نتایج جستجو برای: lysosomal storage diseases

تعداد نتایج: 1035749  

Journal: :International Journal of Molecular Medicine 2012

2015
Sofie M.A. Walenbergh Tom Houben Tim Hendrikx Mike L.J. Jeurissen Patrick J. van Gorp Nathalie Vaes Steven W.M. Olde Damink Fons Verheyen Ger H. Koek Dieter Lutjohann Alena Grebe Eicke Latz Ronit Shiri-Sverdlov Sofie M. A. Walenbergh Mike L. J. Jeurissen Steven W. M. Olde Damink Dieter Lütjohann

Recently, the importance of lysosomes in the context of the metabolic syndrome has received increased attention. Increased lysosomal cholesterol storage and cholesterol crystallization inside macrophages have been linked to several metabolic diseases, such as atherosclerosis and non-alcoholic fatty liver disease (NAFLD). Two-hydroxypropyl-β-cyclodextrin (HP-B-CD) is able to redirect lysosomal c...

2015
Sofie M. A. Walenbergh Tom Houben Tim Hendrikx Mike L. J. Jeurissen Patrick J. van Gorp Nathalie Vaes Steven W. M. Olde Damink Fons Verheyen Ger H. Koek Dieter Lütjohann Alena Grebe Eicke Latz Ronit Shiri-Sverdlov Amedeo Lonardo Giovanni Targher

Recently, the importance of lysosomes in the context of the metabolic syndrome has received increased attention. Increased lysosomal cholesterol storage and cholesterol crystallization inside macrophages have been linked to several metabolic diseases, such as atherosclerosis and non-alcoholic fatty liver disease (NAFLD). Two-hydroxypropyl-β-cyclodextrin (HP-B-CD) is able to redirect lysosomal c...

2016
Fiona Karen Harlan Jason Scott Lusk Breanna Michelle Mohr Anthony Peter Guzikowski Robert Hardy Batchelor Ying Jiang John Joseph Naleway

Lysosomes are acidic cytoplasmic organelles that are present in all nucleated mammalian cells and are involved in a variety of cellular processes including repair of the plasma membrane, defense against pathogens, cholesterol homeostasis, bone remodeling, metabolism, apoptosis and cell signaling. Defects in lysosomal enzyme activity have been associated with a variety of neurological diseases i...

Journal: :Human molecular genetics 2008
Carmine Settembre Alessandro Fraldi Luca Jahreiss Carmine Spampanato Consuelo Venturi Diego Medina Raquel de Pablo Carlo Tacchetti David C Rubinsztein Andrea Ballabio

Most lysosomal storage disorders (LSDs) are caused by deficiencies of lysosomal hydrolases. While LSDs were among the first inherited diseases for which the underlying biochemical defects were identified, the mechanisms from enzyme deficiency to cell death are poorly understood. Here we show that lysosomal storage impairs autophagic delivery of bulk cytosolic contents to lysosomes. By studying ...

2012
Fiona L. Wilkinson Rebecca J. Holley Kia J. Langford-Smith Soumya Badrinath Aiyin Liao Alex Langford-Smith Jonathan D. Cooper Simon A. Jones J. Ed Wraith Rob F. Wynn Catherine L. R. Merry Brian W. Bigger

Mucopolysaccharide diseases (MPS) are caused by deficiency of glycosaminoglycan (GAG) degrading enzymes, leading to GAG accumulation. Neurodegenerative MPS diseases exhibit cognitive decline, behavioural problems and shortened lifespan. We have characterised neuropathological changes in mouse models of MPSI, IIIA and IIIB to provide a better understanding of these events.Wild-type (WT), MPSI, I...

2010
Robert Lowe Robert C. Glen John B. O. Mitchell

Phospholipidosis is an adverse effect caused by numerous cationic amphiphilic drugs and can affect many cell types. It is characterized by the excess accumulation of phospholipids and is most reliably identified by electron microscopy of cells revealing the presence of lamellar inclusion bodies. The development of phospholipidosis can cause a delay in the drug development process, and the impor...

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