Inhibition of T-Type Voltage Sensitive Calcium Channel Reduces Load-Induced OA in Mice and Suppresses the Catabolic Effect of Bone Mechanical Stress on Chondrocytes

Author(s)Srinivasan, Padma P.
Author(s)Parajuli, Ashutosh
Author(s)Price, Christopher
Author(s)Wang, Liyun
Author(s)Duncan, Randall L.
Author(s)Kirn-Safran, Catherine B.
Ordered AuthorPadma P. Srinivasan, Ashutosh Parajuli, Christopher Price, Liyun Wang, Randall L. Duncan, Catherine B. Kirn-Safran
UD AuthorSrinivasan, Padma P.en_US
UD AuthorParajuli, Ashutoshen_US
UD AuthorPrice, Christopheren_US
UD AuthorWang, Liyunen_US
UD AuthorDuncan, Randall L.en_US
UD AuthorKirn-Safran, Catherine B.en_US
Date Accessioned2016-04-12T14:14:09Z
Date Available2016-04-12T14:14:09Z
Copyright DateCopyright © 2015 Srinivasan et al.en_US
Publication Date2015-05-26
DescriptionPublisher's PDF.en_US
AbstractVoltage-sensitive calcium channels (VSCC) regulate cellular calcium influx, one of the earliest responses to mechanical stimulation in osteoblasts. Here, we postulate that T-type VSCCs play an essential role in bone mechanical response to load and participate in events leading to the pathology of load-induced OA. Repetitive mechanical insult was used to induce OA in Cav3.2 T-VSCC null and wild-type control mouse knees. Osteoblasts (MC3T3- E1) and chondrocytes were treated with a selective T-VSCC inhibitor and subjected to fluid shear stress to determine how blocking of T-VSCCs alters the expression profile of each cell type upon mechanical stimulation. Conditioned-media (CM) obtained from static and sheared MC3T3-E1 was used to assess the effect of osteoblast-derived factors on the chondrocyte phenotype. T-VSCC null knees exhibited significantly lower focal articular cartilage damage than age-matched controls. In vitro inhibition of T-VSCC significantly reduced the expression of both early and late mechanoresponsive genes in osteoblasts but had no effect on gene expression in chondrocytes. Furthermore, treatment of chondrocytes with CM obtained from sheared osteoblasts induced expression of markers of hypertrophy in chondrocytes and this was nearly abolished when osteoblasts were pre-treated with the T-VSCC-specific inhibitor. These results indicate that T-VSCC plays a role in signaling events associated with induction of OA and is essential to the release of osteoblast-derived factors that promote an early OA phenotype in chondrocytes. Further, these findings suggest that local inhibition of T-VSCC may serve as a therapy for blocking load-induced bone formation that results in cartilage degenerationen_US
DepartmentUniversity of Delaware. Department of Biological Sciences.en_US
DepartmentUniversity of Delaware. Biomedical Engineering Program.en_US
DepartmentUniversity of Delaware. Department of Mechanical Engineering.en_US
CitationSrinivasan PP, Parajuli A, Price C, Wang L, Duncan RL, Kirn-Safran CB (2015) Inhibition of TType Voltage Sensitive Calcium Channel Reduces Load-Induced OA in Mice and Suppresses the Catabolic Effect of Bone Mechanical Stress on Chondrocytes. PLoS ONE 10(5): e0127290. doi:10.1371/journal.pone.0127290en_US
DOI10.1371/journal.pone.0127290en_US
ISSN1932-6203en_US
URLhttp://udspace.udel.edu/handle/19716/17613
Languageen_USen_US
PublisherPLOS (Public Library of Science)en_US
dc.rightsCC BY 4.0en_US
dc.sourcePLOS Oneen_US
dc.source.urihttp://journals.plos.org/plosone/en_US
TitleInhibition of T-Type Voltage Sensitive Calcium Channel Reduces Load-Induced OA in Mice and Suppresses the Catabolic Effect of Bone Mechanical Stress on Chondrocytesen_US
TypeArticleen_US
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