"While rodent models have been useful, we are not 150-pound rats. And even though we are not balls of cells either, you can often get much better information from these balls of cells than from rodents.
"We believe that the future of brain research will include less reliance on animals, more reliance on human, cell-based models.”
Dr Hartung said the brains had even started to produce ‘a primitive type of thinking.’
'It has the beauty that we can do this from essentially anybody. We have been doing this from five different donors so far, among them also people with genetic diseases'
Obviously there's no input or output,” he added. “It is meaningless electrical activity but the neurons are trying to communicate with each other.”
The brains are made from skin cells of adults which have been reprogrammed back to a stem-cell like state, then grown into brain cells which then transform into mini-brains within eight weeks.
The team said that cells from people with certain genetic traits could also be grown to provide a model for diseases like Alzheimer’s,Parkinson’s or multiple sclerosis.
"It also has the beauty that we can do this from essentially anybody,” added Dr Hartung. “We have been doing this from five different donors so far, among them also people with genetic diseases. So we can test for the first time the combination of genetic traits together with the effect of substances, because many disease are not explained by genes along.
“We have been doing work on Parkinson's as an example, which we're publishing, because we can really replicate some of the hallmarks of Parkinson's in human brain model."
The brains even showed spontaneous electrophysiological activity, which could be recorded with electrodes. To test them, the researchers placed a mini-brain on an array of electrodes and listened to the spontaneous electrical communication of the neurons as test drugs were added.
The research was presented at the annual Advancement for American Science Annual Conference (AAAS) in Washington.
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