TRPV4: molecular conductor of a diverse orchestra

JPM White, M Cibelli, L Urban, B Nilius… - Physiological …, 2016 - journals.physiology.org
Transient receptor potential vanilloid type 4 (TRPV4) is a calcium-permeable nonselective
cation channel, originally described in 2000 by research teams led by Schultz (Nat Cell Biol …

The puzzle of TRPV4 channelopathies

B Nilius, T Voets - EMBO reports, 2013 - embopress.org
Hereditary channelopathies, that is, mutations in channel genes that alter channel function
and are causal for the pathogenesis of the disease, have been described for several …

TRPV4-Rho GTPase complex structures reveal mechanisms of gating and disease

DH Kwon, F Zhang, BA McCray, S Feng… - Nature …, 2023 - nature.com
Crosstalk between ion channels and small GTPases is critical during homeostasis and
disease, but little is known about the structural underpinnings of these interactions. TRPV4 is …

TRPV4: a physio and pathophysiologically significant ion channel

T Rosenbaum, M Benítez-Angeles… - International journal of …, 2020 - mdpi.com
Transient Receptor Potential (TRP) channels are a family of ion channels whose members
are distributed among all kinds of animals, from invertebrates to vertebrates. The importance …

TRPing to the point of clarity: understanding the function of the complex TRPV4 ion channel

TL Toft-Bertelsen, N MacAulay - Cells, 2021 - mdpi.com
The transient receptor potential vanilloid 4 channel (TRPV4) belongs to the mammalian TRP
superfamily of cation channels. TRPV4 is ubiquitously expressed, activated by a disparate …

Combined NGS Approaches Identify Mutations in the Intraflagellar Transport Gene IFT140 in Skeletal Ciliopathies with Early Progressive Kidney Disease

M Schmidts, V Frank, T Eisenberger, S Al Turki… - Human …, 2013 - Wiley Online Library
Ciliopathies are genetically heterogeneous disorders characterized by variable expressivity
and overlaps between different disease entities. This is exemplified by the short rib …

Mutations in TRPV4 cause an inherited arthropathy of hands and feet

SR Lamandé, Y Yuan, IL Gresshoff, L Rowley… - Nature …, 2011 - nature.com
Familial digital arthropathy-brachydactyly (FDAB) is a dominantly inherited condition that is
characterized by aggressive osteoarthropathy of the fingers and toes and consequent …

Transient receptor potential vanilloid 4 (TRPV4) activation by arachidonic acid requires protein kinase A–mediated phosphorylation

S Cao, A Anishkin, NS Zinkevich, Y Nishijima… - Journal of Biological …, 2018 - ASBMB
Transient receptor potential vanilloid 4 (TRPV4) is a Ca 2+-permeable channel of the
transient receptor potential (TRP) superfamily activated by diverse stimuli, including warm …

TRPV4‐associated skeletal dysplasias

G Nishimura, E Lausch, R Savarirayan… - American Journal of …, 2012 - Wiley Online Library
Dominant mutations in the TRPV4 gene result in a bone dysplasia family and form a
continuous phenotypic spectrum that includes, in decreasing severity, lethal, and nonlethal …

Structural and biochemical consequences of disease-causing mutations in the ankyrin repeat domain of the human TRPV4 channel

H Inada, E Procko, M Sotomayor, R Gaudet - Biochemistry, 2012 - ACS Publications
The TRPV4 calcium-permeable cation channel plays important physiological roles in
osmosensation, mechanosensation, cell barrier formation, and bone homeostasis. Recent …