Novel research identifies gene targets of stress hormones in the brain

A magnified image of developing young human neurons. The mineralocorticoid receptor, coloured red, was found in the cell nucleus of these neurons.
Credit: University of Bristol / Hans Reul

Chronic stress is a well-known cause for mental health disorders.  New research has moved a step forward in understanding how glucocorticoid hormones (‘stress hormones’) act upon the brain and what their function is. The findings could lead to more effective strategies in the prevention and treatment of mental health disorders.

The study, led by academics at the University of Bristol and published today [6 August] in Nature Communications, has discovered a link between corticosteroid receptors – the mineralocorticoid receptor (MR) and the glucocorticoid receptor (GR) – and ciliary and neuroplasticity genes in the hippocampus, a region of the brain involved in stress coping and learning and memory.

The aim of the research was to find out what genes MR and GR interact with across the entire hippocampus genome during normal circadian variation and after exposure to acute stress. The research team also wanted to discover whether any interaction would result in changes in the expression and functional properties of these genes.

The study combined advanced next-generation sequencing, bioinformatics and pathway analysis technologies to enable a greater understanding into glucocorticoid hormone action, via MRs and GRs, on gene activity in the hippocampus.

The researchers found a previously unknown link between the MR and cilia function. Cilia are small hair-like structures that protrude from cell bodies. Effective cilia function is vitally important for brain development and ongoing brain plasticity, but how their structure and function is regulated in neurons is largely unknown.

The discovery of the novel role of MR in cilia structure and function in relation to neuronal development has increased knowledge of the role of these cell structures in the brain and could help resolve cilia-related (developmental) disorders in the future.

The team also found that MR and GR interact with many genes which are involved in neuroplasticity processes, such as neuron-to-neuron communication and learning and memory processes. Some of these genes, however, have been linked to the development of mental health disorders like major depression, anxiety, PTSD as well as schizophrenia spectrum disorders. Consequently, glucocorticoid hormone dysfunction, as observed in chronic stress, could have a harmful effect on mental health through their action on these vulnerability genes, providing a potential new mechanism to explain the long-known involvement of glucocorticoids in the aetiology of mental health disorders.

Although further research on the role glucocorticoid hormones play in the regulation of these genes is needed, the findings fill the gap between the long-known involvement of glucocorticoids in mental health disorders and the existence of vulnerability genes.

Hans Reul, Professor of Neuroscience in Bristol Medical School: Translational Health Sciences (THS), said: “This research is a substantial step forward in our efforts to understand how these powerful glucocorticoid hormones act upon the brain and what their function is.

“We hope that our findings will trigger new targeted research into the role these hormones play in the aetiology of severe mental disorders like depression, anxiety and PTSD.”

Next steps for the research include studying how glucocorticoid hormone action via MR and GR on the hippocampus genome changes under chronic stress conditions and, thanks to a new BBSRC grant, glucocorticoid action via MR and GR upon the female brain genome.  Very little is known about this research area in females as most studies on stress and glucocorticoid hormones have been conducted in males.

The study, supported by the BBSRC and a Wellcome Trust Neural Dynamics PhD studentship, was carried out by the Neuro-Epigenetics Research Group led by Professor Hans Reul and Dr Karen Mifsud, in collaboration with Bristol’s Stem Cell Biology Group – Dr Oscar Cordero Llana and Ms Andriana Gialeli – and sequencing specialists and bioinformaticians at the University of Oxford.

Journal: Nature Communications
DOI: doi.org/10.1038/s41467-021-24967-z
Subject of Research: Not applicable
Article Title: Distinct regulation of hippocampal neuroplasticity and ciliary genes by corticosteroid receptors
Article Publication Date: 5-Aug-2021

Media Contact

Joanne Fryer
joanne.fryer@bristol.ac.uk
Office: 0117 428 2489
Cell: 07747768805

www.bristol.ac.uk

Media Contact

Joanne Fryer
University of Bristol

All latest news from the category: Life Sciences and Chemistry

Articles and reports from the Life Sciences and chemistry area deal with applied and basic research into modern biology, chemistry and human medicine.

Valuable information can be found on a range of life sciences fields including bacteriology, biochemistry, bionics, bioinformatics, biophysics, biotechnology, genetics, geobotany, human biology, marine biology, microbiology, molecular biology, cellular biology, zoology, bioinorganic chemistry, microchemistry and environmental chemistry.

Back to home

Comments (0)

Write a comment

Newest articles

Innovative vortex beam technology

…unleashes ultra-secure, high-capacity data transmission. Scientists have developed a breakthrough optical technology that could dramatically enhance the capacity and security of data transmission (Fig. 1). By utilizing a new type…

Tiny dancers: Scientists synchronise bacterial motion

Researchers at TU Delft have discovered that E. coli bacteria can synchronise their movements, creating order in seemingly random biological systems. By trapping individual bacteria in micro-engineered circular cavities and…

Primary investigation on ram-rotor detonation engine

Detonation is a supersonic combustion wave, characterized by a shock wave driven by the energy release from closely coupled chemical reactions. It is a typical form of pressure gain combustion,…