Document Detail


Macrophages and tissue injury: agents of defense or destruction?
MedLine Citation:
PMID:  20887196     Owner:  NLM     Status:  In-Process    
Abstract/OtherAbstract:
The past several years have seen the accumulation of evidence demonstrating that tissue injury induced by diverse toxicants is due not only to their direct effects on target tissues but also indirectly to the actions of resident and infiltrating macrophages. These cells release an array of mediators with cytotoxic, pro- and anti-inflammatory, angiogenic, fibrogenic, and mitogenic activity, which function to fight infections, limit tissue injury, and promote wound healing. However, following exposure to toxicants, macrophages can become hyperresponsive, resulting in uncontrolled or dysregulated release of mediators that exacerbate acute tissue injury and/or promote the development of chronic diseases such as fibrosis and cancer. Evidence suggests that the diverse activity of macrophages is mediated by distinct subpopulations that develop in response to signals within their microenvironment. Understanding the precise roles of these different macrophage populations in the pathogenic response to toxicants is key to designing effective treatments for minimizing tissue damage and chronic disease and for facilitating wound repair.
Authors:
Debra L Laskin; Vasanthi R Sunil; Carol R Gardner; Jeffrey D Laskin
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural    
Journal Detail:
Title:  Annual review of pharmacology and toxicology     Volume:  51     ISSN:  1545-4304     ISO Abbreviation:  Annu. Rev. Pharmacol. Toxicol.     Publication Date:  2011 Feb 
Date Detail:
Created Date:  2011-01-07     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7607088     Medline TA:  Annu Rev Pharmacol Toxicol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  267-88     Citation Subset:  IM    
Affiliation:
Department of Pharmacology and Toxicology, Rutgers University, Piscataway, New Jersey 08854, USA. laskin@eohsi.rutgers.edu
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MeSH Terms
Descriptor/Qualifier:
Grant Support
ID/Acronym/Agency:
AR055073/AR/NIAMS NIH HHS; CA132624/CA/NCI NIH HHS; ES004738/ES/NIEHS NIH HHS; ES005022/ES/NIEHS NIH HHS; GM034310/GM/NIGMS NIH HHS

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