Author:
Nickel Nils,Jonigk Danny,Kempf Tibor,Bockmeyer Clemens L,Maegel Lavinia,Rische Johanna,Laenger Florian,Lehmann Ulrich,Sauer Clemens,Greer Mark,Welte Tobias,Hoeper Marius M,Golpon Heiko A
Abstract
Abstract
Background
Growth-differentiation factor-15 (GDF-15) is a stress-responsive, transforming growth factor-β-related cytokine, which has recently been reported to be elevated in serum of patients with idiopathic pulmonary arterial hypertension (IPAH). The aim of the study was to examine the expression and biological roles of GDF-15 in the lung of patients with pulmonary arterial hypertension (PAH).
Methods
GDF-15 expression in normal lungs and lung specimens of PAH patients were studied by real-time RT-PCR and immunohistochemistry. Using laser-assisted micro-dissection, GDF-15 expression was further analyzed within vascular compartments of PAH lungs. To elucidate the role of GDF-15 on endothelial cells, human pulmonary microvascular endothelial cells (HPMEC) were exposed to hypoxia and laminar shear stress. The effects of GDF-15 on the proliferation and cell death of HPMEC were studied using recombinant GDF-15 protein.
Results
GDF-15 expression was found to be increased in lung specimens from PAH patients, com-pared to normal lungs. GDF-15 was abundantly expressed in pulmonary vascular endothelial cells with a strong signal in the core of plexiform lesions. HPMEC responded with marked upregulation of GDF-15 to hypoxia and laminar shear stress. Apoptotic cell death of HPMEC was diminished, whereas HPMEC proliferation was either increased or decreased depending of the concentration of recombinant GDF-15 protein.
Conclusions
GDF-15 expression is increased in PAH lungs and appears predominantly located in vascular endothelial cells. The expression pattern as well as the observed effects on proliferation and apoptosis of pulmonary endothelial cells suggest a role of GDF-15 in the homeostasis of endothelial cells in PAH patients.
Publisher
Springer Science and Business Media LLC
Reference41 articles.
1. Bottner M, Laaff M, Schechinger B, Rappold G, Unsicker K, Suter-Crazzolara C: Charac-terization of the rat, mouse, and human genes of growth/differentiation factor-15/macrophage inhibiting cytokine-1 (GDF-15/MIC-1). Gene. 1999, 237: 105-111. 10.1016/S0378-1119(99)00309-1.
2. Strelau J, Bottner M, Lingor P, Suter-Crazzolara C, Galter D, Jaszai J, et al: GDF-15/MIC-1 a novel member of the TGF-beta superfamily. J Neural Transm Suppl. 2000, 273-276.
3. Bella AJ, Lin G, Lin CS, Hickling DR, Morash C, Lue TF: Nerve growth factor modulation of the cavernous nerve response to injury. J Sex Med. 2009, 6: 347-352. 10.1111/j.1743-6109.2008.01194.x.
4. Koniaris LG: Induction of MIC-1/growth differentiation factor-15 following bile duct injury. J Gastrointest Surg. 2003, 7: 901-905. 10.1007/s11605-003-0037-5.
5. Zimmers TA, Jin X, Hsiao EC, McGrath SA, Esquela AF, Koniaris LG: Growth differen-tiation factor-15/macrophage inhibitory cytokine-1 induction after kidney and lung injury. Shock. 2005, 23: 543-548.
Cited by
81 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献