Sixt Group
Morphodynamics of Immune Cells
Immune cells zip through our bodies at high speeds to fight off infections and diseases. The Sixt group works at the interface of cell biology and immunology to investigate how cells are able to migrate through tissues.
Most cells in our bodies are stationary, forming solid tissues and encapsulated organs. One exception are leukocytes, immune cells essential for both the innate and adaptive immune responses to infections. Leukocytes migrate with extraordinary speed and are used by the Sixt group as a model to study cell migration. The group works at the interface of cell biology, immunology, and biophysics, and aims to identify basic mechanistic principles that are equally important for developmental processes and cancer cells. One research focus is how the cell’s internal skeleton generates and transduces the force to change shape, move the cell body and interact with other cells. The group also investigates how cells navigate along guidance cues, specifically how they orient their polarity axis in response to chemotactic gradients. In their work, the members of the Sixt group combine genetics, pharmacology, micro-engineering, surface chemistry, and advanced imaging approaches, as well as in vivo imaging techniques.
Group Leader
Administrative Support
On this site:
Team
Current Projects
Environmental control of leukocyte migration | Cellular force generation and transduction | Interpretation of chemo-attractive gradients
Publications
Morandell J, Schwarz LA, Basilico B, Tasciyan S, Dimchev GA, Nicolas A, Sommer CM, Kreuzinger C, Dotter C, Knaus L, Dobler Z, Cacci E, Schur FK, Danzl JG, Novarino G. 2021. Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development. Nature Communications. 12(1), 3058. View
Leithner AF, Altenburger L, Hauschild R, Assen FP, Rottner K, TEB S, Diz-Muñoz A, Stein J, Sixt MK. 2021. Dendritic cell actin dynamics control contact duration and priming efficiency at the immunological synapse. Journal of Cell Biology. 220(4), e202006081. View
Gärtner FR, Sixt MK. 2021. Engaging the front wheels to drive through fibrous terrain. Developmental Cell. 56(6), 723–725. View
Vaahtomeri K, Moussion C, Hauschild R, Sixt MK. 2021. Shape and function of interstitial chemokine CCL21 gradients are independent of heparan sulfates produced by lymphatic endothelium. Frontiers in Immunology. 12, 630002. View
Düllberg CF, Auer A, Canigova N, Loibl K, Loose M. 2021. In vitro reconstitution reveals phosphoinositides as cargo-release factors and activators of the ARF6 GAP ADAP1. PNAS. 118(1), e2010054118. View
Career
since 2013 Professor, IST Austria
2010 – 2013 Assistant Professor, IST Austria
2008 – 2010 Endowed Professor, Peter Hans Hofschneider Foundation for Experimental Biomedicine
2005 – 2010 Group Leader, Max Planck Institute of Biochemistry, Martinsried, Germany
2003 – 2005 Postdoc, Institute for Experimental Pathology, Lund, Sweden
2003 MD, University of Erlangen, Germany
2002 Approbation in human Medicine
Selected Distinctions
2016 ERC Consolidator Grant
2014 EMBO Member
2013 European Biophysical Societies Association (EBSA) Young Investigator Medal
2013 Elected member of the Young Academy of the Austrian Academy of Sciences (ÖAW)
2012 Ignaz L. Lieben Award
2011 ERC Starting Grant
2011 FWF START Award
2008 Endowed Professor of the Peter Hans Hofschneider Foundation
2003 Novartis dissertation prize
