International audienceThe autosomal dominant dementia familial encephalopathy with neuroserpin inclusion bodies is characterized by the accumulation of ordered polymers of mutant neuroserpin within the endoplasmic reticulum of neurones. We show here that intracellular neuroserpin polymers activate NF-kappaB by a pathway that is independent of the IRE1, ATF6, and PERK limbs of the canonical unfolded protein response but is dependent on intracellular calcium. This pathway provides a mechanism for cells to sense and react to the accumulation of folded structures of mutant serpins within the endoplasmic reticulum. Our results provide strong support for the endoplasmic reticulum overload response being independent of the unfolded protein respons...
The serpinopathies are due to misfolding and intracellular polymerisation of mutant serpin variants ...
The endoplasmic reticulum (ER) is the main cellular organelle involved in protein synthesis, assembl...
Neurodegenerative diseases, such as Alzheimer's disease, Huntington's disease, Parkinson's disease, ...
International audienceThe autosomal dominant dementia familial encephalopathy with neuroserpin inclu...
Neuroserpin is a 55 kDa glycoprotein that is secreted from axons of the central and peripheral nervo...
International audienceMutants of neuroserpin are retained as polymers within the endoplasmic reticul...
Intraneuronal deposition of aggregated proteins in tauopathies, Parkinson disease, or familial encep...
The neurodegenerative condition FENIB (familiar encephalopathy with neuroserpin inclusion bodies) is...
Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is a progressive neurodegenerative...
Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is an autosomal dominant dementia ...
International audienceEndoplasmic reticulum (ER) dysfunction is important in the pathogenesis of man...
Accumulation of β-amyloid (Aβ) peptide has long been considered as one of the toxic factors contribu...
Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is a rare disease characterized by...
A feature of neurodegenerative diseases is the intraneuronal accumulation of misfolded proteins. In ...
The serpinopathies are due to misfolding and intracellular polymerisation of mutant serpin variants ...
The endoplasmic reticulum (ER) is the main cellular organelle involved in protein synthesis, assembl...
Neurodegenerative diseases, such as Alzheimer's disease, Huntington's disease, Parkinson's disease, ...
International audienceThe autosomal dominant dementia familial encephalopathy with neuroserpin inclu...
Neuroserpin is a 55 kDa glycoprotein that is secreted from axons of the central and peripheral nervo...
International audienceMutants of neuroserpin are retained as polymers within the endoplasmic reticul...
Intraneuronal deposition of aggregated proteins in tauopathies, Parkinson disease, or familial encep...
The neurodegenerative condition FENIB (familiar encephalopathy with neuroserpin inclusion bodies) is...
Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is a progressive neurodegenerative...
Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is an autosomal dominant dementia ...
International audienceEndoplasmic reticulum (ER) dysfunction is important in the pathogenesis of man...
Accumulation of β-amyloid (Aβ) peptide has long been considered as one of the toxic factors contribu...
Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is a rare disease characterized by...
A feature of neurodegenerative diseases is the intraneuronal accumulation of misfolded proteins. In ...
The serpinopathies are due to misfolding and intracellular polymerisation of mutant serpin variants ...
The endoplasmic reticulum (ER) is the main cellular organelle involved in protein synthesis, assembl...
Neurodegenerative diseases, such as Alzheimer's disease, Huntington's disease, Parkinson's disease, ...