to maintain a plasma iron concentration that secures adequate supplies while preventing organ iron overload. The homeostatic system must react to signals from pathways that consume iron (e.g. the erythropoiesis) and send signals to cells that supply iron (e.g. duodenal enterocytes, which absorb iron from the diet; macrophages which recycle iron from senescent erythrocytes, and hepatocytes which are the major iron stores). The small hepatic peptide hormone hepcidin (Hamp, LEAP1) orchestrates these iron fluxes and controls the amount of available extracellular iron by interacting with the iron exporter ferroportin: binding of hepcidin induces ferroportin internalization and degradation.

 

Goals

Recent research started to move towards network/systems-based analysis of iron metabolism by integrating DNA microarray approaches, mouse models and high through-put siRNA screens. The overall aim is a more detailed understanding of regulatory mechanisms involved in iron homeostasis and the identification of novel regulators of iron metabolism. We then aim to translate new results into understanding human disease and to contribute to clinical patient management.

Specifically, we plan to investigate three themes:

  1. molecular mechanisms underlying hereditary hemochromatosis;
  2. signalling pathways underlying hepcidin regulation and
  3. the hepcidin/ferroportin regulatory system.

 

 

Research Focus 1

Hereditary hemochromatosis

One research focus of our lab aims to investigate molecular mechanisms underlying hereditary hemochromatosis. Using conditional Hfe knock-out mouse lines we will investigate hepatic as well as extra-hepatic functions of the broadly expressed Hfe protein. 
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Research Focus 2

Hepcidin regulation

We further focus on the identification of signalling pathways underlying hepcidin regulation. High-throughput siRNA screening is applied to identify novel regulators of hepcidin expression. 

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Research Focus 3

Hepcidin-mediated ferroportin regulation 

A third research focus is on the identification of molecular mechanisms that control hepcidin-mediated ferroportin regulation. 

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Research Focus 4

MicroRNAs in iron metabolism

Identification of the role of microRNAs in iron metabolism 
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Important publications

Opens external link in new windowComputerized image analysis of iron-stained macrophages.
Benesova K, Schaefer SM, Mall MA, Muckenthaler MU
Ann Hematol 2013 Sep;92(9):1195-9. doi: 10.1007/s00277-013-1740-2. Epub 2013 Apr 17

 

Opens external link in new windowMycn and hdac2 cooperate to repress mir-183 signaling in neuroblastoma
Lodrini M, Oehme I, Schroeder C, Milde T, Schier MC, Kopp-Schneider A, Schulte JH, Fischer M, De Preter K, Pattyn F, Castoldi M, Muckenthaler MU, Kulozik AE, Westermann F, Witt O, Deubzer HE
Nucleic Acids Res 2013 Jul; 41:6018-6033

 

Opens external link in new windowNotch1 activation clinically antagonizes the unfavorable effect of pten inactivation in bfm-treated children with precursor t-cell acute lymphoblastic leukemia.
Bandapalli OR, Zimmermann M, Kox C, Stanulla M, Schrappe M, Ludwig WD, Koehler R, Muckenthaler MU, Kulozik AE
Haematologica 2013 Jun;98:928-936

 

Opens external link in new windowIron refractory iron deficiency anemia.
De Falco L, Sanchez M, Silvestri L, Kannengiesser C, Muckenthaler MU, Iolascon A, Gouya L, Camaschella C, Beaumont C
Haematologica 2013 Jun;98:845-853

 

Opens external link in new windowThe murine growth differentiation factor 15 is not essential for systemic iron homeostasis in phlebotomized mice
Casanovas G, Spasic MV, Casu C, Rivella S, Strelau J, Unsicker K, Muckenthaler MU.
Haematologica. 2013 Mar;98(3):444-7. doi: 10.3324/haematol.2012.069807. Epub 2012 Sep 14

 

Opens external link in new windowNovel mutations in the ferritin-l iron-responsive element that only mildly impair irp binding cause hereditary hyperferritinaemia cataract syndrome.
Luscieti S, Tolle G, Aranda J, Campos CB, Risse F, Moran E, Muckenthaler MU, Sanchez M
Orphanet J Rare Dis 2013 Feb 19;8:30

 

Opens external link in new windowSmad6 and smad7 are co-regulated with hepcidin in mouse models of iron overload.
Vujic Spasic M, Sparla R, Mleczko-Sanecka K, Migas MC, Breitkopf-Heinlein K, Dooley S, Vaulont S, Fleming RE, Muckenthaler MU
Biochim Biophys Acta 2013 Jan;1832:76-84

 

Opens external link in new windowPegylated interferon-α induced hypoferremia is associated with the immediate response to treatment in hepatitis C.
Ryan JD, Altamura S, Devitt E, Mullins S, Lawless MW, Muckenthaler MU, Crowe J.
Hepatology. 2012 Aug;56(2):492-500. doi: 10.1002/hep.25666. Epub 2012 Jun 11

 

Opens external link in new windowHfe deficiency impairs pulmonary neutrophil recruitment in response to inflammation.
Benesova K, Vujić Spasić M, Schaefer SM, Stolte J, Baehr-Ivacevic T, Waldow K, Zhou Z, Klingmueller U, Benes V, Mall MA, Muckenthaler MU.
PLoS One. 2012;7(6):e39363. Epub 2012 Jun 21

 

Opens external link in new windowThe hemochromatosis proteins HFE, TfR2, and HJV form a membrane-associated protein complex for hepcidin regulation.
D'Alessio F, Hentze MW, Muckenthaler MU.
J Hepatol. 2012 Jun 21.

 

Opens external link in new windowRegulation of iron homeostasis by microRNAs.
Castoldi M, Muckenthaler MU.
Cell Mol Life Sci. 2012 Jun 9.

 

Opens external link in new windowQuantitative magnetic analysis reveals ferritin-like iron as the most predominant iron-containing species in the murine Hfe-haemochromatosis.
Gutiérrez L, Vujić Spasić M, Muckenthaler MU, Lázaro FJ.
Biochim Biophys Acta. 2012 Jul;1822(7):1147-53. Epub 2012 Mar 20.

 

Opens external link in new windowIron regulatory protein-1 and -2: transcriptome-wide definition of binding mRNAs and shaping of the cellular proteome by IRPs.
Sanchez, M., B. Galy, B. Schwanhaeusser, J. Blake, T. Bähr-Ivacevic, V. Benes, M. Selbach, M.U. Muckenthaler and M.W. Hentze.
Blood 118: e168-79, Nov 2011 

 

Opens external link in new windowGrowth differentiation factor 15 in patients with congenital dyserythropoietic anaemia (CDA) type II.
Casanovas G, Swinkels DW, Altamura S, Schwarz K, Laarakkers CM, Gross HJ, Wiesneth M, Heimpel H, Muckenthaler MU.
J Mol Med (Berl). 2011 Aug;89(8):811-6

 

Opens external link in new windowThe liver-specific microRNA miR-122 controls systemic iron homeostasis in mice.
Castoldi M, Vujić Spasić M, Altamura S, Elmén J, Lindow M, Kiss J, Stolte J, Sparla R, D'Alessandro LA, Klingmüller U, Fleming RE, Longerich T, Gröne HJ, Benes V, Kauppinen S, Hentze MW, Muckenthaler MU.
J Clin Invest. 2011 Apr 1;121(4):1386-96

 

Opens external link in new windowSystems analysis of iron metabolism: the network of iron pools and fluxes. 
Lopes TJ, Luganskaja T, Vujić Spasić M, Hentze MW, Muckenthaler MU, Schümann K, Reich JG 
BMC Syst Biol. 2010 Aug 13;4:112

 

Opens external link in new windowTwo to tango: regulation of mammalian iron metabolism
Hentze, M.W., M.U. Muckenthaler, B. Galy and C. Camaschella. 
Cell 142, 24-38, 2010

 

Opens external link in new windowThe IronChip evaluation package: a package of perl modules for robust analysis of custom microarrays. 
Vainshtein, Y., M. Sanchez, A. Brazma, M.W. Hentze, T. Dandekar and M.U. Muckenthaler. 
BMC Bioinf. 11, 112, 2010

 

Opens external link in new windowSMAD7 controls iron metabolism as a potent inhibitor of hepcidin expression
Mleczko-Sanecka, K., G. Casanovas, A. Ragab, K. Breitkopf, M. Boutros, S. Dooley, M.W. Hentze and M.U. Muckenthaler. 
Blood
 115, 2657-2665, 2010 

 

Opens external link in new windowBone morphogenetic protein (BMP)-responsive elements located in the proximal and distal hepcidin promoter are critical for its response to HJV/BMP/SMAD
Casanovas G, Mleczko-Sanecka K, Altamura S, Hentze MW, Muckenthaler MU. 
J Mol Med
. 2009 Feb; 87, 471-480

 

Opens external link in new windowHfe acts in hepatocytes to prevent hemochromatosis
Maja Vujić Spasić, Judit Kiss, Thomas Herrmann, Bruno Galy, Stefanie Martinache, Jens Stolte, Hermann-Josef Gröne, Wolfgang Stremmel, Matthias W. Hentze and Martina U. Muckenthaler
Cell Metabolism 2008 Feb;7(2):173-8

 

Opens external link in new windowCa2+ channel blockers reverse iron overload by a novel mechanism via divalent metal transporter (DMT)-1.
Ludwiczek, S., I. Theurl, M. U. Muckenthaler, M. Jakab, S. Mair, M. Theurl, M. Paulmichl, M.W. Hentze, M. Ritter and G. Weiss. 
Nature Medicine 2007 Apr;13(4):448-54

 

 Opens external link in new windowSTAT-3 mediates hepatic hepcidin expression and its inflammatory stimulation
Verga Falzacappa, M.V., Vujic Spasic, M., Hess, R., Stolte, J., Hentze, M.W. and Muckenthaler, M.U. 
Blood
 2007 Jan 1;109(1):353-8

 

 Opens external link in new windowPhysiologic systemic iron metabolism in mice deficient for duodenal Hfe
Vujic Spasic, M., Kiss, J., Herrmann, T., Hess, R., Stolte, J., Galy, B., Rathkolb, B., Wolf, E., Stremmel, W., Hentze, M.W. and Muckenthaler, M.U. 
Blood
 2007 May 15;109(10):4511-7. Epub 2007 Jan 30

 

Opens external link in new windowPrevious publications

 

Opens external link in new windowResearch group's MMPU link to EMBL web page

 

 

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