کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1904923 | 1534680 | 2012 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: The importance of ether-phospholipids: A view from the perspective of mouse models The importance of ether-phospholipids: A view from the perspective of mouse models](/preview/png/1904923.png)
Ether-phospholipids represent an important group of phospholipids characterized by an alkyl or an alkenyl bond at the sn-1 position of the glycerol backbone. Plasmalogens are the most abundant form of alkenyl-glycerophospholipids, and their synthesis requires functional peroxisomes. Defects in the biosynthesis of plasmalogens are the biochemical hallmark of the human peroxisomal disorder Rhizomelic Chondrodysplasia Punctata (RCDP), which is characterized by defects in eye, bone and nervous tissue. The generation and characterization of mouse models with defects in plasmalogen levels have significantly advanced our understanding of the role and importance of plasmalogens as well as pathogenetic mechanisms underlying RCDP. A review of the current mouse models and the description of the combined knowledge gathered from the histopathological and biochemical studies is presented and discussed. Further characterization of the role and functions of plasmalogens will contribute to the elucidation of disease pathogenesis in peroxisomal and non-peroxisomal disorders. This article is part of a Special Issue entitled: Metabolic Functions and Biogenesis of Peroxisomes in Health and Disease.
► Plasmalogens are a special subclass of phospholipids containing a vinyl-ether bond.
► A deficiency in plasmalogens affects multiple tissues and a myriad of human disorders.
► Several mouse mutants have been generated to serve as models for human disorders.
► There is a good correlation between the human disorders and the mouse mutants.
► Plasmalogen loss may modulate tissue pathology in several neurologic disorders.
Journal: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - Volume 1822, Issue 9, September 2012, Pages 1501–1508