Fibrillar islet amyloid polypeptide (amylin) is internalised by macrophages but resists proteolytic degradation

Cell and Tissue Research

Volumn 291, Issue 2, 1998, Pages 285-294

  Badman, M K ^a   Pryce, R A ^a   Charge S B P ^a   Morris, J F ^a   Clark, A ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Amyloid; Diabetes; Islet amyloid polypeptide; Lysosomes; Macrophages; Macrosialin; Mouse (C34 HEH 101 H); Phagocytosis

Indexed keywords

AMYLIN; CYTOCHALASIN B; NOCODAZOLE; POLYINOSINIC ACID;

ANIMAL CELL; ARTICLE; CELL CULTURE; ELECTRON MICROSCOPY; FIBER; IMMUNOCYTOCHEMISTRY; IMMUNOREACTIVITY; INTERNALIZATION; LYSOSOME; MALE; MICROSCOPY; MICROTUBULE ASSEMBLY; MOUSE; NONHUMAN; PERITONEUM MACROPHAGE; PRIORITY JOURNAL; PSEUDOPODIUM;

AMYLOID; ANIMALS; CELLS, CULTURED; CYTOCHALASIN B; DIABETES MELLITUS, TYPE 2; ENDOCYTOSIS; ENDOPEPTIDASES; HUMANS; LYSOSOMES; MACROPHAGES, PERITONEAL; MALE; MICE; MICE, INBRED STRAINS; MICROTUBULES; NOCODAZOLE; PANCREAS; POLY I;

EID: 0031889824     PISSN: 0302766X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004410050998     Document Type: Article

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