PURPOSE. To investigate microenvironment changes of the lacrimal gland after obstruction of lacrimal gland ducts. METHODS. The ducts of rat exorbital lacrimal gland were ligated by sutures for different durations. After that, the sutures in some animals were released, and they were observed for 21 days to evaluate the recovery of the lacrimal gland. Slit lamp and tear secretion test was performed to evaluate ocular surface and lacrimal gland function. The lacrimal gland and cornea were harvested and processed for hematoxylin and eosin staining, oil red O staining, LipidTOX staining, Masson staining, quantitative real time polymerase chain reaction, and immunofluorescence staining. RESULTS. After the lacrimal gland ducts were blocked, tear secretion and the weight of the lacrimal gland were reduced. Incidence of corneal neovascularization increased after seven days. Intraglandular ducts dilated and acini destroyed. Long-term ligation induced fibrosis and lipid accumulation of the lacrimal glands. Inflammatory cell infiltrated and inflammatory factors upregulated. Proliferative and apoptotic cells increased. Structure of myoepithelial cells and basement membrane was destroyed. The p63 expression increased whereas Pax6 expression decreased. After suture release, tear secretion and structure of acini could recover in less than seven days after ligation, with a decrease in inflammatory cell infiltration and fibrosis relief. Apoptotic cells and proliferative cells increased at five days thereafter. The structure of the myoepithelial cells and basement membrane could not recover three days after ligation, and the number of mesenchymal cells increased in ligation after five to 14 days. CONCLUSIONS. Blockage of the lacrimal gland ducts results in dystrophy of lacrimal gland acini cells, inflammation, and lipid accumulation of the lacrimal gland microenvironment. Long-term duct blockage will cause irreversible lacrimal gland failure.
机构:
Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Ophthalmol Otorhinolaringol & Head & Neck Su, Ribeirao Preto, SP, BrazilHarvard Univ, Sch Med, Schepens Eye Res Inst, Boston, MA 02114 USA
Rocha, Eduardo M.
Alves, Monica
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Univ Estadual Campinas, Fac Med Sci, Dept Clin Med, Lab Clin Physiopathol, Campinas, SP, BrazilHarvard Univ, Sch Med, Schepens Eye Res Inst, Boston, MA 02114 USA
Alves, Monica
Rios, J. David
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Harvard Univ, Sch Med, Schepens Eye Res Inst, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Ophthalmol, Boston, MA 02114 USAHarvard Univ, Sch Med, Schepens Eye Res Inst, Boston, MA 02114 USA
Rios, J. David
Dartt, Darlene A.
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Harvard Univ, Sch Med, Schepens Eye Res Inst, Boston, MA 02114 USA
Harvard Univ, Sch Med, Dept Ophthalmol, Boston, MA 02114 USAHarvard Univ, Sch Med, Schepens Eye Res Inst, Boston, MA 02114 USA