Mutant presenilin 2 transgenic mice: A large increase in the levels of Aβ342 is presumably associated with the low density membrane domain that contains decreased levels of glycerophospholipids and sphingomyelin

Naoya Sawamura, Maho Morishima-Kawashima, Hatsue Waki, Kimio Kobayashi, Takashi Kuramochi, Matthew P. Frosch, Kai Ding, Mamoru Ito, Tae Wan Kim, Rudolph E. Tanzi, Fumitaka Oyama, Takeshi Tabira, Susumu Ando, Yasuo Ihara

研究成果: Article

72 引用 (Scopus)

抄録

The N141I mutation in presenilin (PS) 2 is tightly linked with a form of autosomal dominant familial Alzheimer's disease in the Volga German families. We previously reported that mouse brains harboring mutant PS2 contained increased levels of amyloid β protein (Aβ) 42 in the Tris-saline-soluble fraction (Oyama, F., Sawamura, N., Kobayashi, K., Morishima-Kawashima, M., Kuramochi, T., Ito, M., Tomita, T., Maruyama, K., Saido, T. C., Iwatsubo, T., Capell, A., Walter, J., Grinberg, J., Ueyama, Y., Haass, C. and Ihara, Y. (1998) J. Neurochem. 71, 313-322). Here, using a new extraction protocol, we quantitated the A/β40 and Aβ42 levels in the Tris-saline-insoluble fraction. The insoluble Aβ levels were found to be higher than the soluble Aβ levels, and the insoluble Aβ42 levels were markedly increased in mutant PS2 transgenic mice. To investigate the origin of the insoluble Aβ42, we prepared the detergent-insoluble, low density membrane fraction. This fraction from two independent lines of mutant PS2 transgenic mice contained remarkably increased levels of Aβ42 and significantly low levels of glycerophospholipids and sphingomyelin. This unexpected finding suggests that a large increase in the levels of Aβ42 in mutant PS2 mice is presumably induced through alterations of the lipid composition in the low density membrane domain in the brain.

元の言語English
ページ(範囲)27901-27908
ページ数8
ジャーナルJournal of Biological Chemistry
275
発行部数36
DOI
出版物ステータスPublished - 2000 9 8
外部発表Yes

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Presenilin-2
Glycerophospholipids
Sphingomyelins
Transgenic Mice
Brain
Membranes
Serum Amyloid A Protein
Detergents
Alzheimer Disease
Lipids
Mutation
Chemical analysis

ASJC Scopus subject areas

  • Biochemistry

これを引用

Mutant presenilin 2 transgenic mice : A large increase in the levels of Aβ342 is presumably associated with the low density membrane domain that contains decreased levels of glycerophospholipids and sphingomyelin. / Sawamura, Naoya; Morishima-Kawashima, Maho; Waki, Hatsue; Kobayashi, Kimio; Kuramochi, Takashi; Frosch, Matthew P.; Ding, Kai; Ito, Mamoru; Kim, Tae Wan; Tanzi, Rudolph E.; Oyama, Fumitaka; Tabira, Takeshi; Ando, Susumu; Ihara, Yasuo.

:: Journal of Biological Chemistry, 巻 275, 番号 36, 08.09.2000, p. 27901-27908.

研究成果: Article

Sawamura, N, Morishima-Kawashima, M, Waki, H, Kobayashi, K, Kuramochi, T, Frosch, MP, Ding, K, Ito, M, Kim, TW, Tanzi, RE, Oyama, F, Tabira, T, Ando, S & Ihara, Y 2000, 'Mutant presenilin 2 transgenic mice: A large increase in the levels of Aβ342 is presumably associated with the low density membrane domain that contains decreased levels of glycerophospholipids and sphingomyelin', Journal of Biological Chemistry, 巻. 275, 番号 36, pp. 27901-27908. https://doi.org/10.1074/jbc.M004308200
Sawamura, Naoya ; Morishima-Kawashima, Maho ; Waki, Hatsue ; Kobayashi, Kimio ; Kuramochi, Takashi ; Frosch, Matthew P. ; Ding, Kai ; Ito, Mamoru ; Kim, Tae Wan ; Tanzi, Rudolph E. ; Oyama, Fumitaka ; Tabira, Takeshi ; Ando, Susumu ; Ihara, Yasuo. / Mutant presenilin 2 transgenic mice : A large increase in the levels of Aβ342 is presumably associated with the low density membrane domain that contains decreased levels of glycerophospholipids and sphingomyelin. :: Journal of Biological Chemistry. 2000 ; 巻 275, 番号 36. pp. 27901-27908.
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title = "Mutant presenilin 2 transgenic mice: A large increase in the levels of Aβ342 is presumably associated with the low density membrane domain that contains decreased levels of glycerophospholipids and sphingomyelin",
abstract = "The N141I mutation in presenilin (PS) 2 is tightly linked with a form of autosomal dominant familial Alzheimer's disease in the Volga German families. We previously reported that mouse brains harboring mutant PS2 contained increased levels of amyloid β protein (Aβ) 42 in the Tris-saline-soluble fraction (Oyama, F., Sawamura, N., Kobayashi, K., Morishima-Kawashima, M., Kuramochi, T., Ito, M., Tomita, T., Maruyama, K., Saido, T. C., Iwatsubo, T., Capell, A., Walter, J., Grinberg, J., Ueyama, Y., Haass, C. and Ihara, Y. (1998) J. Neurochem. 71, 313-322). Here, using a new extraction protocol, we quantitated the A/β40 and Aβ42 levels in the Tris-saline-insoluble fraction. The insoluble Aβ levels were found to be higher than the soluble Aβ levels, and the insoluble Aβ42 levels were markedly increased in mutant PS2 transgenic mice. To investigate the origin of the insoluble Aβ42, we prepared the detergent-insoluble, low density membrane fraction. This fraction from two independent lines of mutant PS2 transgenic mice contained remarkably increased levels of Aβ42 and significantly low levels of glycerophospholipids and sphingomyelin. This unexpected finding suggests that a large increase in the levels of Aβ42 in mutant PS2 mice is presumably induced through alterations of the lipid composition in the low density membrane domain in the brain.",
author = "Naoya Sawamura and Maho Morishima-Kawashima and Hatsue Waki and Kimio Kobayashi and Takashi Kuramochi and Frosch, {Matthew P.} and Kai Ding and Mamoru Ito and Kim, {Tae Wan} and Tanzi, {Rudolph E.} and Fumitaka Oyama and Takeshi Tabira and Susumu Ando and Yasuo Ihara",
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T2 - A large increase in the levels of Aβ342 is presumably associated with the low density membrane domain that contains decreased levels of glycerophospholipids and sphingomyelin

AU - Sawamura, Naoya

AU - Morishima-Kawashima, Maho

AU - Waki, Hatsue

AU - Kobayashi, Kimio

AU - Kuramochi, Takashi

AU - Frosch, Matthew P.

AU - Ding, Kai

AU - Ito, Mamoru

AU - Kim, Tae Wan

AU - Tanzi, Rudolph E.

AU - Oyama, Fumitaka

AU - Tabira, Takeshi

AU - Ando, Susumu

AU - Ihara, Yasuo

PY - 2000/9/8

Y1 - 2000/9/8

N2 - The N141I mutation in presenilin (PS) 2 is tightly linked with a form of autosomal dominant familial Alzheimer's disease in the Volga German families. We previously reported that mouse brains harboring mutant PS2 contained increased levels of amyloid β protein (Aβ) 42 in the Tris-saline-soluble fraction (Oyama, F., Sawamura, N., Kobayashi, K., Morishima-Kawashima, M., Kuramochi, T., Ito, M., Tomita, T., Maruyama, K., Saido, T. C., Iwatsubo, T., Capell, A., Walter, J., Grinberg, J., Ueyama, Y., Haass, C. and Ihara, Y. (1998) J. Neurochem. 71, 313-322). Here, using a new extraction protocol, we quantitated the A/β40 and Aβ42 levels in the Tris-saline-insoluble fraction. The insoluble Aβ levels were found to be higher than the soluble Aβ levels, and the insoluble Aβ42 levels were markedly increased in mutant PS2 transgenic mice. To investigate the origin of the insoluble Aβ42, we prepared the detergent-insoluble, low density membrane fraction. This fraction from two independent lines of mutant PS2 transgenic mice contained remarkably increased levels of Aβ42 and significantly low levels of glycerophospholipids and sphingomyelin. This unexpected finding suggests that a large increase in the levels of Aβ42 in mutant PS2 mice is presumably induced through alterations of the lipid composition in the low density membrane domain in the brain.

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