Correlation Between Decrease in Protein Levels of Ubiquitin Ligase HRD1 and Amyloid-β Production
Endoplasmic reticulum-associated degradation (ERAD) is a quality control mechanism in which unfolded proteins are retro-translocated to the cytosol for degradation. Our recent study showed that suppression of expression of ubiquitin ligase HRD1, which is involved in ERAD, caused amyloid precursor pr...
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| Main Authors: | , , , |
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| Format: | Book |
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Elsevier,
2010-01-01T00:00:00Z.
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| Summary: | Endoplasmic reticulum-associated degradation (ERAD) is a quality control mechanism in which unfolded proteins are retro-translocated to the cytosol for degradation. Our recent study showed that suppression of expression of ubiquitin ligase HRD1, which is involved in ERAD, caused amyloid precursor protein (APP) accumulation and amyloid-β (Aβ) production. Furthermore, HRD1 protein levels were significantly lower in the cerebral cortex of Alzheimer's disease (AD) patients. To assess whether HRD1 is involved in AD pathology, we analyzed the relationship between HRD1 protein levels and Aβ production. We found that the HRD1 level was negatively correlated with the Aβ level, suggesting the possible involvement of HRD1 in Aβ generation. Keywords:: HRD1, endoplasmic reticulum-associated degradation (ERAD), amyloid-β |
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| Item Description: | 1347-8613 10.1254/jphs.10118SC |