2016
DOI: 10.1016/j.ddmod.2017.01.003
|View full text |Cite
|
Sign up to set email alerts
|

Modeling cytokine regulatory network dynamics driving neuroinflammation in central nervous system disorders

Abstract: A central goal of pharmacological efforts to treat central nervous system (CNS) diseases is to develop systemic therapeutics that can restore CNS homeostasis. Achieving this goal requires a fundamental understanding of CNS function within the organismal context so as to leverage the mechanistic insights on the molecular basis of cellular and tissue functions towards novel drug target identification. The immune system constitutes a key link between the periphery and CNS, and many neurological disorders and neur… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2016
2016
2022
2022

Publication Types

Select...
5
2

Relationship

2
5

Authors

Journals

citations
Cited by 9 publications
(3 citation statements)
references
References 62 publications
0
3
0
Order By: Relevance
“…Even if astrocyte-mediated feedback regulation of microglial inflammation were not exclusively controlled by TGFβ, our model illustrates a plausible mechanism from the perspective of the observed process dynamics. Furthermore, we have argued that computational modeling can be utilized for numerous purposes other than accurately recapitulating or predicting the precise mechanisms of function (Anderson and Vadigepalli, in press ). Alternatively, as in our study, modeling can be used to show that negative feedback processes—regardless of their precise molecular mechanisms—are sufficient to explain the effect of IL-10 occlusion on the adaptive response to CNS insult.…”
Section: Discussionmentioning
confidence: 99%
“…Even if astrocyte-mediated feedback regulation of microglial inflammation were not exclusively controlled by TGFβ, our model illustrates a plausible mechanism from the perspective of the observed process dynamics. Furthermore, we have argued that computational modeling can be utilized for numerous purposes other than accurately recapitulating or predicting the precise mechanisms of function (Anderson and Vadigepalli, in press ). Alternatively, as in our study, modeling can be used to show that negative feedback processes—regardless of their precise molecular mechanisms—are sufficient to explain the effect of IL-10 occlusion on the adaptive response to CNS insult.…”
Section: Discussionmentioning
confidence: 99%
“…All of these processes are currently the subject of multiscale modeling at varying degrees of sophistication (Anderson and Vadigepalli, 2016 ; Linninger et al, 2016 ; Calvetti et al, 2018 ; Durka et al, 2018 ; Zhao et al, 2018 ). Although it would not be practical to incorporate these many types of simulation within NEURON, there will be possibilities for cross-simulator communication providing complex multiphysics simulations in the future (Djurfeldt et al, 2010 ).…”
Section: Discussionmentioning
confidence: 99%
“…In the last couple of decades, several modeling approaches have been put forward to better understand processes underlying neurodegeneration and neural tissue resilience ( Kolodkin et al., 2012 ; Anderson and Vadigepalli, 2016 ; Lloret-Villas et al., 2017 ). The modeling approaches vary widely and address aspects ranging from nervous system energy metabolism ( Cloutier et al., 2009 ; Lewis et al., 2010 ), protein degradation ( Cloutier and Wellstead, 2012 ; Ouzounoglou et al., 2014 ), and blood-brain barrier transport ( Garg and Verma, 2006 ; Martins et al., 2012 ) to tauopathy ( Proctor and Gray, 2010 ; Yuraszeck et al, 2010 ).…”
Section: Introductionmentioning
confidence: 99%