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Parallel Measurement of Circadian Clock Gene Expression and Hormone Secretion in Human Primary Cell Cultures
Published on: November 11, 2016
Modulation of the circadian clock by glucocorticoid receptor isoforms in the H295R cell line
Zsolt Nagy1, Alexa Marta2, Henriett Butz3
12nd Department of Medicine, Faculty of Medicine, Semmelweis University, Budapest, Hungary; Hungarian Academy of Sciences-Semmelweis University "Lendulet" Hereditary Endocrine Tumors Research Group, Budapest, Hungary.
Abstract:
Peripheral clocks are set by different nervous, hormonal and metabolic stimuli, and regulate the circadian expression of several genes. We investigated whether a peripheral clock could be induced in the human adrenocortical cell line H295R and whether glucocorticoid receptor isoforms (GRα and GRß) are involved in this clock system. After synchronization of cells with serum shock, the rhythmic oscillation of clock genes PER1, PER2, REV-ERBα, and ARNTL was confirmed. In addition, H295R cells even without serum shock showed rhythmic expression of PER1, PER2, CRY1 and ARNTL. Glucocorticoid treatment induced a rapid response of PER1, PER2 and CRY1 in a GRα-dependent manner. Continuous glucocorticoid stimulation after 6h caused suppression of REV-ERBα. Administration of a GR antagonist, RU486, disrupted the circadian oscillation of clock genes and prevented the acute changes in PER1, PER2 and CRY1 levels. Overexpression of the GRß isoform alone did not alter the expression of the examined clock genes, but did prevent the GRα-related suppression of REV-ERBα. These alterations occurred independently from ACTH and CRH. Our data demonstrate that a peripheral clock system is present in a human adrenocortical cell line and that periodic oscillations of clock genes are influenced by glucocorticoids, mainly through GRα.
Insights
Human adrenocortical cells (H295R) possess a peripheral clock system. Glucocorticoids, primarily via the GRα receptor, influence circadian gene expression in these cells.
Area of Science:
- Endocrinology
- Chronobiology
- Molecular Biology
Background:
- Peripheral clocks regulate circadian gene expression via various stimuli.
- The role of glucocorticoid receptor isoforms in adrenocortical circadian rhythms is not well understood.
Purpose of the Study:
- To investigate the presence of a peripheral clock in human H295R adrenocortical cells.
- To determine the involvement of glucocorticoid receptor alpha (GRα) and beta (GRß) in this clock system.
Main Methods:
- Synchronization of H295R cells using serum shock.
- Analysis of rhythmic expression of core clock genes (PER1, PER2, REV-ERBα, ARNTL, CRY1).
- Treatment with glucocorticoids and a GR antagonist (RU486), and GR isoform overexpression.
Main Results:
- H295R cells exhibit endogenous rhythmic expression of clock genes.
- Glucocorticoid treatment rapidly affects PER1, PER2, and CRY1 via GRα.
- Glucocorticoids suppress REV-ERBα, an effect modulated by GRß.
- RU486 disrupts circadian gene oscillations and acute responses.
Conclusions:
- A peripheral clock system exists in human adrenocortical cells.
- Glucocorticoids, acting mainly through GRα, influence circadian clock gene oscillations.
- GRß plays a modulatory role in glucocorticoid-mediated effects on the adrenocortical clock.
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