Macrophages in Drosophila embryos and L2 cells exhibit scavenger receptor-mediated endocytosis

John M. Abrams, Alison Lux, Hermann Steller, Monty Krieger

Research output: Contribution to journalArticle

81 Citations (Scopus)

Abstract

Mammalian macrophage scavenger receptors exhibit unusually broad binding specificity and are implicated in atherosclerosis and host defense. Scavenger receptor-like endocytosis was observed in Drosophila melanogaster embryos and in primary embryonic cell cultures. This receptor activity was expressed primarily by macrophages. The Drosophila Schneider L2, but not the Kc, cell line also exhibited a scavenger receptor-mediated endocytic pathway similar to its mammalian counterpart. L2 receptors mediated high-affinity internalization and subsequent temperature- and chloroquine-sensitive degradation of 125I-labeled acetylated low density lipoprotein and displayed characteristic ligand specificity. These findings suggest that scavenger receptors mediate important, well-conserved functions and raise the possibility that they may be pattern recognition receptors that arose early in the evolution of host defense mechanisms. They also establish additional systems for the investigation of endocytosis in Drosophila and scavenger receptor function in disease, host defense, and development.

Original languageEnglish (US)
Pages (from-to)10375-10379
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume89
Issue number21
StatePublished - 1992

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Scavenger Receptors
Endocytosis
Drosophila
Embryonic Structures
Macrophages
Pattern Recognition Receptors
Primary Cell Culture
Chloroquine
Drosophila melanogaster
Atherosclerosis
Ligands
Cell Line
Temperature

ASJC Scopus subject areas

  • Genetics
  • General

Cite this

Macrophages in Drosophila embryos and L2 cells exhibit scavenger receptor-mediated endocytosis. / Abrams, John M.; Lux, Alison; Steller, Hermann; Krieger, Monty.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 89, No. 21, 1992, p. 10375-10379.

Research output: Contribution to journalArticle

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