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一个发育调控程序,限制了胎羊动脉导管中弹性蛋白的不溶性化和板层的形成。

A developmentally regulated program restricting insolubilization of elastin and formation of laminae in the fetal lamb ductus arteriosus.

作者信息

Zhu L, Dagher E, Johnson D J, Bedell-Hogan D, Keeley F W, Kagan H M, Rabinovitch M

机构信息

Department of Pathology, University of Toronto, Ontario, Canada.

出版信息

Lab Invest. 1993 Mar;68(3):321-31.

PMID:8095564
Abstract

BACKGROUND

The ductus arteriosus (DA) is a fetal vessel in which the elastic laminae fail to assemble normally in late gestation. This feature is associated with the development of intimal cushions, structures that partially occlude the DA lumen and assure that the vessel will close completely when it constricts postnatally.

EXPERIMENTAL DESIGN

We studied the fetal lamb DA at two different gestational time-points, 100 days before, and 138 days coincident with intimal cushion formation (term = 145 days) to establish the ultrastructural basis for the 'disassembly' of elastic laminae apparent on light microscopy and to determine further whether the mechanism was due to increased elastolytic activity, decreased synthesis of tropoelastin, or impaired insolubilization of tropoelastin.

RESULTS

Morphometric ultrastructural analyses of tissue from the 138-day gestation fetal lambs revealed that the volume density of elastin in the DA vessel wall was only 40% of that in the aorta (Ao) and 50% of that in the pulmonary artery (PA). Moreover, only 16% of the elastin present contributed to the formation of laminae when compared to 80% in the Ao and 50% in the PA. Despite the morphologic appearance of 'fragmented' elastin, there was no evidence of increased elastolytic activity in the DA at either gestational time-point as judged by solubilization of a [3H] elastin substrate. The reduced elastin apparent was morphologically accompanied by an increase in soluble (tropo) elastin in DA compared with Ao and PA, as measured by enzyme linked immunosorbent assay, in tissue from both 100- and 138-day gestation lambs. Lack of differences in tropoelastin mRNA levels when comparing the 3 vessels suggested that the enzyme linked immunosorbent assay measurements reflected increased DA tropoelastin accumulation owing to lack of insolubilization rather than an increase in synthesis. Reduced insolubilization of newly synthesized elastin was evident in the DA compared with the Ao at 100 days gestation and in the DA compared with both Ao and PA at 138 days gestation in association with reduced desmosine levels.

CONCLUSIONS

The mechanism of the decrease in tropoelastin insolubilization was unrelated to lysyl oxidase activity in the tissue and represents a unique developmental program.

摘要

背景

动脉导管(DA)是一种胎儿血管,在妊娠晚期其弹性膜无法正常组装。这一特征与内膜垫的形成有关,内膜垫是部分阻塞DA管腔的结构,可确保该血管在出生后收缩时完全闭合。

实验设计

我们在两个不同的妊娠时间点研究了胎羊的DA,一个是在内膜垫形成前100天,另一个是在内膜垫形成时的138天(足月为145天),以建立光镜下可见的弹性膜“拆解”的超微结构基础,并进一步确定其机制是由于弹性蛋白酶活性增加、原弹性蛋白合成减少还是原弹性蛋白不溶性化受损。

结果

对妊娠138天的胎羊组织进行形态计量超微结构分析发现,DA血管壁中弹性蛋白的体积密度仅为主动脉(Ao)的40%,肺动脉(PA)的50%。此外,与Ao中的80%和PA中的50%相比,DA中仅16%的弹性蛋白参与了弹性膜的形成。尽管弹性蛋白在形态上呈现“碎片化”,但通过[3H]弹性蛋白底物的溶解判断,在两个妊娠时间点的DA中均没有证据表明弹性蛋白酶活性增加。与Ao和PA相比,通过酶联免疫吸附测定法测量,在妊娠100天和138天的胎羊组织中,DA中可溶性(原)弹性蛋白在形态上增加,而弹性蛋白明显减少。比较这三种血管时,原弹性蛋白mRNA水平没有差异,这表明酶联免疫吸附测定法的测量结果反映了由于不溶性化缺乏而非合成增加导致的DA中原弹性蛋白积累增加。与Ao相比,在妊娠100天时DA中新合成弹性蛋白的不溶性化减少,与Ao和PA相比,在妊娠138天时DA中新合成弹性蛋白的不溶性化减少,同时与锁链素水平降低有关。

结论

原弹性蛋白不溶性化减少的机制与组织中的赖氨酰氧化酶活性无关,代表了一种独特的发育程序。

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