Innate immune processes are sufficient for driving silicosis in mice

Journal of Leukocyte Biology

Volumn 88, Issue 3, 2010, Pages 547-557

  Beamer, Celine A ^a   Migliaccio, Christopher T ^a   Jessop, Forrest ^a   Trapkus, Melanie ^a   Yuan, Dorothy ^b   Holian, Andrij ^a  

^a UNIVERSITY OF MONTANA   (United States)

^b UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

Cytokine; Fibrosis; Inflammasome; Inflammation; Lung; Lymphocyte

Indexed keywords

RAG1 PROTEIN; RNA; SILICON DIOXIDE;

ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; C57BL 6 MOUSE; CELL SUSPENSION; CONTROLLED STUDY; EXPOSURE; HISTOPATHOLOGY; IMMUNOPHENOTYPING; INNATE IMMUNITY; LUNG LAVAGE; LYMPHOCYTE ACTIVATION; LYMPHOCYTE DEPLETION; LYMPHOCYTOPENIA; MICROARRAY ANALYSIS; MOUSE; NATURAL KILLER CELL; NONHUMAN; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA ISOLATION; SILICOSIS;

ADMINISTRATION, INTRANASAL; ANIMALS; B-LYMPHOCYTES; CELL COUNT; CYTOKINES; GENE EXPRESSION REGULATION; IMMUNITY, INNATE; INFLAMMATION MEDIATORS; KILLER CELLS, NATURAL; LUNG; LYMPHOCYTE ACTIVATION; LYMPHOCYTE DEPLETION; MICE; MICE, INBRED C57BL; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; ORGAN SIZE; PULMONARY FIBROSIS; SILICON DIOXIDE; SILICOSIS; T-LYMPHOCYTES; TIME FACTORS;

MURINAE; MUS;

EID: 77957165679     PISSN: 07415400     EISSN: None     Source Type: Journal    
DOI: 10.1189/jlb.0210108     Document Type: Article

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