Using commercially available DNA slides, a team of researchers directed by Anand Swaroop, Ph.D., have established the first-ever gene profile of the aging human retina, an important step in understanding the mechanisms of aging and its impact on vision disorders.

In the August issue of Investigative Ophthalmology and Visual Science, Swaroop and colleagues show that retinal aging is associated, in particular, with expression changes of genes involved in stress response and energy metabolism.

The term gene expression means that in any given cell, only a portion of the genes are expressed or switched on. For example, a person's pancreas and retina have the same genes, but only the pancreas can turn on the genes that allow it to make insulin.

Swaroop believes that the findings will help scientists understand whether age predisposes one to changes in the retina that, in turn, lead to age-related diseases. For vision researchers, one of the most pressing disorders is age-related macular degeneration (AMD), a progressive eye disease that affects the retina and results in the loss of one's fine central vision.

"While we still don't know what causes AMD, we do know that the strongest factors are age and family history," says. Swaroop. "We are likely to find that AMD is caused by a complex interaction between genetic and environmental risk factors."

Microarray technology is an important tool for gene profiling because it allows rapid comparison of thousands of genes, something that was unheard of even few years ago. Shigeo Yoshida, M.D., Ph.D., a post-doctoral research fellow in Swaroop's laboratory, examined microarray slides containing DNA from 2,400 human genes.

After identifying the genes expressed in the retina (about half, or 1,200 genes), the res
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Contact: Kara Gavin
kegavin@umich.edu
734-764-2220
University of Michigan Health System
26-Jun-2002