Differential proteome analysis in adolescent idiopathic scoliosis patients with thoracolumbar/lumbar curvatures

• Main Authors: Hiroto Makino, Shoji Seki, Isao Kitajima, Hiraku Motomura, Makiko Nogami, Yasuhito Yahara, Naoko Ejiri, Tomoatsu Kimura
• Format: Article
• Language: English
• Published: BMC 2019-05-01
• Series: BMC Musculoskeletal Disorders
• Subjects: Adolescent idiopathic scoliosis; Vitamin D binding protein; Two-dimensional fluorescence difference gel electrophoresis; Thoracolumbar curvature
• Online Access: http://link.springer.com/article/10.1186/s12891-019-2640-y
• ISSN: 1471-2474

Abstract Background Although the pathogenesis of adolescent idiopathic scoliosis (AIS) remains unclear, there are little evidences of the pathogenesis in patients with thoracolumbar/lumbar AIS. The purpose of this study was to identify proteins or proteomes that may be causally related to the pathogenesis of AIS with structured thoracolumbar/lumbar curvature using two-dimensional fluorescence difference gel electrophoresis (2D-DIGE). Methods A total of 20 control volunteers and 61 AIS in patients with thoracolumbar/lumbar curvature were included. First, the plasma samples of each five AIS with pure thoracolumbar/lumbar curvature and control samples were subjected to 2D-DIGE analysis. Protein spots that were expressed differently by the AIS and control groups were selected and identified by nanoscale liquid chromatography–tandem mass spectrometry (nanoLC-MS/MS) analysis. To characterize the differently-expressed proteins in AIS patients, we performed functional pathway analysis using the Protein ANalysis THrough Evolutionary Relationships (PANTHER) system. Additionally, the proteins were compared between control and AIS using western blotting. Lastly, prospectively collected 15 control and 41 AIS with thoracolumbar/lumbar curvature samples were compared to the differentially expressed proteins. Results A total of 3862 ± 137 spots were detected, of which 11 spots met the criteria when compared with controls. Nine proteins were identified by nanoLC-MS/MS. Functional analysis showed the association of the proteins in AIS patients with blood coagulation using the PANTHER system. Of the proteins, vitamin D binding protein (DBP) significantly correlated with Cobb angle in thoracolumbar/lumbar curvatures. DBP expression of the prospectively collected AIS samples were significantly higher than those of controls (P < 0.05). Conclusions This study suggests that DBP and several coagulation-related proteins may play a role in the pathogenesis of AIS. DBP appears to be a marker of severity of AIS with thoracolumbar/lumbar curvature.