Angiopoietin-2 impairs collateral artery growth associated with the suppression of the infiltration of macrophages in mouse hindlimb ischaemia
- Xiaoyong Tan†1, 2,
- Kai Yan†3,
- Meiping Ren1, 2,
- Ni Chen1, 2,
- Yongjie Li1, 2,
- Xin Deng1, 2,
- Liqun Wang1, 2,
- Rong Li1, 2,
- Mao Luo1, 2,
- Yong Liu1, 2,
- Yan Liu1, 2 and
- Jianbo Wu1, 2, 4Email author
© The Author(s) 2016
Received: 17 May 2016
Accepted: 10 October 2016
Published: 26 October 2016
Angiopoietin-2 (Ang-2), a ligand of the Tie-2 receptor, plays an important role in maintaining endothelial cells and in destabilizing blood vessels. Collateral artery growth (arteriogenesis) is a key adaptive response to arterial occlusion. It is unknown whether the destabilization of blood vessels by Ang-2 can affect arteriogenesis and modulate mononuclear cell function. This study aimed to investigate the effects of Ang-2 on collateral artery growth.
Hindlimb ischaemia model was produced in C57BL/6 mice by femoral artery ligation. Blood flow perfusion was measured using a laser Doppler perfusion imager quantitative RT-PCR analysis was applied to identify the level of angiogenic factors.
After the induction of hindlimb ischaemia, blood flow recovery was impaired in mice treated with recombinant Ang-2 protein; this was accompanied by a reduction of peri-collateral macrophage infiltration. In addition, quantitative RT-PCR analysis revealed that Ang-2 treatment decreased monocyte chemotactic protein-1 (MCP-1), platelet-derived growth factor-BB (PDGF-BB) mRNA levels in ischaemic adductor muscles. Ang-2 can lead to macrophage M1/M2 polarization shift inhibition in the ischaemic muscles. Furthermore, Ang-2 reduced the in vitro inflammatory response in macrophages and vascular cells involved in arteriogenesis.
Our results demonstrate that Ang-2 is essential for efficient arteriogenesis, which controls macrophage infiltration.
KeywordsAngiopoietin-2 Ischaemia Arteriogenesis Macrophage
Neovascularization is a complex process that involves vasculogenesis, angiogenesis, and arteriogenesis [1–3]. The principal stimuli for blood perfusion include tissue ischaemia and hypoxia, inflammation, and vascular shear stress. Angiogenesis is the growth of new blood vessels from pre-existing blood vessels, whereas arteriogenesis is the enlargement of existing blood vessels to form collaterals and requires the recruitment of pro-inflammatory cells. A number of local and circulating angiogenic factors are involved in arteriogenesis, including vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), and angiopoietins. Previous studies have demonstrated that angiopoietin-2 (Ang-2) regulates both angiogenesis and arteriogenesis , with the concentration of Ang-2 being an important determinant of which effect is observed. However, the role of Ang-2 in neovascularization in vivo remains controversial [5–7] and needs to be elucidated. Given that published studies have predominantly used transgenic mice to compare the effects of normal versus loss of Ang-2 expression on collateral remodelling, relatively little is known about the impact of enhanced Ang-2 expression on this process.
There have been conflicting reports concerning the role of Ang-2 in postnatal neovascularization. For example, Ang-2 was shown to increase the length, but not the density, of neovessels in a corneal implant model . However, in a model of hindlimb ischaemia, collateral formation was impaired in Ang-2 transgenic mice . Moreover, still others have reported that the selective inhibition of Ang-2 activity promotes blood reperfusion following ischaemia through the recruitment of inflammatory cells and combination with VEGF [5, 9]. Finally, Ang-2 was shown to increase vascular destabilization and regression by inhibiting pericyte recruitment and Tie-2–mediated phosphorylation of focal adhesion kinase [10–12]. However, no studies have implicated Ang-2 in controlling signalling pathways that initiate ischemia-mediated vessel stabilization and blood flow perfusion.
Therefore, we hypothesized that Ang-2 plays an important role in the regulation of blood flow recovery during ischaemia through the modulation of collateral artery growth. In this study, we studied the effects of r-Ang-2 on blood flow perfusion and the density of pre-existing collateral vessels in a murine hindlimb ischaemia model. We also studied post-ischaemic alterations in gene expression and macrophage recruitment to examine the potential mechanisms by which r-Ang-2 regulates arteriogenesis.
Mouse hindlimb ischaemia model
Male C57BL/6 mice were anaesthetized with sodium pentobarbital (60 mg/kg body weight, intraperitoneally) or isoflurane (5 % by inhalation) and administered a single subcutaneous dose of buprenorphine hydrochloride (0.1 mg/kg) for analgesia. Additional sodium pentobarbital (12 mg/kg body weight) or 5 % isoflurane was given as needed to maintain anaesthesia. Mice were euthanized by cervical dislocation at the end of the experiment while still anaesthetized. Mice were subjected to unilateral hindlimb ischaemia as previously described . Recombinant human Ang-2 (50 µg/mL) or vehicle (PBS) was injected intraperitoneally every other day beginning 1 day before surgery. Real-time PCR was performed on mouse hindlimb muscles. In some experiments, mouse hindlimbs were also used for immunostaining. All protocols for animal use were reviewed and approved by the Animal Care Committee of Southwest Medical University in accordance with Institutional Animal Care and Use Committee guidelines.
Laser Doppler perfusion images
The ratio of blood flow in the ischaemic (left) limb to the normoxic (right) limb was measured using a laser Doppler perfusion imager (LDPI) (Moor Instruments, Devon, UK) as previously described [14, 15]. Non-invasive perfusion imaging of the adductor thigh region and the plantar foot of both limbs was performed under 1.125 % isoflurane/O2 anaesthesia at 37 ± 0.5 °C, before, immediately after, and at 1, 3, and 7 days following femoral artery ligation. Regions of interest were drawn to facilitate the analysis of specific anatomic regions. To minimize data variability caused by ambient light and temperature, the LDPI index was expressed as the ratio of left limb (ischaemic) to right limb (normoxic) blood flow.
Assessment of ischaemic muscles histology
Mice were euthanized 7 days after surgery. The ischaemic gastrocnemius muscles were excised, embedded in paraffin or TISSUE TEK OCT compound, and stored at −80 °C. Cross-sections were prepared for immunohistochemical analysis. Capillary density was determined by immunostaining with anti-PECAM-1 antibody. The number of PECAM-1+ vessels was quantified in 5 microscopic fields in each of 3 cross-sections from each tissue specimen using ImagePro Plus software. Adductor muscle cryostat sections were obtained, and incubated with primary antibodies anti-Mac-3 (1:500, Pharmingen) and α-SMA (1:100, Santa Cruz Biotech). The secondary antibodies used were goat ant-rat IgG AlexaFluor 488-conjugated antibody and goat ant-rabbit IgG AlexaFluor 568-conjugated antibody (Molecular Probes, Invitrogen). Images were captured by a fluorescence microscopy (Leica).
In some experiments, cross-sections were stained with hematoxylin-eosin (HE). Photomicrographs were taken using a microscope (Leica), the collateral diameters were measured in 5 randomly selected fields per section. The mean value of these measurements was taken as a single point for each animal.
Quantitative real-time PCR
Total RNA was extracted from hindlimb muscles using TRIzol (Invitrogen). RNA was pre-treated with deoxyribonuclease I (Invitrogen Life Technologies), and a SuperScript kit (Invitrogen Life Technologies) was used to synthesize cDNA according to the manufacturer’s recommendations. Each sample was analysed in duplicate with ribosomal 18S RNA used as an internal control. All fold changes in gene expression were determined using the 2−ΔΔCT method. The values are presented as the mean ± SEM. All primers are listed in Additional file 1: Table S1.
Macrophages were obtained by flushing the peritoneal cavity with phosphate-buffered saline (PBS) 4 days after intraperitoneal injection with 1 mL of a 3 % thioglycollate solution (Difco Laboratories, Sparks, MD). Macrophage migration assays were performed using transwell migration chambers with 8.0-μm porous membranes (Corning Costar, Corning, NY, USA). Cells (2 × 104) were added to the upper chambers and were treated with r-Ang-2 (200 nmol/L) or vehicle control. In some experiments, cells were pre-treated with r-Ang-2 for 30 min, followed by stimulation with MCP-1 (100 ng/mL). After incubation for 24 h at 37 °C in a humidified chamber with 5 % CO2, the porous membranes were rinsed, and the cells remaining in the upper chamber were removed with a cotton swab. The membranes were then fixed and stained with 0.5 % crystal violet. The cells that had migrated to the lower chamber were counted.
The migration of human coronary artery smooth muscle cells (VSMCs) was measured using a previously described method . Briefly, cells were grown to confluence on 6-well plates. Parallel lines were then drawn with a marker on the back of each well, and linear wounds were made perpendicular to these lines in the cell monolayers by scraping each well with a sterile 200-µL pipette tip. Cells were then rinsed twice with serum-free medium to remove cellular debris. Images of the intersections between the parallel lines and wounds were obtained using an Olympus inverted microscope. The cells were then incubated with or without Ang-2 (200 ng/mL) for 30 min in the presence or absence of PDGF-BB (20 ng/mL). After 12 h, images of each intersection were obtained again. ImageJ software was then used to measure the distance between the two edges of each wound. The data are presented as the moving distance, which is the difference in the distances between the two edges at the same crossing at 0 and 12 h.
Enzyme-linked immunosorbent assay
A human Ang-2 ELISA kit (R&D Systems) was used to quantify Ang-2 according to the manufacturer’s instructions.
The data are expressed as the mean ± SEM of at least triplicate experiments. Groups were compared using the two-tailed Student’s t test.
r-Ang-2 impaired blood reperfusion following ischaemia
Hindlimb ischaemia was induced in C57BL/6 mice by ligation and excision of the femoral artery, after which mice received either r-Ang-2 or vehicle control.
r-Ang-2 suppresses the infiltration of inflammatory cells
To further study the effects of r-Ang-2 on macrophage migration, we isolated thioglycollate-elicited macrophages from C57BL/6 mice and used a modified Boyden chamber assay that required macrophages to migrate through a porous membrane. In the absence of adding Ang-2, MCP-1 significantly stimulated macrophage migration. However, pre-treatment with r-Ang-2 abrogated MCP-1-induced migration, whereas treatment with Ang-2 alone did not significantly alter macrophage migration (Fig. 2e, f).These results supported the functional significance of r-Ang-2 by inhibiting pericollateral macrophage recruitment.
r-Ang-2 modulates post-ischaemic gene regulation
Effects of r-Ang-2 on in vitro VSMC migration
In this study, we assessed the role of Ang-2 in arteriogenesis using a mouse hindlimb ischaemia model. Our findings indicate that Ang-2 reduced the diameter of collateral arterioles in ischaemic adductor muscles following ligation of the femoral artery. This change is associated with reductions in arteriogenesis but leaves angiogenesis intact. Furthermore, we found that Ang-2 reduced MCP-1-induced macrophage migration and PDGF-BB-induced VSMC migration in vitro. Therefore, we conclude that Ang-2 is important for arteriogenesis induced by acute loss of hindlimb perfusion.
The angiopoietin/Tie system is essential for vascular development and maturation . Ang-1/Tie-2 signalling promotes blood vessel stabilization and the recruitment of mural cells, whereas Ang-2 acts as an Ang-1 antagonist and destabilizes vessels [18, 19]. However, the complex role of Ang-2 in vascular remodelling still remains unknown. We found that treatment with r-Ang-2 impaired the recovery of blood flow in the ischaemic hindlimb, suggesting that Ang-2 is involved in collateral artery growth after arterial ligation. However, effects of Ang-2 in hindlimb ischaemia remain controversial. For example, Tressel et al. showed that the Ang-2 inhibitor, L1-10, induced in ischemic tissue plays a critical role in blood flow recovery by stimulating inflammation and arteriogenesis . However, Reiss et al. found that transgenic overexpression of Ang-2 impaired revascularization during hindlimb ischaemia. The importance of local variations in Ang-2 concentration might be an important determinant of whether vessel growth or regression occurs . Our findings with r-Ang-2 in this study are in agreement with another murine study of Ang-2 overexpression and support the in vivo relevance of Ang-2-mediated destabilization of collateral arteries. We did not observe an increase in capillary density in ischaemic gastrocnemius muscle in response to r-Ang-2 treatment. In addition, our finding that the expression of several major growth factors was transiently downregulated following Ang-2 treatment further supports the initial role of Ang-2 in neovascularization. However, Ang-2 exhibits an opposing role regulating angiogenesis through its receptor Tie-2 and integrin signalling . Thus, these data suggest that Ang-2 mediates blood flow recovery mainly through arteriogenesis without affecting angiogenesis.
The reduced diameter of collateral arterioles in ischaemic adductor muscles in mice treated with r-Ang-2 could be the result of inhibited mural cell recruitment. However, it is unclear whether Ang-2 has a direct effect on the recruitment of VSMCs and pericytes . A recent study showed that Ang-2 induced pericyte apoptosis via α3β1 integrin signalling in a model of diabetic retinopathy . In the present study, we further evaluated the effect of Ang-2 on VSMC migration. In the absence of exogenous Ang-2, PDGF-BB significantly enhanced the migration of VSMCs. However, in the absence of exogenous PDGF-BB, Ang-2 did not significant impact migration. The inhibitory effect of Ang-2 could be mediated by the uncoupling of PDGF receptor-β (PDGFR-β)-integrin crosstalk, as has been described [20, 22]. This mechanism was not resolved in our experiments. Additional studies are necessary to more precisely define the molecular events underlying Ang-2-mediated, integrin-dependent downregulation of PDGFR-β signalling.
There is evidence that Ang-2 acts as a chemoattractant for regulating monocyte/macrophage infiltration [5, 23], suggesting that treatment with r-Ang-2 may increase macrophage recruitment to remodelling collateral arterioles. However, our data did not support this mechanism because we observed reduced macrophage content in ischaemic adductor muscles in vivo. Moreover, Ang-2 treatment abrogated MCP-1-induced macrophage migration in vitro, whereas treatment with Ang-2 alone had no significant effects on migration. In the present study demonstrate that Ang-2 can lead to M1/M2 shift inhibition in the ischemic muscles. Our data suggest that Ang-2-mediated reductions in MCP-1 may impair monocyte recruitment and, therefore, arteriogenesis.
A limitation to the present study is that we cannot at this time definitively determine the inhibitory effect of Ang-2 on arteriogenic activity depends on macrophages compared with pericytes. Additionally, we only detected the effect of Ang-2 at this early time point. Future studies are required in which monocyte/macrophage populations are depleted and late adaptive responses to hind limb ischaemia assessed. In addition, cross-breeding of Apo E knockout mice with Ang-2 knockout or Ang-2 transgenic mice will provide additional evidence for the role of Ang-2 in atherogenesis. Despite these limitations, we believe our study provides a preliminary results of Ang-2 involved in the complex processes contributing to collateral formation.
We found that Ang-2-treated mice exhibited impaired collateral remodelling after femoral artery ligation, as well as a reduction in the diameter of pre-existing collaterals. Ang-2 treatment also altered the expression of several growth factor genes and reduced pro-arteriogenic inflammatory responses. These findings indicate that Ang-2 could be a key regulator of post-ischaemic blood flow recovery by inhibiting the inflammatory factors required for arteriogenesis, and this may lead to potential therapeutic strategies for managing ischaemic cardiovascular diseases.
monocyte chemotactic protein-1
platelet-derived growth factor BB
platelet-derived growth factor receptor-β
vascular endothelial growth factor-A
vascular endothelial growth factor-C
vascular smooth muscle cell
XT, KY and JW designed the research study, analyzed the data and wrote the paper; XT, KY, NC, YL, XD, LW, RL, ML, MR, YL and YL performed the acquisition of data; XT, KY, NC and JW analyzed and interpreted the data. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
All data produced for the purpose of this project are available for consultation and for the public, upon request to the corresponding author (J.W) at firstname.lastname@example.org.
Ethical approval and consent to participate
The research was approved by the Southwest Medical University ethics committee, and were conducted in accordance with the guidelines of the World Medical Association’s Declaration of Helsinki.
This work was supported by American Heart Association Scientist Development Grant (10SDG2570037), National Natural Science Foundation of China Grant (81172050, 81570263), and Grant of Sichuan Province Science and Technology Agency Grant (2014FZ0104) to J. Wu.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Carmeliet P. Mechanisms of angiogenesis and arteriogenesis. Nat Med. 2000;6:389–95.View ArticlePubMedGoogle Scholar
- Heil M, Eitenmüller I, Schmitz-Rixen T, Schaper W. Arteriogenesis versus angiogenesis: similarities and differences. J Cell Mol Med. 2006;10:45–55.View ArticlePubMedGoogle Scholar
- Peirce SM, Skalak TC. Microvascular remodeling: a complex continuum spanning angiogenesis to arteriogenesis. Microcirculation. 2003;10:99–111.View ArticlePubMedGoogle Scholar
- Tressel SL, Huang RP, Tomsen N, Jo H. Laminar shear inhibits tubule formation and migration of endothelial cells by an angiopoietin-2 dependent mechanism. Arterioscler Thromb Vasc Biol. 2007;27:2150–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Tressel SL, Kim H, Ni CW, Chang K, Velasquez-Castano JC, Taylor WR, Yoon YS, Jo H. Angiopoietin-2 stimulates blood flow recovery after femoral artery occlusion by inducing inflammation and arteriogenesis. Arterioscler Thromb Vasc Biol. 2008;28:1989–95.View ArticlePubMedPubMed CentralGoogle Scholar
- Reiss Y, Droste J, Heil M, Tribulova S, Schmidt MH, Schaper W, Dumont DJ, Plate KH. Angiopoietin-2 impairs revascularization after limb ischemia. Circ Res. 2007;101:88–96.View ArticlePubMedGoogle Scholar
- Beck H, Acker T, Wiessner C, Allegrini PR, Plate KH. Expression of angiopoietin-1, angiopoietin-2, and Tie receptors after middle cerebral artery occlusion in the rat. Am J Pathol. 2000;157:1473–83.View ArticlePubMedPubMed CentralGoogle Scholar
- Asahara T, Chen D, Takahashi T, Fujikawa K, Kearney M, Magner M, Yancopoulos GD, Isner JM. Tie2 receptor ligands, angiopoietin-1 and angiopoietin-2, modulate VEGF-induced postnatal neovascularization. Circ Res. 1998;83:233–40.View ArticlePubMedGoogle Scholar
- Lekas M, Lekas P, Mei SH, Deng Y, Dumont DJ, Stewart DJ. Tie2-dependent neovascularization of the ischemic hindlimb is mediated by angiopoietin-2. PLoS ONE. 2012;7(9):e43568.View ArticlePubMedPubMed CentralGoogle Scholar
- Hammes HP, Lin J, Wagner P, Feng Y, Vom Hagen F, Krzizok T, Renner O, Breier G, Brownlee M, Deutsch U. Angiopoietin-2 causes pericyte dropout in the normal retina: evidence for involvement in diabetic retinopathy. Diabetes. 2004;53(4):1104–10.View ArticlePubMedGoogle Scholar
- Thomas M, Felcht M, Kruse K, Kretschmer S, Deppermann C, Biesdorf A, Rohr K, Benest AV, Fiedler U, Augustin HG. Angiopoietin-2 stimulation of endothelial cells induces ∝vβ3 integrin internalization and degradation. J Biol Chem. 2010;285(31):23842–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Felcht M, Luck R, Schering A, Seidel P, Srivastava K, Hu J, Bartol A, Kienast Y, Vettel C, Loos EK, Kutschera S, Bartels S, Appak S, Besemfelder E, Terhardt D, Chavakis E, Wieland T, Klein C, Thomas M, Uemura A, Goerdt S, Augustin HG. Angiopoietin-2 differentially regulates angiogenesis through Tie2 and integrin signaling. J Clin Invest. 2012;122(6):1991–2005.View ArticlePubMedPubMed CentralGoogle Scholar
- Wu J, Strawn TL, Luo M, Wang L, Li R, Ren M, Xia J, Zhang Z, Ma W, Luo T, Lawrence DA, Fay WP. Plasminogen activator inhibitor-1 inhibits angiogenic signaling by uncoupling vascular endothelial growth factor receptor-2-αVβ3 integrin cross talk. Arterioscler Thromb Vasc Biol. 2015;35(1):111–20.View ArticlePubMedGoogle Scholar
- Chalothorn D, Zhang H, Clayton JA, Thomas SA, Faber JE. Catecholamines augment collateral vessel growth and angiogenesis in hindlimb ischemia. Am J Physiol Heart Circ Physiol. 2005;289:H947–59.View ArticlePubMedGoogle Scholar
- Chalothorn D, Zhang H, Smith JE, Edwards JC, Faber JE. Chloride intracellular channel-4 is a determinant of native collateral formation in skeletal muscle and brain. Circ Res. 2009;105(1):89–98.View ArticlePubMedPubMed CentralGoogle Scholar
- Liang CC, Park AY, Guan JL. In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro. Nat Protoc. 2007;2:329–33.View ArticlePubMedGoogle Scholar
- Wong AL, Haroon ZA, Werner S, Dewhirst MW, Greenberg CS, Peters KG. Tie2 expression and phosphorylation in angiogenic and quiescent adult tissues. Circ Res. 1997;81(4):567–74.View ArticlePubMedGoogle Scholar
- Augustin HG, Koh GY, Thurston G, Alitalo K. Control of vascular morphogenesis and homeostasis through the angiopoietin-Tie system. Nat Rev Mol Cell Biol. 2009;10(3):165–77.View ArticlePubMedGoogle Scholar
- Suri C, Jones PF, Patan S, Bartunkova S, Maisonpierre PC, Davis S, Sato TN, Yancopoulos GD. Requisite role of angiopoietin-1, a ligand for the Tie2 receptor, during embryonic angiogenesis. Cell. 1996;87(7):1171–80.View ArticlePubMedGoogle Scholar
- Shimoda H, Bernas MJ, Witte MH, Gale NW, Yancopoulos GD, Kato S. Abnormal recruitment of periendothelial cells to lymphatic capillaries in digestive organs of angiopoietin-2-deficient mice. Cell Tissue Res. 2007;328:329–37.View ArticlePubMedGoogle Scholar
- Park SW, Yun JH, Kim JH, Kim KW, Cho CH, Kim JH. Angiopoietin 2 induces pericyte apoptosis via α3β1 integrin signaling in diabetic retinopathy. Diabetes. 2014;63(9):3057–68.View ArticlePubMedGoogle Scholar
- Ishigaki T, Imanaka-Yoshida K, Shimojo N, Matsushima S, Taki W, Yoshida T. Tenascin-C enhances crosstalk signaling of integrin αvβ3/PDGFR-β complex by SRC recruitment promoting PDGF-induced proliferation and migration in smooth muscle cells. J Cell Physiol. 2011;226(10):2617–24.View ArticlePubMedGoogle Scholar
- Scholz A. Angiopoietin-2 promotes myeloid cell infiltration in a β2-integrin-dependent manner. Blood. 2011;118:5050–9.View ArticlePubMedGoogle Scholar