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抑制香叶基香叶基化可阻断肺血管平滑肌细胞的生长并促进其凋亡。

Inhibiting geranylgeranylation blocks growth and promotes apoptosis in pulmonary vascular smooth muscle cells.

作者信息

Stark W W, Blaskovich M A, Johnson B A, Qian Y, Vasudevan A, Pitt B, Hamilton A D, Sebti S M, Davies P

机构信息

Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, USA.

出版信息

Am J Physiol. 1998 Jul;275(1):L55-63. doi: 10.1152/ajplung.1998.275.1.L55.

Abstract

The activity of small GTP-binding proteins is regulated by a critical step in posttranslational processing, namely, the addition of isoprenoid lipids farnesyl and geranylgeranyl, mediated by the enzymes farnesyltransferase (FTase) and geranylgeranyltransferase I (GGTase I), respectively. We have developed compounds that inhibit these enzymes specifically and in this study sought to determine their effects on smooth muscle cells (SMC) from the pulmonary microvasculature. We found that the GGTase I inhibitor GGTI-298 suppressed protein geranylgeranylation and blocked serum-dependent growth as measured by thymidine uptake and cell counts. In the absence of serum, however, GGTI-298 induced apoptosis in these cells as measured by both DNA staining and flow cytometry. The FTase inhibitor FTI-277 selectively inhibited protein farnesylation but had a minor effect on growth and no effect on apoptosis. To further investigate the role of geranylgeranylated proteins in apoptosis, we added the cholesterol synthesis inhibitor lovastatin, which inhibits the biosynthesis of farnesyl and geranylgeranyl pyrophosphates. This also induced apoptosis, but when geranylgeraniol was added to replenish cellular pools of geranylgeranyl pyrophosphate, apoptosis was reduced to baseline. In contrast, farnesol achieved only partial rescue of the cells. These results imply that geranylgeranylated proteins are required for growth and protect SMC against apoptosis. GGTase I inhibitors may be useful in preventing hyperplastic remodeling and may have the potential to induce the apoptotic regression of established vascular lesions.

摘要

小GTP结合蛋白的活性受翻译后加工关键步骤的调控,即分别由法尼基转移酶(FTase)和香叶基香叶基转移酶I(GGTase I)介导添加类异戊二烯脂质法尼基和香叶基香叶基。我们已开发出特异性抑制这些酶的化合物,在本研究中试图确定它们对肺微血管平滑肌细胞(SMC)的影响。我们发现,GGTase I抑制剂GGTI-298可抑制蛋白质香叶基香叶基化,并通过胸苷摄取和细胞计数测量来阻断血清依赖性生长。然而,在无血清情况下,通过DNA染色和流式细胞术测量,GGTI-298可诱导这些细胞凋亡。FTase抑制剂FTI-277选择性抑制蛋白质法尼基化,但对生长影响较小,对凋亡无影响。为进一步研究香叶基香叶基化蛋白在凋亡中的作用,我们添加了胆固醇合成抑制剂洛伐他汀,其抑制法尼基和香叶基香叶基焦磷酸的生物合成。这也诱导了凋亡,但当添加香叶基香叶醇以补充细胞内香叶基香叶基焦磷酸池时,凋亡减少至基线水平。相比之下,法尼醇仅部分挽救了细胞。这些结果表明,香叶基香叶基化蛋白对生长是必需的,并保护SMC免受凋亡。GGTase I抑制剂可能有助于预防增生性重塑,并可能有潜力诱导已形成的血管病变发生凋亡性消退。

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