Detection of galectin-3 in tear fluid at disease states and immunohistochemical and lectin histochemical analysis in human corneal and conjunctival epithelium
E. Hrdlickova-cela et al., Detection of galectin-3 in tear fluid at disease states and immunohistochemical and lectin histochemical analysis in human corneal and conjunctival epithelium, BR J OPHTH, 85(11), 2001, pp. 1336-1340
Background/aim-Components of the tear fluid contribute to the biochemical d
efence system of the eye. To reveal whether the immune mediator and lipopol
ysaccharide binding galectin-3 is present in tears, tear samples were colle
cted from eyes in healthy and pathological states. Investigation of express
ion of galectin-3 and galectin-3 reactive glycoligands in normal human conj
unctival and corneal epithelia was also initiated as a step to understand t
he role of galectin-3 in ocular surface pathology.
Methods-Immunoblot analysis using either a rabbit polyclonal or a mouse mon
oclonal antibody against galectin-3 was employed to detect galectin-3 in te
ar fluid. Galectin-3 expression in tissue specimens was detected by immunoc
ytochemistry employing A1D6 mouse monoclonal antibody, and galectin-3 react
ive glycoligands were visualised by lectin histochemistry using labelled ga
lectin-3.
Results-Galectin-3 was found only in tears from patients with ocular surfac
e disorders. It was expressed in normal corneal and conjunctival epithelia
but not in lacrimal glands. Inflammatory leucocytes and goblet cells found
in galectin-3 containing tear fluid also expressed galectin-3. Galectin-3 b
inding sites were detected on the surface of conjunctival and corneal epith
elial cells co-localising with desmoglein.
Conclusions-This study revealed expression of galectin-3 in tear fluid obta
ined from patients with eye diseases. The role of this endogenous lectin (p
roduced by inflammatory as well as epithelial cells) in antimicrobial actio
n and inflammation modulation could be expected.