Weller N K, Karnovsky M J
Am J Pathol. 1986 Jan;122(1):92-100.
We have developed an improved isolation procedure for rat lung alveolar Type II (ATII) cells which yields a more representative sample of ATII cells with respect to their densities. This procedure includes an initial selection on a density gradient of approximately the complete density range of rat lung ATII cells. Subsequently, to exclude contaminating macrophages and lymphocytes from this fraction, the authors have exploited the fact that the contaminating cells have leukocyte common antigen (LC) on their surfaces, whereas the ATII cells do not. Our procedure yields 2 X 10(7) ATII cells per rat in a fraction which is 90% pure; the cells are immediately available for biochemical or pharmacologic analysis and represent a 90-95% recovery of the ATII cells loaded onto the density gradient. The cells retain their in vivo morphologic characteristics, including their polarity.
我们已经开发出一种改进的大鼠肺Ⅱ型肺泡(ATII)细胞分离程序,该程序能产生密度更具代表性的ATII细胞样本。此程序包括在大约大鼠肺ATII细胞完整密度范围内的密度梯度上进行初始筛选。随后,为了从该部分中排除污染的巨噬细胞和淋巴细胞,作者利用了污染细胞表面有白细胞共同抗原(LC)而ATII细胞没有这一事实。我们的程序每只大鼠可在纯度为90%的部分中获得2×10⁷个ATII细胞;这些细胞可立即用于生化或药理学分析,并且代表加载到密度梯度上的ATII细胞90 - 95%的回收率。这些细胞保留了它们在体内的形态特征,包括极性。