The difference in gliosis induced by β-amyloid and Tau treatments in astrocyte cultures derived from senescence accelerated and normal mouse strains

Biogerontology

Volumn 10, Issue 6, 2009, Pages 695-710

  Lü, Lanhai ^a   Mak, Ying T ^b   Fang, Marong ^c   Yew, David T ^b  

^a SUN YAT SEN UNIVERSITY   (China)

^b CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^c ZHEJIANG UNIVERSITY   (China)

Author keywords

Aging prone; Alzheimer's disease; Astrocyte; Astrogliosis; Neurodegenerative insult

Indexed keywords

AMYLOID BETA PROTEIN; CASPASE 3; HEXOKINASE 1; LACTATE DEHYDROGENASE; MICROTUBULE ASSOCIATED PROTEIN 2; PROTEIN KINASE C; TAU PROTEIN;

ANIMAL CELL; ARTICLE; ASTROCYTE; CELL COUNT; CELL CULTURE; CELL DEATH; CELL LOSS; CELL STRUCTURE; CONTROLLED STUDY; GLIOSIS; MOUSE; NONHUMAN; PRIORITY JOURNAL; SENESCENCE;

AGING, PREMATURE; AMYLOID BETA-PEPTIDES; ANIMALS; ASTROCYTES; BIOLOGICAL MARKERS; BLOTTING, WESTERN; CASPASE 3; CELL AGING; CELLS, CULTURED; DISEASE MODELS, ANIMAL; GLIOSIS; HEXOKINASE; HUMANS; IMMUNOHISTOCHEMISTRY; L-LACTATE DEHYDROGENASE; MICE; MICE, MUTANT STRAINS; MICROTUBULE-ASSOCIATED PROTEINS; NERVE GROWTH FACTORS; NERVE TISSUE PROTEINS; PEPTIDE FRAGMENTS; PROTEIN KINASE C; S100 PROTEINS; TAU PROTEINS;

EID: 71349087864     PISSN: 13895729     EISSN: 15736768     Source Type: Journal    
DOI: 10.1007/s10522-009-9217-3     Document Type: Article

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