Das Lab:Research

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'''Projects'' <br>
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'''How Competing Negative and Positive Feedbacks Regulate Lymphocyte Selection''' <br>
'''How Competing Negative and Positive Feedbacks Regulate Lymphocyte Selection''' <br>

Revision as of 14:35, 26 January 2013

Systems Immunology

Immune responses in metazoans involve hierarchical kinetic non-linear processes across multiple length and time scales from interaction between molecules to coordinated movements of immune cells in lymph nodes. Therefore, combining mathematical techniques designed to examine such complex systems with wet lab experiments is a necessary step to decipher mechanisms as well as to gain systems level understanding into the immune system. We use mathematical techniques based on statistical physics, engineering, and nonlinear dynamics in synergistic collaboration with our experimental colleagues to understand responses in innate and adaptive immune system. The focus of our current research are knowing, (i) how Natural Killer (NK) cells, an important player of our innate immunity providing resistance against viral infections and tumors, mount decisive (activation or tolerance) in response to diverse stimuli, (ii) the mechanisms underlying the interaction of membrane lipid metabolism with receptor signaling in shaping the T cell (a key orchestrator of our adaptive immunity) repertoire in mammals, (iii) the key regulators of the homeostatic relationship between the host immune system and the resident microbiota in the metazoan gut.


Projects

How Competing Negative and Positive Feedbacks Regulate Lymphocyte Selection

   T cells, key orchestrators of adaptive immunity, sense pathogen-derived antigen peptides through T cell receptors (TCRs) providing protection against pathogens and cancer cells. Developing T cells express TCRs of random antigen specificity that interact with self-peptides with a wide range of affinity. A strict selection process warrants generation of a functional, protective but self-tolerant T cell repertoire by removing T cell precursors failing to interact or stimulated strongly by self-peptides, and inducing survival and maturation for low-affinity/mild TCR signals. How different TCR signals can have such vastly different outcomes is ill understood. TCR engagement activates a complex signaling network with multiple hierarchical nonlinear processes. Among crucial TCR effectors, the oligomeric enzyme Interleukin-2 inducible T cell kinase (Itk) controls early (min scale) TCR signaling. Transient Itk activation is controlled by a positive feedback feeding into a negative feedback. Both are mediated by the soluble small messenger molecule inositol(1,3,4,5)tetrakisphosphate (IP4) generated via signal-dependent metabolism of membrane lipids (Huang et al, Science 2007). We combine computational modeling and biochemical experiments to elucidate the role of antigen affinity and Itk oligomerization in regulating duration and amplitude of Itk and T cell activation. Our results suggest that high affinity peptides cause strong but short-lived Itk activation necessary to induce downstream Ras and MAPK activation. Low affinity antigens cause prolonged Itk activation with smaller amplitudes. This is sufficient to activate Erk, an essential mediator for survival in developing T cells. Our findings also suggest that certain modes of Itk oligomerization can inhibit signaling by low-affinity peptides. Regulation of transient Itk activation by IP4 may point to a novel mechanism used by different cell signaling networks to generate specific functional decisions. In developing T cells, it may contribute to an enigmatic TCR signal splitter that determines whether TCR engagement causes death or survival and maturation.

    We are collaborating with Karsten Sauer's lab at the Scripps Insitute on this project.
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