Copyright © 2015 Lippincott Williams & Wilkins. Unauthorized commercial reproduction of this slide is prohibited Supplemental PowerPoint Slides Dysregulated COL3A1 and RPL8, RPS16, RPS23 in Disc Degeneration Revealed by Bioinformatics Methods Zongde Yang1#MD,Xin Chen2#MM,Qiulin Zhang1#MD,Bin Cai 1MD,Kai Chen1 MD,Ziqiang Chen 1MD,Yushu Bai 1MD,Zhicai Shi1*MD,Ming Li1*MD 1Department of Spine surgery, Changhai Hospital, Second Military Medical University, Shanghai , China; 2 Department of neurosurgery, Changhai Hospital, Second Military Medical University, Shanghai , China;

Key points: 1. Totally 326 differentially expressed genes were obtained from annulus cells. 2. Totally 35 differentially expressed genes were screened from nucleus pulposus cells. 3. Dysregulated COL3A1 may be related to skeletal system in disc degeneration. 4. Dysregulated RPL8, RPS16 and RPS23 may lead to a disorder of protein synthesis. Mini abstract: Our bioinformatics analysis base on gene expression profile revealed the involvement of COL3A1 in skeletal system process, and ribosomal proteins (RP) including RPL8, RPS16 and RPS23 in the biological processes of translation, translational elongation and RNA processing respectively in the progression of DD, suggesting the potential use of being specific therapeutic molecular targets in the treatment of DD.

The biological processes involved by COL3A1 in two different cells

Densely connected module extracted from the protein-protein interaction network. The green nodes are differentially expression genes.