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Samuel C. Silverstein

Researcher at Columbia University

Publications -  187
Citations -  20897

Samuel C. Silverstein is an academic researcher from Columbia University. The author has contributed to research in topics: Receptor & Phagocytosis. The author has an hindex of 81, co-authored 187 publications receiving 20319 citations. Previous affiliations of Samuel C. Silverstein include NewYork–Presbyterian Hospital & Stanford University.

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Adult mouse astrocytes degrade amyloid-beta in vitro and in situ.

TL;DR: It is shown that cultured adult mouse astrocytes migrate in response to monocyte chemoattractant protein-1 (MCP-1), a chemokine present in AD lesions, and cease migration upon interaction with immobilized Aβ1–42, which suggests a novel mechanism for the accumulation of Astrocytes around Aβ deposits.
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Scavenger receptor-mediated adhesion of microglia to β-amyloid fibrils

TL;DR: It is reported that class A scavenger receptors mediate adhesion of rodent microglia and human monocytes to β-amyloid fibril-coated surfaces leading to secretion of reactive oxygen species and cell immobilization.
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Legionnaires' Disease Bacterium (Legionella pneumophila) Multiplies Intracellularly in Human Monocytes

TL;DR: Findings indicate that L. pneumophila falls into a select category of bacterial pathogens that evade host defenses by parasitizing monocytes, and it remains to be determined whether cell-mediated immunity plays a dominant role in host defense against L.neumophila as it does against other intracellular pathogens.
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Identification of the C3bi receptor of human monocytes and macrophages by using monoclonal antibodies.

TL;DR: The C3bi receptor of human M phi is a complex composed of two polypeptides, Mr 185,000 and 105,000, and monoclonal antibodies reacting with four distinct antigenic determinants of this complex are identified.
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Studies on the mechanism of phagocytosis. I. Requirements for circumferential attachment of particle-bound ligands to specific receptors on the macrophage plasma membrane.

TL;DR: Results indicate that attachment of a particle to specific receptors on the macrophage plasma membrane is not sufficient to trigger ingestion of that particle, and that ingestion requires the sequential, circumferential interaction of particle-bound ligands with specific plasma membrane receptors not involved in the initial attachment process.