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Updated: Sep 21, 2026

Chromatin Immunoprecipitation (ChIP) to Assay Dynamic Histone Modification in Activated Gene Expression in Human Cells
Published on: July 29, 2010
Alterations in hepatic chromatin template availability during infection
Abstract:
Hepatic chromatin was isolated from rats at various times after inoculation with either live or heat-killed bacteria. The chromatin was assayed under conditions that allow determination of the DNA template available to support in vitro transcription. Both a fulminant Diplococcus pneumoniae and a milder Salmonella typhimurium infection produced time-related increases in hepatic chromatin template availability when compared to chromatin isolated from rats inoculated with heat-killed bacteria. Both timing and magnitude of increased template availability correlated with the severity of the infection. The earliest change observed was a 50 percent rise in availability noted 4 h after inoculation with D. pneumoniae. This preceded the onset of fever, as well as other known heaptic consequences of systemic infection. After 24 h of infection the maximum rise of 90 percent occurred. Similar changes developed during S. typhimurium infection, but were slower in onset and smaller in magnitude. Adrenalectomy prior to infection enhanced the severity of the disease but markedly blunted the increase in template availability. The data are consistent with the hypothesis that systemic infection regulates the hepatic metabolic response to infection through transcriptional control and that a permissive or stimulatory action of glucocorticoids is involved in the increases in template availability effected.
Insights
Systemic bacterial infections increase hepatic chromatin template availability, impacting gene transcription. Glucocorticoids play a role in this response, suggesting transcriptional control regulates the liver
Area of Science:
- Molecular Biology
- Immunology
- Genetics
Background:
- Systemic infections trigger complex host responses.
- Hepatic gene expression is crucial for metabolic adaptation during infection.
Purpose of the Study:
- To investigate changes in hepatic chromatin template availability during bacterial infections.
- To explore the role of glucocorticoids in infection-induced transcriptional regulation.
Main Methods:
- Isolation of hepatic chromatin from rats at various time points post-bacterial inoculation.
- Assay of chromatin to determine DNA template availability for in vitro transcription.
- Adrenalectomy performed prior to infection to assess glucocorticoid involvement.
Main Results:
- Bacterial infections (Diplococcus pneumoniae, Salmonella typhimurium) increased hepatic chromatin template availability in a time- and severity-dependent manner.
- Earliest changes (50% increase) observed 4 hours post-D. pneumoniae inoculation, preceding clinical signs.
- Maximum increase (90%) noted at 24 hours; S. typhimurium showed slower, less pronounced effects.
- Adrenalectomy exacerbated disease but blunted the increase in template availability.
Conclusions:
- Systemic infections regulate hepatic metabolic responses via transcriptional control.
- Glucocorticoids are involved in mediating infection-induced increases in hepatic chromatin template availability.
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