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一种从小鼠中分离II型细胞和克拉拉细胞的改良方法。

An improved method for the isolation of type II and Clara cells from mice.

作者信息

Belinsky S A, Lechner J F, Johnson N F

机构信息

Inhalation Toxicology Research Institute, Albuquerque, New Mexico 87185, USA.

出版信息

In Vitro Cell Dev Biol Anim. 1995 May;31(5):361-6. doi: 10.1007/BF02634285.

Abstract

Identifying the causal events and temporal aspects of lung cancer development requires the ability to isolate target and nontarget cells for comparative analyses. Current methodology can either isolate only one pure specific cell population from a lung or multiple cell types at lower purity. Previous studies in our laboratory have identified the alveolar type II cell as the progenitor cell for tumor development in the A/J mouse. The purpose of this study was to develop new protocols for the isolation and culture of type II and Clara cells from the mouse lung. Both type II and Clara cells were obtained in high purity using a sequential centrifugal elutriation protocol. In the first elutriation, cell fractions were collected using a Standard chamber. The type II and Clara cell fractions were then elutriated separately (two different separations) using a Sanderson chamber. The final purity of the type II and Clara cell preparations was 73% and 76%, respectively. Colonies of 4 to 20 Clara cells exhibiting epithelial morphology were evident 1 wk after plating in low serum medium. The growth of type II cells required the addition of bronchioalveolar lavage fluid and acidic fibroblast growth factor to the medium. The isolation of viable mouse type II and Clara cells in high purity should facilitate the identification of cell-specific changes in gene expressions or in enzymatic pathways following in vivo or in vitro exposure to environmental carcinogens.

摘要

确定肺癌发生的因果事件和时间特征需要具备分离靶细胞和非靶细胞以进行比较分析的能力。目前的方法要么只能从肺中分离出一种纯的特定细胞群体,要么以较低的纯度分离出多种细胞类型。我们实验室之前的研究已确定肺泡II型细胞是A/J小鼠肿瘤发生的祖细胞。本研究的目的是开发从小鼠肺中分离和培养II型细胞和克拉拉细胞的新方案。使用连续离心淘析方案可获得高纯度的II型细胞和克拉拉细胞。在第一次淘析中,使用标准腔室收集细胞组分。然后使用桑德森腔室分别淘析II型细胞和克拉拉细胞组分(两次不同的分离)。II型细胞和克拉拉细胞制剂的最终纯度分别为73%和76%。接种于低血清培养基1周后,可见4至20个呈现上皮形态的克拉拉细胞形成的集落。II型细胞的生长需要向培养基中添加支气管肺泡灌洗液和酸性成纤维细胞生长因子。高纯度地分离有活力的小鼠II型细胞和克拉拉细胞应有助于识别体内或体外暴露于环境致癌物后基因表达或酶促途径中的细胞特异性变化。

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