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Abstract |
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Objective— Cardiac ankyrin repeat protein (CARP) is a transcription factor-related protein that has been studied most extensively in the heart. In the present study, we investigated the expression and the potential function of CARP in human and murine atherosclerosis.
Methods and Results— CARP expression was observed by in situ hybridization in endothelial cells lining human atherosclerotic plaques, whereas lesion macrophages were devoid of CARP. Furthermore, we established that CARP mRNA and smooth muscle (SM) actin antigen both colocalized in a subset of intimal smooth muscle cells (SMCs), whereas no CARP mRNA was encountered in quiescent SMCs in the media. The CARP mRNA-expressing intimal SMCs were distinct from intimal SMCs that synthesized the activation marker osteopontin or proliferating cell nuclear antigen. In addition, we showed that activin A, a member of the TGFß superfamily that prevents SMC-rich lesion formation, induced CARP mRNA expression in cultured SMCs.
Conclusions— Based on our data and the knowledge that CARP reduces the proliferation of cultured SMCs, we propose that CARP is involved in inhibition of vascular lesion formation.
Key Words: cardiac ankyrin repeat protein endothelial cells smooth muscle cells activin A atherogenesis
Introduction |
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Until now, the function of CARP has been studied most extensively in the heart. Increased CARP expression is found in hypertrophy of the heart under physiological conditions (cardiogenesis) or pathophysiological conditions.3–7 Even though there are conflicting data on modulation of cardiac gene expression by CARP, a detailed analysis revealed that CARP prevents the activation of the MLC-2v promoter by binding the transcription factor YB-1 and consequently inhibits the activity of YB-1.4 Regulation of CARP expression in the heart is at least in part directed by the transcription factors Nkx2.5 and GATA-4, which are known to cooperate in the regulation of various cardiac genes.6,9–11 In skeletal muscle, CARP expression is induced in subcompartments of the muscle during normal morphogenesis or after denervation.2 In addition, in a myogenic cell line, CARP expression was upregulated on differentiation of these cells.2 In summary, CARP has been proposed to play a role in heart and skeletal muscle (re)differentiation.
During atherosclerosis, endothelial cells and SMCs become activated and play a key role in intima formation. Activated endothelial cells attract inflammatory cells, and SMCs proliferate and migrate into the subendothelial space. A potential role for CARP in atherosclerosis is suggested from the knowledge that endothelial cells and SMCs synthesize CARP on stimulation. Specifically, in cultured endothelial cells, inflammatory cytokines, such as interleukin-1 and tumor necrosis factor-, have been shown to increase CARP expression.1 In cultured SMCs, CARP expression is enhanced by transforming growth factor (TGF)-ß via the Smad signal transduction pathway, involving a TGF-ß-response element in the CARP promoter. Importantly, adenovirus-mediated overexpression of CARP results in decreased proliferation of SMCs.8 Furthermore, CARP mRNA synthesis increased in balloon-injured rat aorta, as determined by reverse-transcription polymerase chain reaction (RT-PCR). Collectively, these data suggest a role for CARP during atherogenesis.8 However, the cellular origin and exact localization of CARP expression in the (atherosclerotic) vessel wall has not been assessed. Therefore, we have investigated CARP expression in human and murine atherosclerotic lesions and demonstrate that only a subset of endothelial cells and SMCs express CARP. We have recently shown that activin A, a TGF-ß family member, prevents the formation of SMC-rich vascular lesions by maintaining the contractile SMC phenotype.12 In the current study we show induction of CARP mRNA expression in cultured SMCs on stimulation with activin A and we hypothesize a role for CARP downstream of activin A in preventing lesion formation.
Methods |
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Murine vascular tissues were obtained from APOE*3-Leiden mice that were fed a Western-type (ie, high-fat/cholesterol) diet, resulting in the formation of macrophage-derived foam cell-rich lesions that contained limited numbers of intimal SMCs, as has been described by van Vlijmen et al.13 After 16 to 24 weeks of this Western-type diet, the mice were sacrificed, and hearts and aortas were harvested. Sections were taken at the aortic valves. At this time point, blood cholesterol levels of the APOE*3-Leiden mice were 38.5±7.8 mmol/L, in contrast to 6.9±0.2 mmol/L in control mice. In addition, murine lesions were obtained from mice of a C57Bl6 genetic background that underwent carotid artery ligation. The carotid artery ligation model has been developed by Kumar and Lindner and results in the induction of SMC-rich lesions containing hardly any macrophages in the intima.14 Murine tissues were fixed by perfusion fixation with 4% (v/v) paraformaldehyde in PBS and were paraffin-embedded after resection. The sections (5 µm) were mounted on SuperFrost Plus glass slides.
Immunohistochemistry
Antibody 1A4 (DAKO) recognizes human and murine SM -actin and was used to detect SMCs, HAM56 (DAKO) recognizes human macrophages, and PC10 detects proliferating cell nuclear antigen (PCNA) (DAKO). Immunohistochemistry was performed on sections that were rehydrated and blocked with 10% (v/v) preimmune goat serum (DAKO). Subsequently, the sections were incubated overnight at 4°C with specific antibodies in Tris-buffered saline (10 mmol/L Tris-HCl, pH 8.0, 150 mmol/L NaCl), followed by incubations with biotinylated secondary antibodies that were detected with streptavidin-horseradish peroxidase conjugates (DAKO). Peroxidase activity was visualized with amino-ethyl carbazole and hydrogen peroxide. The PCNA protocol involved antigen retrieval in 10 mmol/L citrate buffer at pH 6.0. The sections were counterstained with hematoxylin, except for the PCNA staining.
In Situ Hybridization
Riboprobes were synthesized and radiolabeled with [35S]-UTP (Amersham). For human CARP, a probe corresponding with the 454- to 1261-bp fragment of GenBank No. was used. For murine CARP, bp 218 to 872 of GenBank No. was used, and for murine osteopontin, bp 1 to 663 of GenBank No. was used as probes. Both antisense and sense riboprobes were assayed, of which the latter ones served as controls for specificity of the signal. In situ hybridization was performed by standard procedures.15
To combine in situ hybridization and immunohistochemistry, human sections were blocked with 10% (v/v) preimmune goat serum in Tris-buffered saline after the last washing step of the in situ hybridization protocol. Thereafter, antibodies were applied, and the immunohistochemical protocol was continued. After visualization of peroxidase activity, the sections were covered with nuclear research emulsion (ILFORD Imaging UK Limited) and exposed. After the slides were developed, these double-stained sections were counterstained with hematoxylin. In all in situ hybridization experiments, for each specimen 3 to 6 consecutive sections were applied.
Cell Culture
SMCs were obtained from human saphenous vein or iliac artery explant cultures and maintained at 37°C in a humidified 5% CO2 chamber in 40% (v/v) Medium-199 with L-glutamine/L-amino acids, 40% (v/v) RPMI 1640 HEPES-buffered/L-glutamine, and 20% (v/v) human serum supplemented with penicillin and streptomycin (GIBCO BRL). Cultured SMCs were characterized by immunofluorescence with the anti-SM -actin 1A4 antibody.15 The SMCs show uniform fibrillar staining. Confluent SMC cultures were made quiescent by incubation overnight in serum-free medium, supplemented with insulin (5 µg/mL), transferrin (5 µg/mL), selenite (5 ng/mL; GIBCO-BRL), and vitamin C (0.2 mmol/L). Subsequently, 100 ng/mL recombinant human activin A and 10 ng/mL TGFß (Roche Diagnostics) was added to the culture medium during 0, 2, 8, 24, and 48 hours of the venous SMCs. The arterial SMCs were stimulated with various concentrations activin A (0, 10, 50, and 100 ng/mL) for 6 hours. Purified, recombinant human activin A (lot #15365 to 361) was obtained from Dr. Pawson through the National Hormone and Pituitary Program, the National Institute of Diabetes and Digestive and Kidney Disease, and the US Department of Agriculture (Bethesda, Md).
RNA Isolation and Northern Blotting
Total RNA was isolated from cultured cells by using the TRIzolTM method (GIBCO-BRL). Ten micrograms of total RNA per lane was subjected to electrophoresis on a formaldehyde-agarose gel and transferred to Hybond nylon membranes (Amersham). The blot was prehybridized at 42°C in formamide-containing buffers according to standard procedures. Probes were radiolabeled with [32P]-ATP (Amersham) applying the random primer labeling mix (GIBCO BRL). To detect human CARP mRNA, a cDNA probe of 807 bp (454- to 1261-bp fragment of GenBank No. ) was applied and for GAPDH a fragment of 65 bp (480 to 545 bp of GenBank No. ). SM -actin and SM22 mRNA were detected with a radiolabeled oligonucleotide and a random hexamer-radiolabeled cDNA probe, respectively, as has been described previously.15
RT-PCR
cDNA was generated by reverse transcription of RNA samples by using oligo dT primers and Superscript II (GIBCO-BRL). CARP and hypoxanthine guanine phosphoribosyltransferase (HPRT) sequences were amplified from the cDNA samples with Taq DNA polymerase (Amersham) and transcript specific primers sets (CARP: 5'-GGGCCAACTCCAGGGATTCC-3', rev: 5'-GGCCATGCCTTCAAAATGCCA-3' and HPRT; fwd: 5'-TAATTATGGACAGGACTGAACG-3', rev: 5'-CACAATCAAGACATTCTTTCCAG-3'). A standard PCR program with 65°C as annealing temperature resulted after 35 cycles in CARP and HPRT-specific products that were analyzed by agarose gel electrophoresis.
Results |
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To assess the expression profile of CARP in SMCs and macrophages, two consecutive sections were assayed for CARP mRNA and simultaneously stained with specific antibodies to detect either SMCs (C) or macrophages (F). Obviously, the CARP-positive cells, lining the lumen of the vessel, are CARP-expressing endothelial cells (F). The intima of this advanced lesion contains a thin fibrous cap, a large macrophage infiltrate, extracellular lipid pools, and a small acellular core. Colocalization of CARP mRNA (black dots) and the SMC marker SM -actin (red) show that CARP is expressed in a subset of intimal SMCs (C). CARP-positive intimal SMCs were seen in the fibrous cap (C) and in the SMC-rich shoulder of the lesion (see online Figure IIA, which can be accessed at http://atvb.ahajournals.org). CARP expression is absent in medial SMCs and, in addition, has never been observed in macrophages (illustrated inF).
To establish whether CARP expression correlates with the proliferative state of SMCs in the intima, PCNA staining was performed (Figure II). The subset of CARP-expressing SMCs did not colocalize with the population of PCNA-positive cells in the intima, suggesting that CARP is not involved in SMC proliferation.
CARP Expression in Murine Atherosclerotic and Restenotic Lesions
To further delineate the expression profile of CARP in atherogenesis, we analyzed CARP expression in murine diet-induced atherosclerotic lesions and in lesions formed in a restenosis model. In APOE*3-Leiden transgenic mice, a Western-type diet results in the formation of lesions containing lipid-laden macrophages. Interestingly, the occasional SMCs present in these lesions, which form a fibrous cap, do express CARP . Clearly, CARP mRNA colocalizes with SM -actin as shown in a consecutive section . CARP is only expressed in intimal SMCs and was never observed in medial SMCs or macrophages in this murine model, which is similar to our observations with human atherosclerotic specimens. Determination of the number of CARP-positive SMCs at different time periods of Western-type diet revealed that CARP reaches optimal expression after 16 weeks of diet, which correlates with the increased presence of intimal SMCs in these lesions (see online Figure IIIA, which can be accessed at http://atvb.ahajournals.org).
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To evaluate the expression of CARP in intimal SMCs in further detail, we studied its expression pattern in lesions generated in the murine carotid artery ligation model. In the SMC-rich lesions induced in this model, CARP mRNA expression is present in a subset of intimal SMCs, indicating that intimal SMCs do not form a homogenous population. To correlate CARP expression with a SMC phenotype, we analyzed in consecutive sections the expression of osteopontin and PCNA, which are markers for proliferative SMCs.17,18 In murine lesions, osteopontin may be considered a relatively broad activation marker, whereas PCNA is only expressed during a short period of the cell cycle. A typical lesion is presented , showing that the expression of CARP (D) does neither colocalize with osteopontin (E) nor with PCNA (F), which may indicate that CARP expression is not associated with intimal SMC proliferation. Analysis of temporal and spatial expression of CARP revealed that after 1 week of ligation, most CARP-positive cells are present in the media (Figure IIIB). At this time point, hardly any intima has been formed. Yet, medial SMCs are activated, express osteopontin (data not shown), and have started to proliferate and migrate to initiate the formation of a lesion. After 2.5 and 4 weeks of ligation, an extensive intima is present containing a subpopulation of CARP-positive SMCs. Already at 2.5 weeks, the medial SMCs are quiescent again and accordingly show only an occasional CARP-expressing SMC.
Note that we do not observe CARP expressing endothelial cells in the murine lesions. This could be either the result of the low number of endothelial cells present in the murine lesions, a different timeframe of CARP expression in the mouse, or a species difference between mice and humans.
Effect of Activin A Stimulation on CARP Expression
CARP expression is induced in SMCs by TGF-ß via the Smad signal transduction pathway, which is mediated by a TGF-ß response element in the CARP promoter.8 Activin A is a member of the TGF-ß superfamily, and its signaling is mediated through the same Smad proteins as TGF-ß signaling. To assess a potential effect of activin A on CARP expression, we added purified activin A for 2 to 48 hours to cultured SMCs and performed Northern blotting analyses. The intensity of the bands, as determined by phosphorimager analysis and after correction for the GAPDH control, was plotted in line graphs (See online Figure IV, which can be accessed at http://atvb.ahajournals.org). Activin A increased steady-state CARP mRNA levels in SMCs, showing a 2.8-fold augmented expression from 8 to 48 hours. SM -actin and SM22 were continuously increasing (ultimately 10.8-fold and 2.9-fold, respectively) after 48 hours of activin A treatment, indicating the transition of the cellular phenotype into a contractile, nonproliferative SMC phenotype.15 TGF-ß was added to the cultured SMCs as a control, leading to similar increase in CARP and SM -actin expression levels (both 2.9-fold). In addition, activin A stimulation of arterial SMCs induced CARP expression in a concentration-dependent manner as determined by RT-PCR . Induction of CARP expression was already observed at an activin A concentration of 10 ng/mL and was optimal at 50 ng/mL.
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Discussion |
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Top Abstract Introduction Methods Results Discussion References |
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Based on these data, we propose that the transient expression of CARP in intimal SMCs may be involved in preventing vascular lesion formation.
Received August 28, 2002; accepted September 6, 2002.
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