Introduction
Stem cell factor (SCF, KIT ligand, steel factor) is a growth factor activating receptor tyrosine kinase c-Kit, which is structurally related to the platelet-derived growth factor (PDGF) receptor and is widely recognized for its role in stem cell biology [
1]. SCF produced in bone marrow by endothelial and perivascular stromal cells is a major player in forming a niche for c-Kit-positive hematopoietic stem cells [
2]. Furthermore, SCF and c-Kit are important for differentiation and function of mast cells [
3] and demonstrate multiple other biological activities. In particular, rapidly accumulating data point to the role of SCF/c-Kit in regulation of vascular wall homeostasis, which is however less investigated as compared to other effects of SCF and c-Kit.
Major vascular wall cells such as endothelial cells (EC) and vascular smooth muscle cells (VSMC) are both producers and targets of SCF [
4‐
8]. Treatment of ECs with SCF stimulates pro-angiogenic reactions including survival and migration of ECs, as well as formation of endothelial capillary tubes [
9]. In vivo data show that c-Kit deficiency inhibits proliferation of ECs and suppresses angiogenesis [
10]. Furthermore, SCF and c-Kit protect VSMCs from apoptosis [
11] and regulate contractile phenotype of these cells [
5]. SCF and c-Kit play a role in vascular disease and repair as suggested by enhanced expression of c-Kit by resident cells, as well as recruitment of circulating c-Kit-positive cells in various vascular pathologies including atherosclerosis [
12,
13], in-stent restenosis [
14], restenosis of artificial vessel grafts [
15], aortic aneurysms [
16], idiopathic pulmonary arterial hypertension [
17] and aging [
18]. Altogether, available data support the notion that SCF and c-Kit play important and multifaceted roles in vascular biology and pathology thus justifying research into the factors and mechanisms regulating expression and function of these proteins.
Accumulation of oxidized low-density lipoprotein (LDL) within arterial wall is a hallmark of atherosclerosis. Phospholipids within LDL particles are prone to oxidation due to the high contents of polyunsaturated fatty acids. Oxidized phospholipids (OxPLs) are generated by enzymatic or non-enzymatic oxidation of esterified fatty acids and demonstrate a variety of activities in vitro and in vivo [
19,
20]. The relevance of OxPLs to vascular pathology is illustrated by their ability to stimulate monocyte–endothelial interactions, inhibit endothelium-dependent relaxation of vessels, promote formation of foam cells, induce phenotypic modulation and migration of VSMCs, enhance thrombogenic activity of ECs and platelets and stimulate angiogenesis [
21]. These effects are mediated by multiple signaling pathways including cellular stress reactions called unfolded protein response (UPR) and electrophilic stress response (ESR). The major transcriptional factors mediating UPR and ESR in OxPL-treated ECs are ATF4 and NRF2, respectively [
22,
23]. OxPLs are known to accumulate in human and animal atherosclerotic vessels at high concentrations comparable to those inducing biological effects in vitro [
24]. In this work, we asked a question whether OxPLs can stimulate production of SCF. Our data show that phospholipid oxidation products increase expression of SCF by endothelial and monocytic cells and that transcription factor NRF2 plays an important role in OxPL-induced upregulation of SCF.
Discussion
Production of SCF by ECs is stimulated by inflammatory agonists and bacterial products [
7,
12,
31]. In this work, we describe for the first time additional stimuli promoting expression of SCF, namely OxPLs and electrophilic prostanoids. These compounds accumulate in atherosclerotic vessels and are relevant to the initiation and progression of the disease [
21,
32]. We observed upregulation of SCF in genetically hypercholesterolemic mice, which supports the notion that oxidized lipids upregulate SCF in atherosclerotic vessels. Induction of SCF by OxPLs potentially can have broad impact on atherogenesis due to ability of this growth factor to regulate viability, migration and differentiation of ECs and VSMCs, as well as recruit local and circulating progenitor and stem cells [
5,
6,
9]. Furthermore, SCF is a key factor regulating differentiation of mast cells, as well as their recruitment into the arterial wall where mast cells play a role both in initiation and advanced stages of atherogenesis [
33]. The importance of mast cells for atherogenesis was confirmed by decreased atherosclerosis in hyperlipidemic mice deficient in mast cells [
34‐
36]. Altogether, available data suggest that upregulation of SCF can modulate several key mechanisms promoting development and progression of lesions.
OxPLs do not induce the major inflammatory pathway NFκB that is activated by inflammatory cytokines and bacterial products [
19,
21], suggesting the involvement of additional mechanisms of SCF induction. In support of this possibility, we characterize NRF2-dependent transcription as a potential mechanism of SCF regulation by OxPLs. The involvement of NRF2 was shown using several approaches targeting different steps both upstream and downstream of NRF2 activation, including inhibition of protein kinase CK2 that is important for activation of electrophilic stress response by OxPLs [
28], knockdown of key players in ESR such as KEAP-1 and NRF2, silencing of transcriptional repressor BACH1 by miR-155 and analysis of SCF expression in vivo in arteries of NRF2 knockout mice. All these data consistently support our hypothesis about the importance of the NRF2 pathway in upregulation of SCF by lipid oxidation products.
Previously, we have shown that the ESR pathway plays an important role in upregulation of VEGF in ECs treated with OxPLs [
37]. Both VEGF and SCF protect endothelium from apoptosis and stimulate its regeneration by local mechanisms (migration, proliferation) as well as by mobilizing and attracting circulating progenitor cells. Thus, we hypothesize that the expression of VEGF and SCF in response to cellular stress induced by oxidized lipids represents a compensatory reaction aiming at the endothelial protection and repair. Our data show that these protective effects are mediated via the NRF2 pathway. However, prolonged secretion of VEGF and SCF potentially can attract monocytes, smooth muscle and mast cells and also stimulate plaque neovascularization thus leading to disease progression. Further in vivo studies are required in order to dissect specific role of OxPL-induced SCF in early and advanced stages of atherosclerosis.
Materials and methods
Materials, cell culture and lipid preparation
Tunicamycin, brefeldin, homocysteine, 4,5,6,7-tetrabromo-2-azabenzimidazole (TBB), imatinib and polyethylenimine (PEI) were obtained from Sigma-Aldrich. Human umbilical vein ECs (HUVECs), human carotid artery ECs (HCAECs) and human aortic ECS (HAECs) (all from Lonza) were grown at 37 °C in 5% CO
2 in medium M199 containing 20% FCS, 1 U/ml heparin, ECGS growth supplement (Promocell), 2 mmol/l glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin and used up to passage 5. 1-Palmitoyl-2-arachidonoyl-
sn-glycero-3-phosphocholine (PAPC) (Avanti Polar Lipids) was oxidized by an exposure to air. Formation of OxPAPC was controlled by electrospray ionization-mass spectrometry and thin-layer chromatography [
38]. For cell stimulation, the lipids were resuspended in medium M199 containing 2% fetal calf serum (FCS).
cDNA synthesis and qRT-PCR analysis of RNA
ECs were treated either with indicated concentration of OxPAPC in medium M199 containing 2% serum or with control medium for 4 h. Trizol reagent (Invitrogen) was used for RNA isolation. Microarray (Affymetrix Gene Profiling Array) profiling of mRNAs and data analysis were done at the Medical University of Vienna Genomics Core Facility. GeneAmp RNA-PCR kit and Fast SYBR Green Master Mix were used for analysis of mRNA by qRT-PCR. All these reagents were purchased from Applied Biosystems. Sequences of primers are available upon request. StepOnePlus real-time PCR cycler (Applied Biosystems) was used for quantitative real-time PCR.
Transfection with siRNA and miRNA mimic
ECs were transfected with 50 nM of either siRNA, miRNA mimic, or control oligonucleotide (all from Qiagen) in plain M199 medium for 4 h using polyethylenimine (PEI) reagent [
39]. All stimulations were performed 24 h after transfection.
ELISA and Western blotting
R&D Systems ELISA kit was used for measurements of the SCF level in cell lysates and conditioned medium. The degree of c-Kit autophosphorylation was analyzed by PathScan® Phospho-c-Kit (Tyr719) sandwich ELISA kit. Signal detection was performed spectrophotometrically at 450 nm. For SCF analysis, protein samples were denatured in Laemmli buffer and separated in SDS-polyacrylamide gels with following electroblotting to PVDF membrane (Millipore). Protein blots were probed with anti-SCF antibodies (Cell Signaling Technology). Horseradish peroxidase conjugated IgG (GE Healtcare) and SuperSignal West Femto Substrate (Pierce) were used for detection of bound primary antibodies. Chemiluminescense was detected by using FluorChem HD2 imager (Alpha Innotech).
Mice
Sixteen weeks old male C57BL/6 and ApoE−/− mice (six animals per group) were fed either a standard laboratory chow diet (6.5% fat) or a proatherogenic diet containing 15% fat and 1.25% cholesterol (Sniff) for 8 weeks. Twelve months old C57BL/6 and ApoE−/− mice hold on chow diet were used for comparison of mRNA levels in aged animals. Six months old C57BL/6 and NRF2−/− mice hold on chow diet were used for comparison of the SCF mRNA levels. Total RNA was prepared from homogenized aortas using Trizol reagent (Invitrogen) and analyzed as described above. Experiments were approved by the Medical University of Vienna animal experimentation committee and the Austrian Ministry of Science.
Statistical analysis
Two-tailed Student’s t test was used for analysis; p value less than 0.05 was considered significant. All data are represented as means ± standard deviations.
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