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Isolation of highly pure alveolar epithelial type I and type II cells from rat lungs

2004; Elsevier BV; Volume: 84; Issue: 6 Linguagem: Inglês

10.1038/labinvest.3700095

1530-0307

Jiwang Chen, Zhongming Chen, Telugu Narasaraju, Nili Jin, Lin Liu,

MicroRNA in disease regulation

There are no ideal cell lines available for alveolar epithelial type I and II cells (AEC I and II) at the present time. The current methods for isolating AEC I and II give limited purities. Here, we reported improved and reproducible methods for the isolation of highly pure AEC I and II from rat lungs. AEC I and II were released from lung tissues using different concentrations of elastase digestion. Macrophages and leukocytes were removed by rat IgG 'panning' and anti-rat leukocyte common antigen antibodies. For AEC II isolation, polyclonal rabbit anti-T1α (an AEC I apical membrane protein) antibodies were used to remove AEC I contamination. For AEC I isolation, positive immunomagnetic selection by polyclonal anti-T1α antibodies was used. The purities of AEC I and II were 91±4 and 97±1%, respectively. The yield per rat was ∼2 × 106 for AEC I and ∼33 × 106 for AEC II. The viabilities of these cell preparations were more than 96%. The protocol for AEC II isolation is also suitable to obtain pure AEC II (93–95%) from hyperoxia-injured and recovering lungs. The purified AEC I and II can be used for gene expression profiling and functional studies. It also offers an important tool to the field of lung biology.