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PMID: 1730752 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Immunocytochemical characterization of the endocytic and phagolysosomal compartments in peritoneal macrophages.

The Journal of cell biology ·Vol. 116 ·No. 1 ·1992-01-00 ·Pages 95-112

Rabinowitz S, Horstmann H, Gordon S, Griffiths G

Abstract

We have used endocytic and phagocytic tracers in an EM immunocytochemical study to define the compartments of the phagocytic and endocytic pathways in mouse peritoneal macrophages. Endocytosed BSA-gold appeared successively in early endosomes, spherical endosomal vesicles, a late endosomal tubuloreticular compartment (TC), and terminal lysosomes. The TC appeared as an elaborate structure enriched for the lysosomal membrane glycoproteins Lamp 1 and Lamp 2, and expressing significant levels of rab7, a late endosome-specific GTP-binding protein. The cation-independent mannose-6-phosphate receptor was restricted to specialized regions of the TC that were predominantly adjacent to the Golgi complex. Both the early endosome and the TC had coated bud structures whose composition and function are presently unknown. Phagolysosomes containing latex beads expressed the same membrane antigens and received endocytic tracers simultaneously with the TC. Since the membrane surrounding both organelles was also in direct continuity, we assume that both structures form one functional compartment. Macrosialin, an antigen confined to macrophages and dendritic cells, was heavily expressed in TC and phagolysosomal membranes with low levels being detected in other endosomal compartments and on the cell surface. Treatment of cells with wheat germ agglutinin drastically altered the morphology of the TC, giving rise to sheets of tightly adherent membrane and greatly expanded vesicles, in which cell-associated wheat germ agglutinin was concentrated. The spherical endosomal carrier vesicles loaded with internalized gold tracers clustered nearby, often making contact without fusing. Since the delivery of endocytic tracer to the TC was significantly delayed these experiments suggest that the lectin is somehow preventing the endosome vesicles from fusing with the TC. Collectively, our data argue first that the PLC is equivalent to the "tubular lysosomes" commonly described in macrophages, and second that the meeting of the phagocytic and endocytic pathway occurs in this compartment.

MeSH Terms
Animals Antigens, CD Biomarkers Cells, Cultured Endocytosis Fluorescein-5-isothiocyanate Lysosome-Associated Membrane Glycoproteins Lysosomes/physiology,ultrastructure Macrophages/physiology,ultrastructure Male Membrane Glycoproteins/analysis Mice Mice, Inbred C57BL Microscopy, Electron Models, Biological Phagocytosis Wheat Germ Agglutinins
Chemicals
Antigens, CD Biomarkers Lysosome-Associated Membrane Glycoproteins Membrane Glycoproteins Wheat Germ Agglutinins fluorescein isothiocyanate-wheat germ agglutinin Fluorescein-5-isothiocyanate
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rabinowitz S
Sir William Dunn School of Pathology, Oxford, England.
Horstmann H
Gordon S
Griffiths G
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1992-01-00
Pages
95-112
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2289258
Subset
IM
Grants
Wellcome Trust · United Kingdom
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