HUMAN RESIDENT LANGERHANS CELLS DISPLAY A LYSOSOMAL COMPARTMENT ENRICHED IN MHC CLASS-II

Citation
Mj. Kleijmeer et al., HUMAN RESIDENT LANGERHANS CELLS DISPLAY A LYSOSOMAL COMPARTMENT ENRICHED IN MHC CLASS-II, Journal of investigative dermatology, 103(4), 1994, pp. 516-523
Citations number
48
Categorie Soggetti
Dermatology & Venereal Diseases
ISSN journal
0022202X
Volume
103
Issue
4
Year of publication
1994
Pages
516 - 523
Database
ISI
SICI code
0022-202X(1994)103:4<516:HRLCDA>2.0.ZU;2-Q
Abstract
Langerhans cells are the antigen-presenting cells of the skin, belongi ng to the family of dendritic cells, which present exogenous antigens in the context of major histocompatibility complex class II (MHC-II) m olecules to CD4(+) T lymphocytes. Langerhans cells are potent stimulat ors of different T-cell responses including primary immune responses. Culturing of Langerhans cells leads to modulation of their phenotype a nd function, as they seem more capable of activating T cells, whereas freshly isolated Langerhans cells are specialized in the endocytosing and processing of antigen. We studied the intracellular distribution o f MHC-II: molecules and invariant chain (I-chain) in resident Langerha ns cells using immunogold labeling of ultrathin cryosections of human epidermis and found the majority of intracellular MHC-II molecules pre sent on membranes of rough endoplasmic reticulum and in so-called MHC- II-enriched compartments (MIIC). The MIIC appeared to be negative for the cation-independent mannose 6-phosphate receptor and positive for t he lysosomal enzyme beta-hexosaminidase and acquired the endocytotic t racer, cationized horseradish peroxidase, only after 60 min of interna lization. Taken together, these data show that MIIC in Langerhans cell s share characteristics with lysosomes. I-chain, which is associated w ith MHC-II molecules in early biosynthetic compartments, was found in the rough endoplasmic reticulum and Golgi complex, but was detected on ly occasionally in MIIC and at the plasma membrane. MIIC with internal membrane vesicles showed some I-chain labeling, suggesting that these are newly formed MIIC in which degradation of the I-chain is not yet complete.