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Researchers Induce Heart Cells to Proliferate; Findings Could Lead to Strategies to Regenerate Tissue After Heart Attack.

Europe Intelligence Wire

| May 02, 2005 | COPYRIGHT 2005 Financial Times Ltd. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

(From AScribe)

BOSTON -- In the best documented effort to date, researchers from the Howard Hughes Medical Institute at Children's Hospital Boston and Harvard Medical School have successfully induced adult heart-muscle cells to divide and multiply.

Heart-muscle cells, or cardiomyocytes, were previously considered incapable of replicating in mammals after birth, which is why heart attack is such a problem: once killed, heart tissue can't regenerate. Dr. Mark Keating and Dr. Felix Engel now show that an enzyme known as p38 MAP kinase suppresses cardiomyocyte replication, and that inhibiting p38 enables these cells to proliferate. Their report appears in the May 15 issue of Genes & Development (published online May 3).

Keating, Engel and colleagues first showed in fetal rats that increased p38 activity correlates with reduced cardiac growth, and that reduced p38 activity correlates with accelerated cardiac growth. Then, working with adult cardiomyocytes, they demonstrated p38's role in every major step of cell replication.

First, in cultures of cardiomyocytes from rats, they showed that activation of p38 reduced DNA synthesis, the first key step in cell replication, and that inhibition of p38 increased DNA synthesis. Second, they showed that p38 regulates the activity of genes required for mitosis (division of the cell nucleus in two), a second key step in replication. When mice were bred to lack p38, mitosis in their cardiomyocytes increased by more than 90 percent. Finally, p38 inhibition promoted cytokinesis, the last step of replication in which the entire cell divides to form two separate cells. Growth factors were needed to get the full effect.

"This is just one baby step toward regenerative therapy, but it's an important one," says Keating. "Inhibiting p38 is now a candidate therapeutic strategy."

When a human heart is injured, it cannot ''grow back'' the damaged muscle, which is instead replaced by scar tissue. Too much scarring can impair the heart's ability to pump and can lead to life-threatening arrhythmias. "If you ...

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