Changes in phospholipid composition within the dystrophic muscle by matrix-assisted laser desorption/ionization mass spectrometry and mass spectrometry imaging

被引:73
作者
Touboul, D
Piednoël, H
Voisin, V
De La Porte, S
Brunelle, A
Halgand, F
Laprévote, O
机构
[1] CNRS, Inst Chim Subst Nat, Lab Spectrometrie Masse, F-91198 Gif Sur Yvette, France
[2] CNRS, Lab Neurobiol Cellulaire & Mol, Inst Neurobiol Alfred Fessard, F-91198 Gif Sur Yvette, France
关键词
Duchenne muscular dystrophy; glycerophosphatidylcholine; fatty acid; imaging mass spectrometry; MALDI-ToF;
D O I
10.1255/ejms.671
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Duchenne muscular dystrophy (DMD) is a neuromuscular disease linked to the lack of dystrophin, a submembrane protein, leading to muscle weakness and associated with a defect of the lipid metabolism. A study of the fatty acid composition of glycerophosphatidylcholines by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-ToF-MS) and tandem mass spectrometry (MS/MS) enabled us to characterize a change in the lipid composition of dystrophic cells at the time of the differentiation. This modification has been used as a marker to identify with profiling and imaging MALDI-ToF MS regenerating areas in sections of an mdx mouse leg muscle. It is the first time that such a slight change in fatty acid composition has been observed directly on tissue slices using mass spectrometry. This approach will be useful in monitoring the treatment of muscular regeneration.
引用
收藏
页码:657 / 664
页数:8
相关论文
共 28 条
[1]   MYOTUBE PHOSPHOLIPID-SYNTHESIS AND SARCOLEMMAL ATPASE ACTIVITY IN DYSTROPHIC (MDX) MOUSE MUSCLE [J].
ANDERSON, JE .
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1991, 69 (12) :835-841
[2]   Function and genetics of dystrophin and dystrophin-related proteins in muscle [J].
Blake, DJ ;
Weir, A ;
Newey, SE ;
Davies, KE .
PHYSIOLOGICAL REVIEWS, 2002, 82 (02) :291-329
[3]  
Brunelle A, 1997, RAPID COMMUN MASS SP, V11, P353, DOI 10.1002/(SICI)1097-0231(19970228)11:4<353::AID-RCM865>3.0.CO
[4]  
2-4
[5]   X-CHROMOSOME-LINKED MUSCULAR-DYSTROPHY (MDX) IN THE MOUSE [J].
BULFIELD, G ;
SILLER, WG ;
WIGHT, PAL ;
MOORE, KJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (04) :1189-1192
[6]   Molecular imaging of biological samples: Localization of peptides and proteins using MALDI-TOF MS [J].
Caprioli, RM ;
Farmer, TB ;
Gile, J .
ANALYTICAL CHEMISTRY, 1997, 69 (23) :4751-4760
[7]   DEFECTIVE [U-14 C] PALMITIC ACID OXIDATION IN DUCHENNE MUSCULAR-DYSTROPHY [J].
CARROLL, JE ;
NORRIS, BJ ;
BROOKE, MH .
NEUROLOGY, 1985, 35 (01) :96-97
[8]   Integrating histology and imaging mass spectrometry [J].
Chaurand, P ;
Schwartz, SA ;
Billheimer, D ;
Xu, BGJ ;
Crecelius, A ;
Caprioli, RM .
ANALYTICAL CHEMISTRY, 2004, 76 (04) :1145-1155
[9]   Direct profiling of proteins in biological tissue sections by MALDI mass spectrometry [J].
Chaurand, P ;
Stoeckli, M ;
Caprioli, RM .
ANALYTICAL CHEMISTRY, 1999, 71 (23) :5263-5270
[10]   DIRECT DETERMINATION OF PHOSPHOLIPID STRUCTURES IN MICROORGANISMS BY FAST-ATOM-BOMBARDMENT TRIPLE QUADRUPOLE MASS-SPECTROMETRY [J].
COLE, MJ ;
ENKE, CG .
ANALYTICAL CHEMISTRY, 1991, 63 (10) :1032-1038