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Blood, 1 March 2007, Vol. 109, No. 5, pp. 1962-1970. Prepublished online as a Blood First Edition Paper on October 24, 2006; DOI 10.1182/blood-2005-10-038893.
HEMOSTASIS, THROMBOSIS, AND VASCULAR BIOLOGY Cooperation between VEGF and ß3 integrin during cardiac vascular development1 Moores UCSD Cancer Center, University of California, San Diego; 2 Core Microscopy Facility, The Scripps Research Institute, La Jolla, CA
In the developing myocardium, vascular endothelial growth factor (VEGF)–dependent neovascularization occurs by division of existing vessels, a process that persists for several weeks following birth. During this remodeling phase, mRNA expression of ß3 integrin in the heart decreases significantly as vessel maturation progresses. However, in male mice lacking ß3, coronary capillaries fail to mature and continue to exhibit irregular endothelial thickness, endothelial protrusions into the lumen, and expanded cytoplasmic vacuoles. Surprisingly, this phenotype was not seen in female ß3-null mice. Enhanced VEGF signaling contributes to the ß3-null phenotype, because these vessels can be normalized by inhibitors of VEGF or Flk-1. Moreover, intravenous injection of VEGF induces a similar angiogenic phenotype in hearts of adult wild-type mice. These findings show a clear vascular phenotype in the hearts of mice lacking ß3 and suggest this integrin plays a critical role in coronary vascular development and the vascular response to VEGF.
Integrins often cooperate with angiogenic growth factor receptors and are critical components of signaling pathways leading to angiogenesis.1 Integrins provide physical and chemical links between cells and extracellular matrix, serving as structural organizers, mechanotransducers, and signaling molecules. In this context, integrin-mediated signaling could uniquely affect the structure and function of an individual cell based on its microenvironment (extracellular matrix components, tissue oxygenation, and growth factor concentration) and expression of particular integrin subunits and/or growth factor receptors. Integrin  vß3 is either absent or expressed at low levels on normal endothelial cells in vivo but is significantly elevated on the angiogenic blood vessels associated with wounds, inflammatory sites,2 or tumors.3 Accordingly, integrin vß3 antagonists promote tumor regression by inducing apoptosis of angiogenic blood vessels while sparing the quiescent endothelial cells on pre-existing vessels.3,4 These results support the concept that vß3 regulates endothelial-cell survival to support tumor growth and angiogenesis.
However, in apparent disagreement with studies using To address the role of ß3 integrin during physiologic angiogenesis, we examined the vascular proliferation that occurs in the heart during the first few postnatal weeks. In this time frame, the vasculature in the heart remodels dramatically as the number of capillaries increases significantly by division of pre-existing vessels.13 This neonatal vascular remodeling phase supports homogeneous oxygen delivery for hypertrophying cardiomyocytes and has been associated with high levels of basic fibroblast growth factor (bFGF) and VEGF expression.13 In fact, development during the first 4 postnatal weeks requires VEGF activity, because VEGF gene ablation or receptor blockade during this period resulted in growth arrest and lethality in mice.14 The adult coronary vasculature can also remodel in response to VEGF, because adenoviral VEGF expression induces a rapid increase in Flk-1 expression on normal cardiac capillaries, which stimulates formation of mother vessels and subsequent division into daughter vessels.15 The mature adult heart also has the capacity to remodel in response to oxygen demand, because coronary capillary density can substantially increase due to chronic exercise.16 Hypoxia promotes cardiac capillary-cell growth in part by inducing myocyte VEGF expression,17 suggesting an intricate feedback system for localized control of angiogenesis. Aside from an enhanced responsiveness to vascular insult, no study has defined a vascular phenotype for the ß3-null mice. Here, we report that coronary capillaries in the adult male ß3-null mouse fail to mature, and they resemble the immature vessels observed during early postnatal development. Dysregulated VEGF and Flk-1 signaling contributes to the vascular phenotype in the ß3-null mouse, because inhibitors of this pathway can induce capillary maturation. Furthermore, intravenous injection of VEGF into normal mice induces a similar vascular phenotype in coronary capillaries, suggesting that coronary blood vessels (compared with those from other organs) are highly reactive to changes in VEGF concentration. We report here that expression of ß3 integrin in the heart decreases significantly during the first few postnatal weeks, concurrent with the cessation of physiologic angiogenesis and maturation of coronary capillaries. Together, these findings support a role for ß3 integrin in cardiac vascular development as well as responsiveness to VEGF signaling.
Pharmacologic agents The SU1498 Flk inhibitor (20 mg/kg intraperitoneally daily, 385 nM) and Cyclo-VEGI (CBO-P11) VEGF inhibitor (2 mg/kg intraperitoneally daily, 13 nM) were purchased from Calbiochem (San Diego, CA). The SKI-606 Src family kinase inhibitor18,19 was injected twice daily (10 mg/kg intraperitoneally, 236 nM). These dosing conditions effectively block tumor-cell extravasation in mice.20 Mice Mice with gene-targeted deletion of ß3-integrin are available from The Jackson Laboratory (Bar Harbor, ME). ß3-deficient mice on the SV129 background were provided by Drs D. Sheppard and R. Hynes and were genotyped as previously described.7 Ultrastructural analysis by scanning electron microscopy Mice were killed and perfused via the left ventricle with saline followed by phosphate buffer containing 2% paraformaldehyde and 4% glutaraldehyde. Tissue was excised, immersion fixed overnight, transferred to 0.1 M sodium cacodylate buffer (pH 7.3) containing 1% osmium tetroxide for 2 hours, and then dehydrated in graded alcohols. Tissue was freeze-fractured in liquid nitrogen, stored in 100% ethanol, and subjected to critical point drying and sputter coating. Samples were viewed on a Hitachi S-2700 scanning electron microscope (Hitachi, Schaumburg, IL). Ultrastructural analysis by transmission electron microscopy Mice were killed and perfused via the left ventricle with 0.1 M sodium cacodylate buffer (pH 7.3) containing 4% paraformaldehyde and 1.5% glutaraldehyde. Tissue was excised and fixed for 2 hours, transferred to 5% glutaraldehyde overnight, and then into 1% osmium tetroxide for 1 hour. Blocks were washed, dehydrated, cleared in propylene oxide, infiltrated with Epon-Araldite, and embedded in resin. Ultrathin sections were stained with uranyl acetate and lead citrate and viewed using a Philips CM-100 transmission electron microscope (Philips, Mahwah, NJ). Negatives were scanned on an Epson 1680 scanner (Epson, Long Beach, CA) using Adobe Photoshop 7.0 software (Adobe Systems, San Jose, CA). Immunohistochemistry
Routine immunostaining and imaging of frozen sections was performed as previously described1 using primary antibodies from BD Biosciences (San Diego, CA): integrin ß3/CD61 (550541); Flk-1 (550549); PECAM-1/CD31 (550274); rat IgG2a, Analysis of mRNA expression Total RNA was isolated with TRIZOL (Invitrogen, Carlsbad, CA), and reverse transcriptase–polymerase chain reaction (RT-PCR) was performed using Invitrogen Superscript III kit. Real-time PCR reactions were performed using Absolute QPCR Mix (ABgene, Rochester, NY) and cDNA analyzed using a Cepheid (Sunnyvale, CA) SmartCycler. Primer sequences are listed in Table 1. GAPDH was evaluated using 1 cycle (92°C, 900 seconds) and 40 cycles (95°C, 15 seconds; 60°C, 60 seconds). VEGF, Flk, and Flt were evaluated using 1 cycle (92°C, 900 seconds) and 40 cycles (95°C, 15 seconds; 60°C, 30 seconds; 72°C, 30 seconds). Cycle threshold was determined for each sample, samples were normalized to GAPDH, and relative gene expression levels were determined as previously described.21
For integrin ß3 mRNA expression, quantitative PCR was performed on a Cepheid SmartCycler using 1 cycle (92°C, 900 seconds) and 40 cycles (95°C, 15 seconds; 66°C, 30 seconds, 72°C, 45 seconds) with SYBR Green (Molecular Probes, Carlsbad, CA) at 1:10 000. Primers were from Maxim Biotech (San Francisco, CA): 5'-GGAAGCAGCGCCCAGATCAC and 3'-TTGTCCACGAAGGCCCCAAA. Statistical analysis Data are presented as mean ± SE, with statistical significance determined from the Student t test (P < .05). Appropriate statistics for the frequency of events measured in a population were used to compute standard error for the data in Figures 1, 3, and 7, according to Primer of Biostatistics.22
Myocardial vascular development in mice persists for several weeks following birth and is dependent on bFGF and VEGF signaling pathways.13 Vascular remodeling in the postnatal heart is characterized by division of existing vessels to support significant cardiac myocyte hypertrophy. Figure 1A. illustrates the significant reorganization of endothelial cells (identified by PECAM-1/CD31 staining) between 1 and 6 weeks of age, providing a uniform distribution of capillaries adjacent to each myocyte to support homogeneous tissue oxygenation in the adult heart tissue.
To observe the properties of these angiogenic vessels throughout the cardiac vascular hierarchy, transmission electron microscopy (TEM) was employed. For quantification, a blinded observer examined several hundred coronary capillaries per heart by TEM to determine what percentage contained angiogenic/immature vessels as evidenced by the presence of luminal protrusions, enlarged vacuoles, or thickened endothelium. Consistent with previous findings,13 we found that coronary capillaries continue to remodel for several weeks following birth. Specifically, neonate and weanling mice of either sex have a significant percentage of immature or angiogenic coronary capillaries (6% to 12%) compared with adult and senescent mice (3% to 6%) (Figure 1B).
Integrin To determine the temporal expression and localization of this integrin during development in wild-type mice, we evaluated the protein expression of ß3 integrin in the heart at different developmental stages. Figure 2A.shows validation of the hamster anti–mouse ß3 integrin antibody for immunohistochemistry, because the antibody positively stains the wild-type but not ß3 knockout heart. This reagent produced similar staining patterns using either immunofluorescence or immunoperoxidase staining. Similar to mRNA expression (Figure 1C), ß3 protein expression in the heart decreased with age (Figure 2B). In adult hearts, ß3 staining was detected only in nonendothelial cells on coronary arteries (Figure 2A-B). In the late-stage embryo hearts, the most obvious ß3-positive staining was evident near areas of vascular remodeling where vascular structures of different sizes were clustered (Figure 2C, arrows). In addition, ß3 staining in the late-stage embryo heart was associated with arteries (Figure 2D, left panel), interstitial cells (Figure 2D, middle panel), and myocytes (Figure 2D, right panel).
To test whether the loss of ß3 expression is required for coronary maturation, we examined hearts from mice lacking ß3 integrin. Previous findings have suggested that ß3-null mice have no vascular defect.5,7–9 After examining the coronary vasculature of ß3-null mice during the phase of VEGF-dependent postnatal vascular remodeling in the heart, we found that myocyte growth and angiogenesis was similar between genotypes. Specifically, there is no evidence that the vascular organization or coronary capillary density is different in the ß3-null mouse heart after careful evaluation using immunohistochemistry and intravenous lectin perfusion (data not shown). However, adult ß3-null males but not females have considerably more immature vessels than their wild-type counterparts (13% ± 1% versus 5% ± 1% of vessels examined for ß3-null and wild-type male mice, respectively). While the percentage of immature coronary capillaries decreases with age, 27-week-old senescent male ß3-null mice continue to exhibit 10% ± 2% immature vessels (Figure 3). This immature blood vessel phenotype appears to be restricted to the capillaries in the hearts of male ß3-null mice, because capillaries in liver, lung, brain, or skin did not contain thickened endothelial cells, luminal filopodia, or expanded vacuoles (not shown). Previously, we have used electron microscopy to observe vascular leak in the heart at the ultrastructural level.20,23 We identified leak as gaps between adjacent endothelial cells exposing basement membrane, attraction of platelets, platelet activation and aggregation, capillary occlusion or collapse, extravasation of blood cells, and interstitial edema. In the current study, we examined a large number of electron micrographs, but we did not observe these signs of vascular leak in the ß3-null mouse heart. Thus, it appears that vascular leak is not a consequence of the immature capillaries in ß3-null mice.
By 5 weeks of age in wild-type mice, the coronary vasculature is composed of mature vessels with consistent endothelial-cell thickness and a smooth luminal surface with very few protrusions (Figure 4A-B). In contrast, coronary capillaries in adult male mice lacking ß3 integrin closely resemble angiogenic blood vessels and immature blood vessels previously reported in neonatal mice.13 To our surprise, we observed no such defect in female mice lacking vß3. While normal blood vessels have a uniform endothelial thickness (Figure 4A-B), endothelial-cell thickness in male ß3-null hearts varies considerably (Figure 4C-D). The thickened endothelium is often associated with the more frequent appearance of organelles such as mitochondria or ribosomes (Figure 4C-D). Like the invasive filopodia, these are characteristics of activated, angiogenic endothelial cells, such as those on immature neonatal blood vessels.24
The filopodia observed in ß3-null mouse coronary capillaries are exclusively luminal processes, as opposed to the outward sprouting of endothelial cells often associated with some angiogenic blood vessels. The luminal protrusions appear to originate from cell-cell junctions (Figure 4D, arrow) as well as from the continuous cytoplasm within a single endothelial cell (Figure 4C, arrow). An example of a single endothelial cell from which luminal protrusions are extending from cell junctions on either side as well as from the middle of the cytoplasm (arrows) is shown in Figure 4E. Despite the immature vascular phenotype, adhesive junctions between adjacent endothelial cells appear to remain intact (Figure 4D-E), suggesting that the vascular barrier is not disrupted. In many cases, filopodia protruding into the lumen often appear to extend toward (Figure 4F) and make additional adhesive contacts with adjacent filopodia or endothelial-cell membrane (Figure 4G-H). Electron-dense patches between endothelial cells are representative of adhesive contacts,25 suggesting that the tips of these filopodia are actively forming intercellular junctions leading to communication or adhesion events within these capillaries. These interactions between filopodia often appear to partition a portion of the capillary lumen, which is consistent with angiogenesis by the division of existing vessels. Some ß3-null coronary capillaries appear to contain expanded vacuoles of varying size (Figure 5A-D). Because no cell-cell junctional staining is visible, these vacuoles appear to be contained within the cytoplasm of a single endothelial cell. Although less frequent, we did observe capillaries that appear to be dividing by intussusception (Figure 5E), the formation of transluminal pillars to facilitate vessel division.26
These ultrastructural observations made using TEM were also confirmed using scanning electron microscopy (SEM). Hearts from adult wild-type mice reveal normal coronary capillaries with smooth luminal surfaces (Figure 6A-B). However, invasive filopodia extending into the lumen of coronary capillaries can be observed in the adult male ß3-null mouse heart (Figure 6C-E, arrows). In some ß3-null vessels, filopodia appear to bridge across the lumen to contact the opposing vessel wall (Figure 6E, arrow). Pockets consistent with the extended vacuoles observed via TEM can also be observed (Figure 6F, asterisk).
Enhanced responsiveness to VEGF in the ß3-null mice has previously been attributed to increased endothelial-cell expression of Flk-1.5,9 Therefore, we evaluated Flk-1, Flt-1, and VEGF mRNA levels in total left ventricle homogenates from adult ß3-null male mice compared with wild type. We found no significant differences in VEGF, Flt-1, or Flk-1 mRNA expression levels between adult male wild-type and ß3-null mice (Table 2). However, we did detect a 60% reduction in VEGF mRNA expression in female ß3-null mice relative to wild-type mice (Table 2), which may represent a compensatory mechanism to facilitate vessel maturation not observed in male mice.
Together, these findings suggest that the immature blood vessel phenotype may be due to increased sensitivity to VEGF rather than an increase in either VEGF or VEGF receptor expression in the male ß3-null mice. To determine whether VEGF signaling directly contributes to the angiogenic phenotype in the ß3-null mouse, we treated mice with inhibitors of either VEGF or Flk-1 and examined their coronary arteries to quantify the level of vascular maturation by enumerating the frequency of luminal protrusions, thickened endothelium, or enlarged vacuoles. We found that the angiogenic phenotype in adult male ß3-null mice could be suppressed by treatment with inhibitors of either VEGF or Flk-1 but not by treatment with inhibitors of other downstream signaling molecules such as Src family kinases (Figure 7). This experiment confirms that blocking VEGF (or Flk-1) activity in the ß3-null male mouse is sufficient to inhibit the immature, angiogenic characteristics of the endothelial cells lining the capillaries in the heart.
Because the hypersensitivity to VEGF in the ß3-null male mouse could effectively be normalized by treatment with inhibitors of either VEGF or Flk-1, we tested whether the mature endothelium in a wild-type mouse could likewise remodel in the presence of increased VEGF concentration. Therefore, we performed a direct intravenous injection of VEGF and examined the coronary endothelial cells for the presence of luminal protrusions, thickened endothelium, or enlarged vacuoles. We found that simple injection of VEGF induces these angiogenic characteristics in the wild-type mouse heart to a similar extent as we observed in the male ß3-null mouse (Figure 7). This finding suggests that increased VEGF concentration alone is sufficient to induce an immature or angiogenic phenotype in the coronary capillaries in an otherwise normal mouse. However, when we injected VEGF into female wild-type or ß3-null mice, we did not observe the angiogenic phenotype in the coronary capillaries (Figure 7). These data are consistent with the concept that females are protected from the occurrence or progression of some types of vascular disease. This finding warrants further investigation to determine how VEGF signaling in blood vessels in females may differ from counterparts in males. Taking all data into account, there appears to be a fine balance of VEGF signaling that dictates the morphology of the endothelial luminal surface.
We have established that cooperative signaling between growth factors and integrins regulates blood vessel development in the postnatal heart. This regulatory phase of VEGF-mediated vascular development depends in part on integrin ß3, because (1) ß3 expression decreases as vessels mature in wild-type mice, (2) male mice lacking ß3 show immature capillary vessels throughout adulthood, (3) immature capillaries can be induced in wild-type mice via intravenous injection of VEGF, and (4) the ß3-null phenotype can be normalized by treatment with VEGF or Flk-1 inhibitors. We report a vascular phenotype consisting of immature coronary capillaries selectively in the hearts of male ß3-null mice. The endothelial cells within these vessels contain luminal protrusions that fuse to divide the vessel lumen, similar in appearance to the VEGF-dependent vascular remodeling that occurs during the first few postnatal weeks. Female ß3-null mice express 60% lower levels of VEGF mRNA in their hearts, suggesting a possible compensatory mechanism accounting for their lack of a vascular phenotype. Our findings raise important questions: What role do ß3 integrins play during vascular development, and how do ß3 integrins influence growth factor receptor signaling and angiogenesis?
Integrin vß3 is highly expressed on angiogenic blood vessels, such as those associated with tumors,3 ischemic tissues,27 or inflammatory sites.2 During development, ß3 integrin expression is restricted to a limited number of tissues compared with v expression.28 Previous studies report that ß3 mRNA expression levels are not detectable on a whole tissue basis except for the liver in the developing embryo.28 In situ hybridization shows very localized ß3 expression in platelet-precursor megakaryocytes in the liver and in the border between developing smooth muscle and submucosa in the gastrointestinal tract.28 Endothelial cells in culture often express ß3 integrin, although these cells are grown under proliferative culture conditions rather than the quiescent situation in vivo. Although ß3 integrin mRNA expression has been detected in vitro on cultured myocytes, fibroblasts, and endothelial cells isolated from adult hearts,29 ß3 is not normally expressed in adult blood vessels, except for microvessels in the lung.30,31 Following myocardial infarction, ß3 mRNA expression has been detected in the heart on vascular structures at the edge of the infarct zone.32 In this study, we report that ß3 mRNA and protein expression in the left ventricle decreases significantly with age following birth on a similar time line as the maturation of coronary capillaries (Figures 1–2).
Immunohistochemical staining suggests that ß3 protein expression is associated only with arteries in the adult heart but with a variety of cell types in the developing heart (Figure 2). These data raise the interesting question: If ß3 expression is not present on capillaries, why are capillaries affected in ß3-null mice? There are several possible explanations: (1) ß3 may indeed be expressed on capillaries, but below levels of detection using immunohistochemistry, yet it is possible that relatively low ß3 expression on adult endothelium may provide an important signal to maintain vessel maturity. (2) ß3 may be absent on capillaries, but lack of expression may be relevant on supporting stromal cells or other cell types that influence vascular maturation. It is feasible that supporting stromal cells contribute to normal vascular development by their direct interaction with vascular cells or by producing and releasing growth factors, cytokines, or extracellular matrix. Myocytes, smooth muscle cells, or fibroblasts may secrete growth factors that influence capillary maturation. This possibility is supported by the established roles of bFGF and VEGF during postnatal vascular development in the heart13 and by our own data in Figure 7 suggesting that inhibitors of Flk-1 signaling can offset the loss of ß3 integrin. (3) The lack of ß3 expression may change the fate of endothelial cells or angiogenic precursor cells at the stem-cell level. The lack of ß3 on endothelial-cell precursors could potentially prevent the later evolution of these cells into mature, quiescent endothelium. Generating a mouse with endothelial-specific knockout of ß3 integrin may provide means to address these issues as well as determine whether the lack of Regulation of growth factor signaling and angiogenesis by ß3 integrins
Previous studies show that antagonists of Reynolds and coworkers have previously reported that lung endothelial cells isolated from ß3-null mice show increased expression of Flk-1, which they suggest as an explanation for the enhanced angiogenic response in these mice.5 It is possible that cultured cells grown under proliferative conditions may show differential expression or activity of a variety of proteins that are not relevant to those expressed on endothelial cells within blood vessels. It is unclear whether the coronary capillary phenotype we observe is due to altered endothelial-cell expression of Flk-1 that we cannot resolve in our whole tissue homogenates or whether Flk-1 expression is not altered in these mice in vivo. To investigate whether localized changes in Flk-1 expression may account for the angiogenic phenotype in the ß3-null male mice, we evaluated whether Flk-1 protein expression was increased in the coronary capillaries in ß3-null mice compared with wild type. However, immunostaining revealed no overt differences in Flk-1 expression or localization between genotypes (data not shown). Consistent with this, we found no significant differences in Flk-1 mRNA expression in ß3-null mice (Table 2). Interestingly, we found Flk-1 protein expression on capillaries in the heart but not on arteries, arterioles, venules, or veins (data not shown). This differential expression suggests that the angiogenic or vascular permeability responses to VEGF via Flk-1 may occur solely within the capillary compartment in the adult heart. To address the mechanism of increased VEGF sensitivity, we have shown that inhibiting VEGF signaling via treatment with an Flk-1 inhibitor is sufficient to normalize the immature capillary phenotype (Figure 7). We also report that female ß3-null mice that do not exhibit this phenotype have lower VEGF expression (Table 2). Lastly, we show that injecting normal mice with VEGF can induce this phenotype (Figure 7). Together, these studies suggest that a balance between VEGF expression and Flk-1 activity can dictate capillary maturation in the postnatal heart and that ß3 integrin expression plays a role in this VEGF/Flk-1 balance. Some but not all aspects of the male ß3-null cardiac vascular phenotype are consistent with postnatal or VEGF-induced capillary remodeling. While ß3-null capillaries exhibit endothelial thickening and luminal protrusions, these apparently do not result in increased capillary density. This suggests that the ß3-null coronary vasculature is not receiving all of the necessary signals to induce actual vessel division and capillary proliferation, such as removal of pericyte coverage or disruption of the underlying basement membrane. This concept is consistent with the hypothesis that increased endothelial-cell VEGF responsiveness is responsible for the angiogenic vessel phenotype, which can be normalized in ß3-null mice by treatment with pharmacologic inhibitors of Flk-1 or VEGF or induced in wild-type mice by intravenous injection with VEGF. Compared with adenoviral VEGF expression, intravenous VEGF injection provides a much more transient stimulus, and thus may induce an endothelial-cell reaction, but would not be expected to produce a long-term angiogenic response. A sex-specific vascular phenotype Female ß3-null mice, which display no overt phenotype, express lower levels of VEGF in the heart compared with their male counterparts. Interestingly, male (but not female) wild-type mice subjected to intravenous VEGF for just 2 hours develop the same angiogenic phenotype. Taken together, these findings suggest that the balance between VEGF concentration and VEGF receptor activation can shift cardiac endothelial cells from a quiescent to an angiogenic phenotype. The finding that VEGF did not induce this phenotype in female mice could be attributed to the fact that estrogen modulates cytokine-induced activation of endothelial cells38 and influences angiogenesis and VEGF receptor expression in coronary vessels.39 A recent review by Cid and coworkers examines the impact of estrogens on the vascular endothelium.40 Furthermore, steroid hormones can regulate expression of many genes (including integrins41) by altering their mRNA stability.42 It is possible that estrogen participates in a feedback mechanism regulating VEGF signaling, which could explain sex-specific influence of ß3-null expression. However, if hormones protect young ß3-null females, this difference should balance out in old age. However, we found that even senescent (more than 20-week-old) ß3-null females had normal coronary capillary endothelial cells (not shown), suggesting that ß3 integrins may be required for proper cardiovascular development rather than maintenance of a quiescent endothelium. Previous reports on ß3-null mice have not specified whether experiments used male or female mice. In these studies, individual experiments may have pooled data from both sexes, thereby masking the magnitude of consequences of ß3-null expression. Our only clue as to the mechanism for this sex-specific genotype is our finding that female ß3-null mice have lower VEGF mRNA expression in their hearts despite equivalent Flk-1 expression. Our data may provide unique insight as to sex-specific responses to ischemic insult, hypoxia, and VEGF regulation during cardiovascular disease and cancer. Notably, we have provided the first demonstration of a sex-specific phenotype in an integrin knockout mouse. The relationship between integrins, hormones, and growth factors warrants further investigation despite significant advances in our understanding of the molecular and cellular basis of cardiovascular sex differences.43 Conclusions Our data support a role for ß3 integrin in dictating sensitivity to VEGF signaling, because we can block the capillary phenotype in ß3-null mice by treatment with a Flk-1 inhibitor and can induce this phenotype in normal mice by injection with VEGF. It is this finding that is particularly interesting, because previous studies have not adequately addressed whether ß3 expression on tumor-associated blood vessels is a proangiogenic or antiangiogenic response. We have used TEM to examine tumor-associated blood vessels that express high levels of ß3 and found endothelial-cell protrusions similar to the ones in immature coronary vessels (data not shown). In this respect, our data suggest that increased ß3 expression on small vessels may serve to counteract angiogenic stimuli and promote vessel quiescence rather than potentiate blood vessel proliferation. The endothelial-cell abnormalities in ß3-null mice do not appear to impact cardiac development and function, suggesting that the physiologic significance may be modest. However, modest changes in ß3 expression could impart angiogenic properties to endothelial cells and thus could contribute to the pathologic progression of disease. In fact, ß3 integrin is not expressed on normal blood vessels,3,27 but its expression increases in tumor endothelium,3 cardiac blood vessels following myocardial infarction,32 and cerebral blood vessels following ischemic stroke.27 Our data show malformed vessels in integrin knockout mice not previously known to have a vascular phenotype and suggest a new link between integrins and VEGF. Because female mice appear to produce less VEGF in their hearts, regulation of VEGF expression may play a compensatory role in vascular homeostasis, which is itself a very important observation. Our data raise the following new and important questions: What does the dysregulation of VEGF do? How is VEGF sensitivity in the heart different from that in other organs? Is vascular development and remodeling in the heart unique? Understanding these issues will be critical for treating cardiovascular disease and cancer, for which VEGF is a current therapeutic target. In summary, we have defined a vascular phenotype for male ß3-null mice in which coronary capillary maturation does not occur during the first few postnatal weeks, suggesting a role for integrin ß3 during VEGF-dependent postnatal vascular remodeling in the heart. The capillary maturation process is dependent on VEGF and Flk-1 signaling, because inhibitors of these pathways normalize the immature coronary capillaries in ß3-null mice and intravenous injection of VEGF into normal wild-type mice induces a similar angiogenic phenotype. Together, these studies suggest that ß3 integrin plays a critical role in vascular development/maturation and regulating the vascular sensitivity to VEGF in the heart.
Contribution: S.M.W. designed research, performed research, collected data, analyzed data, and wrote the paper; J.N.L. designed research, performed research, and collected data; L.A.B., K.M.L.-F., and J.C. performed research and collected data; M.R.W. performed electron microscopy; and D.A.C. designed research, analyzed data, and wrote the paper. Conflict-of-interest disclosure: The authors declare no competing financial interests. Correspondence: David Cheresh, Moores UCSD Cancer Center, 3855 Health Sciences Dr #0803, La Jolla CA 92093-0803; dcheresh{at}ucsd.edu.
This work was supported by National Institutes of Health (NIH) grants CA50286, CA45726, CA95262, HL57900, and HL78912 (D.A.C.) and 1F32HL69701 (S.M.W.). We thank Peggy Hogan and Theresa Fassel for technical assistance and Steve Barlow for performing the scanning electron microscopy at the San Diego State University Electron Microscopy Facility. Dean Sheppard and Richard Hynes kindly provided founder mice for our ß3-null mouse colony.
Submitted October 21, 2005; accepted October 13, 2006.
Prepublished online as Blood First Edition Paper, October 24, 2006
DOI: 10.1182/blood-2005-10-038893
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Abstract
Introduction
isotype control (559073); and hamster IgG1, 
