Transferrin (Tf), the plasma iron transport protein which supports cel
l proliferation and differentiation and has bacteriostatic, antioxidan
t and anti-inflammatory activity, has been found in relatively high co
ncentrations in the intraocular fluids. Intraocular synthesis of Tf ha
s recently been demonstrated, although the intraocular tissue(s) respo
nsible have not been identified, We designed this study to determine w
hether certain ocular tissues can make and secrete transferrin. Transf
errin content of aqueous and Vitreous humors and whole lenses was dete
rmined by ELISA. Transferrin secretion by cultured epithelia from lens
and ciliary body was also measured. In addition, Northern blots of RN
A from cultured lens epithelial cells, ciliary body pigmented and non-
pigmented epithelial cells, and from whole iris, ciliary body and reti
na were probed with riboprobes for Tf mRNA and 18S rRNA. Transferrin m
ade up 23% and 16% of total canine aqueous and vitreous protein. All o
cular tissues and cultured cells tested contained mRNA for Tf, however
Tf was secreted into the bathing medium from lens epithelial cell cul
tures, but not from either the pigmented or non-pigmented epithelial c
ells of the ciliary body Cycloheximide inhibited secretion of Tf from
the lens epithelial cells. Lenses from inflamed eyes contained higher
levels of Tf than their contralateral controls. This is the first expe
rimental demonstration that an intraocular tissue can make and secrete
Tf. Transferrin secretion by the lens may contribute significantly to
the IOF content of this important intraocular protein.