Evidence map›Paper›PMID 41574606›Full record

ArticleJCI insight2026

Small molecule inhibition rescues the skeletal dysplasia phenotype of Trpv4 mutant mice.

Lisette Nevarez, Taylor K Ismaili, Jennifer Zieba, Jorge Martin, Davis Wachtell, Derick Diaz, Jocelyn A Ramirez, Valeria Aceves, Joshua Ito, Ryan S Gray and 4 more

Abstract read
In one paragraph

Article in JCI insight, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Lisette NevarezDepartment of Molecular, Cell and Developmental Biology, UCLA, Los Angeles, California, USA.
Taylor K IsmailiActio Biosciences, San Diego, California, USA.
Jennifer ZiebaDepartment of Orthopaedic Surgery, UCLA, Los Angeles, California, USA.
Jorge MartinDepartment of Orthopaedic Surgery, UCLA, Los Angeles, California, USA.
Davis WachtellDepartment of Orthopaedic Surgery, UCLA, Los Angeles, California, USA.
Derick DiazDepartment of Molecular, Cell and Developmental Biology, UCLA, Los Angeles, California, USA.
Jocelyn A RamirezActio Biosciences, San Diego, California, USA.
Valeria AcevesDepartment of Nutritional Sciences, Dell Pediatric Research Institute, The University of Texas at Austin, Dell Medical School, Austin, Texas, USA.
Joshua ItoDepartment of Nutritional Sciences, Dell Pediatric Research Institute, The University of Texas at Austin, Dell Medical School, Austin, Texas, USA.
Ryan S GrayDepartment of Nutritional Sciences, Dell Pediatric Research Institute, The University of Texas at Austin, Dell Medical School, Austin, Texas, USA.
David GoldsteinActio Biosciences, San Diego, California, USA.
Sunil SahdeoActio Biosciences, San Diego, California, USA.
Deborah KrakowDepartment of Orthopaedic Surgery, UCLA, Los Angeles, California, USA.
Daniel H CohnDepartment of Molecular, Cell and Developmental Biology, UCLA, Los Angeles, California, USA.

Funding

Towards a Mechanistic Undestanding of Adolscent Idiopathic ScoliosisR01AR072009 · NIAMS · UNIVERSITY OF TEXAS AT AUSTIN · PI Ryan Scott Gray · 2017 to 2026
$3.9M
NIAMS NIH HHS R01 AR072009
6 · The paper itself

Abstract

The TRPV4 skeletal dysplasias are characterized by short stature, short limbs with prominent large joints, and progressive scoliosis. They result from dominant missense mutations that activate the TRPV4 calcium permeable ion channel. As a platform to understand the mechanism of disease and to test the hypothesis that channel inhibition could treat these disorders, we developed a knock-in mouse that conditionally expresses the p.R594H Trpv4 mutation. Embryonic, chondrocyte-specific induction of the mutation using Col2a1-Cre resulted in a skeletal dysplasia affecting the long bones, spine, and craniofacial skeletal elements, consistent with the human skeletal dysplasia phenotypes produced by TRPV4 mutations. Cartilage growth plate histological abnormalities included disorganized proliferating chondrocyte columns and reduced hypertrophic chondrocyte development, reflecting abnormal endochondral ossification. In vivo treatment with the TRPV4-specific inhibitor GSK2798745 markedly improved the radiographic skeletal phenotype and rescued the growth plate histological abnormalities. ScRNA-Seq of chondrocyte transcripts from affected mice identified calcium-mediated effects on multiple signaling pathways as potential mechanisms underlying the defects in linear and cartilage appositional growth observed in both mutant mice and patients. These results provide preclinical evidence demonstrating TRPV4 inhibition as a rational, mechanism-based therapeutic strategy to ameliorate disease progression and severity in the TRPV4 skeletal dysplasias.

Indexed as

Bone Diseases, DevelopmentalOsteochondrodysplasiasTRPV Cation ChannelsAnimalsCartilageChondrocytesDisease Models, AnimalFemaleGene Knock-In TechniquesGrowth PlateHumansLeucineMiceMice, TransgenicMutationPhenotypeLeucineN-(1-((4-(2-(((2,4-dichlorophenyl)sulfonyl)amino)-3-hydroxypropanoyl)-1-piperazinyl)carbonyl)-3-methylbutyl)-1-benzothiophene-2-carboxamideSulfonamidesTrpv4 protein, mouseTRPV Cation ChannelsBone biologyBone developmentCalcium channelsCartilageCell biologyGenetics

Identifiers

PMID41574606
PMCPMC12892883

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.