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表面活性蛋白B肽对肺泡细胞摄取脂质体的影响。

Effect of SP-B peptides on the uptake of liposomes by alveolar cells.

作者信息

Poelma D L, Walther F J, Waring A J, Haitsma J J, Zimmermann L J, Lachmann B, van Iwaarden J F

机构信息

Department of Anesthesiology, Erasmus MC-Faculty, Rotterdam, The Netherlands.

出版信息

Neonatology. 2007;91(4):233-40. doi: 10.1159/000098170. Epub 2006 Dec 22.

Abstract

BACKGROUND

Exogenous surfactant has been accepted worldwide as a therapy of RDS in premature and term infants. Exogenous surfactant is usually derived from lung extracts containing phospholipids and the surfactant proteins SP-B and SP-C. Synthetic peptides of SP-B and SP-C are being tested with the aim to develop a completely synthetic surfactant preparation. Nevertheless, the effects of these peptides on the endogenous surfactant metabolism remain unknown.

OBJECTIVES

The effect of synthetic SP-B peptides on uptake of surfactant-like liposomes was investigated in alveolar cells. Native SP-B and seven SP-B peptides were included: monomeric and dimeric SP-B(1-25) (Cys-11 --> Ala-11), SP-B(63-78)and Ala-SP-B(63-78) (Cys-71 --> Ala-71;Cys-77 --> Ala-77)and their serine mutants.

METHODS

In vitro, alveolar macrophages (AM) and alveolar type II cells (ATII) were incubated with liposomes containing SP-B or one of its peptides. In vivo, rats received intratracheally various SP-B peptides (SP-B/lipid ratio 1:33 w/w) incorporated in fluorescent surfactant-like liposomes. One hour after instillation, AM and ATII were isolated and cell-associated fluorescence was determined using flow cytometry. Confocal laser microscopy was performed to ensure internalization of the liposomes.

RESULTS

In vitro uptake by AM or ATII was not influenced by the SP-B peptides. In vivo, SP-B(1-25) and Ser-SP-B(1-25) increased the uptake by AM whereas dSP-B(1-25) decreased the uptake. Neither SP-B(1-25) nor dSP-B(1-25 )affected total uptake by ATII. The overall uptake by SP-B(63-78) variants was not changed.

CONCLUSIONS

Surface-active synthetic SP-B peptides do not interfere with the normal uptake of surfactant by ATII.

摘要

背景

外源性表面活性剂已在全球范围内被接受作为治疗早产儿和足月儿呼吸窘迫综合征(RDS)的方法。外源性表面活性剂通常来源于含有磷脂以及表面活性蛋白SP-B和SP-C的肺提取物。目前正在对SP-B和SP-C的合成肽进行测试,目的是开发一种完全合成的表面活性剂制剂。然而,这些肽对内源性表面活性剂代谢的影响尚不清楚。

目的

研究合成的SP-B肽对肺泡细胞摄取表面活性剂样脂质体的影响。纳入了天然SP-B和7种SP-B肽:单体和二聚体SP-B(1-25)(Cys-11→Ala-11)、SP-B(63-78)以及Ala-SP-B(63-78)(Cys-71→Ala-71;Cys-77→Ala-77)及其丝氨酸突变体。

方法

在体外,将肺泡巨噬细胞(AM)和II型肺泡上皮细胞(ATII)与含有SP-B或其一种肽的脂质体一起孵育。在体内,给大鼠气管内注入掺入荧光表面活性剂样脂质体的各种SP-B肽(SP-B/脂质比例为1:33 w/w)。滴注1小时后,分离出AM和ATII,并使用流式细胞术测定细胞相关荧光。进行共聚焦激光显微镜检查以确保脂质体的内化。

结果

在体外,AM或ATII的摄取不受SP-B肽的影响。在体内,SP-B(1-25)和Ser-SP-B(1-25)增加了AM的摄取,而dSP-B(1-25)降低了摄取。SP-B(1-25)和dSP-B(1-25)均未影响ATII的总摄取。SP-B(63-78)变体的总体摄取没有变化。

结论

具有表面活性的合成SP-B肽不会干扰ATII对表面活性剂的正常摄取。

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