Early Gene Expression of Immune Proteins in Chondrocytes Differentiation from Rat Bone Marrow Stromal Cells
To study an effective differentiation condition of chondrocytes(Ch) from rat bone marrow stromal cells(MSC) in vitro by immunohistochemistry, in situ hybridization and RTPCR, and identify gene expression pattern of immune proteins in this process via cDNA microarray analysis. The results suggested that Dexamethasone (Dex) had an ability to promote cell proliferation. The group of TGF-β could highly express collagen Ⅱ while its cell proliferation was weaker than that of Dex group. These indicated that TGF-βhad the ability to differentiate MSC into Ch.The group of combination of TGF-βand Dex could both express collagen Ⅱ and maintain proliferation. Analysis by cDNA microarray revealed that 7genes of immune proteins out of the 2242 rat genes had differential expression during this process, including membrane-spanning 4-domainssubfamily A; T-cell receptor active alpha-chain C-region, TRA29; MHC class I-related protein; pepti dylprolyl isomerase C-associated protein; C8b;complement component 4 binding protein α and β.This study showed that combination cultural condition in which MSC were induced into Ch lineage was effective to repair of articular cartilage. Various immune genes were involved in Ch differentiation. This would provide foundation for repair of articular cartilage defect with Ch.
Bone marrow stromal cell Chondrocyte Dexamethasone
Jia Tanghong Sun Yuping Wang Yunshan Ma Xiaoli Shen Hong Cao Yilin
Jinan Central Hospital, Shandong University,Jinan, China Research Lab of Tissue Engineering of Shanghai,Shanghai,China
国际会议
武汉
英文
230-233
2007-07-06（万方平台首次上网日期，不代表论文的发表时间）