People Have Better Touch Sensitivity with DFNA2 Hearing
Loss
December 2011
People with a certain form of inherited hearing loss have increased
sensitivity to low frequency vibration, according to a new German study. The
findings reveal that in order to be able to "feel", specialized cells in the
skin must be tuned like instruments in an orchestra.
The study from Professor Thomas Jentsch of the Leibniz-Institut für
Molekulare Pharmakologie (FMP)/Max Delbrück Center for Molecular Medicine (MDC)
Berlin-Buch and Professor Gary Lewin (MDC), conducted in cooperation with
clinicians from Madrid, Spain and Nijmegen, the Netherlands, was published
in Nature Neuroscience.
The researchers looked at Spanish and Dutch families who have a history
of hereditary DFNA2 hearing loss, which is caused by a mutation that
disrupts the function of many hair cells in the inner ear. This mutation,
the researchers suspected, might also affect the sense of touch.
In normal humans, the hairs in the inner ear vibrate to the pressure of
the sound waves. The vibrations cause an influx of positively charged
potassium ions into the hair cells. This electric current produces a nerve
signal that is transmitted to the brain, and a person hears.
The potassium ions flow through a channel in the cell membrane and again
out of the hair cells. This potassium channel, a protein molecule called
KCNQ4, is destroyed by the mutation in hearing-impaired people. The sensory
cells gradually die off due to overload.
"We have found that KCNQ4 is present not only in the ear, but also in
some sensory cells of the skin," Thomas Jentsch explained. "This gave us the
idea that the mutation might also affect the sense of touch. And this is
exactly what we were able to show in our research, which we conducted in a
close collaboration with the lab of Gary Lewin, a colleague from the MDC who
is specialized in touch sensation."
Touch conveys a variety of precise and important information about our
environment. Humans distinguish between a rough and smooth surface by the
vibrations that occur in the skin when the surface is stroked. For the
different touch stimuli, there are sensory cells in the skin with different
structures; through the deformation of the delicate structures, electric
nerve signals are generated. However, exactly how this happens is still a
mystery.
As a first step to uncovering how the signals are generated, the
researchers in the Jentsch lab created a mouse model for deafness by
generating a mouse line that carries the same mutation in the potassium
channel as a patient with this form of genetic hearing loss. The touch
receptors in the skin where the KCNQ4 potassium channel is found did not die
off due to the defective channel like they did in the ear, but instead
showed an altered electric response to the mechanical stimuli in the mutated
mouse. They reacted much more sensitively to vibration stimuli in the low
frequency range. The outlet valve for potassium ions normally functions here
as a filter to dampen the excitability of the cells preferentially at low
frequencies. This normally tunes these mechanoreceptors to moderately high
frequencies in normal people. In mice lacking functional KCNQ4 channels,
these receptors can no longer distinguish between low and high frequencies.
The Spanish and Dutch deaf patients with mutations in the potassium
channel who were examined by Stefan Lechner and Matthias Heidenreich showed
exactly the same effect. They could even perceive very slow vibrations that
their healthy siblings could not perceive. Due to mutations in the KCNQ4
channel gene, the fine tuning of the mechanoreceptors for normal touch
sensation was altered.
The sensation of touch varies greatly from person to person - some people
are much more sensitive to touch than others. DFNA2 patients are extremely
sensitive to vibrations, according to Gary Lewin and Thomas Jentsch.
However, the researchers noted, "Although the receptors we studied became
more sensitive due to the loss of the potassium channel, this may be
outweighed by the disadvantage of the wrong 'tuning to other frequencies'.
With KCNQ4 we have for the first time identified a human gene that changes
the traits of the touch sensations."
SOURCE: Max-Delbrück-Centrum für Molekulare Medizin (MDC)