Yang Jun, Davies Rachel J, Southwood Mark, Long Lu, Yang Xudong, Sobolewski Anastasia, Upton Paul D, Trembath Richard C, Morrell Nicholas W
Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke's and Papworth Hospitals, Cambridge CB2 2QQ, United Kingdom.
Circ Res. 2008 May 23;102(10):1212-21. doi: 10.1161/CIRCRESAHA.108.173567. Epub 2008 Apr 24.
Heterozygous germ line mutations in the gene encoding the bone morphogenetic protein (BMP) type II receptor occur in more than 80% of patients with familial pulmonary arterial hypertension. Because inhibitors of DNA binding (Id) genes are major targets of BMP/Smad signaling, we studied the regulation of these transcription factors in pulmonary artery smooth muscle cells harboring mutations in BMP type II receptor and control cells. Mutant cells demonstrated a marked deficiency in BMP4-stimulated Id1 and Id2 gene and protein expression compared with control cells. Mutant cells were deficient in Smad1/5 signaling in response to BMPs but also in extracellular signal-regulated kinase (ERK)1/2 activation. We provide evidence for an important interaction between Smad1/5 and ERK1/2 signaling in the regulation of Id gene expression. Thus, BMP4-induced Id1 expression was negatively regulated by ERK1/2 activation. The mechanism involves ERK1/2-dependent phosphorylation of the Smad1 linker region (serine 206), which limits C-terminal serine 463/465 phosphorylation and inhibits Smad nuclear accumulation. Furthermore, activation of ERK1/2 by platelet-derived growth factor BB also caused Smad1 linker region phosphorylation and inhibited BMP4-induced Id1 gene expression. In contrast, Id2 expression was positively regulated by ERK1/2. Moreover, we show that both BMP type II receptor mutation and Id1 knockdown leads to loss of growth suppression by BMPs. Taken together, these findings indicate an important interaction between ERK1/2 and Smad1/5 in the regulation of Id genes. Platelet-derived growth factor, via ERK1/2, further impairs the deficiency in Smad signaling found in BMP type II receptor mutant cells. The integration of these signals at the level of Id gene expression may contribute to the pathogenesis of familial pulmonary arterial hypertension.
在超过80%的家族性肺动脉高压患者中,编码骨形态发生蛋白(BMP)II型受体的基因存在杂合性种系突变。由于DNA结合抑制因子(Id)基因是BMP/Smad信号通路的主要靶点,我们研究了在携带BMP II型受体突变的肺动脉平滑肌细胞和对照细胞中这些转录因子的调控情况。与对照细胞相比,突变细胞在BMP4刺激下的Id1和Id2基因及蛋白表达明显不足。突变细胞对BMPs的反应中Smad1/5信号通路存在缺陷,但在细胞外信号调节激酶(ERK)1/2激活方面也有缺陷。我们提供了证据表明Smad1/5和ERK1/2信号通路在Id基因表达调控中存在重要相互作用。因此,ERK1/2激活对BMP4诱导的Id1表达起负调控作用。其机制涉及ERK1/2依赖的Smad1连接区(丝氨酸206)磷酸化,这限制了C末端丝氨酸463/465的磷酸化并抑制Smad核内积累。此外,血小板衍生生长因子BB激活ERK1/2也导致Smad1连接区磷酸化并抑制BMP4诱导的Id1基因表达。相反,ERK1/2对Id2表达起正调控作用。此外,我们表明BMP II型受体突变和Id1基因敲低均导致BMPs对生长抑制作用的丧失。综上所述,这些发现表明ERK1/2和Smad1/5在Id基因调控中存在重要相互作用。血小板衍生生长因子通过ERK1/2进一步损害了BMP II型受体突变细胞中发现的Smad信号通路缺陷。这些信号在Id基因表达水平的整合可能有助于家族性肺动脉高压的发病机制。