s is also performed to explore which model parameters greatly influence system behaviors. All in all, the main aim of this study is establishing a multi-scale BMS-345541 site modeling framework capable of simulating main characteristics of critical components in human endotoxemia to examine the balance and distribution of inflammatory cytokines in a population of heterogeneous leukocytes and the interplay between circadian controls and endotoxin treatments through a novel quantity based on the cellto-cell variability. Model 16522807 Construction Assumptions and biological evidence The model is principally constructed based on our previous studies. First of all, high-dimensional transcriptional profiling data from human blood leukocytes following LPS administration are decomposed into 11741928 four significant expression patterns. These patterns capture the essence of three inflammatory phases including a pro-inflammatory response, a counter-regulatory/antiinflammatory response, and a dysregulation in leukocyte bioenergetics . They define the basic elements characterizing how leukocytes respond to endotoxemia. A number of assumptions have been made to construct the model, namely: peripheral blood leukocytes can be approximated as a community of leukocytes whose main behavior is characterized by asynchronous and stochastic activities without intra-cellular spatial localization; the dynamics of the proinflammatory response, the counter-regulatory response, and the dysregulation in leukocyte bioenergetics can be characterized by patterns of corresponding pro-inflammatory cytokines, anti-inflammatory cytokines, and bio-energetic proteins; different types of pro-inflammatory cytokines, anti-inflammatory cytokines, and bioenergetic proteins are represented by corresponding average delegators as P, A, and E, respectively, whose main behaviors are associated with asynchronous and stochastic activities. Lastly, it has been observed that after LPS challenge, many pro-inflammatory cytokines exhibit similar dynamics as is observed in their corresponding mRNA temporal profiles e.g. TNFa, IL6, IL8, etc. IL10, an anti-inflammatory cytokine, shows a slight difference between its mRNA and protein temporal profiles. While mRNA levels of IL10 dropped during the first hour post-LPS 
and its protein levels rose very modestly, both profiles still exhibit up-regulation overall. Consequently, in this context, we hypothesize that the common dynamics of pro- and anti-inflammatory cytokines can be characterized by their average mRNA expression profiles. Such expression dynamics of inflammatory cytokines are assumed to be mainly regulated by the activation of relevant transcription factors. Nuclear factor-kappa B was selected as the representative signaling controller underpinning the manifestation of transcriptional responses due to its essential role in the immune system and extensive prior computational analyses. Furthermore, NFkB activity is primarily modulated by the activity of its kinase and its inhibitor through the Toll-like receptor signaling pathway a pivotal pathway subjected to crosstalk from other signals and pathways . Such regulation can be characterized by the ubiquitous paradigm of a two-feedback mechanism: a positiveand a negative- feedback. Therefore, we hypothesize that the dynamics of inflammatory cytokines are mainly regulated by intra-cellular signaling cascades and transcription factors whose activities can be characterized by the paradigm of a two-feedback regulatory mechan
