Kreisberg J I, Mills J W, Jarrell J A, Rabito C A, Leaf A
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5445-7. doi: 10.1073/pnas.77.9.5445.
In order to study the relationship between cell swelling and cell death due to ischemia, we have developed an in vitro model by using primary cultures of renal tubular epithelial cells. With this model, we have studied two components of ischemia--namely, anoxia along with substrate deprivation. After 2 hr of anoxia in the absence of substrate, the cultured cells swelled and blebbed. Cells similarly treated in the presence of 8% polyethylene glycol, an oncotic agent, did not swell and bleb, and when cells were counted 18 hr later, similar numbers of cells were seen as in the untreated cultures. However, tubule cells exposed to anoxia without 8% polyethylene glycol had 50% fewer cells 18 hr later. Therefore, if cell swelling is prevented during 2 hr of anoxia, cell viability is improved.
为了研究缺血导致的细胞肿胀与细胞死亡之间的关系,我们利用肾小管上皮细胞原代培养建立了一个体外模型。通过这个模型,我们研究了缺血的两个组成部分,即缺氧和底物剥夺。在无底物条件下缺氧2小时后,培养的细胞肿胀并出现气泡。在存在8%聚乙二醇(一种渗透剂)的情况下进行类似处理的细胞没有肿胀和出现气泡,并且在18小时后计数时,可见的细胞数量与未处理的培养物相似。然而,暴露于无8%聚乙二醇缺氧环境的肾小管细胞在18小时后细胞数量减少了50%。因此,如果在缺氧2小时期间防止细胞肿胀,细胞活力会得到改善。