Impact of direct cell co‐cultures on human adipose‐derived stromal cells and nucleus pulposus cells. Issue 11 (2nd August 2013)

• Record Type: Journal Article
• Authors: Sun, Zhen; Liu, Zhi‐Heng; Zhao, Xu‐Hong; Sun, Lu; Chen, Yu‐Fei; Zhang, Wei‐Lin; Gao, Yang; Zhang, Yong‐Zhao; Wan, Zhong‐Yuan; Samartzis, Dino; Wang, Hai‐Qiang; Luo, Zhuo‐Jing
• Is Part Of: Journal of orthopaedic research. Volume 31:Issue 11(2013:Nov.)
• Page Start: 1804
• Page End: 1813
• Publication Date: 2013-08-02
• Subjects: direct co‐culture -- intervertebral disc degeneration -- adipose‐derived stem cells -- nucleus pulposus; Orthopedics -- Periodicals; Musculoskeletal system -- Periodicals; 616.7
• DOI: 10.1002/jor.22439
• Languages: English
• ISSNs: 0736-0266

Abstract

ABSTRACT: Biologic and cellular treatment strategies aiming for curing intervertebral disc degeneration (IDD) have been proposed recently. Given the convenient availability and expansion potential, adipose‐derived stromal cells (ADSCs) might be an ideal cell candidate. However, the interaction between ADSCs and nucleus pulposus (NP) cells still remains ambiguous, especially in direct co‐cultures of the two types of cells. Nevertheless, NP markers in ADSCs after co‐cultures were unidentified. Here, we addressed the interaction of human ADSCs and NP cells in a direct co‐culture system for the first time. As a result, ADSCs could differentiate to the NP cell phenotype with a significant up‐regulated expression of multiple genes and proteins in extracellular matrix (ECM) ( SOX9, COL2A1, ACAN, and COL6A2 ), relative NP markers ( FOXF1, PAX1, CA12, and HBB ) and pertinent growth factors ( CDMP‐1, TGF‐β1, IGF‐1, and CTGF ). Moreover, the gene expression of COL2A1, ACAN, and COL6A2 of degenerate NP cells was also up‐regulated. Collectively, these results suggest that direct co‐cultures of ADSCs and NP cells may exert a reciprocal impact, that is, both stimulating ADSCs differentiation to the NP cell phenotype and inducing NP cells to regain functional phenotype. Accordingly, ADSCs might be a potential candidate in the development of cellular treatment strategies for IDD. © 2013 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 31:1804–1813, 2013