人牙周韧带成纤维细胞对放线菌产生的细胞致死膨胀毒素的反应分析。

The Penn dental journal Pub Date : 2001-01-01
R Lukasiewicz
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引用次数: 0

摘要

已经发现少数不同的细菌病原体产生细胞致死膨胀毒素(CDT)。已有大量证据表明,CDTs可导致多种真核细胞在细胞周期的G2期发生不可逆的阻滞。对CDT敏感的细胞,如中国仓鼠卵巢(CHO)细胞,在接触这种毒素后几天内就会死亡。最近的研究表明,CDT是放线菌的潜在毒力因子,放线菌是一种与青少年牙周炎(JP)相关的细菌。研究放线菌对人牙周韧带成纤维细胞(HPDLFs)的影响。在HPDLFs暴露于生理水平的CDT后,利用一种测定四氮唑化合物转化为可溶性甲醛产物的方法来评估细胞活力,该方法可以在分光光度计上读取。通过台盼蓝染色和血细胞计测量CDT暴露后的细胞活力。CHO细胞作为平行对照,表明从放线菌comitans中获得的CDT具有活性。结果表明,HPDLFs对细胞致死性扩张毒素具有抗性。HPDLFs对CDT的抵抗可能源于成纤维细胞的低周转率。然而,这一课题还有待进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the human periodontal ligament fibroblast response to the cytolethal distending toxin produced by actinobacillus actinomycetemcomitans.

A small number of diverse bacterial pathogens have been found to produce cytolethal distending toxin (CDT). Much evidence has been obtained to show that CDTs cause a variety of eukaryotic cells to become irreversibly blocked in the G2 phase of the cell cycle. Cells which are sensitive to CDT, such as Chinese hamster ovary (CHO) cells, die within a few days after exposure to the toxin. Recent research has shown that CDT is a potential virulence factor for Actinobacillus actinomycetemcomitans, a bacterial species associated with juvenile periodontitis (JP). This research investigates the effects A. actinomycetemcomitans CDT has on human periodontal ligament fibroblasts (HPDLFs). After HPDLFs were exposed to physiologic levels of CDT, cell viability was assessed utilizing an assay that measured the conversion of a tetrazolium compound into a soluble formazan product, which could be read on a spectrophotometer. Cell viability was also measured after exposure to CDT through trypan blue staining and the use of a hemocytometer. CHO cells were utilized as a parallel control to show that the CDT obtained from A. actinomycetemcomitans was active. The results obtained indicate that the HPDLFs are resistant to the cytolethal distending toxin. The possible resistance the HPDLFs have to the CDT may stem from the low turnover rate of the fibroblasts. However, further research must be completed on this topic.

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