M. Dechesne R. Sepulchre

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Systems and models in chronobiology A delay model for the circadian rhythm M. Dechesne R. Sepulchre Department of Electrical Engineering and Computer Science Monteore Institute University of Liège 24th Benelux Meeting on Systems and Control Houalize, 22-24 March 2005

Outline Introduction Biological modeling for the circadian oscillator Results Systems viewpoint: Why is it useful? Application to the analysis of the circadian rhythm Conclusion

Introduction Outline Introduction Biological modeling for the circadian oscillator Results Systems viewpoint: Why is it useful? Application to the analysis of the circadian rhythm Conclusion

Introduction Circadian rhythms (1) Denition and roles Denition Biological rhythms with a period τ 24h Roles Circadian rhythms control Sleep Muscular activity and metabolism Food ingestion... Moreover, there are possible links with various pathologies

Introduction Circadian rhythms (2) Properties Property Comment Ubiquitous All eukaryotes and some prokaryotes Entrainment Zeitgeber=light/temperature cycles Genetic Single-gene clock mechanisms mutants isolated Precision τ < 0.1% Robustness T, IC... A cell-autonomous circadian oscillator Cellular nature mechanism exists and appears to be a fundamental unit even among multicellular organisms

Outline Introduction Biological modeling for the circadian oscillator Results Systems viewpoint: Why is it useful? Application to the analysis of the circadian rhythm Conclusion

Biological modeling for the circadian oscillator Simple model Biochemical principle!#"$#&%('( (P N ) v s V 1 V 3 k 2 k 1 (M) k s P ER 0 (P 0 ) P ER 1 (P 1 ) v m V 2 V 4 P ER 2 (P 2 ) v d from Goldbeter, Biochemical oscillations and cellular rhythms, Cambridge University Press, 1996

Biological modeling for the circadian oscillator Simple model Equations K n I Ṁ = v s K n I + P n N M v m k m + M Ṗ 0 = k s M V 1 P 0 K 1 + P 0 + V 2 P 1 K 2 + P 1 Ṗ 1 = V 1 P 0 K 1 + P 0 V 2 P 1 K 2 + P 1 V 3 P 1 K 3 + P 1 + V 4 P 2 K 4 + P 2 Ṗ 2 = V 3 P 1 K 3 + P 1 V 4 P 2 K 4 + P 2 k 1 P 2 + k 2 P N v d P 2 k d + P 2 Ṗ N = k 1 P 2 k 2 P N 5 nonlinear ODEs 17 parameters

Biological modeling for the circadian oscillator Evolutions of the model Drosophilia 10 nonlinear ODEs 34 parameters

Biological modeling for the circadian oscillator Evolutions of the model Drosophilia Mammals 10 nonlinear ODEs 34 parameters 19 nonlinear ODEs 59 parameters

Results Results (1) Oscillations and limit cycle Oscillations Limit Cycle

Results Results (2) Entrainment

Results Results (3) Bifurcation diagram

Systems viewpoint: Why is it useful? Outline Introduction Biological modeling for the circadian oscillator Results Systems viewpoint: Why is it useful? Application to the analysis of the circadian rhythm Conclusion

Systems viewpoint: Why is it useful? Limitations of current mathematical modeling Very complicated systems (strongly nonlinear, several variables and parameters) restricted to numerical simulations Impossible to test all parameter combinations Mathematically (and computationally) dicult to study interconnections Exhibit some properties, but NOT explain them

Systems viewpoint: Why is it useful? System approach Principle Developing or using system models and tools for the analysis of biological system (and particularly oscillatory systems)

Systems viewpoint: Why is it useful? System approach Links with system question By nature, cells are open systems, i.e. with inputs and outputs Many unexplained properties are related to fundamental systems questions: Why is there an entrainment? Why is the system robust to certain parameters variation (T, initial conditions...)? Why is it robust to molecular noise? And to external disturbance? How can we guess from observed properties, the values of unknown parameters? Why is there a synchronization in networks of oscillators? What kind of synchronized behaviour may we expect given a particular network conguration?

Application to the analysis of the circadian rhythm Outline Introduction Biological modeling for the circadian oscillator Results Systems viewpoint: Why is it useful? Application to the analysis of the circadian rhythm Conclusion

Application to the analysis of the circadian rhythm Recent approaches Classical methods for the analysis of limit cycles Limitations: either useless in high dimension (and so for interconnections) or unable to handle global treatment Abstract models Limitations: Acts more as a black box i.e. it is possible to obtain qualitative information, but no quantitative one. Development of new methods Monotone Systems (P. de Leenheer, D. Angeli, E. Sontag) Piecewise Linear Systems - PLS (J. Goncalves) Dissipative Systems (R. Sepulchre, G.B. Stan) = dedicated I/O approaches

Application to the analysis of the circadian rhythm Recent approaches Classical methods for the analysis of limit cycles Limitations: either useless in high dimension (and so for interconnections) or unable to handle global treatment Abstract models Limitations: Acts more as a black box i.e. it is possible to obtain qualitative information, but no quantitative one. Development of new methods Monotone Systems (P. de Leenheer, D. Angeli, E. Sontag) Piecewise Linear Systems - PLS (J. Goncalves) Dissipative Systems (R. Sepulchre, G.B. Stan) = dedicated I/O approaches

Application to the analysis of the circadian rhythm Recent approaches Classical methods for the analysis of limit cycles Limitations: either useless in high dimension (and so for interconnections) or unable to handle global treatment Abstract models Limitations: Acts more as a black box i.e. it is possible to obtain qualitative information, but no quantitative one. Development of new methods Monotone Systems (P. de Leenheer, D. Angeli, E. Sontag) Piecewise Linear Systems - PLS (J. Goncalves) Dissipative Systems (R. Sepulchre, G.B. Stan) = dedicated I/O approaches

Application to the analysis of the circadian rhythm A delay model for the circadian rhythm Variation on Goldbeter's model: 2 variables vs vm NL $ &%' &( θ NL K n I Ṁ = v s K n I + P n v mm Ṗ = v P M(t τ) m v d P "!# vd from T. olde Scheper and al., A Mathematical Model for the Intracellular Circadian Rhythm Generator, J. of Neuroscience, 1999

Application to the analysis of the circadian rhythm A delay model for the circadian rhythm Further simplication : 1 variable V H v = 0 + u 1 τs+1 y V 2 K y NL e sθ φ(u NL) u NL H NL K n I Ṁ = v s K n I + M(t τ) n v mm This model is equivalent to the famous Mackey and Glass' model for Red Blood Cell regulation

Conclusion Outline Introduction Biological modeling for the circadian oscillator Results Systems viewpoint: Why is it useful? Application to the analysis of the circadian rhythm Conclusion

Conclusion Conclusion and perspectives There remains many unsolved questions in the exploding eld of mathematical biology. Most of these are natural in the framework of systems modeling: synchronization, robustness, entrainment... Our research group currently develops methods based on an input/output approach to answer (some of) those questions and classify basic oscillatory mechanisms. We are tempting to analyze a new mechanism based on a delay and a specic regulatory nonlinearity in the feedback loop.

Conclusion Thank you Thank you for your attention... :-)