Pulmonary, Critical Care and Sleep Division, Tufts Medical Center, 800 Washington St., #257, Boston, MA 02111.
Am J Physiol Lung Cell Mol Physiol. 2014 Feb 15;306(4):L309-15. doi: 10.1152/ajplung.00321.2013. Epub 2013 Dec 27.
The monoamine serotonin (5-HT) has been previously implicated in pulmonary arterial remodeling and is considered a potential therapeutic target for the disease pulmonary arterial hypertension (PAH). More recently, it has been recognized that the enzyme tissue transglutaminase (TG2) mediates cross-linking of proteins with 5-HT, a posttranslational process of monoaminylation known as "serotonylation." TG2 activity and serotonylation of protein participate in both smooth muscle proliferation and contraction produced by 5-HT. Indeed, markedly increased TG2 activity has now been identified in lung tissue of an experimental rodent model of pulmonary hypertension, and elevated serotonylation of fibronectin and the signaling molecule Rho, downstream products of transglutamidation, have been found in blood of patients with PAH. The basic mechanism by which TG2 is activated and the potential role(s) of serotonylated proteins in pulmonary hypertension remain a mystery. In the present review we have tried to address the current understanding of 5-HT metabolism in pulmonary hypertension and relate it to what is currently known about the evolving cellular process of serotonylation.
单胺类物质 5-羟色胺(5-HT)先前被认为与肺血管重塑有关,被认为是肺动脉高压(PAH)疾病的潜在治疗靶点。最近,人们已经认识到组织转谷氨酰胺酶(TG2)介导 5-HT 与蛋白质的交联,这是一种被称为“单胺化”的翻译后过程。TG2 活性和蛋白质的单胺化参与了 5-HT 引起的平滑肌增殖和收缩。事实上,在肺动脉高压的实验性啮齿动物模型的肺组织中,已经发现 TG2 活性显著增加,并且在 PAH 患者的血液中发现了纤维连接蛋白和信号分子 Rho 的单胺化,这是转谷氨酰胺作用的下游产物。TG2 被激活的基本机制以及在肺动脉高压中单胺化蛋白的潜在作用仍然是一个谜。在本综述中,我们试图阐述目前对肺动脉高压中 5-HT 代谢的理解,并将其与目前对单胺化这一不断发展的细胞过程的了解联系起来。