MECHANISMS OF PHAGOCYTOSIS IN MACROPHAGES
Phagocytosis of pathogens by macrophages initiates the innate immune response, which in turn orchestrates the adaptive response. In order to discriminate between infectious agents and self, macrophages have evolved a restricted number of phagocytic receptors, like the mannose receptor, that recogniz...
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Published in | Annual review of immunology Vol. 17; no. 1; pp. 593 - 623 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Palo Alto, CA 94303-0139
Annual Reviews
01.01.1999
4139 El Camino Way, P.O. Box 10139 Annual Reviews, Inc USA |
Subjects | |
Online Access | Get full text |
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Summary: | Phagocytosis of pathogens by macrophages initiates the innate immune
response, which in turn orchestrates the adaptive response. In order to
discriminate between infectious agents and self, macrophages have evolved a
restricted number of phagocytic receptors, like the mannose receptor, that
recognize conserved motifs on pathogens. Pathogens are also phagocytosed by
complement receptors after relatively nonspecific opsonization with complement
and by Fc receptors after specific opsonization with antibodies. All these
receptors induce rearrangements in the actin cytoskeleton that lead to the
internalization of the particle. However, important differences in the
molecular mechanisms underlying phagocytosis by different receptors are now
being appreciated. These include differences in the cytoskeletal elements that
mediate ingestion, differences in vacuole maturation, and differences in
inflammatory responses. Infectious agents, such as
M. tuberculosis
,
Legionella pneumophila
, and
Salmonella typhimurium
, enter
macrophages via heterogeneous pathways and modify vacuolar maturation in a
manner that favors their survival. Macrophages also play an important role in
the recognition and clearance of apoptotic cells; a notable feature of this
process is the absence of an inflammatory response. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 ObjectType-Review-3 content type line 23 ObjectType-Feature-3 ObjectType-Review-1 |
ISSN: | 0732-0582 1545-3278 |
DOI: | 10.1146/annurev.immunol.17.1.593 |