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1 Division of Inhalation Toxicology, Institute of Environmental Medicine, Karolinska Institutet, SE-171 77 Stockholm; 2 Division of Clinical and Oral Bacteriology, Department of Immunology, Microbiology, Pathology and Infectious Diseases, Huddinge University Hospital, SE-141 86 Huddinge, Sweden; and 3 Faculty of Microbiology, University of Costa Rica, San Juan, Costa Rica
Phagocytosis of three types of
fluorescein-labeled test particles by rat alveolar macrophages
(AM) were studied: spherical silica (3.2 µm), heat-killed
Candida albicans (3.8 µm), and heat-killed Cryptococcus neoformans (6.1 µm) opsonized with specific
IgG. These particles should attach to scavenger, mannose, and Fc
receptors, respectively. Both control AM and AM pretreated for 20 h with interferon-
(12.5 or 50 U/ml) were studied. The sum of the
number of attached and ingested particles per AM (accumulated
attachment) was used as a measure of the attachment process, and the
number of ingested particles per AM divided by the accumulated
attachment (ingested fraction) was used as a measure of the ingestion
process. The average ingestion time (IT), which is also a measure of
the ingestion process, was calculated from the experimental data. The
ingestion process was independent of the attachment process. IT
increased with the time of observation. This is explained by the fact
that IT determined from observation times shorter than the whole
distribution of IT for a certain particle results in a shorter IT than
the real average IT. C. albicans (mannose receptor) had the
fastest ingestion process, C. neoformans opsonized with specific IgG (Fc receptor) had ingestion that was nearly as fast, and
the silica particles (scavenger receptors) had the slowest ingestion
process. Treatment with interferon-
markedly impaired the attachment
process for all three types of particles (and three types of receptors)
but clearly impaired the ingestion process only for silica particles
(scavenger receptors).
macrophage receptors; interferon-
; Candida albicans; Cryptococcus neoformans
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