Interleukin-1β Expression Is Required for Lysophosphatidic Acid-Induced Lymphangiogenesis in Human Umbilical Vein Endothelial Cells

Lysophosphatidic acid (LPA) is a lipid mediator which binds to G-protein-coupled receptors and regulates various cellular responses, including inflammation of endothelial cells. Interleukin- (IL-) 1β, a proinflammatory cytokine, is elevated upon LPA treatment in human umbilical vein endothelial cells (HUVECs). Previous studies indicated that LPA upregulates vascular endothelial growth factor- (VEGF-) C and lymphatic marker expressions in HUVECs. However, the relationships between LPA-induced VEGF-C and IL-1β expressions are not clear. In this paper, we demonstrated that, in the presence of AF12198, an inhibitor of the IL-1 receptor abolished LPA-induced VEGF-C and lymphatic marker expressions in HUVECs. Furthermore, LPA-induced in vitro tube formation of HUVECs was also suppressed by pretreatment with AF12198. Our results suggest that LPA-stimulated lymphangiogenesis in HUVECs is mediated through IL-1β-induced VEGF-C expression.

Lymphangiogenesis, the process of growth and formation of new lymphatic vessels [14], occurs in normally developing tissues and pathological processes, particularly inflammation, wound healing, and cancer metastasis [15,16]. Like angiogenesis, lymphangiogenesis is regulated by various growth factors, cytokines, and hormones [17]. Among these regulators, vascular endothelial growth factor-(VEGF-) C is considered to be a major regulator of the lymphangiogenic process [18,19]. In transgenic mouse skin and mature chick chorioallantoic membrane models, VEGF-C is known to induce both lymphangiogenesis and angiogenesis [20,21]. Several recent studies reported that lymphatic vessels accumulate adjacent to tumor tissues highly expressing VEGF-C, and an increase in the lymphatic diameter may contribute to promotion of tumor metastasis [22]. We demonstrated that LPA stimulates VEGF-C and lymphatic markers, including Prox-1, LYVE-1, and podoplanin expressions in human umbilical vein endothelial cells (HUVECs) [23,24]. In addition, sphingosine-1phosphate (S1P), another bioactive lysophospholipid, was also demonstrated to induce lymphangiogenesis [25]. Those results indicate that bioactive lipids may be important lymphangiogenic regulators.

International Journal of Inflammation
Despite studies suggesting connections between inflammation and lymphangiogenesis, the molecular mechanisms that regulate lymphatic vessel formation remain largely unclear. Proinflammatory cytokines, such as interleukin-(IL-) 1β and tumor necrosis factor-(TNF-) α, were shown to enhance the expression of VEGF-C by fibroblasts [26]. Moreover, IL-1β-induced lymphangiogenesis is mediated through VEGFR-3 in the mouse cornea [27]. Those findings suggest that cytokines are important mediators of lymphangiogenesis.
In our previous studies, we demonstrated that LPA upregulates VEGF-C and lymphatic marker expressions in HUVECs [23,24]. Moreover, we also demonstrated that LPA upregulates IL-1β messenger (m) RNA expression in HUVECs [28]. In this study, we postulated that IL-1β, the main proinflammatory cytokine, regulates LPA-induced lymphangiogenesis in HUVECs. In this report, we showed that LPA upregulated VEGF-C and lymphatic marker expressions in HUVECs in LPA1/3-, EGFR transactivation-, and IL-1-dependent manners. Furthermore, we also demonstrated that LPA-induced HUVEC tube formation in vitro was suppressed by pretreatment with these inhibitors. These data demonstrate for the first time that IL-1β may act as an essential mediator for LPA-induced lymphangiogenesis in HUVECs.

Cell
Culture. Human umbilical cords were kindly provided by National Taiwan University Hospital (Institutional Review Board approval no. 9561709146). HUVECs were isolated from fresh umbilical cords by treatment with 0.1% collagenase type I (Sigma) in cord buffer at 37 • C for 30 min. Then endothelial cells (ECs) were collected and centrifuged. HUVECs were cultured on 1% gelatin-coated (Sigma) 10 cm plates in 60% M199 medium supplemented with 100 U/mL penicillin, 100 mg/mL streptomycin, 20% FBS, and 20% EGM. Cells underwent one passage weekly. Cells were subcultured after trypsinization and used in experiments until passage 4.

Determination of IL-1β Protein Expression by an Enzyme-
Linked Immunosorbent Assay (ELISA). Starved HUVECs were pretreated with an inhibitor for 1 h, followed by LPA (5 μM) treatment for an additional 24 h. The conditioned medium was measured by an IL-1β ELISA kit purchased from Cayman Chemical (Ann Arbor, MI).

Determination of VEGF-C Protein Expression by an
ELISA. Starved HUVECs were pretreated with an inhibitor for 1 h, followed by LPA (5 μM) treatment for an additional 24 h, and the conditioned medium was measured by a VEGF-C ELISA kit from R and D Systems (Minneapolis, MN).

Matrigel Tube Formation Assay.
Matrigel (BD Pharmingen, San Diego, CA) at 0.3 mL/well was plated evenly in a 24well plate, and incubated at 37 • C for 30 min before seeding with HUVECs (5 × 10 4 cells/well). Tube formation was studied for 6 h, and photographs were taken. The original magnification was 100x. The Matrigel was fixed, blocked, permeabilized, and stained with rabbit anti-mouse Prox-1 (Abcam), followed by incubation with a goat anti-rabbit AlexaFluor-555-conjugated secondary antibody (Molecular Probes). The Matrigel was thoroughly washed and incubated with Mec13.3, a direct FITC-conjugated rat anti-mouse mAb against PECAM-1 (BD Biosciences, San Jose, CA). After a further series of washes with PBS, samples were mounted on glass slides and viewed using a Zeiss fluorescence microscope (Oberkochen, Germany).

Statistical Analysis.
All experiments were performed at least three times, and the data are expressed as the mean ± SD. An analysis of variance (ANOVA) was performed using Statview 5.0 software. P < .05 was considered statistically significant.

LPA-Induced IL-1β Protein Expression Is Mediated by EGFR Transactivation-, MMP-, LPA1/3-, and IL-1R-Dependent Mechanisms in HUVECs.
Since LPA-induced lymphatic marker expressions are mediated by the IL-1R in HUVECs (Figure 1), we further investigated whether LPA stimulates IL-1β expression and whether LPA1/3 or EGFR transactivation mediates LPA-induced IL-1β expression in HUVECs. We observed that treatment with LPA (5 μM) significantly enhanced IL-1β protein expression in HUVECs. In addition, LPA-induced IL-1β protein expression in HUVECs was blocked by Ki16425, AG1478, GM6001, and AF12198. A Rac inhibitor (toxin B) showed no suppressive effects ( Figure 2). These results indicate that the enhancement of IL-1β protein expression by LPA in HUVECs is mediated by LPA1/3-, EGFR transactivation-, MMP-, and IL-1Rdependent mechanisms. Our previous study indicated that LPA induced MMP activity and EGFR transactivation [13,23,24]. GM6001, a broad-spectrum MMP inhibitor, is known to reduce LPA-induced EGFR transactivation. In this study, we showed that GM6001 and AG1478 could inhibit LPA-induced IL-1β expression. These results indicated that LPA-induced IL-1β expression may act through EGFR transactivation.

LPA-Stimulated VEGF-C Protein Expression Is Mediated by EGFR Transactivation-, MMP-, LPA1/3-, and IL-1R-Dependent Mechanisms in HUVECs.
The present study showed that IL-1β plays an important role in LPA-induced lymphangiogenesis. Moreover, we demonstrated that VEGF-C mediates LPA-induced lymphangiogenesis. Since both IL-1β and VEGF-C mediate LPA-induced lymphangiogenesis, we next investigated whether LPA-stimulated VEGF-C protein expression is mediated by an IL-1 receptor mechanism. LPA-induced VEGF-C protein expression in HUVECs was blocked by Ki16425, AG1478, GM6001, and AF12198. Pretreatment with a Rac inhibitor (toxin B) showed no suppressive effects (Figure 3). These results indicate that the enhancement of VEGF-C protein expression by LPA in HUVECs is also mediated through these pathways. , and toxin B (10 nM) for 1 h, followed by LPA (5 μM) treatment for an additional 24 h. Conditioned medium was measured by an ELISA as described in "Methods". All ELISA data are expressed as the mean ± SD from at least three independent experiments. * P < .05, * * P < .01, and * * * P < .001 indicate a statistically significant difference with the untreated control.

LPA-Stimulated Endothelial Cell Tube Formation In Vitro Is Mediated by EGFR
were pretreated with 100 nM of AG1478, 10 nM of AF12198, 10 μM of GM6001, 10 μM of Ki16425, or 10 nM of toxin B for 1 h, followed by LPA (5 μM) treatment for an additional 24 h, and then Matrigel tube formation assays were performed. After 6 h of plating, Matrigel of each experiment was fixed and subjected to an immunocytochemical assay. By immunostaining with PECAM-1, an endothelial cell marker, expression levels were stimulated by LPA induction and compared to the untreated control ( Figure 4). These results further demonstrated that LPA-induced tube formation in HUVECs is mediated through LPA1/3-, EGFR transactivation-, and IL-1R-dependent mechanisms. According to immunostaining with Prox-1, we observed that LPA upregulated the expression of Prox-1, a lymphatic marker. These enhancement effects were also suppressed by an inhibitor of LPA1/3, EGFR kinase, a broad-spectrum MMP, and IL-1R. However, an inhibitor of Rac (toxin B) showed no suppressive effects (Figure 4). These results demonstrate that LPA-induced tube formation and lymphatic marker expressions are also mediated by LPA1/3-, EGFR transactivation-, and IL-1R-dependent mechanisms.
A previous study indicated that basal mRNA expression levels of lymphatic markers are relatively low in HUVECs , and toxin B (10 nM) for 1 h, followed by LPA (5 μM) treatment for an additional 24 h. Conditioned medium was measured by an ELISA as described in "Methods". All ELISA data are expressed as the mean ± SD from at least three independent experiments. * P < .05, * * P < .01, and * * * P < .001 indicate a statistically significant difference with the untreated control. [29]. In addition, IL-3 induces the transformation of blood endothelial cells (BECs) into lymphatic endothelial cells (LECs). In this study, we also reported that LPA induced lymphatic marker expressions in HUVECs. These findings suggested that non-LECs can be used to study lymphangiogenesis. However, the effects of LPA on adult LECs or endothelial stem cells will be important experiments to carry out.
Both inflammation and lymphangiogenesis are aggravated by enhanced production of cytokines, chemokines, growth factors, and lipid mediators. It was reported that expressions of LPA-induced inflammatory response genes are mediated through a nuclear factor-(NF-) κBdependent pathway [30]. Moreover, our data showed that LPA induces lymphangiogenesis via an IL-1β-dependent pathway. Accordingly, LPA acts as a regulator of both lymphangiogenesis and inflammation. Like LPA, S1P is known to be a proinflammatory agent in the airway epithelium. In addition, S1P also plays a role in regulating lymphatic vessel maturation [31]. S1P1 is expressed in lymphocytes, and S1P regulates migration of T-cells from nonlymphoid tissues to the lymph [system?] [32]. Moreover, human lymphatic ECs (HLECs) express S1P1 and S1P3, and S1P acts as a  lymphatic regulator [25]. These results further confirm that bioactive lipids may be regulators of both inflammation and lymphangiogenesis. The lymphatic vascular system has critical roles in regulating interstitial pressure, homeostasis, and inflammation. Several studies suggested that new lymphatic vessel formation can be caused by chronic inflammation. For example, TNF-α, a proinflammatory factor, was found to be a mediator driving blood vessel remodeling and lymphangiogenesis in inflammation [33]. VEGF-C is mainly derived from inflammatory cells, which are involved in regulating lymphangiogenesis via VEGFR-3 signaling in LECs [34]. Moreover, Prox-1 and podoplanin were shown to be induced by inflammatory cytokines in differentiated ECs [29]. Those results suggest that inflammation evokes the formation of new lymphatic vessels. Cytokines, such as TNF-α and IL-1β, were reported to enhance VEGF-C expression in an NF-κB-dependent manner in HUVECs [26,33]. In addition, IL-1β also induced lymphangiogenesis in mouse corneas through upregulating the production of VEGF-C and VEGF-D [27]. Our previous study demonstrated that LPA induced VEGF-C expression and lymphangiogenesis in human ECs. Furthermore, LPA stimulated IL-8 and MCP-1 expressions via an IL-1dependent pathway [28]. In this study, we clarified that the LPA-induced lymphangiogenesis cascade acts through an IL-1β-dependent pathway which is a crucial pathway involved in the inflammatory response. This is consistent with a previous study demonstrating that IL-1β plays a key role in lymphangiogenesis [27].
As shown in Figure 2, we found LPA-induced IL-1β protein expression in human ECs. However, the enhancement effects were abolished by treatment with AF12198, an inhibitor of the IL-1 receptor, suggesting that the regulation of IL-1 has a positive-feedback mechanism. Our results are consistent with those of the Dinarello and Savage (1989) study showing that IL-1 has a self-augmentation induction mechanism, which allows a positive-feedback mechanism to amplify the effects of cytokines within the local environment [35].
In summary, this study is the first to establish that IL-1β is necessary for LPA-induced VEGF-C expression and lymphangiogenesis in human endothelial cells, which suggests that both LPA and IL-1β may be potent targets for generating therapeutics against lymphangiogenesis and tumor metastasis.

Conclusions
Our data clearly indicate that LPA-induced VEGF-C expression is largely mediated by the IL-1 receptor. Furthermore, LPA stimulated lymphatic marker expressions through upregulating IL-1β protein expression in HUVECs, thereby inducing the progression of lymphangiogenesis ( Figure 5). These findings suggest that LPA plays a critical role in inflammation-induced lymphangiogenesis.