Research Groups

Portrait Lutz Brusch

Lutz Brusch

Spatio-temporal pattern formation in cells and tissues

Previous and Current Research

Feedback regulation is ubiquitous in nature, starting already at the molecular scale and extending all the way up, often linking different spatial scales. Biological systems utilise feedback regulation to let structures and functions self-organise. Such self-organisation often defies our linear-pathway-trained intuition. Mathematical modelling, analysis and computer simulation closely iterated with quantitative experiments can therefore be a fruitful strategy for studying complex regulatory systems.

We have previously applied this theoretical approach in collaboration with experimentalists and found that feedback loops of effector recruitment and activity can couple different Rab GTPases on intracellular organelles in such a way that multistability self-organises (del Conte-Zerial et al., 2008). Therewith, membrane identity is robustly maintained despite of noise and perturbations but can also abruptly switch to a successive identity upon a super-threshold signal. This abrupt switch, as observed for instance in early to late endosome conversion, represents a novel type, termed cut-out switch, which differs from the canonical toggle switch by superposition of negative feedback upon the positive feedback loop and correspondingly novel switch behaviour. Such theoretical insight into biological switches was also applied in the design and analysis of biosynthetic computing circuits (Hayat et al., 2006). Currently, self-organising multistability and switches between different functional states are further explored for pancreas cell differentiation with implications for cell reprogramming in regenerative medicine (Zhou et al., 2011).

More complex spatio-temporal behaviour emerges when regulatory networks couple spatially distributed components. Along this line, a mechanistic model and analysis of ErbB signal transduction and gene regulation revealed that differentiation versus proliferation decisions of cells upon growth factor stimulation arise from spatially distributed signal processing (Nakakuki et al., 2010). We are currently also exploring how feedback regulation and spatio-temporal patterning control tissue morphogenesis and growth (Gin et al., 2010).

Throughout these projects, the mathematical models are inherently nonlinear and only fully disclose their secrets through advanced methods including dynamical systems theory and bifurcation analysis. We continuously develop such analysis methods further, in particular for nonlinear partial differential equation models.

Lutz Brusch research: figure
Fig.: A mechanistic mathematical model of an epithelial cyst (left) gives insight into how intraluminal ion concentration can drive and arrest cyst growth (right, curve shows model simulation compared to experimental data) through an interplay (left) of osmotic fluid transport, ion dilution and stretch-activated cell proliferation.
Future Projects and Goals

This theory group, in close collaborations with experimentalists, will further extend and apply systems biology approaches to uncover the regulatory mechanisms that underlie spatio-temporal patterning processes in cells and tissues.

Open questions that inspire our work are

  • Which capabilities does the eukaryotic cell gain from the closed regulatory loop between signal transduction and compartmentalisation/endocytosis?
  • How is hepatocyte polarity established and remodelled in the regenerating liver?
  • What kind of biochemical and/or biophysical signals does a growing, and moreover a regenerating, tissue feed back from the tissue/organ scale down to a single proliferating cell such that a robust organ size emerges?
Methodological and Technical Expertise
  • Mathematical modelling of processes in cells and tissues using Morpheus
  • Model analysis using dynamical systems theory, especially bifurcation analysis
  • Computer simulation and high performance computing
  • Data analysis and parameter estimation
Selected Publications

Meyer K, Ostrenko O, Bourantas G, Morales-Navarrete H, Porat-Shliom N, Segovia-Miranda F, Nonaka H, Ghaemi A, Verbavatz J-M, Brusch L, Sbalzarini I, Kalaidzidis Y, Weigert R, Zerial M.
A predictive 3D multi-scale model of biliary fluid dynamics in the liver lobule.
Cell Systems 2017; 4:277–290.

Rost F, Albors A R, Mazurov V, Brusch L, Deutsch A, Tanaka E M, Chara O.
Accelerated cell divisions drive the outgrowth of the regenerating spinal cord in axolotls.
eLife 2016; 5: e20357

Chara O, Tanaka EM, Brusch L.
Mathematical modeling of regenerative processes.
Curr. Top. Dev. Biol. 2014; 108: 283-317.

Rost F, Eugster C, Schröter C, Oates AC, Brusch L.
Chevron formation of the zebrafish muscle segments.
J. Exp. Biol. 2014; 217: 3870–3882.

de Back W, Zhou JX, Brusch L.
On the role of lateral stabilization during early patterning in the pancreas.
J. R. Soc. Interface 2012; 10: 20120766.


Since 2008
Group leader at Center for Information Services and High Performance Computing (ZIH), TU Dresden

Postdoctoral work at Center for High Performance Computing, TU Dresden

Postdoctoral work at Centre de Bioingenierie Gilbert Durand, Toulouse

PhD/Postdoctoral work at MPI-PKS, Dresden


Center for Information Services and High Performance Computing (ZIH)
Technische Universität Dresden
Nöthnitzer Straße 46
01062 Dresden