The polymerase chain reaction (PCR) and hot-blotting methods were used
to identify fibroblast growth factor (FGF) receptor-1-specific messen
ger ribonucleic acid (mRNA) sequences in cDNA samples prepared from hu
man corneal endothelial cell cultures with proliferative and senescent
morphology, an ex vivo corneal epithelium sample, two primary corneal
epithelial cell cultures, two third-passage corneal epithelial cell c
ultures, and two stromal fibroblast cultures. The PCR primers used in
this study distinguished mRNAs coding for three amino-terminal motifs
(alpha, beta, and gamma) of the FGF receptor-1 that are derived by alt
ernative splicing from a single genomic sequence. Messenger RNA molecu
les coding for FGF receptor-1 amino-terminal motif were detected in co
rneal endothelial and epithelial cells. The alpha and beta amino-termi
nal motif, but not the gamma amino-terminal motif, mRNAs were detected
in stromal fibroblasts. The gamma motif lacks a known signal sequence
for membrane translocation and is thought to represent an intracellul
ar form of the FGF receptor-1. Identification of mRNA coding for FGF r
eceptor-1 along with the previous identification of basic FGF mRNA and
protein in corneal endothelial, epithelial, and stromal fibroblast ce
lls suggests an autocrine and/or paracrine role for basic FGF in the p
hysiology of the cornea.