Nerve cells like these could be controlled by quantum dots (Image: CNRI/Science Photo Library)
In an unlikely marriage of quantum physics and
neuroscience, tiny particles called quantum dots have been used to
control brain cells for the first time.
Having
such control over the brain could one day provide a non-invasive
treatment for conditions such as Alzheimer's disease, depression and
epilepsy. In the nearer term, quantum dots could be used to treat
blindness by reactivating damaged retinal cells.
"Many brain disorders are caused by imbalanced neural activity," says Lih Lin
at the University of Washington, Seattle. "Manipulation of specific
neurons could permit the restoration of normal activity levels."
Methods
to stimulate the brain artificially already exist, though each has its
drawbacks. Deep brain stimulation is used in Parkinson's disease to
trigger brain cell activity and prevent the abnormal signalling that
causes debilitating tremors, but placing the electrodes required is
highly invasive. Transcranial magnetic stimulation can stimulate brain
cells from
outside
the head, but is not highly targeted and so affects large areas of the
brain at once. Researchers in optogenetics can control genetically
modified brain cells using light but because of these modifications,
the technique is not yet deemed safe to use in humans.
Lin's
team has now come up with an alternative using quantum dots –
light-sensitive, semiconducting particles just a few nanometres in
diameter.
First,
they cultivated prostate cancer cells on a film covered with quantum
dots. The cell membranes of the cancer cells were positioned next to
the dots. The team then shone light onto the nanoparticles.
Energy from the light excites electrons within the quantum dot which causes the surrounding area to become negatively charged (see diagram).
This caused some of the cancer cells' ion channels, which are mediated
by a voltage, to open, allowing ions to rush in or out of the cells.
In
nerve cells, opening ion channels is a crucial step in generating
action potentials – the signals by which the cells communicate in the
brain. If the voltage change is large enough, an action potential is
generated.
When
Lin's team repeated their experiment with nerve cells, they found that
stimulating the quantum dots caused ion channels to open and the nerve
cell to fire.
In
humans, quantum dots would need to be delivered to brain tissue. Lin
claims this shouldn't be a problem. "A significant advantage is that
their surface can be modified with various molecules," she says. These
molecules could be attached to the quantum dots in order to target specific brain cells and could be administered intravenously.
A
key hurdle would be delivering the light source to the brain. For this
reason, Lin reckons the first use for the technique would be in
reactivating damaged cells in the retina, which naturally absorb light.
Co-author Fred Reike, who specialises in retinal disease, says that
quantum dots have great potential in this area because they directly
affect ion channels, which play a key part in the signalling pathways
of vision.
"Quantum dots have a great future for biomedical applications," agrees Kevin Critchley at the University of Leeds, UK, but adds that there are limitations such as potential toxicity issues.
"Based
on what we have observed, we are optimistic about the potential of this
technology in helping us [answer] biological questions, and eventually
diagnose and treat human diseases," Lin says.
Journal reference: Biomedical Optics Express, DOI: 10.1364/boe.3.000447
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