{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Cook D"],"funding":["National Institute on Alcohol Abuse and Alcoholism","National Institute of Biomedical Imaging and Bioengineering"],"pagination":["2275-2287"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9912253"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["62(5)"],"pubmed_abstract":["Recent experimental investigations of liver homeostatic renewal have identified high replication capacity hepatocyte populations as the primary maintainers of liver mass. However, the molecular and cellular processes controlling liver homeostatic renewal remain unknown. To address this problem, we developed and analyzed a mathematical model describing cellular network interactions underlying liver homeostatic renewal. Model simulation results demonstrate that without feedback control, basic homeostatic renewal is not robust to disruptions, leading to tissue loss under persistent/repetitive insults. Consequently, we extended our basic model to incorporate putative regulatory interactions and investigated how such interactions may confer robustness on the homeostatic renewal process. We util"],"journal":["Industrial & engineering chemistry research"],"pubmed_title":["Elucidating the Mechanisms of Dynamic and Robust Control of the Liver Homeostatic Renewal Process: Cell Network Modeling and Analysis."],"pmcid":["PMC9912253"],"funding_grant_id":["R01 AA018873","F31 AA030214","U01 EB023224","T32 AA007463"],"pubmed_authors":["Vadigepalli R","Cook D","Manchel A","Ogunnaike BA"],"additional_accession":[]},"is_claimable":false,"name":"Elucidating the Mechanisms of Dynamic and Robust Control of the Liver Homeostatic Renewal Process: Cell Network Modeling and Analysis.","description":"Recent experimental investigations of liver homeostatic renewal have identified high replication capacity hepatocyte populations as the primary maintainers of liver mass. However, the molecular and cellular processes controlling liver homeostatic renewal remain unknown. To address this problem, we developed and analyzed a mathematical model describing cellular network interactions underlying liver homeostatic renewal. Model simulation results demonstrate that without feedback control, basic homeostatic renewal is not robust to disruptions, leading to tissue loss under persistent/repetitive insults. Consequently, we extended our basic model to incorporate putative regulatory interactions and investigated how such interactions may confer robustness on the homeostatic renewal process. We util","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Feb","modification":"2025-04-21T22:45:02.21Z","creation":"2025-04-05T18:56:27.064Z"},"accession":"S-EPMC9912253","cross_references":{"pubmed":["36787103"],"doi":["10.1021/acs.iecr.2c03579"]}}