Repository logo
  • Log In
    Log in via Symplectic to deposit your publication(s).
Repository logo
  • About
  • Communities & Collections
  • Advanced Search
  • Statistics
  • Log In
    Log in via Symplectic to deposit your publication(s).
  1. Home
  2. Faculty of Medicine
  3. Faculty of Medicine
  4. Epigenetics and chromatin remodeling play a role in lung disease
 
  • Details
Epigenetics and chromatin remodeling play a role in lung disease
File(s)
Epigenetics and chromatin remodeling play a role in lung disease.pdf (2.09 MB)
Published version
Author(s)
Mortaz, E
Masjedi, MR
Barnes, PJ
Adcock, IM
Type
Journal Article
Abstract
Epigenetics is defined as heritable changes that affect gene expression without altering the DNA sequence. Epigenetic regulation of gene expression is facilitated through different mechanisms such as DNA methylation, histone modifications and RNA-associated silencing by small non-coding RNAs. All these mechanisms are crucial for normal development, differentiation and tissue-specific gene expression. These three systems interact and stabilize one another and can initiate and sustain epigenetic silencing, thus determining heritable changes in gene expression. Histone acetylation regulates diverse cellular functions including inflammatory gene expression, DNA repair and cell proliferation. Transcriptional coactivators possess intrinsic histone acetyltransferase activity and this activity drives inflammatory gene expression. Eleven classical histone deacetylases (HDACs) act to regulate the expression of distinct subsets of inflammatory/immune genes. Thus, loss of HDAC activity or the presence of HDAC inhibitors can further enhance inflammatory gene expression by producing a gene-specific change in HAT activity. For example, HDAC2 expression and activity are reduced in lung macrophages, biopsy specimens, and blood cells from patients with severe asthma and smoking asthmatics, as well as in patients with chronic obstructive pulmonary disease (COPD). This may account, at least in part, for the enhanced inflammation and reduced steroid responsiveness seen in these patients. Other proteins, particularly transcription factors, are also acetylated and are targets for deacetylation by HDACs and sirtuins, a related family of 7 predominantly protein deacetylases. Thus the acetylation/deacetylation status of NF-κB and the glucocorticoid receptor can also affect the overall expression pattern of inflammatory genes and regulate the inflammatory response. Understanding and targeting specific enzymes involved in this process might lead to new therapeutic agents, particularly in situations in which current anti-inflammatory therapies are suboptimal.
Date Issued
2011-08-01
Date Acceptance
2011-08-01
Citation
Tanaffos : Journal of Respiratory Disease, Thoracic Surgery, Intensive Care and Tuberculosis, 2011, 10 (4), pp.7-16
URI
http://hdl.handle.net/10044/1/31713
ISSN
2345-3729
Publisher
National Research Institute of Tuberculosis and Lung Disease
Start Page
7
End Page
16
Journal / Book Title
Tanaffos : Journal of Respiratory Disease, Thoracic Surgery, Intensive Care and Tuberculosis
Volume
10
Issue
4
Copyright Statement
© 2011 National Research Institute of Tuberculosis and Lung Disease
Sponsor
Wellcome Trust
Grant Number
093080/Z/10/Z
Subjects
Asthma
COPD
HDAC
Inflammatory cells
Publication Status
Published
About
Spiral Depositing with Spiral Publishing with Spiral Symplectic
Contact us
Open access team Report an issue
Other Services
Scholarly Communications Library Services
logo

Imperial College London

South Kensington Campus

London SW7 2AZ, UK

tel: +44 (0)20 7589 5111

Accessibility Modern slavery statement Cookie Policy

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science

  • Cookie settings
  • Privacy policy
  • End User Agreement
  • Send Feedback