Published ahead of print on March 26, 2008, doi:10.1165/rcmb.2008-0049OC
American Journal of Respiratory Cell and Molecular Biology. Vol. 39, pp. 253-262, 2008
© 2008 American Thoracic Society DOI: 10.1165/rcmb.2008-0049OC
Directed Expression of Transgenes to Alveolar Type I Cells in the Mouse
Jeff N. Vanderbilt1,
Lennell Allen1,
Robert F. Gonzalez1,
Zachary Tigue1,
Jess Edmondson1,
Daniel Ansaldi1,
Anne Marie Gillespie1 and
Leland G. Dobbs1,2,3
1 Cardiovascular Research Institute, and Departments of 2 Medicine and 3 Pediatrics, University of California San Francisco, San Francisco, California
Correspondence and requests for reprints should be addressed to Jeff N. Vanderbilt, Ph.D., University of California San Francisco, 3333 California Street, Suite 150, San Francisco, CA 94118. E-mail: jeff.vanderbilt{at}ucsf.edu
Podoplanin (RTI40, aggrus, T1 , hT1 -2, E11, PA2.26, RANDAM-2, gp36, gp38, gp40, OTS8) is a type I cell marker in rat lung. We show that a bacterial artificial chromosome vector containing the rat podoplanin gene (RTIbac) delivers a pattern of transgene expression in lung that is more restricted to mouse type I cells than that of the endogenous mouse podoplanin gene. RTIbac-transgenic mice expressed rat podoplanin in type I cells; type II cells, airways, and vascular endothelium were negative. A modified bacterial artificial chromosome containing internal ribosome entry site (IRES)-green fluorescent protein (GFP) sequences in the podoplanin 3'UTR expressed rat podoplanin and transgenic GFP in type I cells. RTIbac transgene expression was absent or reduced in pulmonary pleura, lymphatic endothelium, and putative lymphoid-associated stromal tissue, all of which contained abundant mouse podoplanin. Rat podoplanin mRNA levels in normal rat lung and RTIbac transgenic lung were 25-fold higher than in corresponding kidney and brain samples. On Western blots, transgenic rat and endogenous mouse podoplanin displayed very similar patterns of protein expression in various organs. Highest protein levels were observed in lung with 10- to 20-fold less in brain; there were low levels in thymus and kidney. Both GFP and rat podoplanin transgenes were expressed at extrapulmonary sites of endogenous mouse podoplanin gene expression, including choroid plexus, eye ciliary epithelium, and renal glomerulus. Because their pulmonary expression is more restricted than endogenous mouse podoplanin, RTIbac derivatives should be useful for mouse type I cell–specific transgene delivery.
Key Words: alveolar type I cells transgenes podoplanin bacterial artificial chromosome alveolar epithelium
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