نتایج جستجو برای: smpd1

تعداد نتایج: 88  

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2014
Patrick Münzer Oliver Borst Britta Walker Evi Schmid Marion A H Feijge Judith M E M Cosemans Madhumita Chatterjee Eva-Maria Schmidt Sebastian Schmidt Syeda T Towhid Christina Leibrock Margitta Elvers Martin Schaller Peter Seizer Klaus Ferlinz Andreas E May Erich Gulbins Johan W M Heemskerk Meinrad Gawaz Florian Lang

OBJECTIVE Platelet activation is essential for primary hemostasis and acute thrombotic vascular occlusions. On activation, platelets release their prothrombotic granules and expose phosphatidylserine, thus fostering thrombin generation and thrombus formation. In other cell types, both degranulation and phosphatidylserine exposure are modified by sphingomyelinase-dependent formation of ceramide....

2015
Cosima Rhein Christiane Mühle Johannes Kornhuber Martin Reichel Emil Alexov

Loss-of-function mutations in the sphingomyelin phosphodiesterase 1 (SMPD1) gene are associated with decreased catalytic activity of acid sphingomyelinase (ASM) and are the cause of the autosomal recessive lysosomal storage disorder Niemann-Pick disease (NPD) types A and B. Currently, >100 missense mutations in SMPD1 are listed in the Human Gene Mutation Database. However, not every sequence va...

Journal: :International journal of clinical and experimental medicine 2015
Kai Li Bei-Sha Tang Nan-Nan Yang Ji-Feng Kang Zhen-Hua Liu Rui-Qi Liu Xin-Xiang Yan Lu Shen Ji-Feng Guo

PURPOSE The protein encoded by sphingomyelin phosphodiesterase 1, acid lysosomal (SMPD1) is a lysosomal acid sphingomyelinase. While there are increasing evidences to suggest that lysosomal enzyme defects and Parkinson's disease (PD) have strong associations, and recently, SMPD1 p.L302P (c.T911C, NM_000543) was found to be a risk factor for PD in Ashkenazi Jewish ancestry population, we try to ...

2017
Svenja Sydor Jan-Peter Sowa Dominik A. Megger Martin Schlattjan Sami Jafoui Lena Wingerter Alexander Carpinteiro Hideo A. Baba Lars P. Bechmann Barbara Sitek Guido Gerken Erich Gulbins Ali Canbay

OBJECTIVE Alterations in sphingolipid and ceramide metabolism have been associated with various diseases, including nonalcoholic fatty liver disease (NAFLD). Acid sphingomyelinase (ASM) converts the membrane lipid sphingomyelin to ceramide, thereby affecting membrane composition and domain formation. We investigated the ways in which the Asm knockout (Smpd1-/-) genotype affects diet-induced NAF...

2017
Ha-Yeun Chung Anna S. Kollmey Andrea Schrepper Matthias Kohl Markus F. Bläss Sebastian N. Stehr Amelie Lupp Markus H. Gräler Ralf A. Claus

Cardiac dysfunction, in particular of the left ventricle, is a common and early event in sepsis, and is strongly associated with an increase in patients' mortality. Acid sphingomyelinase (SMPD1)-the principal regulator for rapid and transient generation of the lipid mediator ceramide-is involved in both the regulation of host response in sepsis as well as in the pathogenesis of chronic heart fa...

2013
Hamid Galehdari Raheleh Tangestani Sepideh Ghasemian

OBJECTIVE NIEMANN PICK DISEASE (NPD) TYPE A (NPA: MIM #257200) is a lipid storage disorder with an autosomal recessive inheritance and occurrs by defect of the SMPD1 gene encoding sphingomyelinase. Disruption of this enzyme leads to the accumulation of sphingomyelin in brain and liver, which in turn causes dysfunction or damage of tissue. METHODS We report firstly a 2.5 year old boy with NPA ...

Journal: :Frontiers in bioscience 2016
Ming Xu Qiufang Zhang Pin-Lan Li Thaison Nguyen Xiang Li Yang Zhang

Acid sphingomyelinase (ASM; gene symbol Smpd1) has been shown to play a crucial role in autophagy maturation by controlling lysosomal fusion with autophagosomes in coronary arterial smooth muscle cells (CASMCs). However, the underlying molecular mechanism by which ASM controls autophagolysosomal fusion remains unknown. In primary cultured CASMCs, lysosomal Ca2+ induced by 7-ketocholesterol (7-K...

Journal: :Traffic 2010
Cecilia Devlin Nina H Pipalia Xianghai Liao Edward H Schuchman Frederick R Maxfield Ira Tabas

Different primary lysosomal trafficking defects lead to common alterations in lipid trafficking, suggesting cooperative interactions among lysosomal lipids. However, cellular analysis of the functional consequences of this phenomenon is lacking. As a test case, we studied cells with defective Niemann-Pick C1 (NPC1) protein, a cholesterol trafficking protein whose defect gives rise to lysosomal ...

2015
Marcel Kramer Stefanie Quickert Christoph Sponholz Uwe Menzel Klaus Huse Matthias Platzer Michael Bauer Ralf A. Claus

Acid sphingomyelinase (ASM or sphingomyelin phosphodiesterase, SMPD) activity engages a critical role for regulation of immune response and development of organ failure in critically ill patients. Beside genetic variation in the human gene encoding ASM (SMPD1), alternative splicing of the mRNA is involved in regulation of enzymatic activity. Here we show that the patterns of alternatively splic...

Journal: :Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2008
Verena Brand Saisudha Koka Camelia Lang Verena Jendrossek Stephan M Huber Erich Gulbins Florian Lang

Plasmodia express a sphingomyelinase, which is apparently required for their development. On the other hand, the sphingomyelinase product ceramide has previously been shown to delay parasite development. Moreover, ceramide triggers suicidal erythrocyte death or eryptosis, characterized by exposure of phosphatidylserine at the erythrocyte surface and cell shrinkage. Accelerated eryptosis of infe...

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