Identification of phosphocholine plasmalogen as a lipid component in mammalian pulmonary surfactant using high-resolution 31P NMR spectroscopy.
Identification of phosphocholine plasmalogen as a lipid component in mammalian pulmonary surfactant using high-resolution 31P NMR spectroscopy.
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使用高分辨率 31P NMR 光谱鉴定磷酸胆碱缩醛磷脂作为哺乳动物肺表面活性剂中的脂质成分。
DOI:
10.1021/bi00052a005
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发表时间:
1993
期刊:
影响因子:
2.9
通讯作者:
Dluhy,RA
中科院分区:
文献类型:
--
作者:
Rana,FR;Harwood,JS;Mautone,AJ;Dluhy,RA
Revised Manuscript Received November 10, 1992 abstract: High-resolution 31P NMR spectroscopy was used toanalyze the phospholipid composition of mammalian pulmonary surfactant from two different sources. Under conditions which considerably narrow the usually broad 31P phospholipid signals, solution-phase NMR spectra of these surfactant preparations unequivocally demonstrate that a phosphocholine plasmalogen (ie, 1-O-(1'-alkenyl)-2-acyl-szt-glycero-3-phosphocholine) exists as a major secondary component (~ 4 mol%) in mammalian pulmonary surfactant. Phosphocholine (PC) plasmalogen was identified in preparations obtained from both adult cow lung surfactant extract as well as in ovine (lamb) fetal pulmonary liquid. PC plasmalogenshave not previously been identified any mammalian pulmonary surfactant preparation. Theamount of PC plasmalogen in these preparations occurs at fractional levels that are comparable to that of phosphoglycerol (£), which previously had been thought of as the second-most common phospholipid class in pulmonary surfactant. Thepresence of PC plasmalogen in pulmonary surfactant may have important physiological ramifications and immediately suggests new directions for biochemical and biophysical investigations of pulmonary surfactant.Pulmonary surfactant is a complex mixtureof lipids (90 wt%), proteins (8 wt%), and carbohydrates (2 wt%) which is synthesized and secreted by alveolarepithelial type II cells. The function of this heterogeneous surfactant mixture is to reduce the surface tension at the air-alveolar interface inthe lungs to near zero, thereby providing the necessary mechanical stability to the broncho-alveolarunits required for breathing (Scarpelli, 1988). Inadequate synthesis and release of pulmonary surfactant is responsible for the respiratory distress experienced by premature infants as well as some forms of adult respiratory distress syndrome. Greater than 85% of the lipids found in pulmonary surfactant are phospholipids (King, 1984). To date, phosphocholines and phosphoglycerols (PC’s and PC’s) 1 have been identified as the primary phospholipid classes which are present inmammalian pulmonary surfactant. PC’s comprise roughly 70-85% of pulmonary surfactantby weight, with the specific PC species 1, 2-dipalmitoyl-in-glycero-3-phosphocholine (DPPC) making up more than 60% of the total PC component. The class of lipids containingPG and their headgroup may comprise up to 10% of the pulmonary surfactant phospholipids. The other phospholipid classes (PE, SM, PI, PS, and CL) occur at relatively low levels [< 2-5 mol%(King, 1984)]. At least four proteins, termed SP-A, SP-B, SP-C, and SP-D, have also been isolated from pulmonary
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影响因子:
2.9
作者:
Pastrana,B;Mautone,AJ;Mendelsohn,R
通讯作者:
Mendelsohn,R
影响因子:
2.1
作者:
K. Keough;E. Farrell;M. Cox;G. Harrell;H. Taeusch
通讯作者:
H. Taeusch
影响因子:
2.9
作者:
J. Johansson;T. Curstedt;B. Robertson;H. Jörnvall
通讯作者:
H. Jörnvall
影响因子:
3.4
作者:
A. Salmon;T. Wiedmann
通讯作者:
T. Wiedmann
DOI:
10.1016/0005-2736(87)90349-x
发表时间:
1987
期刊:
Biochimica et biophysica acta
影响因子:
--
作者:
Mautone,AJ;Reilly,KE;Mendelsohn,R
通讯作者:
Mendelsohn,R