A vitellogenic-like carboxypeptidase expressed by human macrophages is localized in endoplasmic reticulum and membrane ruffles

International Journal of Experimental Pathology

Volumn 87, Issue 1, 2006, Pages 29-39

  Harris, James ^a,d   Schwinn, Nicole ^a,e   Mahoney, James A ^b   Lin, Hsi Hsien ^a,f   Shaw, Michael ^a   Howard, Chris J ^c   Da Silva, Rosangela P ^a   Gordon, Siamon ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c INSTITUTE FOR ANIMAL HEALTH   (United Kingdom)

^d UNIVERSITY OF NEW MEXICO SCHOOL OF MEDICINE   (United States)

^e UNIVERSITY OF HEIDELBERG   (Germany)

^f CHANG GUNG UNIVERSITY   (Taiwan)

Author keywords

Antigen processing presentation; Lamellipodia; Membrane ruffles; Secretory pathway; Serine carboxypeptidase

Indexed keywords

ACTIN; CARBOXYPEPTIDASE; CC338 MONOCLONAL ANTIBODY; MACROPHAGE INFLAMMATORY PROTEIN 1ALPHA; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; MANNOSE; MONOCLONAL ANTIBODY; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG; VITELLOGENIC LIKE CARBOXYPEPTIDASE; CPVL PROTEIN, HUMAN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ANTIGEN PRESENTATION; ARTICLE; CANDIDA ALBICANS; CELL MATURATION; CELL MEMBRANE; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; ENZYME LOCALIZATION; HUMAN; HUMAN CELL; LAMELLIPODIUM; MACROPHAGE; MONOCYTE; MOUSE; NONHUMAN; PHAGOSOME; PRIORITY JOURNAL; PROTEIN GLYCOSYLATION; UPREGULATION; CELL DIFFERENTIATION; CHEMISTRY; CONFOCAL MICROSCOPY; CYTOLOGY; CYTOSOL; ELECTRON MICROSCOPY; ENZYME LINKED IMMUNOSORBENT ASSAY; FLOW CYTOMETRY; IMMUNOLOGY; ISOLATION AND PURIFICATION; METHODOLOGY; PHAGOCYTOSIS; PSEUDOPODIUM; SECRETION; ULTRASTRUCTURE; WESTERN BLOTTING;

ANTIBODIES, MONOCLONAL; ANTIGEN PRESENTATION; BLOTTING, WESTERN; CARBOXYPEPTIDASES; CELL DIFFERENTIATION; CELL MEMBRANE; CYTOSOL; ENDOPLASMIC RETICULUM; ENZYME-LINKED IMMUNOSORBENT ASSAY; FLOW CYTOMETRY; MACROPHAGES; MICROSCOPY, CONFOCAL; MICROSCOPY, ELECTRON; MONOCYTES; PHAGOCYTOSIS; PSEUDOPODIA;

EID: 33644958581     PISSN: 09599673     EISSN: 13652613     Source Type: Journal    
DOI: 10.1111/j.0959-9673.2006.00450.x     Document Type: Article

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