نتایج جستجو برای: neuroserpin

تعداد نتایج: 162  

Journal: :Journal of cell science 2008
Nathalie Lebeurrier Séverine Launay Richard Macrez Eric Maubert Hélène Legros Arnaud Leclerc Soazik P Jamin Jean-Yves Picard Stéphane Marret Vincent Laudenbach Philipp Berger Peter Sonderegger Carine Ali Nathalie di Clemente Denis Vivien

The balance between tissue-type plasminogen activator (tPA) and one of its inhibitors, neuroserpin, has crucial roles in the central nervous system, including the control of neuronal migration, neuronal plasticity and neuronal death. In the present study, we demonstrate that the activation of the transforming growth factor-beta (TGFbeta)-related BMPR-IB (also known as BMPR1B and Alk6)- and Smad...

Journal: :Genetics 2013
Angela Schipanski Sascha Lange Alexandra Segref Aljona Gutschmidt David A Lomas Elena Miranda Michaela Schweizer Thorsten Hoppe Markus Glatzel

Intraneuronal deposition of aggregated proteins in tauopathies, Parkinson disease, or familial encephalopathy with neuroserpin inclusion bodies (FENIB) leads to impaired protein homeostasis (proteostasis). FENIB represents a conformational dementia, caused by intraneuronal polymerization of mutant variants of the serine protease inhibitor neuroserpin. In contrast to the aggregation process, the...

2013
Jiao Ma Dan Yu Yu Tong Meng Mao

Hypoxia-ischemia (HI) occurring in immature brains stimulates the expression of tissue-type plasminogen activator (tPA). Neuroserpin is a selected inhibitor of tPA in the central nerves system. However, the role that neuroserpin plays and the possible mechanisms involved during neonatal HI are poorly defi ned. In this study, an oxygen-glucose deprivation and reoxygenation (OGD/R) model was gene...

Journal: :The Journal of biological chemistry 2009
Heike Kroeger Elena Miranda Ian MacLeod Juan Pérez Damian C Crowther Stefan J Marciniak David A Lomas

The serpinopathies are a family of diseases characterized by the accumulation of ordered polymers of mutant protein within the endoplasmic reticulum. They are a diverse group including alpha(1)-antitrypsin deficiency and the inherited dementia familial encephalopathy with neuroserpin inclusion bodies or FENIB. We have used transient transfection of COS7 cells and mouse embryonic fibroblasts, PC...

Journal: :Journal of neuropathology and experimental neurology 2000
M Takao M D Benson J R Murrell M Yazaki P Piccardo F W Unverzagt R L Davis P D Holohan D A Lawrence R Richardson M R Farlow B Ghetti

Mutations in the Neuroserpin gene have been reported to cause familial presenile dementia. We describe a new family in which the S52R Neuroserpin mutation is associated with progressive myoclonus epilepsy in 2 siblings. The proband presented myoclonus and epilepsy at age 24, his brother and mother presented a similar disorder when they were 25. A clinical diagnosis of progressive myoclonus epil...

Journal: :Circulation 2002
Zhenggang Zhang Li Zhang Manuel Yepes Quan Jiang Qingjiang Li Polly Arniego Timothy A Coleman Daniel A Lawrence Michael Chopp

BACKGROUND After stroke, the thrombolytic effect of tissue-type plasminogen activator (tPA) in the intravascular space is beneficial, whereas its extravascular effect on ischemic neurons is deleterious. We tested the hypothesis that neuroserpin, a natural inhibitor of tPA, reduces tPA-induced neuronal toxicity and increases its therapeutic window for treatment of embolic stroke. METHODS AND R...

Journal: :BMC Neurology 2007
John W Cole Adam C Naj Jeffrey R O'Connell Oscar C Stine John D Sorkin Marcella A Wozniak Barney J Stern Manuel Yepes Daniel A Lawrence Laurie J Reinhart Dudley K Strickland Braxton D Mitchell Steven J Kittner

BACKGROUND Neuroserpin, primarily localized to CNS neurons, inhibits the adverse effects of tissue-type plasminogen activator (tPA) on the neurovascular unit and has neuroprotective effects in animal models of ischemic stroke. We sought to evaluate the association of neuroserpin polymorphisms with risk for ischemic stroke among young women. METHODS A population-based case-control study of str...

2017
Costanza Giampietro Maria Chiara Lionetti Giulio Costantini Federico Mutti Stefano Zapperi Caterina A. M. La Porta

Intraneural accumulation of misfolded proteins is a common feature of several neurodegenerative pathologies including Alzheimer's and Parkinson's diseases, and Familial Encephalopathy with Neuroserpin Inclusion Bodies (FENIB). FENIB is a rare disease due to a point mutation in neuroserpin which accelerates protein aggregation in the endoplasmic reticulum (ER). Here we show that cholesterol depl...

2015
Rosina Noto Maria Grazia Santangelo Matteo Levantino Antonio Cupane Maria Rosalia Mangione Daniele Parisi Stefano Ricagno Martino Bolognesi Mauro Manno Vincenzo Martorana

Neuroserpin (NS) is a serine protease inhibitor (SERPIN) involved in different neurological pathologies, including the Familial Encephalopathy with Neuroserpin Inclusion Bodies (FENIB), related to the aberrant polymerization of NS mutants. Here we present an in vitro and in silico characterization of native neuroserpin and its dysfunctional conformation isoforms: the proteolytically cleaved con...

Journal: :Neurology 2007
H M Nielsen L Minthon E Londos K Blennow E Miranda J Perez D C Crowther D A Lomas S M Janciauskiene

OBJECTIVE Serine protease inhibitors (serpins), the acute phase reactants and regulators of the proteolytic processing of proteins, have been recognized as potential contributors to the pathogenesis of Alzheimer disease (AD). We measured plasma and CSF levels of serpins in controls and patients with dementia. METHODS Using rocket immunoelectrophoresis, ELISA, and Luminex xMAP technology, we a...

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