Histopathologic and immunohistochemical findings in gelatinous drop-like corneal dystrophy

Ophthalmic Res. 1990;22(6):371-6. doi: 10.1159/000267049.

Abstract

A cornea with gelatinous drop-like corneal dystrophy was examined by histochemical and immunohistochemical techniques. Pretreatment of the sections with potassium permanganate did not decrease the staining with Congo red dye. Immunohistochemically, amyloid deposits in the cornea with this disease almost did not stain with antibodies to amyloid protein AA and AA-3. However, the corneal epithelium reacted distinctly with antibodies to amyloid protein AA and AA-3. Cross-reactivity with antibodies to protein AA and serum precursor of protein AA has been reported and protein AA-3 is the synthesized peptide corresponding to the amino acid sequence 37-47 of the human amyloid protein AA molecule. The present study suggests at least that corneal epithelial cells with gelatinous drop-like corneal dystrophy may produce a precursor of amyloid related to protein AA-3.

MeSH terms

  • Adult
  • Antibodies, Monoclonal / immunology
  • Cornea / pathology*
  • Corneal Dystrophies, Hereditary / metabolism
  • Corneal Dystrophies, Hereditary / pathology*
  • Corneal Dystrophies, Hereditary / surgery
  • Corneal Stroma / metabolism
  • Corneal Stroma / pathology
  • Corneal Transplantation
  • Epithelium / metabolism
  • Epithelium / pathology
  • Female
  • Humans
  • Immunoenzyme Techniques
  • Male
  • Potassium Permanganate
  • Serum Amyloid A Protein / metabolism*
  • beta 2-Microglobulin / metabolism

Substances

  • Antibodies, Monoclonal
  • Serum Amyloid A Protein
  • beta 2-Microglobulin
  • Potassium Permanganate