Macrophage Migration Inhibitory Factor Mediates Hypoxia-Induced Pulmonary Hypertension
- 38 Downloads
Pulmonary hypertension (PH) is a devastating disease leading to progressive hypoxemia, right ventricular failure, and death. Hypoxia can play a pivotal role in PH etiology, inducing pulmonary vessel constriction and remodeling. These events lead to increased pulmonary vessel wall thickness, elevated vascular resistance and right ventricular hypertrophy. The current study examined the association of the inflammatory cytokine macrophage migration inhibitory factor (MIF) with chronic lung disease and its role in the development of hypoxia-induced PH. We found that plasma MIF in patients with primary PH or PH secondary to interstitial lung disease (ILD) was significantly higher than in the control group (P = 0.004 and 0.007, respectively). MIF involvement with hypoxia-induced fibroblast proliferation was examined in both a human cell-line and primary mouse cells from wild-type (mif+/+) and MIF-knockout (mif−/−) mice. In vitro, hypoxia-increased MIF mRNA, extracellular MIF protein accumulation and cell proliferation. Inhibition of MIF inflammatory activity reduced hypoxia-induced cell proliferation. However, hypoxia only increased proliferation of mif−/− cells when they were supplemented with media from mif+/+ cells. This growth increase was suppressed by MIF inhibition. In vivo, chronic exposure of mice to a normobaric atmosphere of 10% oxygen increased lung tissue expression of mRNA encoding MIF and accumulation of MIF in plasma. Inhibition of the MIF inflammatory active site, during hypoxic exposure, significantly reduced pulmonary vascular remodeling, cardiac hypertrophy and right ventricular systolic pressure. The data suggest that MIF plays a critical role in hypoxia-induced PH, and its inhibition may be beneficial in preventing the development and progression of the disease.
Pulmonary hypertension (PH) is a devastating disease associated with progressive hypoxemia and right ventricular failure. PH is usually classified as primary (idiopathic) or secondary. The World Health Organization (WHO) has proposed a classification system for PH based on common clinical features (1). This classification adds to our understanding of the mechanisms involved and provides a good starting point in developing a rational clinical approach to the management of PH. Clinically the diagnosis of pulmonary arterial hypertension (primary PH) is made when these secondary causes have been clinically excluded. PH can occur in association with chronic lung disorders, with hypoxia playing a pivotal role in the etiology. Reduced oxygen tension provokes pulmonary vessel constriction and if persistent induces pulmonary vascular remodeling resulting in increased vessel wall thickness and pulmonary vascular resistance which in turn lead to right ventricular failure, decreased left ventricular preload and reduced cardiac output (2,3). A major factor in the rapid progression of PH symptoms may be due in part to the creation of a vicious cycle: PH can be initiated by hypoxia, itself causes hypoxia, and hypoxia in return exacerbates PH.
Current evidence suggests that hypoxia-induced pulmonary vascular remodeling is a chronic inflammatory process (2,4,5). Macrophage migration inhibitory factor (MIF) is a potent proinflammatory cytokine involved in both chronic and late stage acute inflammation (6), and we have shown previously that the lungs can be a major source of this inflammatory protein (7). The expression of MIF is induced by hypoxia inducible factor-1 α (HIF-1α) (8,9), and MIF itself can amplify hypoxia induced HIF-1α stabilization, leading to a positive feedback and expression of further MIF and other HIF-1 related factors (10,11). Once released into the extracellular environment, MIF can increase proliferation of cells including fibroblasts (12), endothelial cells (13) and smooth muscle cells (14,15), which are the main components of the vascular wall.
Therefore, in this study, we examined the involvement of extracellular MIF in the development of PH, examining plasma MIF concentrations from patients with PH both at baseline and following exercise. We then used in vitro hypoxia-induced cell proliferation and an in vivo mouse model to reveal the critical role of MIF in hypoxia-induced pulmonary vascular remodeling and hypertension.
Materials and Methods
The human studies and animal use received prior approval from the Institutional Review Board and Institutional Animal Care and Use Committee, respectively, at the Feinstein Institute for Medical Research.
Patients with (a) primary PH (2 males, 5 females, aged 42–75 years) with a right heart catheterization diagnosis of mean pulmonary artery pressure >25 mmHg at rest or >30 mmHg with exercise and pulmonary capillary wedge pressure <18 mmHg, without other cardiopulmonary disease or known secondary causes for PH; (b) interstitial lung disease (ILD; 3 males, 2 females, aged 35–72 years) characterized by signs of ILD on high resolution computed tomography, and total lung capacity less than 60%; or (c) PH secondary to ILD (2 males, 4 females, aged 54–76 years) meeting both diagnostic criteria for ILD and PH described above, were examined. Plasma MIF concentrations were compared with results from our previously published control subjects (n = 53) from a randomly recruited population (16). The control group comprised individuals who consented to participate, as volunteers, in response to an invitation sent to 1000 randomly selected individuals. No additional exclusion criteria other than unwillingness to participate in the study were applied in the selection of the control group.
Patients walked on a treadmill to a speed adjusted to their target heart rate. Oxygen saturation and 3-lead electrocardiogram were measured continuously. To maintain oxygen saturation >90%, supplemental oxygen was administered if needed. The test was terminated if the target heart rate was reached or the patient could not continue due to dyspnea and/or muscle fatigue. Venous blood samples were drawn from an antecubital vein pre- and postexercise.
Human lung fibroblasts (CCL-210) were cultured in Eagle’s Minimum Essential Medium (EMEM) with 10% fetal bovine serum at 37°C, 5% CO2. Primary lung fibroblasts isolated from MIF knockout (mif−/−) (17) or wild type C57BL6 mice (mif+/+) were established by outgrowth from lung explants (18) and used during passages 2–6.
Fibroblast proliferation was assessed by 5-bromo-2-deoxyuridine (BrdU) incorporation (Calbiochem, Gibbstown, NJ, USA). In some experiments, hemocytometer cell counts were also performed, to confirm the results of the BrdU assay.
Hypoxia In Vitro
Cells were cultured in a microenvironment of 37°C, 5%CO2, 100% humidity and either normoxia or 1% O2. To examine the effects of hypoxia on MIF expression, cell-cycle synchronized human fibroblasts (CCL-210) were cultured in normoxia or hypoxia for 24 h. Culture medium was assayed for MIF protein by ELISA, and cellular MIF gene expression assessed using real-time qPCR (primers: human MIF forward: ACCGCTCCTACAGCAAGC; human MIF reverse: CGCGTTCATG TCGTAATAGTTG).
MIF involvement in cell proliferation was assessed in normoxia and hypoxia by incubating cells with a specific MIF inhibitor ISO-92 (19) or DMSO (vehicle control). Additionally, growth of primary lung fibroblasts (mif−/− and mif+/+) cultured in normoxia and hypoxia was assessed. Fibroblasts (mif−/−) were also cultured under hypoxic conditions, in medium preconditioned by fibroblasts (mif+/+) cultured in hypoxia. In some cases, MIF inflammatory activity was inhibited by ISO-92.
Hypoxia In Vivo
C57BL6 mice (male, 8–10 wks; Taconic, Hudson, NY, USA) were randomly divided into 4 groups and housed in room air or 10% normobaric hypoxia for 3–42 d. At the time of euthanasia, animals were anesthetized with isoflurane and 100% oxygen. The right ventricular systolic pressure (RVSP) was measured trans-diaphragmatically. All ventricular pressure measurements were made with the animals breathing 100% oxygen to ensure that the measurements reflected changes in pulmonary resistance due to remodeling rather than hypoxia-induced constriction. Blood was then drawn from the right ventricle and plasma stored for MIF measurement. Postmortem, the hearts were removed, dissected and weighed; and the weights were expressed as a ratio of the right ventricle to the septum + left ventricle (RV/S + LV). The lungs were harvested; the left lung being used to assess MIF mRNA expression (qPCR; primers: mouse MIF forward: ACAGCATCGG CAAGATCG, mouse MIF reverse: GGCCACACAGCAGCTTACT), and the right lung fixed, at inflation, for lung vascular histology.
To investigate the effects of MIF inhibition, mice were randomized into 4 groups and administered DMSO (control) or ISO-92 (1.8 mg/kg/d, subcutaneous [s.c.]) via an osmotic delivery device (Alzet, CA, USA) inserted subcutaneously on the dorsum of the animals. Immediately after pump implantation, the mice were housed in 10% normobaric hypoxia for two different time periods (10 d and 21 d). At the indicated times, the RVSP, RV/S + LV, and vascular changes were determined.
Vascular Wall Thickness and Muscularization
The muscular layer of the lung vessel wall was revealed by immunostaining with an anti-α-smooth muscle actin (anti-α-SMA) antibody (Abcam, Cambridge, MA, USA). External diameter (ED) and internal diameter (ID) of 50 pulmonary small vessels (with ED of 40–100 µm) per animal were measured by an independent investigator blinded to the sample origin. Total wall thickness (WT), that is, mean distance between ED and ID was assessed and the percentage wall thickness (WT%) calculated (20).
MIF in human plasma and cell culture medium was evaluated using the Quantikine MIF Immunoassay (R&D systems, Minneapolis, MN, USA). MIF in mouse plasma was quantitated using Western blotting.
Data are presented as mean ± standard deviation. Student t test or oneway ANOVA were used to evaluate statistical significance between two and multiple groups respectively. Differences with P values <0.05 were considered significant.
Plasma MIF Concentrations in Patients with Chronic Lung Disease
MIF Expression in a Mouse Hypoxia Model of Pulmonary Vascular Remodeling and Hypertension
MIF Involvement in Fibroblast Proliferation In Vitro
Reduction of Pulmonary Vascular Remodeling and Hypertension by MIF Inhibitor in the Mouse Hypoxia Model
Pulmonary hypertension is a potentially lethal disease with poor prognosis. PH can be idiopathic or associated with other conditions, such as scleroderma (21), sickle cell disease (22) or ILD (23), and is often “silent” with a long period from the onset of vascular proliferation to the earliest emergence of symptoms (24). The symptoms of PH, often subtle in the early stages of the disease, include chronic fatigue, dyspnea, angina, palpitation, and so on, none of which are typical, and this makes the differential diagnosis difficult from other cardiopulmonary diseases. Once diagnosed, individuals with PH demonstrate rapid deterioration, with a median length of survival for patients with primary PH of only 2.8 years, and an estimated 5-year survival rate of 21–34% (25,26). There are limited therapeutic options in PH, and the limitation of current treatment suggests the need for a better understanding of the pathogenesis and identification of new therapeutic targets (27).
MIF is a potent regulator of the immuno-response (28, 29, 30) that plays a critical role in the lethality associated with sepsis (17,31,32), and is increasingly recognized as playing a role in altered physiological states from Alzheimer’s disease (33) to sperm maturation (34). Our previous studies have identified the lung as a major source of this inflammatory protein (7). Here, we present data showing that MIF mediates hypoxia-induced pulmonary hypertension. We examined MIF concentrations in human plasma from patients with PH both at baseline and after exercise and used in vitro cell proliferation and development of PH in a mouse model to define the role of MIF in hypoxia-induced pulmonary vascular remodeling and hypertension.
Inflammatory mechanisms appear to play a significant role in pulmonary hypertension (4,5,35,36). Therefore, in our initial studies, we examined plasma MIF in individuals with primary PH or ILD alone, or PH secondary to ILD to determine if there was an association between increased concentrations of this inflammatory molecule and the disease. While the study groups were small, individuals with chronic lung disease had increased baseline plasma MIF concentrations and those individuals with more severe disease (PH secondary to ILD) significantly increased the plasma MIF after 10 min exercise. This suggested that MIF may, in part, be regulated by tissue oxygenation. However, the increase of MIF after exercise also may be due to other reasons, such as muscle fatigue, probably muscle hypoxia with inappropriately low cardiac output, or redistribution of blood flow to muscle from core organs such as liver and kidneys, and so on.
To examine the role of MIF in the development of PH more fully, we used a mouse model in which the animals were subjected to 10%, normobaric hypoxia. These animals underwent pulmonary vascular remodeling, significantly increasing the vascular wall thickness and vascular muscularization over 42 d. The time-course study revealed that there were significant increases in RVSP by 10 d, and this was accompanied by right ventricular hypertrophy. The increases in RVSP and right ventricular weights were associated with increased mRNA encoding MIF in the lung tissue and increased MIF protein in the plasma. The mRNA encoding MIF in the lungs was significantly increased by d 3 of hypoxia and was 15-fold higher than normal at d 10. By 42 d, the level had decreased considerably but was still at least double the normoxia level. The plasma level of the MIF protein was increased at 10 and 42 d reflecting the increases in RVSP and cardiac hypertrophy evaluations, suggesting that MIF is involved from the early stages in the pulmonary vascular remodeling events.
Increased cell proliferation and angiogenesis are common adaptive changes to hypoxia. Increased cell proliferation can compensate for the cell death caused by oxygen deprivation, whereas new vascular formation increases the blood flow to a hypoxic area. However, disordered new vascular formation can be pathogenic. In the lung vasculature, uncontrolled cell proliferation and angiogenesis during hypoxia leads to vascular wall thickening, lumen narrowing, increased vascular resistance, and PH. Chronic hypoxia induces structural changes to the pulmonary arteries including the appearance of SMC-like myofibroblasts expressing α-SMA, in previously nonmuscularized vessels. While hypoxia-induced remodeling is associated with medial hypertrophy, direct stimulation of SMC proliferation by hypoxia remains somewhat controversial (37). Although there are reports of hypoxia driven smooth muscle cell proliferation (38,39), several in vitro studies have shown that hypoxia does not directly increase SMC proliferation (40, 41, 42) or may actually decrease proliferation (43,44). However, fibroblasts that are less differentiated than the other two main vascular cell types, have a greater proliferative response to hypoxia (44, 45, 46). Fibroblasts are uniquely positioned in the scheme of remodeling being able to rapidly proliferate, contract, migrate, synthesize cytokines and other mediators, and transdifferentiate into other cell types such as the SMC-like myofibroblast (47). Animal models indicate that the adventitia undergoes the earliest and most profound changes under hypoxic conditions (48,49) and in vitro, hypoxia induces fibroblast proliferation in the absence of any exogenous comitogen (50). In addition, several investigators have suggested that MIF can induce fibroblasts proliferation directly (12,51, 52, 53, 54). Therefore, we chose cultures of lung fibroblasts, both a human cell line and primary mouse cells, to examine the inter-relationships between hypoxia, MIF and cell proliferation. The data demonstrate that hypoxia induces both MIF expression and proliferation in the fibroblasts, and this was assessed by BrdU incorporation and confirmed by cell counts using a hemocytometer. These results are consistent with the findings of others regarding MIF production and hypoxia-induced fibroblast proliferation (9). However, we have also demonstrated that inhibition of the MIF inflammatory site can block the hypoxic cell proliferation, which indicates that MIF is a key mediator of fibroblast proliferation under hypoxic conditions. In the current study, two different ways were used to show the critical role of MIF. The first was to use the MIF-specific inhibitor ISO-92, a small synthetic molecule with high affinity for MIF, developed by rational design to fit into the hydrophobic active site of MIF (19). ISO-92, but not the vehicle control DMSO, was able to inhibit hypoxia-driven proliferation in the CCL-210 cells. Treatment of the cells with 100 µmol/L ISO-92 had no effect on the growth of cells cultured in normoxic conditions, nor did it cause accumulation of lactate dehydrogenase in the culture medium (data not shown). These data indicate that ISO-92 did not inhibit cell proliferation by cytotoxic effects, and that hypoxia induces the accumulation in the culture medium of a material (MIF) that then acts in an autocrine manner to stimulate proliferation. To further establish the role of MIF in the fibroblast proliferation, we used primary cell lines established from wild type and MIF-deficient mice. These studies revealed that while mif+/+ fibroblasts increased proliferation in hypoxia, mif−/− did not. However, conditioned medium from mif+/+ fibroblasts grown under hypoxic conditions was able to induce increased proliferation in mif−/− cultured in hypoxia. This increased proliferation was inhibitable by ISO-92. It should be noted that conditioned medium alone was not sufficient to induce mif−/− cell proliferation. Increased cell proliferation occurred only when conditioned medium from hypoxic mif+/+ cells was combined with hypoxic conditions in the mif−/− cells. This finding suggests that there is a hypoxic priming of the cells, which are then responsive to MIF stimulation
As a final illustration of proof of concept that MIF is involved in the hypoxia-induced pulmonary vascular remodeling and hypertension, we administered ISO-92 (or vehicle control) to mice housed under hypoxic conditions. We used specific inhibition of the inflammatory active site rather than evaluation of mif−/− mice for two reasons. First extracellular MIF is known to have inflammatory activities that are associated with the hydrophobic pockets located between adjacent monomers. Blockade of this site can inhibit the activity of the molecule (32,55). Our in vitro studies shown in Figure 6 suggest that the mediator of hypoxia-induced fibroblast growth was extracellular and could be transferred in culture media and inhibited by ISO-92. Second, MIF also has a thioreductase activity (56) and this intracellular activity can be protective in times of oxidative stress (57,58). Thus, to examine the role of extracellular MIF on the hypoxia-induced vascular remodeling, we administered ISO-92 to inhibit the inflammatory site and avoid confounding conditions occurring in the total absence of MIF. Inhibition of the MIF inflammatory site significantly reduced vascular remodeling and right ventricular hypertrophy. The overall benefit being the reduction of right ventricular systolic pressures by approximately 53% at 21 d. In this study, we did not examine optimal dose or timing of drug delivery initiation. The administration conditions used were such that the drug delivery pump was inserted before hypoxic exposure to avoid animals experiencing multiple changes in oxygen tension that would occur with a surgery postinitiation of hypoxia. While future studies will address whether the in vivo vascular changes in smooth muscle actin expressing cells are due reduced smooth muscle cell or myofibroblasts, inhibition of the MIF inflammatory active site clearly suppressed the development of PH.
Overall, the data suggest a key role for MIF in the development of hypoxia-induced pulmonary vascular remodeling and hypertension. Since baseline plasma MIF is increased in individuals with ILD and PH, and can further increased on exercise, MIF may prove to be a useful biomarker in the diagnosis and treatment of hypoxia-driven PH. Perhaps more importantly, inhibition of MIF inflammatory activity may be a useful treatment strategy to inhibit the development and progression of hypoxia-induced vascular remodeling and the devastating consequences of the development of pulmonary hypertension.
The authors declare that they have no competing interests as defined by Molecular Medicine, or other interests that might be perceived to influence the results and discussion reported in this paper.
The authors wish to thank following for their support: Pulmonary Hypertension Association (Fellowship, Y Zhang); The Empire Clinical Research Investigator Program (Fellowships, A Sadoughi and K Omonuwa) and The Feinstein Institute for Medical Research, for intramural funding (EJ Miller, A Talwar).
- 1.McLaughlin VV, et al. (2009) ACCF/AHA 2009 expert consensus document on pulmonary hypertension a report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association developed in collaboration with the American College of Chest Physicians; American Thoracic Society, Inc.; and the Pulmonary Hypertension Association. J. Am. Coll. Cardiol. 53:1573–1619.CrossRefGoogle Scholar
- 5.Sadoughi A, Zhang Y, Miller EJ, Talwar A. (2010) Inflammatory mechanisms in pulmonary hypertension. CML Pulm. Hypertens. 1:93–106.Google Scholar
- 12.Mitchell RA, Metz CN, Peng T, Bucala R. (1999) Sustained mitogen-activated protein kinase (MAPK) and cytoplasmic phospholipase A2 activation by macrophage migration inhibitory factor (MIF). Regulatory role in cell proliferation and glucocorticoid action. J. Biol. Chem. 274:18100–6.CrossRefGoogle Scholar
- 20.Li FH, Xia W, Li AW, Zhao CF, Sun RP. (2007) Inhibition of rho kinase attenuates high flow induced pulmonary hypertension in rats. Chin. Med. J. (Engl) 120:22–9.Google Scholar
- 33.Oyama R, Yamamoto H, Titani K. (2000) Glutamine synthetase, hemoglobin alpha-chain, and macrophage migration inhibitory factor binding to amyloid beta-protein: their identification in rat brain by a novel affinity chromatography and in Alzheimer’s disease brain by immunoprecipitation. Biochim. Biophys. Acta 1479:91–102.CrossRefGoogle Scholar
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it.
The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
To view a copy of this license, visit (https://doi.org/creativecommons.org/licenses/by-nc-nd/4.0/)