Instytut Podstawowych Problemów Techniki
Polskiej Akademii Nauk

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Jakub Pękalski

Institute of Physical Chemistry, Polish Academy of Sciences (PL)

Ostatnie publikacje
1.  Pękalski J., Żuk P.J., Kochańczyk M., Junkin M., Kellogg R., Tay S., Lipniacki T., Spontaneous NF-κB Activation by Autocrine TNFα Signaling: A Computational Analysis, PLOS ONE, ISSN: 1932-6203, DOI: 10.1371/journal.pone.0078887, Vol.8, No.11, pp.e78887-1-14, 2013

Streszczenie:
NF-κB is a key transcription factor that regulates innate immune response. Its activity is tightly controlled by numerous feedback loops, including two negative loops mediated by NF-κB inducible inhibitors, IκBα and A20, which assure oscillatory responses, and by positive feedback loops arising due to the paracrine and autocrine regulation via TNFα, IL-1 and other cytokines. We study the NF-κB system of interlinked negative and positive feedback loops, combining bifurcation analysis of the deterministic approximation with stochastic numerical modeling. Positive feedback assures the existence of limit cycle oscillations in unstimulated wild-type cells and introduces bistability in A20-deficient cells. We demonstrated that cells of significant autocrine potential, i.e., cells characterized by high secretion of TNFα and its receptor TNFR1, may exhibit sustained cytoplasmic–nuclear NF-κB oscillations which start spontaneously due to stochastic fluctuations. In A20-deficient cells even a small TNFα expression rate qualitatively influences system kinetics, leading to long-lasting NF-κB activation in response to a short-pulsed TNFα stimulation. As a consequence, cells with impaired A20 expression or increased TNFα secretion rate are expected to have elevated NF-κB activity even in the absence of stimulation. This may lead to chronic inflammation and promote cancer due to the persistent activation of antiapoptotic genes induced by NF-κB. There is growing evidence that A20 mutations correlate with several types of lymphomas and elevated TNFα secretion is characteristic of many cancers. Interestingly, A20 loss or dysfunction also leaves the organism vulnerable to septic shock and massive apoptosis triggered by the uncontrolled TNFα secretion, which at high levels overcomes the antiapoptotic action of NF-κB. It is thus tempting to speculate that some cancers of deregulated NF-κB signaling may be prone to the pathogen-induced apoptosis.

Afiliacje autorów:
Pękalski J. - Institute of Physical Chemistry, Polish Academy of Sciences (PL)
Żuk P.J. - inna afiliacja
Kochańczyk M. - IPPT PAN
Junkin M. - Eidgenössische Technische Hochschule Zürich (CH)
Kellogg R. - Eidgenössische Technische Hochschule Zürich (CH)
Tay S. - Eidgenössische Technische Hochschule Zürich (CH)
Lipniacki T. - IPPT PAN
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