Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/79408
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Type: Journal article
Title: Inhibition of protein kinase-D promotes cartilage repair at injured growth plate in rats
Author: Chung, R.
Foster, B.
Xian, C.
Citation: Injury-international Journal of the Care of the Injured, 2013; 44(7):914-922
Publisher: Elsevier Sci Ltd
Issue Date: 2013
ISSN: 0020-1383
1879-0267
Statement of
Responsibility: 
Rosa Chung, Bruce K. Foster and Cory J. Xian
Abstract: <h4>Introduction</h4>Injured growth plate cartilage is often repaired by bony tissue, causing bone growth defects in children. Currently, mechanisms for the undesirable repair remain unclear and there are no biological treatments available to prevent the associated bone growth defects. Osterix is known as a vital transcription factor for osteoblast differentiation which is critical for normal bone formation and bone repair, and osterix is known to be regulated by protein kinase-D; however it is unknown whether protein kinase-D-osterix signalling plays any roles in the bony repair of injured growth plate.<h4>Methods</h4>Using a rat model, this study investigated potential roles of protein kinase-D (PKD) in regulating expression of osteogenic transcription factor osterix and the growth plate bony repair. 4 days post injury at the proximal tibial growth plate, rats received four once-daily injections of vehicle or 2.35 mg/kg gö6976 (a PKD inhibitor), and growth plate tissues collected at day 10 were examined histologically and molecularly. In addition, effects of PKD inhibition on osteogenic and chondrogenic differentiation were examined in vitro using rat bone marrow mesenchymal stromal cells.<h4>Results</h4>Compared to vehicle control, PKD inhibition caused a decrease in bone volume (p<0.05), an increase in % of mesenchymal tissue (p<0.01), and an increase in cartilaginous tissue within the injury site. Consistently, gö6976 treatment tended to decrease expression of bone-related genes (osterix, osteocalcin) and increase levels of cartilage-related genes (Sox9, collagen-2a, collagen-10a1). In support, in vitro experiments showed that gö6976 presence in the primary rat marrow stromal cell culture resulted in a decrease of alkaline phosphatase(+) CFU-f colonies formed (p<0.05) and an increase in collagen-2a expression in chondrogenic pellet culture (p<0.05).<h4>Conclusion</h4>These studies suggest that PKD is important for growth plate bony repair and its inhibition after growth plate injury may result in less bone formation and potentially more cartilage repair.
Keywords: Cartilage; Growth Plate; Bone Marrow Cells; Osteoblasts; Animals; Rats; Rats, Sprague-Dawley; Disease Models, Animal; Protein Kinase C; Transcription Factors; Gene Expression; Male; Salter-Harris Fractures
Rights: © 2013 Elsevier Ltd. All rights reserved.
RMID: 0020130359
DOI: 10.1016/j.injury.2013.01.038
Appears in Collections:Medical Sciences publications

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