Rüstow B, Kolleck I, Guthmann F, Haupt R, Kunze D, Stevens P
Institute of Pathological and Clinical Biochemistry, Charité Hospital, Humboldt University of Berlin, Germany.
Biochem J. 1994 Sep 15;302 ( Pt 3)(Pt 3):665-8. doi: 10.1042/bj3020665.
Alveolar surfactant (exposed to air and therefore a prime target of air oxidants) is supplied with antioxidants during its intracellular formation on type-II pneumocytes [Rüstow, Haupt, Stevens and Kunze (1993) Am. J. Physiol. 265, L133-L139]. Plasmalogens can protect animal cells against lipid peroxidation caused by u.v. radiation. It has been suggested that plasmalogens play a direct role in protecting animal cell membranes against oxidative stress [Zoeller, Morand and Raetz (1988) J. Biol. Chem. 263, 11590-11596]. We investigated biosynthesis and secretion of plasmalogens and phospholipids by type-II cells of adult rat lungs. The plasmalogens of type-II cells consist of 93% ethanolamine plasmalogens (EthPlas) and 7% choline plasmalogens (ChoPlas). Plasmalogens isolated from alveolar surfactant, however, consist of 36.5% ChoPlas and 63.5% EthPlas. The different incorporation rates of [14C]hexadecanol into both types of plasmalogen by type-II pneumocytes are reflected in the relative proportions of their total cellular plasmalogen content. Type-II cells cultured in the presence of labelled hexadecanol or labelled hexadecylglycerol and of labelled palmitate secrete labelled ChoPlas and labelled phospholipids, both spontaneously and in response to isoprenaline. The spontaneous and stimulated secretion rates of labelled ChoPlas are 3-6 times higher than those of labelled EthPlas. This higher relative secretion rate of ChoPlas corresponds to its higher proportion in the total plasmalogen content of alveolar surfactant compared with type-II cells. Added extracellular surfactant-specific protein A inhibits the secretion of plasmalogens as well as that of phospholipids by type-II cells. The molecular species of EthPlas and ChoPlas isolated from type-II cells or lung lavage do not differ significantly and consist mainly of molecular species containing poly-unsaturated fatty acids. We conclude that ChoPlas are secreted partly as integral constituents of the alveolar surfactant. Type-II cells select between both types of plasmalogens for secretion as a constituent of surfactant. The intramolecular sorting signal presumably is the choline moiety.
肺泡表面活性物质(暴露于空气中,因此是空气氧化剂的主要靶标)在其于II型肺细胞内形成过程中会获得抗氧化剂[鲁斯托、豪普特、史蒂文斯和昆泽(1993年),《美国生理学杂志》265卷,L133 - L139页]。缩醛磷脂可以保护动物细胞免受紫外线辐射引起的脂质过氧化作用。有人提出缩醛磷脂在保护动物细胞膜免受氧化应激方面发挥直接作用[佐勒、莫兰德和雷茨(1988年),《生物化学杂志》263卷,11590 - 11596页]。我们研究了成年大鼠肺II型细胞中缩醛磷脂和磷脂的生物合成与分泌。II型细胞的缩醛磷脂由93%的乙醇胺缩醛磷脂(EthPlas)和7%的胆碱缩醛磷脂(ChoPlas)组成。然而,从肺泡表面活性物质中分离出的缩醛磷脂由36.5%的ChoPlas和63.5%的EthPlas组成。II型肺细胞对[14C]十六醇掺入两种缩醛磷脂的不同速率反映在它们总细胞缩醛磷脂含量的相对比例中。在存在标记的十六醇或标记的十六烷基甘油以及标记的棕榈酸的情况下培养的II型细胞会自发地以及在异丙肾上腺素刺激下分泌标记的ChoPlas和标记的磷脂。标记的ChoPlas的自发分泌速率和刺激分泌速率比标记的EthPlas高3 - 6倍。ChoPlas这种较高的相对分泌速率与其在肺泡表面活性物质总缩醛磷脂含量中所占比例高于II型细胞相对应。添加细胞外表面活性物质特异性蛋白A会抑制II型细胞分泌缩醛磷脂以及磷脂。从II型细胞或肺灌洗物中分离出的EthPlas和ChoPlas的分子种类没有显著差异,并且主要由含有多不饱和脂肪酸的分子种类组成。我们得出结论,ChoPlas部分作为肺泡表面活性物质的组成成分被分泌。II型细胞在两种缩醛磷脂之间进行选择,以便作为表面活性物质的组成成分进行分泌。分子内分选信号大概是胆碱部分。