Expression of Runx2 and type X collagen in vertebral growth plate of patients with adolescent idiopathic scoliosis.

Abstract

The different expression of type X collagen and Runx2 between the convex and concave side of vertebral growth plate in scoliosis may help to improve our understanding of the role that growth plate tissue play in the development or progression of idiopathic scoliosis. In this investigation, there were significant differences of the total expression of type X collagen, Runx2 protein, and Runx2 mRNA between convex side and concave side growth plates of the apex vertebrae (p < 0.05). The total expression of type X collagen in the concave side growth plates of the lower end vertebrae was higher than that in the same side growth plates of apex (p < 0.05). The total expression of Runx2 in the concave side growth plates in the upper and lower end vertebrae were higher than that in the concave side growth plates of apex (p < 0.05). The expression of type X collagen, Runx2, and Runx2 mRNA, the cell density of type X collagen and Runx2 positive chondrocytes, and histological changes between convex side and concave side of the vertebral growth plate indicated that the vertebral growth plate was affected by mechanical forces, which was a secondary change and could contribute to progression of adolescent idiopathic scoliosis.

• Authors: Shoufeng Wang, Yong Qiu, Zhaolong Ma, Caiwei Xia, Feng Zhu, Zezhang Zhu
• Journal: Connective tissue research (Connect Tissue Res) Vol. 51 Issue 3 Pg. 188-96 (Jun 2010) ISSN: 1607-8438 [Electronic] England
• PMID: 20073986 (Publication Type: Journal Article)

Chemical References

• Collagen Type X
• Core Binding Factor Alpha 1 Subunit
• RNA, Messenger
• RUNX2 protein, human

Topics

• Adolescent
• Cartilage, Articular (metabolism, pathology)
• Child
• Chondrocytes (metabolism, pathology)
• Collagen Type X (genetics, metabolism)
• Core Binding Factor Alpha 1 Subunit (genetics, metabolism)
• Female
• Gene Expression
• Growth Plate (chemistry, metabolism, pathology)
• Humans
• Immunoenzyme Techniques
• In Situ Hybridization
• RNA, Messenger (analysis, metabolism)
• Scoliosis (genetics, metabolism, pathology)
• Spine (metabolism, pathology)