Scrapie in mice deficient in apolipoprotein E or glial fibrillary acidic protein

被引:42
作者
Tatzelt, J
Maeda, N
Pekny, M
Yang, SL
Betsholtz, C
Eliasson, C
Cayetano, J
Camerino, AP
DeArmond, SJ
Prusiner, SB
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT NEUROL, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, DEPT BIOCHEM & BIOPHYS, SAN FRANCISCO, CA 94143 USA
[3] UNIV CALIF SAN FRANCISCO, DEPT PATHOL, SAN FRANCISCO, CA 94143 USA
[4] UNIV N CAROLINA, DEPT PATHOL, CHAPEL HILL, NC 27515 USA
[5] UNIV N CAROLINA, PROGRAM MOL BIOL & BIOTECHNOL, CHAPEL HILL, NC 27515 USA
[6] UNIV N CAROLINA, CURRICULUM GENET, CHAPEL HILL, NC 27515 USA
[7] GOTHENBURG UNIV, DEPT MED BIOCHEM, S-41124 GOTHENBURG, SWEDEN
关键词
D O I
10.1212/WNL.47.2.449
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In the prion diseases, extensive reactive gliosis is often found to be out of proportion to the degree of apparent neuronal damage. To evaluate the role of astrocytic gliosis in experimental scrapie of the mouse, we inoculated mice deficient in apolipoprotein E (apoE) or the glial fibrillary acidic protein (GFAP) with mouse prions. The expression of both apoE and GFAP in astrocytes increases as part of the reactive gliosis that accompanies scrapie. Null mice deficient in either apoE or GFAP inoculated with prions exhibited incubation times indistinguishable from untargeted control mice. The level of PrPSc and its regional deposition in the brains of ill mice deficient in either protein were also similar to control mice. Our findings demonstrate that neither apoE nor GFAP participates in the pathogenesis of the disease or in the production of PrPSc.
引用
收藏
页码:449 / 453
页数:5
相关论文
共 56 条
  • [11] PRION PROTEIN IS NECESSARY FOR NORMAL SYNAPTIC FUNCTION
    COLLINGE, J
    WHITTINGTON, MA
    SIDLE, KCL
    SMITH, CJ
    PALMER, MS
    CLARKE, AR
    JEFFERYS, JGR
    [J]. NATURE, 1994, 370 (6487) : 295 - 297
  • [12] GENE DOSE OF APOLIPOPROTEIN-E TYPE-4 ALLELE AND THE RISK OF ALZHEIMERS-DISEASE IN LATE-ONSET FAMILIES
    CORDER, EH
    SAUNDERS, AM
    STRITTMATTER, WJ
    SCHMECHEL, DE
    GASKELL, PC
    SMALL, GW
    ROSES, AD
    HAINES, JL
    PERICAKVANCE, MA
    [J]. SCIENCE, 1993, 261 (5123) : 921 - 923
  • [13] 3 SCRAPIE PRION ISOLATES EXHIBIT DIFFERENT ACCUMULATION PATTERNS OF THE PRION PROTEIN SCRAPIE ISOFORM
    DEARMOND, SJ
    YANG, SL
    LEE, A
    BOWLER, R
    TARABOULOS, A
    GROTH, D
    PRUSINER, SB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (14) : 6449 - 6453
  • [14] DEARMOND SJ, 1995, AM J PATHOL, V146, P785
  • [15] CHANGES IN THE LOCALIZATION OF BRAIN PRION PROTEINS DURING SCRAPIE INFECTION
    DEARMOND, SJ
    MOBLEY, WC
    DEMOTT, DL
    BARRY, RA
    BECKSTEAD, JH
    PRUSINER, SB
    [J]. NEUROLOGY, 1987, 37 (08) : 1271 - 1280
  • [16] NEUROPATHOLOGICAL CHANGES IN SCRAPIE AND ALZHEIMERS-DISEASE ARE ASSOCIATED WITH INCREASED EXPRESSION OF APOLIPOPROTEIN-E AND CATHEPSIN-D IN ASTROCYTES
    DIEDRICH, JF
    MINNIGAN, H
    CARP, RI
    WHITAKER, JN
    RACE, R
    FREY, W
    HAASE, AT
    [J]. JOURNAL OF VIROLOGY, 1991, 65 (09) : 4759 - 4768
  • [17] TARGETED MUTATION OF THE HPRT GENE IN MOUSE EMBRYONIC STEM-CELLS
    DOETSCHMAN, T
    MAEDA, N
    SMITHIES, O
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (22) : 8583 - 8587
  • [18] DRANOVSKY A, 1995, INT J EXP CLIN INVES, V2, P39
  • [19] Gandy S., 1995, Society for Neuroscience Abstracts, V21, P5
  • [20] PERTURBATION OF THE SECONDARY STRUCTURE OF THE SCRAPIE PRION PROTEIN UNDER CONDITIONS THAT ALTER INFECTIVITY
    GASSET, M
    BALDWIN, MA
    FLETTERICK, RJ
    PRUSINER, SB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) : 1 - 5