The sense of touch is unique in perceiving stimuli both physical (temperature, mechanical) and chemical (compounds that cause pain, itch, et cetera) in nature. In each modality, touch neurons distinguish noxious (painful) from innocuous stimuli, and the sensitization of touch neurons in response to injury and inflammation is the basis for many clinically-relevant chronic pain states. Discovery of the Transient Receptor Potential (TRP) ion channel sensors for temperature has advanced our understanding of thermosensation. However, recent data suggests that thermoTRPs are unlikely to explain all of the thermosensory capability of the somatosensory or other temperature-dependent systems. We have very recently identified components of a mechanically-activated cation channels named Piezos. Piezo2 can account for rapidly-adapting but not slowly-adapting mechanically-activated currents in DRGs. Indeed, mechanosensation remains perhaps the least understood of the mammalian sensory receptor systems. Therefore, the molecular identities of thermosensitive (TS) and mechanosensitive (MS) ion channels and proteins in mammals have been elusive, and the cloning and characterization of these sensors will provide a critical foundation for the study of pain perception and pain relief. Our proposal uses state-of-the-art technologies of screening candidate- and genome-wide full length cDNAs and RNAis to identify novel receptors and potential sensors.

Public Health Relevance

The molecules that mediate detection of touch stimuli have been a long-standing mystery. We do not know the identity of most of the ion channels that sense mechanical force, and only some of the temperature-sensors are identified. We will use genomic screens to find novel proteins that are directly/indirectly activated by temperature and pressure.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE022115-03
Application #
8415779
Study Section
Special Emphasis Panel (ZDE1-JH (12))
Program Officer
Kusiak, John W
Project Start
2011-07-29
Project End
2015-03-31
Budget Start
2013-04-01
Budget End
2014-03-31
Support Year
3
Fiscal Year
2013
Total Cost
$363,840
Indirect Cost
$171,840
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Qiu, Zhaozhu; Dubin, Adrienne E; Mathur, Jayanti et al. (2014) SWELL1, a plasma membrane protein, is an essential component of volume-regulated anion channel. Cell 157:447-58