Fibroblast growth factor receptor-1 and neonatal compensatory lung growth after exposure to 95% oxygen.

Neonatal rats exposed to 95% oxygen (O-2) for 7 days from birth had inhibited lung growth, DNA synthesis, and secondary septation. These parameters were rapidly restored by a period of recovery in air. Northern and Western blot analysis and immunohistochemistry were used to screen for the fibroblast growth factor receptor-1 (FGF-R1) and its high affinity ligand, basic fibroblast growth factor (bFGF), which could have a role in this recovery process. Expression of bFGF in the lung was significantly reduced at the end of the 7-day exposure to 95% O-2 and was increased after 3 days of recovery in air. Expression of FGF-R1 was not affected by exposure to 95% O-2 or recovery in air. We hypothesized that the increase in bFGF after removal from 95% O-2, acting through the FGF-R1, would be critical for compensatory growth. Intraperitoneal injection of soluble truncated FGF-R1 at the onset of the recovery phase arrested compensatory lung DNA synthesis and secondary septation seen in control animals after 3 days of recovery, confirming a role for FGF-R1 in this model of compensatory neonatal lung growth.