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Am J Physiol Lung Cell Mol Physiol 288: L179-L189, 2005. First published September 24, 2004; doi:10.1152/ajplung.00272.2004
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Freshly isolated rat alveolar type I cells, type II cells, and cultured type II cells have distinct molecular phenotypes

Robert Gonzalez,1 Yee Hwa Yang,2,3 Chandi Griffin,2,4 Lennell Allen,1 Zachary Tigue,1 and Leland Dobbs1,2,5

1Cardiovascular Research Institute, Departments of 2Medicine and 5Pediatrics, 3Center of Bioinformatics and Molecular Biostatistics, and 4General Clinical Research Center, University of California San Francisco, San Francisco, California

Submitted 19 July 2004 ; accepted in final form 14 September 2004

We used microarray analysis with Affymetrix rat chips to determine gene expression profiles of freshly isolated rat type I (TI) and TII cells and cultured TII cells. Our goals were 1) to describe molecular phenotypic "fingerprints" of TI and TII cells, 2) to gain insight into possible functional differences between the two cell types through differentially expressed genes, 3) to identify genes that might indicate potential functions of TI cells, since so little is known about this cell type, and 4) to ascertain the similarities and differences in gene expression between cultured TII cells and freshly isolated TI cells. For these experiments, we used preparations of isolated TI and TII cells that contained <2% cross-contamination. With a false discovery rate of 1%, 601 genes demonstrated over twofold different expression between TI and TII cells. Those genes with very high levels of differential expression may be useful as markers of cell phenotype and in generating novel hypotheses about functions of TI and TII cells. We found similar numbers of differentially expressed genes between freshly isolated TI or TII cells and cultured TII cells (698, 637 genes) and freshly isolated TI and TII cells (601 genes). Tests of sameness/difference including cluster dendrograms and log/log identity plots indicated major differences between the phenotypes of freshly isolated TI cell and cultured type II cell populations. The latter results suggest that experiments with TII cells cultured under these conditions should be interpreted with caution with respect to biological relevance to TI or TII cells.

gene expression profiling; transdifferentiation



Address for reprint requests and other correspondence: L. G. Dobbs, Suite 150, UCSF-LH Campus, 3333 California St., San Francisco, CA 94118 (E-mail: dobbs{at}itsa.ucsf.edu)




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