骨髓基质细胞条件培养液调节神经干细胞分化有效成分的蛋白质微阵列分析

顾平;马芹颖;王彦永;温雅;王铭维;崔冬生 ;刘力 ;耿媛

解剖学报 ›› 2008, Vol. 39 ›› Issue (6) : 845-849.

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解剖学报 ›› 2008, Vol. 39 ›› Issue (6) : 845-849.
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骨髓基质细胞条件培养液调节神经干细胞分化有效成分的蛋白质微阵列分析

  • 顾平1,2*; 马芹颖1,2 ;王彦永1,2; 温雅1,2 ;王铭维1,2; 崔冬生2 ;刘力2 ;耿媛2
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PROTEIN MICROARRAY ANALYSIS OF EFFECTIVE INGREDIENT THAT BONE MARROW STROMAL CELLS CONDITIONED MEDIUM REGULATE THE DIFFERENTIATION OF NEURAL STEM CELLS

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Abstract

Objective To detect the cytokines in the bone marrow stromal cells (BMSCs) conditioned medium (neurobasal conditioned medium ,N-CM) that can regulate the differentiation of neural stem cells (NSCs) into high proportional neurons and explore the mechanism that BMSCs regulate the differentiation of NSCs.Methods The collected N-CM was divided into two parts(>5kD and <5kD)by means of ultrafiltration after misce bene. The two parts were used to culture NSCs separately, and the effective part that could regulate the differentiation of NSCs was detected by protein microarray analysis. Results The N-CM>5kD could promote the NSCs to differentiate into high proportional neurons, so this part was detected by protein microarray analysis, 7 cytokines CINC-3, CNTF, IFN-γ, IL-1α, MCP-1, TIMP-1and VEGF were detected to up-regulate 1.5 times compared with the neurobasal medium (molecular weight above 5kD). Conclusion The dissolvable molecules excreted by BMSCs could promote the NSCs to differentiate into neurons. Some cytokines with the molecular weight of above 5kD play a crucial role during this process.

关键词

神经干细胞 / 骨髓基质细胞 / 条件培养液 / 蛋白质微阵列 / 细胞因子 / 超滤浓缩 / 免疫组织化学

Key words

Neural stem cell / Bone marrow stromal cell / Conditioned medium / Protein microarray / Cytokine / Ultrafiltrate concentration / Immunohistochemistry

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顾平;马芹颖;王彦永;温雅;王铭维;崔冬生 ;刘力 ;耿媛. 骨髓基质细胞条件培养液调节神经干细胞分化有效成分的蛋白质微阵列分析[J]. 解剖学报. 2008, 39(6): 845-849
PROTEIN MICROARRAY ANALYSIS OF EFFECTIVE INGREDIENT THAT BONE MARROW STROMAL CELLS CONDITIONED MEDIUM REGULATE THE DIFFERENTIATION OF NEURAL STEM CELLS[J]. Acta Anatomica Sinica. 2008, 39(6): 845-849
中图分类号: R329.21   

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