Fig. 4.

CADM1 isoforms expressed in human lungs and lung epithelial cells. Total RNAs were extracted from rat primary cultured type 1 and type 2 AECs, and were analyzed by RT-PCR using primer sets for calveolon-1 and surfactant protein B (a). Total RNAs from NCI-H441 and RLE-6TN human lung epithelial cell lines, rat type 1 and type 2 AECs and human lung tissues of cases indicated were analyzed by RT-PCR using a primer set encompassing the CADM1 extracellular juxtamembrane region, susceptible to alternative splicing (b). The PCR products were electrophoresed on 3 % agarose gels, together with CADM1 isoform size markers (rightmost lane in B). L, 100 base pair (bp) ladder. RNAs were also PCR-amplified using a primer set for G3PDH to indicate RNA loading per lane