Direkt zum Inhalt
Merck

Follistatin in chondrocytes: the link between TRPV4 channelopathies and skeletal malformations.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology (2014-03-01)
Holly A Leddy, Amy L McNulty, Suk Hee Lee, Nicole E Rothfusz, Bernd Gloss, Margaret L Kirby, Mary R Hutson, Daniel H Cohn, Farshid Guilak, Wolfgang Liedtke
ZUSAMMENFASSUNG

Point mutations in the calcium-permeable TRPV4 ion channel have been identified as the cause of autosomal-dominant human motor neuropathies, arthropathies, and skeletal malformations of varying severity. The objective of this study was to determine the mechanism by which TRPV4 channelopathy mutations cause skeletal dysplasia. The human TRPV4(V620I) channelopathy mutation was transfected into primary porcine chondrocytes and caused significant (2.6-fold) up-regulation of follistatin (FST) expression levels. Pore altering mutations that prevent calcium influx through the channel prevented significant FST up-regulation (1.1-fold). We generated a mouse model of the TRPV4(V620I) mutation, and found significant skeletal deformities (e.g., shortening of tibiae and digits, similar to the human disease brachyolmia) and increases in Fst/TRPV4 mRNA levels (2.8-fold). FST was significantly up-regulated in primary chondrocytes transfected with 3 different dysplasia-causing TRPV4 mutations (2- to 2.3-fold), but was not affected by an arthropathy mutation (1.1-fold). Furthermore, FST-loaded microbeads decreased bone ossification in developing chick femora (6%) and tibiae (11%). FST gene and protein levels were also increased 4-fold in human chondrocytes from an individual natively expressing the TRPV4(T89I) mutation. Taken together, these data strongly support that up-regulation of FST in chondrocytes by skeletal dysplasia-inducing TRPV4 mutations contributes to disease pathogenesis.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Dimethylsulfoxid, Hybri-Max, sterile-filtered, BioReagent, suitable for hybridoma, ≥99.7%
Sigma-Aldrich
Dimethylsulfoxid, ACS reagent, ≥99.9%
Sigma-Aldrich
Dimethylsulfoxid, Molecular Biology
Sigma-Aldrich
Dimethylsulfoxid, suitable for HPLC, ≥99.7%
Sigma-Aldrich
Dimethylsulfoxid, sterile-filtered, BioPerformance Certified, meets EP, USP testing specifications, suitable for hybridoma
Sigma-Aldrich
Dimethylsulfoxid, ReagentPlus®, ≥99.5%
Sigma-Aldrich
Dimethylsulfoxid, anhydrous, ≥99.9%
Sigma-Aldrich
Dimethylsulfoxid, ≥99.5% (GC), suitable for plant cell culture
Sigma-Aldrich
Formaldehyd -Lösung, Molecular Biology, 36.5-38% in H2O
Sigma-Aldrich
Formaldehyd -Lösung, ACS reagent, 37 wt. % in H2O, contains 10-15% Methanol as stabilizer (to prevent polymerization)
SAFC
Formaldehyd -Lösung, contains 10-15% methanol as stabilizer, 37 wt. % in H2O
Sigma-Aldrich
Dimethylsulfoxid, BioUltra, Molecular Biology, ≥99.5% (GC)
Sigma-Aldrich
Natriumselenit, 99%
Sigma-Aldrich
Natriumselenit, BioReagent, suitable for cell culture, ≥98%
Sigma-Aldrich
Formaldehyd -Lösung, Molecular Biology, BioReagent, ≥36.0% in H2O (T)
Sigma-Aldrich
Dimethylsulfoxid, meets EP testing specifications, meets USP testing specifications
Sigma-Aldrich
Natriumselenit, γ-irradiated, lyophilized powder, BioXtra, suitable for cell culture
Sigma-Aldrich
Formaldehyd -Lösung, meets analytical specification of USP, ≥34.5 wt. %
Sigma-Aldrich
Dimethylsulfoxid, PCR Reagent
Sigma-Aldrich
Safranin O, certified by the BSC
Sigma-Aldrich
Phenolrot, powder, BioReagent, suitable for cell culture
Supelco
Formaldehyd -Lösung, stabilized with methanol, ~37 wt. % in H2O, certified reference material
Sigma-Aldrich
Phenolrot, ACS reagent
Sigma-Aldrich
Safranin O, Dye content ≥85 %
Sigma-Aldrich
Gram-Safranin -Lösung, suitable for microscopy
Sigma-Aldrich
Safranin O, suitable for microscopy
Sigma-Aldrich
Formaldehyd -Lösung, tested according to Ph. Eur.
Supelco
Dimethylsulfoxid, analytical standard
Sigma-Aldrich
Natriumselenit, anhydrous, ≥90.0% (RT)
Supelco
Dimethylsulfoxid, for inorganic trace analysis, ≥99.99995% (metals basis)