Y. Representative oscillations are shown on the right. This representation shows overall oscillation pattern. There is no change in the oscillation frequency by changing N/C ratios which is seen by a regular color interval among different N/C ratios. The damping of the oscillation is faster in smaller N/C volume ratios which is supported by disappearance of the periodic color change at the later time in smaller N/C ratios. At higher N/C ratios, however, the oscillation lasts for more than 10 hrs. (B) There is no change in the oscillation frequency (f) with changes in the N/C ratio. (C) The amplitude of the first peak (A0) becomes smaller at larger N/C values. (D) The time to the first peak (tfp) also stays almost unchanged by the change in N/C. (E) The decay time constants of the peaks (tp) and successive amplitudes (td) of oscillation becomes larger at larger N/C ratios. tp and td at larger N/Cs could not be extracted from the simulated oscillation. doi:10.1371/journal.pone.0046911.gIt is clearly seen that all characterizing parameters possess different sensitivities to different spatial parameters. For example, f possesses positive and negative sensitivity to nuclear transport and D, respectively, while it is insensitive to N/C ratios. On the other hand, A0 are negatively sensitive to N/C ratio. Its sensitivity to nuclear transport and D is slightly positive. The sensitivity of the first peak tfp to N/C ratio is slightly positive, and tp and td have the 
same tendency toward positive or negative sensitivity to the same spatial parameters. It is also clearly seen that each characterizing Castanospermine web parameter possesses insensitive regions within a certain range of spatial parameters. For example, f is insensitive within the whole range of N/C ratios tested, while it is insensitive only at the restricted region of D around 10212 m2/s. A0 is insensitive to D at higher values, and tfp is insensitive to N/C volume ratios at lower and higher values and to D at lower values. Thus each characterizing parameter possesses different sensitivities to different spatial parameters and different ranges. It should be noted that tp and td are strongly sensitive to N/C ratios. Larger N/C ratios result in more prolonged oscillation without changing oscillation frequencies.DiscussionWe constructed a 3D computational model to see the effect of spatial parameters on the oscillation pattern of nuclear NF-kB and found that N/C ratios, diffusion coefficient, the locus of IkBs synthesis, and nuclear transport altered oscillation patterns. Neither the location nor localization of IkBs transcription or IKK activation altered the oscillation pattern. Thus, there are at least two categories of spatial parameters that alter and do not alter the oscillation pattern of 
nuclear NF-kB. When the N/C ratio was increased, the decay time constant td increased in our simulation, indicating the persistent oscillation in larger N/C volume ratios. It is reported that in human cancer patients, both nuclear volume and the N/C ratio are increased [52,55]. Thus, the oscillation of NF-kB in cancer cells is potentially prolonged. Although there are discussions on the MedChemExpress 58-49-1 physiological role of persistent oscillation of nuclear NF-kB [64,65], the persistent oscillation will maintain NF-kB-dependent gene expression [65] and lead to the aberrant gene expression. Our simulation results offer one possible mechanism and explanation for the altered gene expression in cancer cells which have larger N/C ratio.Y. Representative oscillations are shown on the right. This representation shows overall oscillation pattern. There is no change in the oscillation frequency by changing N/C ratios which is seen by a regular color interval among different N/C ratios. The damping of the oscillation is faster in smaller N/C volume ratios which is supported by disappearance of the periodic color change at the later time in smaller N/C ratios. At higher N/C ratios, however, the oscillation lasts for more than 10 hrs. (B) There is no change in the oscillation frequency (f) with changes in the N/C ratio. (C) The amplitude of the first peak (A0) becomes smaller at larger N/C values. (D) The time to the first peak (tfp) also stays almost unchanged by the change in N/C. (E) The decay time constants of the peaks (tp) and successive amplitudes (td) of oscillation becomes larger at larger N/C ratios. tp and td at larger N/Cs could not be extracted from the simulated oscillation. doi:10.1371/journal.pone.0046911.gIt is clearly seen that all characterizing parameters possess different sensitivities to different spatial parameters. For example, f possesses positive and negative sensitivity to nuclear transport and D, respectively, while it is insensitive to N/C ratios. On the other hand, A0 are negatively sensitive to N/C ratio. Its sensitivity to nuclear transport and D is slightly positive. The sensitivity of the first peak tfp to N/C ratio is slightly positive, and tp and td have the same tendency toward positive or negative sensitivity to the same spatial parameters. It is also clearly seen that each characterizing parameter possesses insensitive regions within a certain range of spatial parameters. For example, f is insensitive within the whole range of N/C ratios tested, while it is insensitive only at the restricted region of D around 10212 m2/s. A0 is insensitive to D at higher values, and tfp is insensitive to N/C volume ratios at lower and higher values and to D at lower values. Thus each characterizing parameter possesses different sensitivities to different spatial parameters and different ranges. It should be noted that tp and td are strongly sensitive to N/C ratios. Larger N/C ratios result in more prolonged oscillation without changing oscillation frequencies.DiscussionWe constructed a 3D computational model to see the effect of spatial parameters on the oscillation pattern of nuclear NF-kB and found that N/C ratios, diffusion coefficient, the locus of IkBs synthesis, and nuclear transport altered oscillation patterns. Neither the location nor localization of IkBs transcription or IKK activation altered the oscillation pattern. Thus, there are at least two categories of spatial parameters that alter and do not alter the oscillation pattern of nuclear NF-kB. When the N/C ratio was increased, the decay time constant td increased in our simulation, indicating the persistent oscillation in larger N/C volume ratios. It is reported that in human cancer patients, both nuclear volume and the N/C ratio are increased [52,55]. Thus, the oscillation of NF-kB in cancer cells is potentially prolonged. Although there are discussions on the physiological role of persistent oscillation of nuclear NF-kB [64,65], the persistent oscillation will maintain NF-kB-dependent gene expression [65] and lead to the aberrant gene expression. Our simulation results offer one possible mechanism and explanation for the altered gene expression in cancer cells which have larger N/C ratio.
