Gene therapy can fix a defective sense of smell in mice by repairing problems with the hair-like structures on their olfactory neurons, researchers report this week in Nature Medicine1. The study suggests that abnormalities in these structures, called cilia, can be treated, but how the findings can be applied to other organs is unclear. Cilia are found on the surfaces of many types of cell, and they affect various functions, including sensory perception, movement and cell signaling. Damage to cilia as a result of genetic mutation can cause kidney and liver cysts, extra digits, obesity, blindness and hearing loss in mammals. The mutations and cellular mechanisms that contribute to such ciliopathies have been well studied, but “there's been very little work done in the area of therapeutics”, says study leader Jeffrey Martens, a pharmacologist at the University of Michigan in Ann Arbor.
Martens and his colleagues used mice in which a mutant protein causes effects similar to polycystic kidney disease in humans. Mutation of this protein, called intraflagellar transport 88 (IFT88), disrupts cilia expression and function, causing impaired growth, extra digits, blindness and brain abnormalities2. These mice, called Oak Ridge polycystic kidney (ORPK) mice, die by early adulthood. Because olfactory dysfunction is a common effect of ciliopathy, the researchers examined the olfactory neurons of ORPK mice. In healthy mice, numerous cilia project from the olfactory neurons, but ORPK mice had fewer cilia, and those that remained were shortened and malformed. As expected, these mice also had a deficient sense of smell. To reverse this defect, the authors inserted a functional IFT88 protein into an adenovirus and then injected the virus into the noses of ORPK mice. The injection restored normal cilia number and structure as well as sense of smell.