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首页> 外文期刊>Journal of Occupational Medicine and Toxicology >Assessment of long-term cultivated human precision-cut lung slices as an ex vivo system for evaluation of chronic cytotoxicity and functionality
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Assessment of long-term cultivated human precision-cut lung slices as an ex vivo system for evaluation of chronic cytotoxicity and functionality

机译:评估长期培养的人类精密切割肺片作为用于评估慢性细胞毒性和功能的离体系统

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Background Investigation of basic chronic inflammatory mechanisms and development of new therapeutics targeting the respiratory tract requires appropriate testing systems, including those to monitor long- persistence. Human precision-cut lung slices (PCLS) have been demonstrated to mimic the human respiratory tract and have potential of an alternative, ex-vivo system to replace or augment in-vitro testing and animal models. So far, most research on PCLS has been conducted for short cultivation periods (≤72?h), while analyses of slowly metabolized therapeutics require long-term survival of PCLS in culture. In the present study, we evaluated viability, physiology and structural integrity of PCLS cultured for up to 15?days. Methods PCLS were cultured for 15?days and various parameters were assessed at different time points. Results Structural integrity and viability of cultured PCLS remained constant for 15?days. Moreover, bronchoconstriction was inducible over the whole period of cultivation, though with decreased sensitivity (EC501d?=?4?×?10?8?M vs. EC5015d?=?4?×?10?6?M) and reduced maximum of initial airway area (1d?=?0.5% vs. 15d?=?18.7%). In contrast, even though still clearly inducible compared to medium control, LPS-induced TNF-α secretion decreased significantly from day 1 to day 15 of culture. Conclusions Overall, though long-term cultivation of PCLS need further investigation for cytokine secretion, possibly on a cellular level, PCLS are feasible for bronchoconstriction studies and toxicity assays.
机译:背景研究基本的慢性炎症机制和开发针对呼吸道的新疗法需要适当的测试系统,包括监测持久性的系统。人体精密切割肺片(PCLS)已被证明可模仿人体呼吸道,并具有替代,体外系统替代或增强体外测试和动物模型的潜力。到目前为止,对PCLS的大多数研究都是在短培养期(≤72?h)内进行的,而对缓慢代谢的药物的分析则要求PCLS在培养中能够长期存活。在本研究中,我们评估了培养长达15天的PCLS的活力,生理学和结构完整性。方法将PCLS培养15天,并在不同时间点评估各种参数。结果培养的PCLS的结构完整性和生存力保持15天不变。此外,尽管敏感性降低(EC 50 1d?=?4?×?10 ?8 ?M vs.EC < sub> 50 15d?=?4?×?10 ?6 ?M)并减小了初始气道面积的最大值(1d?=?0.5%,而15d?=?18.7% )。相反,即使与培养基对照相比仍可明显诱导,LPS诱导的TNF-α分泌从培养的第1天到第15天显着降低。结论总的来说,尽管长期培养PCLS可能需要在细胞水平上进一步研究细胞因子的分泌,但PCLS在支气管狭窄研究和毒性测定中是可行的。

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