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多聚脱氧核糖核苷酸增强人皮肤成纤维细胞的增殖:A2嘌呤能受体亚型的参与

Polydeoxyribonucleotides enhance the proliferation of human skin fibroblasts: involvement of A2 purinergic receptor subtypes.

作者信息

Thellung S, Florio T, Maragliano A, Cattarini G, Schettini G

机构信息

Institute of Pharmacology, School of Medicine, University of Genova, Italy.

出版信息

Life Sci. 1999;64(18):1661-74. doi: 10.1016/s0024-3205(99)00104-6.

Abstract

It is well-known that nucleotides, nucleosides and purine/pyrimidine bases enhance cell proliferation in vitro. Nevertheless, the molecular mechanisms involved in this mitogenic activity is still controversial, since these compounds are reported both to synergize with growth factor, and to act directly on purinergic receptor inducing per se a proliferative response. It was suggested that cell growth enhancement could be mediated by the A2 purinergic receptor activation. Here we report that a polydeoxyribonucleotide (PDRN) and adenosine are able to increase, the growth rate of human skin fibroblasts in primary cultures. The proliferative activity exerted by PDRN was significantly counteracted by the A2 antagonist 3, 7-Dimethyl-1-propargylxanthine (DMPX), but not by the A1 antagonist 8-cyclopentyl-1,3-dipropylxanthine (PD 116,948, DPCPX). Accordingly, the trophic action of PDRN was mimicked by the A2 agonist N6-[2-(3,5-Dimethoxyphenyl)-2-(methylphenyl)-ethyl]adenosine (DPMA), while the A1 agonist N6-Cyclopenthyladenosine (CPA) did not show any effect. In microfluorimetric studies, we observed that PDRN and adenosine increased the concentration of cytosolic calcium ions. The PDRN-evoked calcium rise was dose-dependent and DMPX sensitive. Taken together, our results suggest that PDRN may operate as a pro-drug providing the cultured cells with an effective amount of mitogenic deoxyribonucleotides, deoxyribonucleosides and bases; moreover, cell proliferation enhancement that has been induced by PDRN seems to be mediated, at least in part, by the activation of purinergic receptors of the A2 subtype.

摘要

众所周知,核苷酸、核苷以及嘌呤/嘧啶碱基可在体外增强细胞增殖。然而,这种促有丝分裂活性所涉及的分子机制仍存在争议,因为据报道这些化合物既能与生长因子协同作用,又能直接作用于嘌呤能受体,本身诱导增殖反应。有人提出细胞生长增强可能由A2嘌呤能受体激活介导。在此我们报告,一种聚脱氧核糖核苷酸(PDRN)和腺苷能够提高原代培养的人皮肤成纤维细胞的生长速率。PDRN发挥的增殖活性被A2拮抗剂3,7 - 二甲基 - 1 - 丙炔基黄嘌呤(DMPX)显著抵消,但未被A1拮抗剂8 - 环戊基 - 1,3 - 二丙基黄嘌呤(PD 116,948,DPCPX)抵消。相应地,A2激动剂N6 - [2 - (3,5 - 二甲氧基苯基)-2 - (甲基苯基)-乙基]腺苷(DPMA)模拟了PDRN的营养作用,而A1激动剂N6 - 环戊基腺苷(CPA)未显示任何作用。在微量荧光测定研究中,我们观察到PDRN和腺苷增加了胞质钙离子浓度。PDRN引起的钙升高呈剂量依赖性且对DMPX敏感。综上所述,我们的结果表明PDRN可能作为一种前体药物,为培养细胞提供有效量的促有丝分裂脱氧核糖核苷酸、脱氧核糖核苷和碱基;此外,PDRN诱导的细胞增殖增强似乎至少部分是由A2亚型嘌呤能受体的激活介导的。

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