Ultrastructural immunocytochemical demonstration of HLA class I antigens in human pathological liver tissue
β Scribed by Rita De Vos; Chris De Wolf-Peeters; Joost J. Den Van Oord; Valeer Desmet
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 617 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
Major histocompatibility complex products Class I (HLA Class I) antigens are not expressed on the surface of normal human hepatocytes but become so in pathological conditions. The purpose of this study was to specify the ultrastructural topography of HLA Class I antigens expreesion.
Nine human liver specimens, known from light microscopic investigation to display membranous positivity for HLA Class I antigens, were p r d for immun6electronmicroscopy using monoclonal anti-HLA Class I in an indirect immunoperoxidase procedure.
H L A Class I antigens were detected on the basolateral membrane of hepatocytes and bile duct cells; some cisternae of the endoplasmic reticulum were also positive. The membranes of normal bile canaliculi of hepatocytes and the apical border of bile duct cells were negative. In one case of presumably drug-induced cholestasis, abnormal cholestatic canaliculi displayed HLA Class I antigens.
These results indicate that HLA Class I antigens are synthesized by the hepatocytes and bile duct cells and incorporated into the plasma membrane; the basolateral expression follows the pattern as in other polarized cells. The expression in cholestatic canaliculi suggests a disturbed polarity of the hepatocyte.
π SIMILAR VOLUMES
Engraftment by recipient's (R) cells has been already demonstrated in gender mismatched liver grafts using fluorescence in situ hybridization (FISH), with contrasting results concerning epithelial cells. Mismatch for human leukocyte antigen (HLA) class I (HLA-I) is quite common in patients with orth
A simple sandwich ELISA method has been developed for the quantification of soluble HLA class I antigens (s-HLA) in human serum. The assay utilizes the monoclonal antibody Q6164, directed to a monomorphic determinant of the HLA a-chain, to capture the antigen and the biotinylated NAMB1 monoclonal an
HLA class I molecules present antigenic peptides to cytotoxic T lymphocytes and thus play an important role in immune surveillance of cells infected with virus or altered by malignant transformation. Immunochemical studies have demonstrated a marked deficiency or lack of expression of class I molecu