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Expression of growth differentiation factor 6 in the human developing fetal spine retreats from vertebral ossifying regions and is restricted to cartilaginous tissues

Authors :
Bojiang Shen
Divya Bhargav
Sarennya Pathmanandavel
Twishi Gulati
Aiqun Wei
Ashish D. Diwan
Lisa A. Williams
Zhimin Fang
Source :
Journal of Orthopaedic Research. 34:279-289
Publication Year :
2015
Publisher :
Wiley, 2015.

Abstract

During embryogenesis vertebral segmentation is initiated by sclerotomal cell migration and condensation around the notochord, forming anlagen of vertebral bodies and intervertebral discs. The factors that govern the segmentation are not clear. Previous research demonstrated that mutations in growth differentiation factor 6 resulted in congenital vertebral fusion, suggesting this factor plays a role in development of vertebral column. In this study, we detected expression and localization of growth differentiation factor 6 in human fetal spinal column, especially in the period of early ossification of vertebrae and the developing intervertebral discs. The extracellular matrix proteins were also examined. Results showed that high levels of growth differentiation factor 6 were expressed in the nucleus pulposus of intervertebral discs and the hypertrophic chondrocytes adjacent to the ossification centre in vertebral bodies, where strong expression of proteoglycan and collagens was also detected. As fetal age increased, the expression of growth differentiation factor 6 was decreased correspondingly with the progress of ossification in vertebral bodies and restricted to cartilaginous regions. This expression pattern and the genetic link to vertebral fusion suggest that growth differentiation factor 6 may play an important role in suppression of ossification to ensure proper vertebral segmentation during spinal development. © 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:279–289, 2016.

Details

ISSN :
07360266
Volume :
34
Database :
OpenAIRE
Journal :
Journal of Orthopaedic Research
Accession number :
edsair.doi...........e3262dcc97c20910a8189605948a0547
Full Text :
https://doi.org/10.1002/jor.22983