منابع مشابه
Lysosomal phospholipase A2 and phospholipidosis.
A lysosomal phospholipase A2, LPLA2, was recently characterized and shown to have substrate specificity for phosphatidylcholine and phosphatidylethanolamine. LPLA2 is ubiquitously expressed but is most highly expressed in alveolar macrophages. Double conditional gene targeting was employed to elucidate the function of LPLA2. LPLA2-deficient mice (Lpla2-/-) were generated by the systemic deletio...
متن کاملLysosomal phospholipase A2 Lysosomal Phospholipase A2 is Selectively Expressed in Alveolar Macrophages*
Lung surfactant is the surface-active agent comprised of phospholipids and proteins that lines pulmonary alveolae. Surfactant stabilizes the alveolar volume by reducing surface tension. Previously, we identified a phospholipase A2, termed LPLA2, with specificity towards phosphatidylcholine and phosphatidylethanolamine. The phospholipase is localized to lysosomes, is calcium independent, has an ...
متن کاملPositional specificity of lysosomal phospholipase A2.
Lysosomal phospholipase A(2) (Lpla2) is highly expressed in alveolar macrophages and may mediate the phospholipid metabolism of surfactant. Studies on the properties of this phospholipase are consistent with the presence of both phospholipase A(1) and phospholipase A(2) activities. These activities were studied through the production of O-acyl compounds, produced by the transacylase activity of...
متن کاملLysosomal phospholipase A2 is selectively expressed in alveolar macrophages.
Lung surfactant is the surface-active agent comprised of phospholipids and proteins that lines pulmonary alveoli. Surfactant stabilizes the alveolar volume by reducing surface tension. Previously, we identified a lysosomal phospholipase A2, termed LPLA2, with specificity toward phosphatidylcholine and phosphatidylethanolamine. The phospholipase is localized to lysosomes, is calcium-independent,...
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ژورنال
عنوان ژورنال: Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
سال: 2019
ISSN: 1388-1981
DOI: 10.1016/j.bbalip.2018.07.012