ESI-MS quantitation of increased sphingomyelin in Niemann-Pick disease type BHDL

被引:27
作者
Lee, CY
Lesimple, A
Larsen, Å
Mamer, O
Genest, J [1 ]
机构
[1] McGill Univ, Cardiovasc Genet Lab, Dept Med, Montreal, PQ, Canada
[2] McGill Univ, Mass Spectrometry Unit, Montreal, PQ, Canada
[3] Univ Oslo, Dept Chem, Oslo, Norway
关键词
electrospray ionization-mass spectrometry; phospholipids; sphingomyelin phosphodiesterase-1 gene; sphingomyelinase; high density lipoprotein;
D O I
10.1194/jlr.M500011-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
HDLs have been proposed to have antiatherogenic properties because of their role in reverse cholesterol transport as lipid acceptors. To elucidate the phospholipid profile of these particles, we used electrospray ionization mass spectrometry to examine the phosphatidylcholine ( PC) and sphingomyelin (SM) composition of HDLs purified from plasma and nascently generated in vitro from fibroblasts. We also quantitatively compared the phospholipids present in these lipoproteins between normal and Niemann-Pick disease type B (NPD-B) subjects characterized by sphingomyelinase (SMase) deficiency. We demonstrated that plasma HDLs from NPD-B were significantly enriched in SM by an average of 28%, particularly the palmitoyl SM ( with an increase of 95%), which accounted for similar to 25-44% of total SM molecular species. Similarly, we observed an increase of similar to 63% in total SM levels in nascent HDLs prepared from NPD-B fibroblasts. Although PC levels in nascent HDLs were comparable between control and NPD-B cells, there was a 95% increase in total PC levels similar to that of SM in plasma HDLs extracted from NPD-B subjects. These data provide insight into the structure of HDLs and identify potential new roles for SMase in lipoprotein metabolism.
引用
收藏
页码:1213 / 1228
页数:16
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