نتایج جستجو برای: sortilin

تعداد نتایج: 403  

Journal: :The Journal of clinical investigation 2014
Martin B Mortensen Mads Kjolby Stine Gunnersen Jakob V Larsen Johan Palmfeldt Erling Falk Anders Nykjaer Jacob F Bentzon

Genome-wide association studies have identified a link between genetic variation at the human chromosomal locus 1p13.3 and coronary artery disease. The gene encoding sortilin (SORT1) has been implicated as the causative gene within the locus, as sortilin regulates hepatic lipoprotein metabolism. Here we demonstrated that sortilin also directly affects atherogenesis, independent of its regulator...

Journal: :Neuron 2010
Fenghua Hu Thihan Padukkavidana Christian B. Vægter Owen A. Brady Yanqiu Zheng Ian R. Mackenzie Howard H. Feldman Anders Nykjaer Stephen M. Strittmatter

VIDEO ABSTRACT The most common inherited form of Frontotemporal Lobar Degeneration (FTLD) known stems from Progranulin (GRN) mutation and exhibits TDP-43 plus ubiquitin aggregates. Despite the causative role of GRN haploinsufficiency in FTLD-TDP, the neurobiology of this secreted glycoprotein is unclear. Here, we examined PGRN binding to the cell surface. PGRN binds to cortical neurons via its ...

2014
Jacob Lauwring Andersen Tenna Juul Schrøder Søren Christensen Dorthe Strandbygård Lone Tjener Pallesen Maria Marta García-Alai Samsa Lindberg Morten Langgård Jørgen Calí Eskildsen Laurent David Lena Tagmose Klaus Baek Simonsen Philip James Maltas Lars Christian Biilmann Rønn Inge E. M. de Jong Ibrahim John Malik Jan Egebjerg Jens-Jacob Karlsson Srinivas Uppalanchi Durga Rao Sakumudi Pradheep Eradi Steven P. Watson Søren Thirup

Sortilin is a type I membrane glycoprotein belonging to the vacuolar protein sorting 10 protein (Vps10p) family of sorting receptors and is most abundantly expressed in the central nervous system. Sortilin has emerged as a key player in the regulation of neuronal viability and has been implicated as a possible therapeutic target in a range of disorders. Here, the identification of AF40431, the ...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2018
Claudia Goettsch Mads Kjolby Elena Aikawa

Cardiovascular disease is a leading cause of morbidity and mortality in the Western world. Studies of sortilin's influence on cardiovascular and metabolic diseases goes far beyond the genome-wide association studies that have revealed an association between cardiovascular diseases and the 1p13 locus that encodes sortilin. Emerging evidence suggests a significant role of sortilin in the pathogen...

2017
Kevin Mahendra Patel

Genome-wide association studies (GWAS) have been used to identify novel genes and loci that contribute to lipid traits and coronary heart disease (CHD) in a causal manner. A locus on chromosome 1p13, which harbors the gene sortilin-1 (SORT1) encoding the protein sortilin is the locus in the human genome with the strongest association with low-density lipoprotein cholesterol (LDL-C) and is also ...

2015

Sortilin protein drives cholesterol uptake in macrophages and promotes atherosclerosis, report Patel et al. A characteristic feature of atherosclerosis is the formation of foam cells that arise from cholesterol-loaded macrophages. But exactly how macrophages take up cholesterol from transporter proteins such as low-density lipoprotein (LDL) is unclear, especially since the deletion of known mac...

2012
Ana M. Santos Noelia López-Sánchez David Martín-Oliva Pedro de la Villa Miguel A. Cuadros José M. Frade

Both proNGF and the neurotrophin receptor p75 (p75(NTR)) are known to regulate photoreceptor cell death caused by exposure of albino mice to intense illumination. ProNGF-induced apoptosis requires the participation of sortilin as a necessary p75(NTR) co-receptor, suggesting that sortilin may participate in the photoreceptor degeneration triggered by intense lighting. We report here that light-e...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2013
Camilla Gustafsen Simon Glerup Lone Tjener Pallesen Ditte Olsen Olav M Andersen Anders Nykjær Peder Madsen Claus Munck Petersen

The development and progression of Alzheimer's disease is linked to excessive production of toxic amyloid-β peptide, initiated by β-secretase cleavage of the amyloid precursor protein (APP). In contrast, soluble APPα (sAPPα) generated by the α-secretase is known to stimulate dendritic branching and enhance synaptic function. Regulation of APP processing, and the shift from neurotrophic to neuro...

2015

Sortilin protein drives cholesterol uptake in macrophages and promotes atherosclerosis, report Patel et al. A characteristic feature of atherosclerosis is the formation of foam cells that arise from cholesterol-loaded macrophages. But exactly how macrophages take up cholesterol from transporter proteins such as low-density lipoprotein (LDL) is unclear, especially since the deletion of known mac...

2017
Xia Hu Zhao-Lan Hu Zheng Li Chun-Sheng Ruan Wen-Ying Qiu Aihua Pan Chang-Qi Li Yan Cai Lu Shen Yaping Chu Bei-Sha Tang Huaibin Cai Xin-Fu Zhou Chao Ma Xiao-Xin Yan

Genetic variations in the vacuolar protein sorting 10 protein (Vps10p) family have been linked to Alzheimer's disease (AD). Here we demonstrate deposition of fragments from the Vps10p member sortilin at senile plaques (SPs) in aged and AD human cerebrum. Sortilin changes were characterized in postmortem brains with antibodies against the extracellular and intracellular C-terminal domains. The t...

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