TY - JOUR
T1 - Radial stretch reveals distinct populations of mechanosensitive mammalian somatosensory neurons
AU - Bhattacharya, Martha R.C.
AU - Bautista, Diana M.
AU - Wu, Karin
AU - Haeberle, Henry
AU - Lumpkin, Ellen A.
AU - Julius, David
PY - 2008/12/16
Y1 - 2008/12/16
N2 - Primary afferent somatosensory neurons mediate our sense of touch in response to changes in ambient pressure. Molecules that detect and transduce thermal stimuli have been recently identified, but mechanisms underlying mechanosensation, particularly in vertebrate organisms, remain enigmatic. Traditionally, mechanically evoked responses in somatosensory neurons have been assessed one cell at a time by recording membrane currents in response to application of focal pressure, suction, or osmotic challenge. Here, we used radial stretch in combination with live-cell calcium imaging to gain a broad overview of mechanosensitive neuronal sub-populations. We found that different stretch intensities activate distinct subsets of sensory neurons as defined by size, molecular markers, or pharmacological attributes. In all subsets, stretch-evoked responses required extracellular calcium, indicating that mechanical force triggers calcium influx. This approach extends the repertoire of stimulus paradigms that can be used to examine mechanotransduction in mammalian sensory neurons, facilitating future physiological and pharmacological studies.
AB - Primary afferent somatosensory neurons mediate our sense of touch in response to changes in ambient pressure. Molecules that detect and transduce thermal stimuli have been recently identified, but mechanisms underlying mechanosensation, particularly in vertebrate organisms, remain enigmatic. Traditionally, mechanically evoked responses in somatosensory neurons have been assessed one cell at a time by recording membrane currents in response to application of focal pressure, suction, or osmotic challenge. Here, we used radial stretch in combination with live-cell calcium imaging to gain a broad overview of mechanosensitive neuronal sub-populations. We found that different stretch intensities activate distinct subsets of sensory neurons as defined by size, molecular markers, or pharmacological attributes. In all subsets, stretch-evoked responses required extracellular calcium, indicating that mechanical force triggers calcium influx. This approach extends the repertoire of stimulus paradigms that can be used to examine mechanotransduction in mammalian sensory neurons, facilitating future physiological and pharmacological studies.
KW - Mechanotransduction
KW - Sensory signaling
KW - Somatosensation
KW - Touch
UR - http://www.scopus.com/inward/record.url?scp=58149401200&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=58149401200&partnerID=8YFLogxK
U2 - 10.1073/pnas.0810801105
DO - 10.1073/pnas.0810801105
M3 - Article
C2 - 19060212
AN - SCOPUS:58149401200
SN - 0027-8424
VL - 105
SP - 20015
EP - 20020
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 50
ER -