Skin genes underlie blistering disorder.
Epidermolysis bullosa (EB) afflicts an estimated 50,000 people in the United States. For now, treatment is limited mainly to bandages and antibiotic ointments, which help shield the delicate skin and protect the blisters from infection (SN: 1/26/85, p.58; 5/17/86, p.318). But three research reports, uncovering the genetic defects responsible for two types of EB, may offer clues to new treatments--and perhaps a cure -- for those who inherit this dire disorder.
Scientists have identified 23 types of EB. Two of the new reports focus on EB simplex, blaming it on a genetic defect in keratin -- the key protein in the springy "inner skeletons" of cells. A third report links dominant dystrophic EB, the most severe form, with a damaged gene for collagen, another structural protein.
The new work represents "a tremendous step forward" in understanding EB, says Miriam Feder, executive director of the Dystrophic Epidermolysis Bullosa Research Association of America, based in New York City. "It opens the door to finding a cure," she says.
In the Sept. 20 CELL, researchers report finding similar mutations in the keratin genes of two unrelated EB simplex patients. When they isolated the mutant gene and spliced it into healthy, keratin-producing skin cells called keratinocytes, it disrupted the cells' normal, filamentous internal scaffolding. And when they inserted the gene into bacteria, the microbes produced defective keratin lacking the ability to assemble into long, helical filaments in a test tube.
The investigators, led by Elaine V. Fuchs of the Howard Hughes Medical Institute at the University of Chicago, conclude that the mutant keratin causes blisters by weakening keratinocytes so that they sometimes dissolve when touched. They suggest that the various types of EB arise from "different ... mutations in different regions" of the keratin gene, resulting in proteins with varying degrees of strength.
Another team, lead by Ervin H. Epstein at the University of California, San Francisco, found a similar type of keratin mutation in one family with 10 EB simplex patients. These researchers, whose report has been accepted for publication in SCIENCE, also found that the mutant keratin failed to form helical filaments.
A third research group, directed by Jouni Uitto of Thomas Jefferson University in Philadelphia, found that 20 members of a Finnish family affected by dominant dystrophic EB bore defective genes for collagen. In the October AMERICAN JOURNAL OF HUMAN GENETICS, they report that all 20 patients had blistering lesions where the skin's outer, epidermal layer had separated from the inner, dermal layer. Because collagen makes up the fibrils that anchor the two skin layers together, Uitto's team concludes that dominant dystrophic EB results from the collagen mutation.
Robert A. Briggaman, a dermatologist at the University of North Carolina in Chapel Hill, calls the three reports "absolutely essential" to finding a cure for EB, although he concedes that the search will be tough. Gene therapy may hold promise, but there's a catch, he says. Fuchs' group found that even tiny amounts of mutant keratin can block the normal protein's assembly into healthy filaments -- which means that physicians would need to inactivate a patient's mutant gene as well as insert a healthy gene.
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|Title Annotation:||epidermolysis bullosa|
|Date:||Sep 28, 1991|
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