This study was designed to demonstrate the expression of the chaperonin containing T-complex polypeptide 1 (CCT) and alpha-smooth muscle actin (alpha-SMA), in normal corneas and corneas treated with ultraviolet radiation (UVR). The wound model chosen is previously characterized, the injury is mild and the cornea heals to transparency. Rabbit corneas were exposed to UVR at the dose producing keratitis. The corneas were allowed to heal for up to 5 days and the paraffin-embedded tissue specimens were double stained and examined morphologically and immunohistochemically. Expression of CCT and alpha-SMA genes was investigated by semiquantitative reverse transcription-polymerase chain reaction (RT-PCR). There was a front of repopulating keratocytes that showed positive staining for alpha-SMA after 3 days. The alpha-SMA mRNA was already strongly expressed after 1 day, whereas the expression level of CCT was increased after 2 days. After 5 days the levels were decreased. By this time the stroma was partly repopulated by keratocytes. In a mild wound, the expression of alpha-SMA mRNA is followed by expression of mRNA of at least one subunit of the complex folding alpha-SMA. At protein level, alpha-SMA is detected in the front line of repopulating keratocytes. Expression levels for both mRNAs decline as the stroma repopulation process progresses.