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Enzyme may link inflammation to new cell fate

Jmdj3 (red) removes lysine methyl groups (green) from chromatin and allows macrophages to become new cell types. NATOLI/ELSEVIER

Gene silencing is the sine qua non of differentiation, and reversal of gene silencing paves the way for a cell to adopt a new fate. In a new study, Francesca De Santa, Giaocchino Natoli, and colleagues (European Institute of Oncology, Milan, Italy) identify a desilencing protein that might let cells find new fates during inflammation.

"Under conditions of chronic inflammation, tissues tend to show altered differentiation," Natoli says. Chronic gastritis, for instance, can lead to the formation of intestinal cells within the stomach lining. And in a rejected kidney transplant, host macrophages turn into endothelial cells, creating new lymphatic vessels.

For macrophages to adopt new fates, a lysine in histone H3 must first be demethylated to relieve the silencing of cell fate determinants. One group of enzymes that removes methyl groups is the JmjC domain proteins, which includes JmjD3, whose exact function has been unclear. In the new work, the authors discovered that JmjD3 was up-regulated during inflammation and that it demethylated cell fate genes.

Jmdj3's target genes included late HoxA genes, which are powerful determinants of cell fate. Additionally, knock down of Jmdj3 inhibited the demethylation of bone morphogenetic protein 2, thus preventing its normal inflammation-induced increase.

The existence of a system to erase controls on terminal differentiation may seem counterintuitive at first, but "it makes a lot of biological sense," says Natoli. In situations in which tissue regeneration is needed, and local stem cells are exhausted, there may be a need to recruit other cell types. New lymphatic vessels, for instance, may be needed to increase the flow of debris out of an injured and inflamed area, Natoli suggests. "Inflammation loosens control over differentiation, and Jmdj3 may be the molecular link between these processes."

Reference:

De Santa, F., et al. 2007. Cell. 130:1083–1094.[CrossRef][Medline]

Richard Robinson

rrobinson{at}nasw.org

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This Article Full Text (PDF, 800K) PPT slides of all figures Alert me when this article is cited Services Email this article Similar articles in this journal Alert me to new content in the JCB Download to citation manager Citing Articles Citing Articles via CrossRef Citing Articles via Google Scholar Google Scholar Articles by Robinson, R. Search for Related Content PubMed Articles by Robinson, R. Social Bookmarking                            What's this?