Prostaglandin Levels in Stimulated Macrophages Are Controlled by Phospholipase A2-activating Protein and by Activation of Phospholipase C and D

Journal of Biological Chemistry

Volumn 276, Issue 8, 2001, Pages 5467-5475

  Ribardo, Deborah A ^b   Crowe, Sheila E ^b   Kuhl, Kristine R ^b   Peterson, Johnny W ^b   Chopra, Ashok K ^a  

^a University of Texas Medical Branch School of Medicine   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

BIOPSY; CELLS; ORGANIC ACIDS; PROTEINS; TUMORS;

MACROPHAGES;

BIOCHEMISTRY;

ANTISENSE OLIGONUCLEOTIDE; ARACHIDONIC ACID; CYCLOOXYGENASE 1; CYCLOOXYGENASE 2; ICOSANOID; INTERLEUKIN 1BETA; LIPOPOLYSACCHARIDE; MELITTIN; PHOSPHOLIPASE A2; PHOSPHOLIPASE A2 ACTIVATING PROTEIN; PHOSPHOLIPASE C; PHOSPHOLIPASE D; PROSTAGLANDIN; PROSTAGLANDIN E2; PROTEIN; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG; AUTACOID; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INTERLEUKIN 1; ISOENZYME; MEMBRANE PROTEIN; PHOSPHOLIPASE A2-ACTIVATING PROTEIN; PROSTAGLANDIN SYNTHASE; PROTEINASE INHIBITOR; PTGS2 PROTEIN, HUMAN;

ANIMAL CELL; ARTICLE; CELL STIMULATION; CONTROLLED STUDY; ENTERITIS; ENZYME ACTIVATION; ENZYME ACTIVITY; EUKARYOTIC CELL; INTESTINE MUCOSA; MACROPHAGE; MOUSE; NONHUMAN; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; AMINO ACID SEQUENCE; ANIMAL; BIOSYNTHESIS; CELL LINE; COLITIS; CROHN DISEASE; DRUG ANTAGONISM; HUMAN; IRRITABLE COLON; MACROPHAGE ACTIVATION; METABOLISM; MOLECULAR GENETICS; PHYSIOLOGY; PROTEIN TRANSPORT; SECRETION;

ANIMALIA; EUKARYOTA; MURINAE;

AMINO ACID SEQUENCE; ANIMALS; ARACHIDONIC ACID; CELL LINE; COLITIS; COLONIC DISEASES, FUNCTIONAL; CROHN DISEASE; CYCLOOXYGENASE 2; DINOPROSTONE; HUMANS; INFLAMMATION MEDIATORS; INTERLEUKIN-1; ISOENZYMES; LIPOPOLYSACCHARIDES; MACROPHAGE ACTIVATION; MACROPHAGES; MELITTEN; MEMBRANE PROTEINS; MICE; MOLECULAR SEQUENCE DATA; NF-KAPPA B; PHOSPHOLIPASE C; PHOSPHOLIPASE D; PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES; PROTEASE INHIBITORS; PROTEIN TRANSPORT; PROTEINS; TUMOR NECROSIS FACTOR-ALPHA;

EID: 0035937177     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M006690200     Document Type: Article

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