Unlike vision, smell, and tastes, the molecular mechanisms of hearing, touch, and blood- pressure or systemic-osmolarity sensing are unknown. How ion channels receive mechanical forces remain obscure, except for bacterial channels MscL, MscS. We are using the rat TRP channel V4 subtype, to help fill this knowledge gap. We have now shown TRPV4's direct response to membrane stretch under Xenopus oocyte patch clamp. We have also developed yeast as a new arena to dissect TRPV4. Our work challenges a previous TRPV4's osmotic-gating model. We plan to define the force-sensing domain within TRPV4, using strategic peptide insertions and chimeras. 2008-11 found TRPV4 gain-of-function mutations to cause two sets of human diseases: skeletal dysplasia (SD) and adult peripheral neuropathy. We examined 14 SD alleles and found the level of increased basal TRPV4 activity parallels the severity of the SD disease. Besides understanding the working of the wild-type TRPV4 channels, we now plan to examine 17 mutations in the ankyrin-repeat domain (ARD), of which crystal structure is known. This work aims towards understanding how ARD mutations can lead to two disparate diseases. In collaboration, we will also use trpV4-/- knock-out mice to test the role of TRPV4 in fracture healing.

Public Health Relevance

Ion-channel mechanosensitivity underlies the physiology and pathology of hearing, touch, the sensing of blood pressure, systemic osmolarity etc. Understanding how a channel protein receives forces is fundamental. The molecular functioning of the mechanosensitive TRPV4 channel has direct impact on human health: TRPV4 mutations cause autosomal dominant brachyolmia, spondylmetaphyseal dysplasias Kozlowski type, metatropic dysplasia, scapuloperoneal spinal muscular atrophies, and Charcot- Marie-Tooth disease type 2C in human.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM096088-03
Application #
8541866
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Nie, Zhongzhen
Project Start
2011-09-15
Project End
2015-08-31
Budget Start
2013-09-01
Budget End
2014-08-31
Support Year
3
Fiscal Year
2013
Total Cost
$275,942
Indirect Cost
$92,592
Name
University of Wisconsin Madison
Department
Genetics
Type
Schools of Earth Sciences/Natur
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Teng, Jinfeng; Loukin, Stephen; Anishkin, Andriy et al. (2015) The force-from-lipid (FFL) principle of mechanosensitivity, at large and in elements. Pflugers Arch 467:27-37
Anishkin, Andriy; Loukin, Stephen H; Teng, Jinfeng et al. (2014) Feeling the hidden mechanical forces in lipid bilayer is an original sense. Proc Natl Acad Sci U S A 111:7898-905
Anishkin, Andriy; Kung, Ching (2013) Stiffened lipid platforms at molecular force foci. Proc Natl Acad Sci U S A 110:4886-92