Literature DB >> 19944693

Acid sphingomyelinase, cell membranes and human disease: lessons from Niemann-Pick disease.

Edward H Schuchman1.   

Abstract

Acid sphingomyelinase (ASM) plays an important role in normal membrane turnover through the hydrolysis of sphingomyelin, and is one of the key enzymes responsible for the production of ceramide. ASM activity is deficient in the genetic disorder Types A and B Niemann-Pick disease (NPD). ASM knockout (ASMKO) mice were originally constructed to study this disorder, and numerous defects in ceramide-related signaling have been shown. Studies in these mice have further suggested that ASM may be involved in the pathogenesis of several common diseases through the reorganization of membrane microdomains. This review will focus on the role of ASM in membrane biology, with a specific emphasis on what a rare genetic disorder (NPD) has taught us about more common events. Copyright 2009 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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Year:  2009        PMID: 19944693     DOI: 10.1016/j.febslet.2009.11.083

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  54 in total

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Authors:  James A Shayman; Robert Kelly; Jessica Kollmeyer; Yongqun He; Akira Abe
Journal:  Prog Lipid Res       Date:  2010-11-11       Impact factor: 16.195

Review 3.  Damage control: cellular mechanisms of plasma membrane repair.

Authors:  Norma W Andrews; Patricia E Almeida; Matthias Corrotte
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Review 4.  Sphingolipids in the DNA damage response.

Authors:  Brittany Carroll; Jane Catalina Donaldson; Lina Obeid
Journal:  Adv Biol Regul       Date:  2014-11-18

5.  Solving the secretory acid sphingomyelinase puzzle: Insights from lysosome-mediated parasite invasion and plasma membrane repair.

Authors:  Norma W Andrews
Journal:  Cell Microbiol       Date:  2019-06-10       Impact factor: 3.715

Review 6.  Gene Therapy for the Treatment of Neurological Disorders: Metabolic Disorders.

Authors:  Dominic J Gessler; Guangping Gao
Journal:  Methods Mol Biol       Date:  2016

7.  Inhibition of Acid Sphingomyelinase Depletes Cellular Phosphatidylserine and Mislocalizes K-Ras from the Plasma Membrane.

Authors:  Kwang-Jin Cho; Dharini van der Hoeven; Yong Zhou; Masashi Maekawa; Xiaoping Ma; Wei Chen; Gregory D Fairn; John F Hancock
Journal:  Mol Cell Biol       Date:  2015-11-16       Impact factor: 4.272

8.  Exocytosis of acid sphingomyelinase by wounded cells promotes endocytosis and plasma membrane repair.

Authors:  Christina Tam; Vincent Idone; Cecilia Devlin; Maria Cecilia Fernandes; Andrew Flannery; Xingxuan He; Edward Schuchman; Ira Tabas; Norma W Andrews
Journal:  J Cell Biol       Date:  2010-06-07       Impact factor: 10.539

9.  Differential association of the Na+/H+ Exchanger Regulatory Factor (NHERF) family of adaptor proteins with the raft- and the non-raft brush border membrane fractions of NHE3.

Authors:  Ayesha Sultan; Min Luo; Qin Yu; Brigitte Riederer; Weiliang Xia; Mingmin Chen; Simone Lissner; Johannes E Gessner; Mark Donowitz; C Chris Yun; Hugo deJonge; Georg Lamprecht; Ursula Seidler
Journal:  Cell Physiol Biochem       Date:  2013

10.  Inhibition of acid sphingomyelinase disrupts LYNUS signaling and triggers autophagy.

Authors:  Matthew J Justice; Irina Bronova; Kelly S Schweitzer; Christophe Poirier; Janice S Blum; Evgeny V Berdyshev; Irina Petrache
Journal:  J Lipid Res       Date:  2018-01-29       Impact factor: 5.922

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