Recent studies show that 40 percent of Americans over the age of 85 have Alzheimer's disease, and that the disease begins 10 to 20 years before people show up at the doctor's office with memory problems.
One major problem with understanding Alzheimer's is not being able to clearly see why the disease starts. A super-resolution "nanoscope" developed by Purdue University researchers now provides a 3D view of brain molecules with 10 times greater detail. This imaging technique could help reveal how the disease progresses and where new treatments could intervene.
The instrument helped Indiana University researchers better understand the structure of plaques that form in the brain of Alzheimer's patients, pinpointing the characteristics that are possibly responsible for damage.
Long before Alzheimer's develops in an individual, waxy deposits called amyloid plaques accumulate in the brain. These clusters interact with surrounding cells, causing inflammation that destroys neurons and creates memory problems. The deposition of these plaques is currently the earliest detectable evidence of pathological change leading to Alzheimer's disease.
"While strictly a research tool for the foreseeable future, this technology has allowed us to see how the plaques are assembled and remodeled during the disease process," said Gary Landreth, professor of anatomy and cell biology at the Indiana University School of Medicine's Stark Neurosciences Research Institute. "It gives insight into the biological causes of the disease, so that we can see if we can stop the formation of these damaging structures in the brain."
The limited resolution in conventional light microscopes and the natural thickness of brain tissue have prevented researchers from clearly observing 3D morphology of amyloid plaques and their interactions with other cells. "Brain tissue is particularly challenging for single molecule super-resolution imaging because it is highly packed with extracellular and intracellular constituents, which distort and scatter light – our source of molecular information," said Fang Huang, Purdue assistant professor of biomedical engineering. "You can image deep into the tissue, but the image is blurry."
The super-resolution nanoscopes, which Huang's research team has already developed to visualize cells, bacteria, and viruses in fine detail, uses "adaptable optics" – deformable mirrors that change shape to compensate for light distortion, called "aberration," that happens when light signals from single molecules travel through different parts of cell or tissue structures at different speeds.
To tackle the challenge of brain tissue, Huang's research team developed new techniques that adjust the mirrors in response to sample depths to compensate for aberration introduced by the tissue. At the same time, these techniques intentionally introduce extra aberration to maintain the position information carried by a single molecule.