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Sökning: onr:"swepub:oai:lup.lub.lu.se:4b2447f2-80e8-4893-9521-c271c8fb6da0" > Unconventional Sour...

Unconventional Source of Neurotoxic Protein Aggregation from Organelle Off-Target Bax∆2 in Alzheimer's Disease

Yao, Qi (författare)
Illinois Institute of Technology
Mascarenhas Dos Santos, Anne Caroline (författare)
Illinois Institute of Technology
Zhang, Huaiyuan (författare)
Illinois Institute of Technology
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Mañas, Adriana (författare)
Lund University,Lunds universitet,Molekylär barnonkologi,Forskargrupper vid Lunds universitet,Molecular Pediatric Oncology,Lund University Research Groups
Hussaini, Ammarah (författare)
Illinois Institute of Technology
Kim, Ujin (författare)
Illinois Institute of Technology
Xu, Congtai (författare)
Illinois Institute of Technology
Basheer, Sana (författare)
Illinois Institute of Technology
Tasaki, Shinya (författare)
Rush University Medical Center Chicago
Xiang, Jialing (författare)
Illinois Institute of Technology
visa färre...
 (creator_code:org_t)
2023
2023
Engelska.
Ingår i: Biomolecules. - 2218-273X. ; 13:6
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Protein aggregates are a hallmark of Alzheimer's disease (AD). Extensive studies have focused on β-amyloid plaques and Tau tangles. Here, we illustrate a novel source of protein aggregates in AD neurons from organelle off-target proteins. Bax is a mitochondrial pore-forming pro-death protein. What happens to Bax if it fails to target mitochondria? We previously showed that a mitochondrial target-deficient alternatively spliced variant, Bax∆2, formed large cytosolic protein aggregates and triggered caspase 8-mediated cell death. Bax∆2 protein levels were low in most normal organs and the proteins were quickly degraded in cancer. Here, we found that 85% of AD patients had Bax∆2 required alternative splicing. Increased Bax∆2 proteins were mostly accumulated in neurons of AD-susceptible brain regions. Intracellularly, Bax∆2 aggregates distributed independently of Tau tangles. Interestingly, Bax∆2 aggregates triggered the formation of stress granules (SGs), a large protein-RNA complex involved in AD pathogenesis. Although the functional domains required for aggregation and cell death are the same as in cancer cells, Bax∆2 relied on SGs, not caspase 8, for neuronal cell death. These results imply that the aggregation of organelle off-target proteins, such as Bax∆2, broadens the scope of traditional AD pathogenic proteins that contribute to the neuronal stress responses and AD pathogenesis.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

Humans
Alzheimer Disease/metabolism
Protein Aggregates
bcl-2-Associated X Protein/genetics
Amyloid beta-Peptides/metabolism
Mitochondria/metabolism
Neurotoxicity Syndromes
tau Proteins/genetics

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