2007
DOI: 10.1096/fj.06-7016com
|View full text |Cite
|
Sign up to set email alerts
|

Acid ceramidase is a novel factor required for early embryo survival

Abstract: Recent studies suggest that the lipid, ceramide, induces the default apoptosis process in eggs. Yet, it is obscure how newly formed embryos overcome this fate. Acid ceramidase (AC) is a key regulatory enzyme involved in ceramide metabolism, and mutations in the AC gene (Asah1) result in Farber Lipogranulomatosis, a fatal human genetic disorder. Our previous studies revealed that AC knockout (Asah1-/-) mice had a lethal phenotype, and herein we reveal the mechanism underlying this observation. A single-cell, po… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

2
78
0

Year Published

2008
2008
2022
2022

Publication Types

Select...
7
3

Relationship

2
8

Authors

Journals

citations
Cited by 98 publications
(80 citation statements)
references
References 26 publications
2
78
0
Order By: Relevance
“…Genetic defects in several of these hydrolytic enzymes cause various disorders with lysosomal accumulation of the substrate lipids, a group of disorders termed the sphingolipidoses [41,[90][91][92][93]. Particularly, some of the known sphingolipidoses might closely associate with aberrant metabolisms of ceramide because of defective activities of ceramide generating/degrading enzymes: Farber's disease, Gaucher disease, and Niemann-Pick type A and B diseases are caused by a deficiency of acid ceramidase [94,95], glucocerebrosidase (acid-β-glucosidase) [96][97][98], acid SMase [99,100], respectively. The salvage pathway is one of the routes for controlling cellular levels of ceramide.…”
Section: Sphingolipidosesmentioning
confidence: 99%
“…Genetic defects in several of these hydrolytic enzymes cause various disorders with lysosomal accumulation of the substrate lipids, a group of disorders termed the sphingolipidoses [41,[90][91][92][93]. Particularly, some of the known sphingolipidoses might closely associate with aberrant metabolisms of ceramide because of defective activities of ceramide generating/degrading enzymes: Farber's disease, Gaucher disease, and Niemann-Pick type A and B diseases are caused by a deficiency of acid ceramidase [94,95], glucocerebrosidase (acid-β-glucosidase) [96][97][98], acid SMase [99,100], respectively. The salvage pathway is one of the routes for controlling cellular levels of ceramide.…”
Section: Sphingolipidosesmentioning
confidence: 99%
“…The AC-deficient mouse (Asah1 Ϫ / Ϫ ) undergoes apoptotic death at the 2-cell stage (E1; Fig. 4 ) because of excessive ceramide accumulation ( 39,102 ), demonstrating that AC is expressed in the embryo and that ceramide degradation is essential for survival beyond the 2-cell stage (E1) ( 102 ). In addition to increasing ceramide pools, loss of AC activity is thought to concurrently reduce pools of sphingosine and sphingosine-1-phosphate, two lipids known to promote cell growth and differentiation ( 103 ).…”
Section: Disorders Of Ceramide Degradationmentioning
confidence: 99%
“…Ceramide may also form membrane channels for proteins like cytochrome C, and stabilize membrane rafts (42). The early embryo is resistant to apoptosis, owing to low levels of ceramide (43,44); however, there has been no measurement of ceramide during fertilization.…”
Section: Lipid Signaling Related To Fertilizationmentioning
confidence: 99%