The role of circulating thrombospondin-1 in patients with precapillary pulmonary hypertension
© The Author(s). 2016
Received: 1 March 2016
Accepted: 21 July 2016
Published: 30 July 2016
The vasoconstrictive protein TSP-1 is released from endothelial cells upon increased shear stress and hypoxia. Both conditions are prevalent in pulmonary hypertension (PH). TSP-1 damages the local microcirculation by disrupting pathways, which are essential for specific medical therapeutics. Furthermore, TSP-1 induces excessive fibrosis and smooth muscle proliferation - a common finding in advanced PH - via TGF-ß and might promote disease progression. The prognostic impact of circulating TSP-1, influence on hemodynamic parameters and interaction with other biomarkers in patients with PH is incompletely understood.
This study examines prospectively circulating TSP-1 in association with hemodynamic parameters, clinical variables and mortality.
Circulating TSP-1 was measured prospectively in 93 patients with precapillary PH undergoing right heart catheterization and in 19 subjects without PH. TSP-1 levels were determined by ELISA and examined in the context of hemodynamic variables. For evaluation of survival, patients were monitored for adverse events on a 3-monthly basis and contacted at the end of the study after 5 years. In addition, levels of big-endothelin and humoral cofactors of TSP-1 release were measured.
Patients with PH had significantly increased TSP-1 levels compared to controls without PH (1114 ± 136 ng/mL vs. 82.1 ± 15.8 ng/mL, p < 0.05). Levels were correlated with mean pulmonary artery pressure (PAPm, r = −0.58, p < 0.001) and pulmonary vascular resistance (PVR, r = 0.33, p = 0.002). Survivors had lower TSP-levels as non-survivors and all cause mortality associated with TSP-1 plasma levels above 2051 ng/mL (p = 0.0002, HR 1.49).
High plasma levels of TSP-1 are associated with increased PAPm, increased PVR and decreased survival. Due to its interaction with therapeutic pathways, studies are warranted to clarify the impact of TSP-1 on of specific medications for PH.
Thrombospondin-1 (TSP-1) is a matricellular protein, which is involved in various processes of inflammation, neovascularization, hypoxia and remodeling [1–3]. A major source of TSP-1 are the alpha-granules of platelets . Nevertheless, it is expressed in numerous cell types like macrophages, endothelial cells, vascular smooth muscle cells and cardiomyocytes [5–7]. Its production increases dramatically under conditions of hypoxia, altered shear stress or exposure to growth factors including platelet derived growth factor and basic fibroblast growth factor . These conditions are all present in pulmonary hypertension. In vitro and in vivo studies revealed three mechanisms of action of TSP-1. First, binding to CD47 disrupts the nitric oxide pathway and vascular endothelial growth factor pathways based on the inhibition of soluble guanylyl cyclase and protein kinase G in vascular smooth muscle cells . Second, in higher concentrations TSP-1 binds and activates CD36, thereby decreasing intracellular cGMP-levels due to interaction with cellular uptake of myristic acid and decreased eNOS-dependent synthesis of nitric oxide . The net result of TSP-1 binding to these receptors is induction of apoptosis and abortion of VEGF and nitric oxide signaling [11–13]. Finally, TSP-1 is able to exert its biological effects by an additional mechanism involving the activation of transforming growth factor ß (TGF-ß) leading to excessive fibrosis . Therefore, TSP-1 is able to diminish the effects of specific therapeutics of PH and promote disease progression of PH.
In this study we investigated the possible associations of circulating TSP-1 with clinical as well as hemodynamic variables and survival in PH. TSP-1 levels were compared between a control group without PH, patients with pulmonary arterial hypertension (PAH), lung disease associated PH (LD) and chronic thromboembolic PH (CTEPH). Furthermore, humoral cofactors of TSP-1 release were measured and analyzed.
Between June 2007 and December 2010, we enrolled prospectively 19 control subjects and 93 patients prospectively from the outpatient clinic for PH at the Department of Pulmonology of the Saarland University Hospital (Homburg / Saar, Germany). The control group consisted of subjects without evidence of any internal disease. In nine out of nineteen controls a right heart catheterization was performed for exclusion of pulmonary hypertension while in nine persons without any medical history of chronic disease or respiratory symptoms, PH was considered absent. Cardiopulmonary function tests including echocardiography and right heart cathererization were within normal range. The patients had incident and prevalent diagnosis of PH and had diagnostic workup according to current guidelines. Cardiovascular diseases aside from PH were excluded prior to inclusion into the study. Diagnosis of PH was based on a mean pulmonary artery pressure above 25 mmHg (PAPm) and a pulmonary artery occlusion pressure (PAOP) below 15 mmHg. Cardiac output was determined by thermodilution method. All patients received pulmonary ventilation/perfusion scintigraphy to diagnose CTEPH. Patients with suspected CTEPH had confirmatory pulmonary angiography. The inclusion into the study was irrespective of operability and plasma samples were taken before planned pulmonary end-arterectomy. Both incident as well as prevalent diagnosis of PH was included. Patients were at least two months clinically and hemodynamically stable before enrollment as indicated by unchanged functional class, lack of hospitalization and stable medication.
The study complies with the declaration of Helsinki and was approved by the local ethics committee (Ethikkommission der Ärztekammer des Saarlandes, Nr. 153/11). Written informed consent was obtained from each patient.
Blood was drawn during right heart catheterization as initial work-up or follow-up. For platelet stabilization, blood samples were collected into tubes containing 1 mL volume of citrate 109 mmol/l, theophylline 15 mmol/l, adenosine 3.7 mmol/l, dipyridamole 0.198 mmol/l. Plasma was separated by immediate centrifugation (2700xg at 4 °C, 20 min) and stored at −80 °C for batch analysis. The local clinical laboratory determined routine parameters.
TSP-1 levels were measured by ELISA in duplicates according to the manufacturers instructions (Quantikine human TSP-1 ELISA, R&D, Minneapolis, USA). Optical density was determined using a Tecan Spectra III reader set to 450 nm and 620 nm reference wavelength. The TSP-1 assay had a minimal detection limit of 0.355 ng/mL. The within run repeatability coefficient of variation was 5.1 %. Inter-assay repeatability was calculated with 11.3 % resulting in an overall variability of 8.2 %.
PGDF-β platelet poor plasma levels were measured by the Quantikine Human PDGF-β Immunoassay (R&D Systems, Minneapolis, USA, Catalog Number DBB00). Big-Endothelin ELISA was obtained from the Biomedica Group (Vienna, Austria, Catalog Number BI-20082), SDF1a and PF-4 ELISA from Ray Biotech, Inc. (Catalog Number ELH-SDF1alpha-001, ELH-PF4-001). Measurements were performed as indicated by the manufacturer.
Continuous variables were tested for normality and variance homogeneity by Shapiro-Wilk test and Hartley´s Fmax test respectively. Non-normally distributed variables are expressed as median (range), normally distributed variables as mean ± SD unless indicated otherwise. Categorical variables are expressed as numbers (percentage). Outliers were defined outside a three-SD interval from mean of the whole dataset. Differences between groups were tested by ANOVA with post-hoc analysis (Dunnett T3 correction) for normally distributed and Mann–Whitney-U-test for non-normally distributed variables. Comparison of categorical variables was performed by Chi-square-test.
Regression analysis was studied for associations of continuous variables. For bivariate regression a non-parametric model was chosen with locally linear curve fitting of the dataset.
Kaplan-Meyer-Analysis for death was performed with an optimized cut-off of TSP-1 by minimized Matthews coefficient. Hazard ratios were calculated using a cox proportional hazard model (efron method). A p-value of less than 0.05 (two-tailed) was considered statistically significant in all tests.
Data storage and processing, calculations, as well as statistical computations were performed by R-Project version 3.2.0.
Basic characteristics of control group and patients grouped by DanaPoint classification
47.2 ± 14.9
59.3 ± 15.8*
55.1 ± 16.9(*)
66.9 ± 13.0*,**
63.0 ± 9.9*,(**)
169.2 ± 10.1
167.1 ± 9.8
165.6 ± 8.9
170.1 ± 11.9
168.4 ± 9.0
71.7 ± 17.3
81.0 ± 20.0(*)
81.6 ± 20.2
82.2 ± 23.7
76.8 ± 11.9
1.81 ± 0.23
1.89 ± 0.24
1.88 ± 0.23
1.92 ± 0.30
1.87 ± 0.17
441 ± 68.4
328 ± 142*
353 ± 110
243 ± 155*,**
347 ± 192(***)
Six minute walking distance (6MWD) was determined according to guidelines. 79 % of patients were in functional class II or III. Six minute walking distance in control patients was 441 ± 68.4 m and significantly lower in patients with PH patients (328 ± 142 m; p < 0.05). Lowest values for 6MWD were observed in patients with lung disease (243 ± 155 m), while patients with PAH had a walking distance of 353 ± 111.3 m.
Current medication is summarized in Table 1. 20.4 % of patients received no specific therapy at enrollment and none of the control group received specific drugs. 75.3 % of patients received one or two specific drugs, mostly endothelin receptor antagonists (ERA) or phosphodiesterase inhibitors (PDEI). Only 4.3 % were on triple therapy.
Circulating TSP-1 and biomarker levels
Circulating biomarkers grouped according to DanaPoint classification
82.1 ± 15.8
799* ± 237
1.22 ± 0.34
2.29 ± 0.53
152 ± 11
905 ± 253
382 ± 173
2.12 ± 0.25
2.81 ± 0.30
3.60 ± 0.72
2.95 ± 0.86
71.6 ± 8.7
128 ± 21.4
121 ± 17.1
116 ± 46.1
128.0 ± 49
1529 ± 662
0.77 ± 0.22
1.01 ± 0.32*
1.06 ± 0.32*
0.95 ± 0.26
0.94 ± 0.35
Uric acid [mg/dL]
5.09 ± 1.41
7.56 ± 2.46*
7.20 ± 2.13*
7.70 ± 2.12*
8.93 ± 4.01*
14.2 ± 1.3
14.2 ± 2.4
14.6 ± 2.5
13.9 ± 2.3
13.5 ± 1.9
199.9 ± 66.0
285.6 ± 91.0*
277.6 ± 62.0*
279.5 ± 70.9*
324.2 ± 173.2*
0.55 ± 0.20
0.80 ± 0.50
0.78 ± 0.47
0.78 ± 0.39
0.88 ± 0.75
Patients with PDEI had lower TSP-1 levels compared to patients without PDEI (1234 vs. 516 ng/mL, p = 0.02). In contrast, ERA therapy had no effect on TSP-1 levels (806 vs. 1188 ng/ml, p = 0.1), while patients on PC-therapy had higher TSP-1 levels (823 vs. 1762 ng/ml, p = 0.01).
Circulating levels of PDGF-β - a potent inductor of TSP-1 - were elevated in PH compared to controls, with PAH showing the highest levels followed by lung disease associated PH. Levels of patients with CTEPH and PAH were elevated but not statistically significant (Table 2).
Platelet factor 4 (PF4) is an established marker of platelet activation and was determined in the same plasma samples. Despite a trend to increased levels in the PH group, none of the subgroups reached statistical significance (Table 2). No correlation of PF4 and TSP-1 was detected (rho = 0.252 with p = 0.471).
Among many biomarkers SDF-1α has been promoted to quantify endothelial shear stress. In patients with PH, SDF-1α was increased significantly, but the subgroup analysis produced no statistical significance for one of the types of PH (Table 2).
Big-endothelin showed significantly increased levels in both PAH and CTEPH patients, while levels in the group with LD did not reach statistical significance. Highest levels of big-endothelin were observed in CTEPH patients. NT-pro-BNP was statistically significantly elevated in PAH and CTEPH. The increased levels of NT-proBNP in the lung disease group were not statistically significant due to the high standard deviations (Table 2).
TSP-1 and hemodynamic parameters
Summary of hemodynamic variables. All pressures are expressed in millimeter mercury
15.4 ± 2.1
54.2 ± 19.0*
57.0 ± 18.4*
44.9 ± 16.5*,**
59.1 ± 21.8*,***
23.6 ± 4.3
76.8 ± 23.4*
79.3 ± 22.0*
67.2 ± 24.2*,(**)
82.7 ± 25.0*,(***)
10.7 ± 2.5
31.3 ± 11.7*
34.3 ± 12.6*
26.6 ± 8.5*,**
26.6 ± 7.9*,**
7.8 ± 2.3
9.8 ± 2.5*
9.7 ± 2.5
10.1 ± 2.7
9.8 ± 2.0
7.7 ± 2.1
44.5 ± 19.6*
47.5 ± 19.0*
34.8 ± 17.1*,**
49.2 ± 22.2*,***
2.67 ± 0.6
2.46 ± 0.7
2.36 ± 0.7
2.67 ± 0.4
2.52 ± 1.0
250 ± 125
1282 ± 690*
1411 ± 730*
923 ± 472*,**
1326 ± 661*
TSP-1 and outcome
The presented study showed, that levels of circulating TSP-1 differ significantly between patients with PH compared to subjects without PH. The subgroup analysis demonstrated the importance of the specific subtype of PH for the interpretation of this biomarker. Furthermore, associations of circulating TSP-1-levels and pulmonary hemodynamics were elaborated. And finally, the association of elevated TSP-1 with increased mortality became evident.
As Bauer and Isenberg showed, TSP-1 is abundantly expressed in lung tissue of patients with PH. In pulmonary endothelium, CD47 controls endothelial NO-synthase. Binding of TSP-1 uncouples eNOS via CD47 and promotes progress of hypoxic PH in animal models . Furthermore, TSP-1 has been shown to deteriorate shear stress dependent vasodilation under hypoxic conditions and is induced by hypoxia in pulmonary vascular endothelium .
In this study we demonstrated a significant increase in plasma levels of TSP-1 in patients with various types of PH. While levels of TSP-1 varied in different subtypes of PH, the common denominator was their hemodynamic state. The univariate non-linear regression analysis showed a significant association of circulating TSP-1 with PVR and CO. This supports the initial hypothesis, that the increase of PVR increases shear stress resulting in a release of TSP-1 from pulmonary endothelial cells. However, hemodynamic parameters to determine shear stress in humans remain scarce. The extent of shear stress in a specific pulmonary vessel is influenced by both right ventricular function and properties of the vascular bed of the lung. PVR and cardiac output remain the best surrogate variables of standard right heart catheterization for estimation of shear stress.
On the other hand it has been shown, that TSP-1 production is minimal at optimal shear rates , explaining nonlinear U-shaped relation of shear stress and TSP-1 release. In this study we showed first clinical evidence for this complex relationship (Fig. 3), but had to omit possibly confounding factors (i.e. age, medication) due to limited data points.
Induction of TSP-1 in endothelial cells has been shown previously  and was confirmed for PAH . Our data contrasts these findings, as an association of TSP-1 with mixed central venous oxygen saturation, which reflects peripheral oxygen depletion, could not be confirmed. Furthermore, the vascular endothelium might not be the only source of TSP-1 in PH, as increasing right ventricular load might release TSP-1 from cardiomyocytes as hemodynamics deteriorate. The release of TSP-1 from the myocardium especially due to ischemia-reperfusion injury has been shown previously  and might limit specificity of TSP-1 as a marker for diagnosis of PH.
Experimental data supported the hypothesis of TSP-1 interfering with the NO-pathway . This abrogates soluble guanylate cyclase and protein kinase G as well as adenylate cyclase [21–23], resulting in direct pulmonary arterial vasoconstriction, disease progression  and disruption of key pharmacological targets of specific therapy.
Examination of drug regimes suggested lower TSP-1 levels on treatment with PDEIs, higher levels on PC-treatment and intermediate levels under ERA treatment. This observation might lead to the assumption, that treatment regime was influential on circulating TSP-1. On the other hand, PC therapy is an invasive therapeutic concept and often withheld until treatment goals are not sufficiently achieved by oral medications. Therefore, these observations might reflect the finding, that TSP-1 was elevated with deteriorating hemodynamics and increased functional class. The influence of medical therapy on TSP-1 levels could not be determined in this study and warrants longitudinal trials observing TSP-1 levels before and after initiation of new drug regimes.
As this study was designed as a cross-sectional observation, we included patients in different stages of disease. While some had newly diagnosed PH, others were in the final stage of their illness. Thus a non-matched comparison of TSP-1 levels between groups seems a serious limitation for this study. The comparison of incident and prevalent PH demonstrated slightly higher levels of TSP-1 in incident PH, statistical significance was not reached. While the groups had similar hemodynamics, the influence of medication, the course of disease and adaptive processes might lead to this finding. The reasons and possibly influence on the prognostic value of TSP-1 was beyond the scope of this cross-sectional pilot study.
Based on the data linking TSP-1 to hemodynamics and the possibility of its negative impact on pathophysiological mechanisms of PH, we sought to gain insight of the prognosis attached to TSP-1 as a biomarker. At the end of the study, survivor and non-survivors were compared and in all groups non-survivors had significantly higher levels of TSP-1 when entering the study (Fig. 4). CTEPH patients demonstrated relatively higher levels in both survivors and non-survivors compared to the other subgroups. It is therefore mandatory to exactly classify the type of PH before using TSP-1 as a potential biomarker.
Survival analysis in this study was based on follow-up in regular intervals up to five years. The patients had received standard therapy according to current guidelines. Cardiovascular mortality was chosen as the primary endpoint, but in this dataset it was identical with all cause mortality. We were able to show a significantly increased mortality in patients with high TSP-1 levels. This data is limited by the sample size of 93 patients and inclusion of further confounding factors or multivariate analysis with established predictors of mortality is obsolete. Nevertheless, the optimized cut-off at 2051 ng/mL yielded a highly significant difference between groups. Though, as discussed above, the circulating levels of TSP-1 might vary between subgroups and therefore a different cut-off can be expected especially in patients with CTEPH. Furthermore, serial measurements are needed to evaluate the true impact on survival and various clinical events in more complex frailty models.
Nevertheless, this data provides valuable information on the relation of TSP-1 with pulmonary hemodynamics, a clinical application of in vitro observations considering crucial pathways in PH and indicates an impact on the prognosis of a serious disease. These observations are the clinical implication of previous studies on the role of TSP-1 in experimental PH [15, 24].
The presented data might form the basis for evaluation of TSP-1 as an indicator for the choice of medication and might facilitate therapeutic decisions. TSP-1 interacts significantly with the NO pathway, thereby leading to uncoupling of specific therapeutic drugs . Observational studies should evaluate TSP-1 as a marker for possible non-responders before initiation of therapy.
In this observational study, we could show that TSP-1 levels are significantly elevated in PH. While the majority of studies focuses on strict selection of PH subgroups, this cross-sectional pilot study was able to compare various groups of precapillary PH. The association of TSP-1 levels with invasive hemodynamic parameters offers insight into the complex mechanisms of this disease. While current biomarkers focus on the consequences of PH such as myocardial damage, TSP-1 might monitor endothelial injury and activation at the very source of the pathology. In a prospective approach we were able to provide five-year survival data from patients with PH. Despite of the limited sample size, patients with elevated circulating TSP-1 levels demonstrated a lower survival rate. Therefore, prospective longitudinal studies are warranted to provide insight in the usability of TSP-1 to predict disease activity and progression and to confirm the usefulness of this marker in various clinical endpoints and decisions.
CI, cardiac index; CTEPH, chronic thrombembolic PH; LD, lung disease associated PH; NO, nitric oxide; PAH, pulmonary arterial hypertension; PAOP, pulmonary artery occlusion pressure; PAP, pulmonary artery pressure; PDGF, platelet derived growth factor; PF-4, platelet factor 4; PH, pulmonary hypertension; PVR/I, pulmonary vascular resistance/index; RAP, right atrial pressure; SAP, systemic artery pressure; SDF-1, stromal derived factor 1; TGF, tissue growth factor; TSP-1, Thrombospondin-1; VEGF, vascular endothelial growth factor
RK: Hypothesis, conception, data acquisition, statistics and interpretation, preparation of manuscript. CF: data acquisition, interpretation, drafting manuscript. RB: interpretation, final approval. HW: conception, data acquisition, interpretation, final approval. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
This study was supported by a grant from HOMFOR 2009 (Homburger Forschungsförderungsprogramm) of the Saarland University.
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- Bréchot N, Gomez E, Bignon M, Khallou-Laschet J, Dussiot M, Cazes A, et al. Modulation of macrophage activation state protects tissue from necrosis during critical limb ischemia in thrombospondin-1-deficient mice. PLoS One [Internet]. 2008;3:e3950. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2597179&tool=pmcentrez&rendertype=abstract. Accessed 26 July 2016.View ArticleGoogle Scholar
- Frangogiannis NG, Ren G, Dewald O, Zymek P, Haudek S, Koerting A, et al. Critical role of endogenous thrombospondin-1 in preventing expansion of healing myocardial infarcts. Circulation. 2005;111:2935–42.View ArticlePubMedGoogle Scholar
- Laderoute KR, Alarcon RM, Brody MD, Calaoagan JM, Chen EY, Knapp a M, et al. Opposing effects of hypoxia on expression of the angiogenic inhibitor thrombospondin 1 and the angiogenic inducer vascular endothelial growth factor. Clin Cancer Res [Internet]. 2000;6:2941–50. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10914744. Accessed 26 July 2016.Google Scholar
- Ahamed J, Janczak CA, Wittkowski KM, Coller BS. In vitro and in vivo evidence that thrombospondin-1 (TSP-1) contributes to stirring- and shear-dependent activation of platelet-derived TGF-beta1. PLoS One [Internet]. 2009;4:e6608. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2719874&tool=pmcentrez&rendertype=abstract. Accessed 26 July 2016.View ArticleGoogle Scholar
- Jaffe E a, Ruggiero JT, Falcone DJ. Monocytes and macrophages synthesize and secrete thrombospondin. Blood [Internet]. 1985;65:79–84. Available from: http://www.ncbi.nlm.nih.gov/pubmed/3965054. Accessed 26 July 2016.Google Scholar
- Kobayashi S, Yamamoto T. The molecular biologic study of the expression of thrombospondin in vascular smooth muscle cells and mesangial cells. J Diabet Complications UNITED STATES. 1991;5:121–3.View ArticleGoogle Scholar
- Mosher DF, Doyle MJ, Jaffe EA. Synthesis and secretion of thrombospondin by cultured human endothelial cells. J Cell Biol [Internet]. 1982;93:343–8. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2112841&tool=pmcentrez&rendertype=abstract. Accessed 26 July 2016.View ArticleGoogle Scholar
- Sezaki S, Hirohata S, Iwabu A, Nakamura K, Toeda K, Miyoshi T, et al. Thrombospondin-1 is induced in rat myocardial infarction and its induction is accelerated by ischemia/reperfusion. Exp Biol Med (Maywood, NJ) [Internet]. 2005;230:621–30. Department of Medicine and Medical Science, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan. http://www.ncbi.nlm.nih.gov/pubmed/16179730.Google Scholar
- Kaur S, Soto-Pantoja DR, Stein EV, Liu C, Elkahloun AG, Pendrak ML, et al. Thrombospondin-1 signaling through CD47 inhibits self-renewal by regulating c-Myc and other stem cell transcription factors. Sci Rep [Internet]. 2013;3:1673. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3628113&tool=pmcentrez&rendertype=abstract. Accessed 26 July 2016.Google Scholar
- Isenberg JS, Jia Y, Fukuyama J, Switzer CH, Wink DA, Roberts DD. Thrombospondin-1 inhibits nitric oxide signaling via CD36 by inhibiting myristic acid uptake. J Biol Chem [Internet]. 2007;282:15404–15. Available from: papers3://publication/doi/10.1074/jbc.M701638200.View ArticleGoogle Scholar
- Isenberg JS, Shiva S, Gladwin M. Thrombospondin-1–CD47 blockade and exogenous nitrite enhance ischemic tissue survival, blood flow and angiogenesis via coupled NO–cGMP pathway activation. Nitric Oxide [Internet]. 2009;21:52–62. Available from: http://linkinghub.elsevier.com/retrieve/pii/S1089860309000731. Accessed 26 July 2016.View ArticleGoogle Scholar
- Isenberg JS, Maxhimer JB, Hyodo F, Pendrak ML, Ridnour LA, DeGraff WG, et al. Thrombospondin-1 and CD47 limit cell and tissue survival of radiation injury. Am J Pathol [Internet]. 2008;173:1100–12. Available from: http://linkinghub.elsevier.com/retrieve/pii/S000294401061499X. Accessed 26 July 2016.View ArticleGoogle Scholar
- Zhang X, Galardi E, Duquette M, Lawler J, Parangi S. Antiangiogenic treatment with three thrombospondin-1 type 1 repeats versus gemcitabine in an orthotopic human pancreatic cancer model. Clin Cancer Res [Internet]. 2005;11:5622–30. 2005/08/03 ed. Department of Surgery and Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA. Available from: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16061881. Accessed 26 July 2016.View ArticleGoogle Scholar
- Belmadani S, Bernal J, Wei CC, Pallero MA, Dell’italia L, Murphy-Ullrich JE, et al. A thrombospondin-1 antagonist of transforming growth factor-beta activation blocks cardiomyopathy in rats with diabetes and elevated angiotensin II. Am J Pathol [Internet]. 2007;171:777–89. 2007/07/21 ed. Department of Physiology and Biophysics, University of Alabama at Birmingham, 668 Volker Hall, 1530 3rd Ave. South, Birmingham, AL 35294–0019, USA. Available from: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=17640965. Accessed 26 July 2016.View ArticleGoogle Scholar
- Bauer PM, Bauer EM, Rogers NM, Yao M, Feijoo-Cuaresma M, Pilewski JM, et al. Activated CD47 promotes pulmonary arterial hypertension through targeting caveolin-1. Cardiovasc Res [Internet]. 2012;93:682–93. 2012/01/05 ed. Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22215724. Accessed 26 July 2016.View ArticleGoogle Scholar
- Labrousse-Arias D, Castillo-González R, Rogers NM, Torres-Capelli M, Barreira B, Aragonés J, et al. HIF-2α-mediated induction of pulmonary thrombospondin-1 contributes to hypoxia-driven vascular remodelling and vasoconstriction. Cardiovasc Res [Internet]. 2015;cvv243. Available from: http://cardiovascres.oxfordjournals.org/lookup/doi/ Accessed 26 July 2016.10.1093/cvr/cvv243. Accessed 26 July 2016.
- Bongrazio M, Da Silva-Azevedo L, Bergmann EC, Baum O, Hinz B, Pries AR, et al. Shear stress modulates the expression of thrombospondin-1 and CD36 in endothelial cells in vitro and during shear stress-induced angiogenesis in vivo. Int J Immunopathol Pharmacol [Internet]. 2006;19:35–48. 2006/03/30 ed. Department of Physiology, Charite Campus Benjamin Franklin--Arnimallee 22, 14195 Berlin, Germany. Available from: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=16569344. Accessed 26 July 2016.Google Scholar
- Phelan MW, Forman LW, Perrine SP, Faller DV. Hypoxia increases thrombospondin-1 transcript and protein in cultured endothelial cells. J Lab Clin Med [Internet]. 1998;132:519–29. 1998/12/16 ed. Cancer Research Center and Department of Medicine, Boston University School of Medicine, MA 02118, USA. Available from: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=9851743. Accessed 26 July 2016.View ArticleGoogle Scholar
- Kaiser R, Grotemeyer K, Kalsch T, Graber S, Wilkens H, Elmas E. Decreased TSP-1 following percutaneous coronary intervention is associated with major adverse cardiac events in ST-elevation myocardial infarction. Clin Hemorheol Microcirc [Internet]. 2013;54:59–73. 2012/07/04 ed. Department of Pulmonology, Saarland University, Homburg/Saar, Germany. email@example.com. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22750995. Accessed 26 July 2016.Google Scholar
- Yao M, Roberts DD, Isenberg JS. Thrombospondin-1 inhibition of vascular smooth muscle cell responses occurs via modulation of both cAMP and cGMP. Pharmacol Res [Internet]. 2011;63:13–22. Elsevier Ltd. Available from: http://dx.doi.org/10.1016/j.phrs.2010.10.014. Accessed 26 July 2016.View ArticleGoogle Scholar
- Kaur S, Martin-Manso G, Pendrak ML, Garfield SH, Isenberg JS, Roberts DD. Thrombospondin-1 inhibits VEGF receptor-2 signaling by disrupting its association with CD47. J Biol Chem. 2010;285:38923–32.View ArticlePubMedPubMed CentralGoogle Scholar
- Miller TW, Isenberg JS, Roberts DD. Thrombospondin-1 is an inhibitor of pharmacological activation of soluble guanylate cyclase. Br J Pharmacol [Internet]. 2010;159:1542–7. Available from: http://doi.wiley.com/10.1111/j.1476-5381.2009.00631.x. Accessed 26 July 2016.View ArticleGoogle Scholar
- Bauer EM, Qin Y, Miller TW, Bandle RW, Csanyi G, Pagano PJ, et al. Thrombospondin-1 supports blood pressure by limiting eNOS activation and endothelial-dependent vasorelaxation. Cardiovasc Res [Internet]. 2010;88:471–81. 2010/07/09 ed. Vascular Medicine Institute of University of Pittsburgh, Pittsburgh, PA, USA. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20610415. Accessed 26 July 2016.View ArticleGoogle Scholar
- Ochoa CD, Yu L, Al-Ansari E, Hales CA, Quinn DA. Thrombospondin-1 null mice are resistant to hypoxia-induced pulmonary hypertension. J Cardiothorac Surg [Internet]. 2010;5:32. Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. firstname.lastname@example.org. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20441584. Accessed 26 July 2016.View ArticleGoogle Scholar