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内膜增生中G蛋白表达的时间顺序。

The temporal sequence of G-protein expression in intimal hyperplasia.

作者信息

Davies M G, Barber L, Dhanraj D N, Gettys T W, Ramkumar V, Hagen P O

机构信息

Vascular Biology and Atherosclerosis Research Laboratory, Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

J Surg Res. 1996 Jun;63(1):115-22. doi: 10.1006/jsre.1996.0233.

Abstract

The universal response of a blood vessel to intimal injury is the development of intimal hyperplasia. The etiology of this lesion is not fully understood but is assumed to involve stimulation of receptors on smooth muscle cells with their subsequent proliferation. Many receptor-mediated processes are coupled to G-proteins but little information exists regarding the expression of G-proteins during the development of intimal hyperplasia. This study examines the kinetics of G-protein expression in experimental vein grafts. Male New Zealand White rabbits had a right carotid interposition bypass graft using the ipsilateral external jugular vein. These were harvested on days 1, 3, 5, 7, 14, and 28 postoperatively for histology (n = 3), for in vitro isometric tension studies of potassium chloride, serotonin, bradykinin, and histamine (n = 3), or for Western blot analysis (n = 3) of the G-protein subunits (alpha(i1), alpha(i2), alpha(i3), alpha(S) and beta). The results show that expression of alpha(i3) developed de novo, was detectable by day 1, and continued to increase through day 7, paralleling the development of intimal hyperplasia. The expression of alpha(S) (52 kDa) increased significantly by day 1 and also continued to increase until day 7. In contrast, expression for alpha(i2), alpha(S) (45 kDa) and beta subunits increased at a much slower rate from 1 to 7 days and remained constant thereafter. No alpha(i1) was detected. The contractile response to potassium chloride was significantly reduced (36% of the response in the jugular vein) over the first 7 days and increased to 196% of the jugular vein response at 14 and 28 days. There was minimal response to serotonin, bradykinin, and histamine over the first 7 days. Contractile responses to serotonin increased while those to bradykinin and histamine decreased from 7 to 28 days. This study demonstrates that there are specific changes in alpha(i) and alpha(S) subunits within 24 hr of grafting and that increases in all G-proteins occur in a time dependent manner up to 7 days postoperatively. Microscopic development of intimal hyperplasia occurs from days 3 to 5 and increases rapidly between 7 and 14 days. Changes in the expression of G-proteins in the vein grafts, particularly the alpha(i3) subunit, parallel this formation of intimal hyperplasia. These alterations in G-protein expression do not appear to correlate with G-protein-mediated, contractile responses in the vein grafts.

摘要

血管对内膜损伤的普遍反应是内膜增生。这种病变的病因尚未完全明了,但推测涉及平滑肌细胞上受体的刺激及其随后的增殖。许多受体介导的过程与G蛋白偶联,但关于内膜增生发展过程中G蛋白表达的信息却很少。本研究检测了实验性静脉移植物中G蛋白表达的动力学。雄性新西兰白兔采用同侧颈外静脉进行右颈动脉搭桥术。术后第1、3、5、7、14和28天采集样本,用于组织学检查(n = 3)、对氯化钾、5-羟色胺、缓激肽和组胺进行体外等长张力研究(n = 3),或对G蛋白亚基(α(i1)、α(i2)、α(i3)、α(S)和β)进行蛋白质印迹分析(n = 3)。结果显示,α(i3)的表达是新生的,在第1天即可检测到,并持续增加至第7天,与内膜增生的发展平行。α(S)(52 kDa)的表达在第1天显著增加,并持续增加至第7天。相比之下,α(i2)、α(S)(45 kDa)和β亚基的表达在第1至7天增加的速度要慢得多,此后保持恒定。未检测到α(i1)。在最初的7天内,对氯化钾的收缩反应显著降低(为颈静脉反应的36%),在第14天和28天增加至颈静脉反应的196%。在最初的7天内,对5-羟色胺、缓激肽和组胺的反应极小。从第7天到28天,对5-羟色胺的收缩反应增加,而对缓激肽和组胺的反应则降低。本研究表明,移植后24小时内α(i)和α(S)亚基有特定变化,并且所有G蛋白的增加在术后7天内呈时间依赖性。内膜增生的微观发展在第3至5天出现,并在第7至14天迅速增加。静脉移植物中G蛋白表达的变化,尤其是α(i3)亚基,与内膜增生的形成平行。G蛋白表达的这些改变似乎与静脉移植物中G蛋白介导的收缩反应无关。

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