Fig. 1. RT-PCR analysis of LTBP expression in human cell lines. Total RNA isolated from different cell lines was reverse transcribed followed by PCR amplification using two different primer pairs per each LTBP. (A) LTBP-x.1 primers amplify products spanning from the last EGF-repeats to the noncoding region, whereas LTBP-x.2 primers amplify regions around the 3^rd 8-Cys repeat (for primer sequences see Table 1). `RPA' and `3rd 8-Cys' probes used in northern blotting and RNase protection assays are indicated under LTBP-4. In B, human lung fibroblast (CCL-137) RNA was used in RT-PCR reaction with the eight different primer pairs. Agarose gel electrophoreses of the amplified fragments are shown. An arrowhead indicates the LTBP-48-Cys^3rd form. The molecular weight markers (nt) are shown on the left. (C) A summary of the arbitrary quantitation of the amounts of different LTBPs in the panel of the indicated cell lines. The amounts of specific products were equalized using G3PDH levels in each cell line, and compared with those of CCL-137 cells. These cell lines included human embryonic lung fibroblasts (CCL-137, WI-38), human skin fibroblasts, SV-40 transformed embryonic lung fibroblasts (VA-13; counterpart of WI-38 cells), human fibrosarcoma cells (HT-1080), human umbilical vein endothelial cells (HUVEC) and immortalized human skin keratinocytes (HaCat). The results, obtained from several independent experiments using two different primer pairs of each LTBP, were combined and are expressed arbitrarily from positive (+) to strong positive (++++).