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J R Soc Interface. 2018 Apr;15(141). doi: 10.1098/rsif.2017.0895.
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本文引用的文献

1
Interfacial curvature effects on the monolayer morphology and dynamics of a clinical lung surfactant.界面曲率对临床用肺表面活性剂单层形态和动力学的影响。
Proc Natl Acad Sci U S A. 2018 Jan 9;115(2):E134-E143. doi: 10.1073/pnas.1715830115. Epub 2017 Dec 26.
2
Interfacial rheology of coexisting solid and fluid monolayers.共存固液单层膜的界面流变学。
Soft Matter. 2017 Feb 15;13(7):1481-1492. doi: 10.1039/c6sm02797k.
3
Fibrinogen: a journey into biotechnology.纤维蛋白原:生物技术之旅。
Soft Matter. 2016 Oct 26;12(42):8639-8653. doi: 10.1039/c6sm01895e.
4
Combined effect of synthetic protein, Mini-B, and cholesterol on a model lung surfactant mixture at the air-water interface.合成蛋白Mini - B与胆固醇对气液界面处模型肺表面活性剂混合物的联合作用。
Biochim Biophys Acta. 2016 Apr;1858(4):904-12. doi: 10.1016/j.bbamem.2016.01.008. Epub 2016 Jan 15.
5
2D dynamical arrest transition in a mixed nanoparticle-phospholipid layer studied in real and momentum spaces.在实空间和动量空间中研究的混合纳米颗粒 - 磷脂层中的二维动态阻滞转变
Sci Rep. 2015 Dec 10;5:17930. doi: 10.1038/srep17930.
6
Visualizing monolayers with a water-soluble fluorophore to quantify adsorption, desorption, and the double layer.使用水溶性荧光团可视化单层,以量化吸附、解吸和双层。
Proc Natl Acad Sci U S A. 2015 Feb 24;112(8):E826-35. doi: 10.1073/pnas.1419033112. Epub 2015 Feb 9.
7
Composition, structure and mechanical properties define performance of pulmonary surfactant membranes and films.组成、结构和机械性能决定了肺表面活性物质膜和片的性能。
Chem Phys Lipids. 2015 Jan;185:153-75. doi: 10.1016/j.chemphyslip.2014.09.002. Epub 2014 Sep 28.
8
Influence of molecular coherence on surface viscosity.分子相干性对表面粘度的影响。
Langmuir. 2014 Jul 29;30(29):8829-38. doi: 10.1021/la501615g. Epub 2014 Jul 14.
9
Interfacial shear rheology of DPPC under physiologically relevant conditions.在生理相关条件下 DPPC 的界面剪切流变学。
Soft Matter. 2014 Jan 7;10(1):175-86. doi: 10.1039/c3sm52091a.
10
Surface shear inviscidity of soluble surfactants.可溶性表面活性剂的表面切变非粘性。
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混合磷脂-纤维蛋白原单层的演变和力学性质。

Evolution and mechanics of mixed phospholipid fibrinogen monolayers.

机构信息

Department of Chemical Engineering, University of California, Santa Barbara, CA, USA

Department of Chemical Engineering, University of California, Santa Barbara, CA, USA.

出版信息

J R Soc Interface. 2018 Apr;15(141). doi: 10.1098/rsif.2017.0895.

DOI:10.1098/rsif.2017.0895
PMID:29618528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5938581/
Abstract

All mammals depend on lung surfactant (LS) to reduce surface tension at the alveolar interface and facilitate respiration. The inactivation of LS in acute respiratory distress syndrome (ARDS) is generally accompanied by elevated levels of fibrinogen and other blood plasma proteins in the alveolar space. Motivated by the mechanical role fibrinogen may play in LS inactivation, we measure the interfacial rheology of mixed monolayers of fibrinogen and dipalmitoylphosphatidylcholine (DPPC), the main constituent of LS, and compare these to the single species monolayers. We find DPPC to be ineffective at displacing preadsorbed fibrinogen, which gives the resulting mixed monolayer a strongly elastic shear response. By contrast, how effectively a pre-existing DPPC monolayer prevents fibrinogen adsorption depends upon its surface pressure. At low DPPC surface pressures, fibrinogen penetrates DPPC monolayers, imparting a mixed viscoelastic shear response. At higher initial DPPC surface pressures, this response becomes increasingly viscous-dominated, and the monolayer retains a more fluid, DPPC-like character. Fluorescence microscopy reveals that the mixed monolayers exhibit qualitatively different morphologies. Fibrinogen has a strong, albeit preparation-dependent, mechanical effect on phospholipid monolayers, which may contribute to LS inactivation and disorders such as ARDS.

摘要

所有哺乳动物都依赖肺表面活性剂(LS)来降低肺泡界面的表面张力,从而促进呼吸。在急性呼吸窘迫综合征(ARDS)中,LS 的失活通常伴随着肺泡空间中纤维蛋白原和其他血浆蛋白水平的升高。鉴于纤维蛋白原在 LS 失活中可能发挥的机械作用,我们测量了纤维蛋白原和二棕榈酰磷脂酰胆碱(DPPC)混合单层的界面流变特性,DPPC 是 LS 的主要成分,并将这些与单种单层进行了比较。我们发现 DPPC 对预吸附的纤维蛋白原没有置换作用,这使得所得混合单层具有强烈的弹性剪切响应。相比之下,预先存在的 DPPC 单层对纤维蛋白原吸附的阻止效果取决于其表面压力。在 DPPC 表面压力较低时,纤维蛋白原渗透 DPPC 单层,赋予混合粘弹性剪切响应。在较高的初始 DPPC 表面压力下,这种响应变得越来越粘性主导,单层保留了更具流动性、类似 DPPC 的特性。荧光显微镜显示混合单层表现出不同的形态。纤维蛋白原对磷脂单层具有强烈的、尽管取决于制备的机械作用,这可能有助于 LS 失活和 ARDS 等疾病。