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聚脱氧核糖核苷酸(PDRN)促进人成骨细胞增殖:骨组织修复的新方案

Polydeoxyribonucleotide (PDRN) promotes human osteoblast proliferation: a new proposal for bone tissue repair.

作者信息

Guizzardi Stefano, Galli Carlo, Govoni Paolo, Boratto Renata, Cattarini Giulia, Martini Desiree, Belletti Silvana, Scandroglio Renato

机构信息

Department of Experimental Medicine--Section of Histology, Via Volturno 39, University of Parma, 43100 Parma, Italy.

出版信息

Life Sci. 2003 Aug 29;73(15):1973-83. doi: 10.1016/s0024-3205(03)00547-2.

Abstract

Several researchers have recently shed new light upon the importance of extracellular nucleotides and nucleosides to stimulate cells growth. PDRN, a mixture of deoxyribonucleotides polymers of different lengths, has recently demonstrated to stimulate "in vitro" fibroblast proliferation and collagen production, probably stimulating the purinergic receptor system. In this work we evaluated the effects of PDRN on human cultured osteoblasts, focusing our attention on cell proliferation and alkaline phosphatase activity. PDRN at a concentration of 100 microg/ml induce an increase in osteoblasts growth after 6 days as compared to control (+21%). The addition of DMPX 50 microM and suramine (P2 inhibitor) 10 microM give different results: suramine has no significant effect, while DPMX reduce, even if partially, the PDRN induced cell growth. The alkaline phosphatase activity shows a gradual enhancement starting from day 0 to day 10, even if PDRN treated cells, examined at day 6, present a sensibly lower phosphatase activity when compared to controls. Our data demonstrate that PDRN acts as an osteoblast growth stimulator. Its action is partially due to a stimulation of the purinergic system mediated by A2 purinoreceptors, however we can not exclude the involvement of other mechanism like salvage pathway.

摘要

最近,几位研究人员对细胞外核苷酸和核苷在刺激细胞生长方面的重要性有了新的认识。PDRN是一种不同长度的脱氧核糖核苷酸聚合物的混合物,最近已证明它能刺激“体外”成纤维细胞增殖和胶原蛋白生成,可能是通过刺激嘌呤能受体系统来实现的。在这项研究中,我们评估了PDRN对人培养成骨细胞的影响,重点关注细胞增殖和碱性磷酸酶活性。与对照组相比,浓度为100微克/毫升的PDRN在6天后可使成骨细胞生长增加(增加21%)。添加50微摩尔的DMPX和10微摩尔的苏拉明(P2抑制剂)会产生不同的结果:苏拉明没有显著影响,而DPMX即使只是部分地降低了PDRN诱导的细胞生长。碱性磷酸酶活性从第0天到第10天呈逐渐增强趋势,即使在第6天检测的PDRN处理细胞与对照组相比,其磷酸酶活性明显较低。我们的数据表明,PDRN可作为成骨细胞生长刺激剂。其作用部分归因于由A2嘌呤受体介导的嘌呤能系统的刺激,然而我们不能排除其他机制如补救途径的参与。

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