Differential expression of the angiogenic Tie receptor family in arthritic and normal synovial tissue
© BioMed Central Ltd 2002
Received: 6 March 2001
Accepted: 27 November 2001
Published: 16 January 2002
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© BioMed Central Ltd 2002
Received: 6 March 2001
Accepted: 27 November 2001
Published: 16 January 2002
Angiopoietins (Ang) are vascular endothelial cell-specific growth factors that play important roles principally during the later stages of angiogenesis. We have compared the distribution of the receptor tyrosine kinase (Tie) and the Ang ligands in synovial tissues from normal subjects and those with rheumatoid arthritis (RA) and osteoarthritis (OA).
Immunohistochemical analysis was used to determine the expression of Ang-1, Ang-2, Tie1 and Tie2 in synovial tissue of normal subjects and those with RA and OA. Ang-1, Ang-2, Tie1 and Tie2 mRNA and protein expression were quantified in synovial tissues and RA synovial tissue fibroblasts with real-time reverse transcription polymerase chain reaction and western blot analysis.
In RA, Ang-1 positive immunostaining on lining cells, macrophages and endothelial cells was significantly higher than in OA and normal synovial tissue. The expression pattern of Ang-2 in synovial tissue was similar in RA and OA, whereas the Ang-2 expression was low in normal tissue. Synovial tissue from subjects with RA and OA showed a significant upregulation of Tie1 on lining cells, macrophages and endothelial cells compared to that from normal subjects. Tie2 was significantly upregulated in the RA and OA synovial tissue lining cells, macrophages and smooth muscle cells compared to normal synovial tissue. Generally Ang-1, Ang-2, Tie1 and Tie2 mRNA levels were higher in RA synovial tissue compared to normal and OA synovial tissues, and RA synovial tissue fibroblasts. Western blot analysis also demonstrated greater Tie1 and Tie2 protein expression in RA and OA synovial tissue compared to RA synovial tissue fibroblasts. In conclusion, the dominance of Ang-1 mRNA and protein expression over Ang-2 is in agreement with an active neovascularization in RA synovial tissue.
Rheumatoid arthritis (RA) is characterized by synovial tissue leukocyte infiltration and angiogenesis . The neovascularization process in RA is dependent on the balance between angiogenic mediators and inhibitors. The angiogenic mediators include growth factors, cytokines, chemokines, adhesion receptors and proteolytic enzymes . These factors, which are released by endothelial cells and macrophages, have been shown to play an important role in the pathogenesis of RA .
Tie receptors constitute a family of endothelial tyrosine kinase receptors [3, 4]. There are two members in this receptor family, termed Tie1 and Tie2 (also known as Tek). Tie1 is an orphan receptor, whereas the ligands of Tie2 receptor have been identified as angiopoietin (Ang)-1 and Ang-2 [5, 6]. Ang-1 has been shown to be responsible for recruiting and sustaining periendothelial support cells . It has been reported that Ang-2 disrupts blood vessel formation in the developing embryo by antagonizing Ang-1-induced autophosphorylation of Tie2 . Transgenic mouse models of Tie2/Ang-1 result in embryonic lethality due to absence of remodeling and sprouting of blood vessels [7, 8]. The physiologic roles of the Tie2 receptor and its ligands are limited to angiogenic processes that occur subsequently to the earlier vasculogenic and angiogenic actions of vascular endothelial growth factor (VEGF) and its receptors . VEGF and the Tie family orchestrate optimal blood vessel formation [9, 10].
Little is known about the role of Tie receptors and the ligands Ang-1 and Ang-2 in RA synovial tissue. To determine which of these angiogenic factors may play a role in RA, we investigated both the distribution and the levels of mRNA for Tie1, Tie2, Ang-1 and Ang-2 in synovial tissue obtained from RA patients, compared with that from subjects with osteoarthritis (OA) and normal tissues.
The patient population details and the methods used for microscopic analysis and statistical analysis are described in the supplementary material.
Synovial tissues (4 μm) were fixed in cold acetone for 20 minutes. Endogenous peroxidase was quenched by treatment with 3% H2O2 for 5 minutes. Synovial tissues were pretreated with either 3% horse or goat serum for one hour at 37°C before application of primary antibody. Indirect immunoperoxidase staining was performed at 37°C for one hour using Vector Elite ABC kits (Vector, Burlingame, CA, USA) and diaminobenzidine (Kirkegaard and Perry, Gaitherburg, MD, USA) as a chromogen [11, 12]. The polyclonal antibodies, goat antihuman Ang-1 and Ang-2, and rabbit antihuman Tie1 and Tie2, were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Additionally, goat antihuman Tie1 and Tie2 antibodies were purchased from R&D Systems (Minneapolis, MN, USA). Antibodies did not cross-react with other members of the Tie family.
Macrophage identity was confirmed by reactivity of cells with the mouse antihuman mAb, CD11c (Becton Dickinson, Mountain View, CA, USA). Rabbit antihuman von Willebrand factor (Dako, Carpinteria, CA, USA) was used to identify endothelium. Isotype-specific IgG was used as a negative control.
Cell culture, RNA purification, reverse transcription, standard dilution preparation, real-time reverse transcription polymerase chain reaction (RT-PCR) quantification (TaqMan) and western blot analysis are detailed in the supplementary material.
The Ang-2 mRNA expression pattern was similar to Ang-2 immunostaining on vascular endothelium. The Ang-2 mRNA expression in RA synovial tissue was similar to that from OA patients, and both were significantly higher than normal. Interestingly, in RA synovial tissue fibroblasts, Ang-2 mRNA was expressed at low levels compared to that found in whole RA, OA or normal synovial tissue (Fig. 2).
Immunohistochemistry studies using the goat antihuman Tie1 antibody purchased from R&D Systems showed predominantly endothelial cell staining, and minimal staining on macrophages and fibroblasts. Tie1 mRNA expression was significantly higher in RA synovial tissue compared to OA synovial tissue (3-fold), normal synovial tissue (9.5-fold) and RA synovial tissue fibroblasts (6-fold). Western blot analysis also confirmed the same pattern of expression.
The Tie receptors and the ligands Ang-1 and Ang-2 appear to be involved in the later stages of vessel growth and remodeling [8, 13]. Transgenic mice with gene deletions [7, 8, 13] or overexpression of Ang-2  exhibit early embryonic lethality secondary to defects in the developing vasculature.
Ang-1 was more highly expressed in synovial tissue from RA patients than in either OA or normal synovial tissues; expression in OA tissue was similar to normal. Positive cells included lining cells, macrophages and endothelial cells. In RA, Ang-1 was most upregulated on endothelial cells. The results obtained from RT-PCR analysis confirmed that RA synovial tissue had significantly higher Ang-1 mRNA expression than OA and normal synovial tissue. Hence, no Ang-1 mRNA expression was detected in RA fibroblasts (Fig. 1). The Tie receptor family is known to be expressed on endothelial cells . Otani et al reported Ang-1 and Ang-2 positive staining on macrophages and endothelial cells in choroidal neovascular membranes. Macrophages are key angiogenesis effector cells that produce a number of growth factor stimulators and inhibitors, proteolytic enzymes and cytokines that can activate one or more steps in the angiogenesis cascade [15–17]. Recent studies have shown that angiopoietins promote postnatal neovascularization by potentiating angiogenic cytokines such as VEGF [9, 10].
In situ hybridization and immunohistochemical analyses of RA synovial biopsies revealed that VEGF mRNA and protein localized to subsynovial macrophages, lining cells, vascular smooth muscle cells and fibroblasts within the pannus, which are the putative target of this cytokine [18, 19]. The localization of Ang-1 is similar to that of VEGF, which further supports the crucial role of the interaction between these two pathways. Ang-1 modulates VEGF-stimulated reorganization of endothelial cells and promotes vascular network maturation [9, 20]. Additionally, both Ang-1 and VEGF are chemotactic and are involved in recruiting endothelial cells to initiate and accelerate endothelialization of blood vessels [21, 22].
We detected Ang-2 immunopositive cells in synovial lining, macrophages and vascular endothelium. Vascular smooth muscle immunostaining was found only in RA. In agreement with our finding, it has been reported that primary cultured macrophages and precursor macrophage cell lines mainly express Ang-2 mRNA . In contrast to Ang-1, Ang-2 was distributed in a similar pattern in RA and OA compared to normal synovial tissues (Fig. 2). The dominance of Ang-2 over Ang-1 mRNA and protein in OA synovial tissue are in agreement with the inactive VEGF receptor 1 pathway (angiogenic pathway) in OA . The Ang-2 mRNA expression pattern correlates with the Ang-2 immunostaining detected on endothelial cells. In RA synovial tissue, Ang-2 showed a lower percentage of staining in all the cell types compared to Ang-1. Low Ang-2 mRNA expression was also detected on RA fibroblasts. Interestingly Ang-2 acts as an agonist for Tie2 receptors expressed on fibroblasts . Since the neovascularization process is dependent on the dominance of angiogenic mediators over inhibitors, the higher Ang-1 mRNA and protein expression compared to Ang-2 in RA synovial tissue is of importance. It has been shown that increasing amounts of Ang-2 can block the chemotactic activity of Ang-1 in endothelial cells . Ang-2 alone did not stimulate corneal neovascularization, but the combination of Ang-2 and VEGF resulted in longer vessels with greater circumferential extent than those seen with VEGF alone . This suggests that Ang-2 expression in the absence of VEGF leads to vessel regression, whereas expression of Ang-2 in the presence of VEGF potentiates angiogenesis.
Using the Santa Cruz Biotechnology antibody, Tie1 expression was detected on all cell components examined, including a percentage of synovial lining cells, macrophages and smooth muscle cells in RA and OA. Synovial tissues from normal subjects, and those with OA, had considerably lower positive immunostaining on endothelial cells compared to RA tissues. Immunohistochemical analysis performed with anti-Tie1 from R&D Systems in synovial tissues supports its expression mainly on endothelial cells. However, western blot analysis for Tie1 also performed with an antibody from R&D Systems, showed higher relative abundance of Tie1 in whole RA and OA synovial tissue homogenates compared to RA fibroblasts (Fig. 3). In accordance with the protein data, the mRNA levels of Tie1 in RA synovial tissue were upregulated compared to OA synovial tissue, normal synovial tissue and RA fibroblasts. Since the ligand for the Tie1 receptor is not known, it is difficult to speculate if there is any correlation between this receptor and Tie2 and its ligands. In agreement with previous studies, the Tie1 receptor was detected on vascular endothelial cells [4, 25] and recently on synovial lining cells . It has been shown that tumor necrosis factor-α and VEGF activate membrane-associated metalloproteinases that release soluble Tie1 from the cell surface of endothelial cells and thereby decrease membrane-bound Tie1 expression . The upregulation of Tie1 mRNA and protein expression in RA is not consistent with these findings and this may be due to the fact that the inflammatory milieu in RA synovial tissue is far more complex than the in vitro system.
Using the Santa Cruz Biotechnology antibody we showed that Tie2 expression was significantly upregulated both in RA and OA synovial tissue lining cells, macrophages, endothelial cells and vascular smooth muscle compared to normal synovial tissue. In accordance with Otani et al. and Uchida et al. we detected Tie2 immunostaining on endothelial cells and fibroblasts in all disease groups. Tie2 immunostaining using antibody from R&D Systems confirmed the expression of this antigen mainly on endothelial cells. Tie2 mRNA and protein expression followed the same pattern of expression as Tie1. There are some possible reasons why the immunohistochemistry studies performed with Santa Cruz Biotechnology/R&D Systems antibodies differ. The Santa Cruz Biotechnology antibodies detected epitopes on the carboxy terminus whereas the R&D Systems antibodies recognized the extracelluar domain (N terminus or the ligand binding domain) of Tie1 and Tie2. There is also some variability between individual RA patient samples, however, we attempted to use the same RA patient samples in performing immunohistochemistry with the two different antibodies. Additionally, the results obtained from the RT-PCR and western blot analysis confirm our findings.
It is noteworthy that the activating ligand, Ang-1 is exclusively higher than Ang-2 at the mRNA and protein levels in RA synovial tissue compared to that from patients with OA and normal subjects. Hypothetically, in RA synovial tissue the dominating Ang-1 induces the Tie2 pathway, whereas in normal synovial tissue higher Ang-2 presence blocks Ang-1 binding to Tie2 and inhibits its autophosphorylation.
In conclusion, the dominance of Ang-1 over Ang-2 expression favors active neovascularization in RA synovial tissue. Multiple pathways are probably required to regulate angiogenesis. It may be that the inhibition of the VEGF and Tie2 pathways might be an effective therapeutic modality in RA.
Synovial tissues from patients with RA and OA, undergoing arthroplasty or synovectomy, who fulfilled the criteria set by the American College of Rheumatology were obtained with Institutional Review Board (IRB) consent [28, 29]. Normal synovial tissues were obtained from fresh autopsies or amputations. Synovial tissues were snap frozen in Optimal Cutting Temperature (OCT) compound (Miles, Elkhart, IN, USA).
Synovial tissue components including lining cells, macrophages, lymphocytes, fibroblasts, smooth muscle cells and endothelial cells were graded for immunostaining by a frequency of staining scale, scored 0–100%, where 0% indicates no staining and 100% indicates that all cells were immunoreactive. Five 400× fields were examined per section by a single pathologist in a blinded study. Selected sections were analyzed by two additional observers.
Data were analyzed using a Kruskal Wallis test. There were 5 to 15 patient samples per group. P values < 0.05 were considered to be significant.
Fibroblasts were isolated from synovial tissues that had been minced and digested in a solution of dispase, collagenase and DNase. Synovial tissue fibroblasts were cultured in Roswell Park Memorial Institute (RPMI)-1640 supplemented with 10% FBS and 1% penicillin/streptomycin (P/S) and used at passage five or older, at which time they were a homogeneous population of fibroblasts.
Human microvascular endothelial cells (HMVECs) (BioWhittaker, CA, USA) were cultured in endothelial cell growth medium-2 for microvascular cells (BioWhittaker, Walkerville, MD, USA) and were used between passages 3 and 12. Upon confluence, the cells were passaged by brief trypsinisation as previously described . HMVECs were used as positive controls for Tie1 and Tie2 protein expression in western blot analysis.
Total RNA was prepared from synovial tissue by an acid phenol method according to the procedure described by Chomczynski and Sacchi . RNA (20 μg) was digested with five units of DNase in 1× reverse transcription buffer (Gibco/Life Technologies, Grand Island, NY, USA) containing eight units of RNase inhibitor (Gibco/Life Technologies, Grand Island, NY, USA) for 30 minutes at 37°C. Sodium acetate (2 M, pH4.0) was added (10% of the total volume), and the solution was extracted with one volume each of water-saturated phenol and chloroform (Fisher, Itasca, IL, USA). The RNA was precipitated with ethanol, washed with 75% ethanol, then air-dried. The pellet was dissolved in water at 1 μg/μl.
Reverse transcription of RNA was performed using 5 μg of RNA in a total volume of 20 μl. The RNA was reverse transcribed by Superscript II RT (Gibco/Life Technologies, Grand Island, NY, USA) according to manufacturer's specification. After 10 minutes at 25°C, the enzyme was incubated at 42°C for 50 minutes and thereafter inactivated at 70°C for 15 minutes. The solution was diluted to 40 μl. All samples were reverse transcribed simultaneously.
The sequence for the designed Tie receptors and ligands
GCC ATT ACC AGT CAG AGG CAG T
CAT GCT AAG AAT TGA GTT AAT
AAT AGG CTC GGT TCC CTT CC
CGC TCG AAT ACG ATG ACT CG
TGC AGA GGC TGC AAG TGC TGG AGA A
CCA CTG AGT GTT GTT TTC CAT GAT
GCC ACG TTC TGG CTG GAT
TCA GGC CTC CTC AGC TGT GGC AT
ACT TCA CTT ACG CGG GCA TT
GGC AAC TTG ACT TCG GTG CT
ACT TAC ATC CCA GGG AGC AGT ACG TGG TC
GGC CTT GGT GTT GAC TCT AGC T
The PCR primer and the TaqMan fluorogenic probe were designed using the Primer Express program v 1.01 (Perkin Elmer Applied Biosystem, CA, USA). The TaqMan probe carries a 5' FAM (6-carboxy-fluorescein) reporter dye and a 3' TAMRA (6-carboxy-tetramethyl-rhodamine) quencher dye (Mega Bases, Chicago, IL, USA) The quantity of cDNA of the gene of interest was directly related to the fluorescence detection of FAM after 40 cycles. The amount of cDNA was calculated using a comparative CT method and the standard curve method  according to Perkin Elmer ABI PRISM 7700 User Bulletin No. 2, 1997. The calibration curves showed a strong linear correlation, with correlation coefficients between 0.96 and 0.99. In both methods, the estimated amount of the gene of interest was normalized by the amount of glyceraldehyde-3-phosphate dehydrogenase to compensate for variations in quantity and for differences in reverse transcription efficiency.
Briefly, 3 μl of the cDNA was in a reaction of 25 μl that contained final concentrations of 1× Platinum PCR buffer (Gibco/Life Technologies, Grand Island, NY, USA), 3.5 mM MgCl2, 200 μM dNTP, 500 nM each primer (Mega Bases, Chicago, IL, USA), 200 nM FAM-TAMRA probe (Mega Bases, IL, USA), 100 nM Blue 636 (BD 636), 0.05 units platinum Taq DNA polymerase (Gibco/Life Technologies, Grand Island, NY, USA). The thermal cycling conditions included 94°C for five minutes, followed by 40 cycles of amplification at 94°C for 30 seconds and 60°C for one minute for denaturing and annealing-extension, respectively. All samples were amplified in triplicate.
Synovial tissues were homogenized in a 50 ml conical centrifuge tube containing 3 ml of Complete Mini protease inhibitor cocktail homogenization buffer (Roche, Indianapolis, IN, USA). Synovial tissue homogenization was completed on ice using a motorized homogenizer, followed by sonication for 30 seconds. Homogenates were centrifuged at 2000 ×g for 10 minutes, filtered through a 0.45 μm pore size filter (Bedpore, Bedford, MA, USA) and stored at -80°C until use. Complete Mini protease inhibitor cocktail (1 ml) was added to one million RA fibroblasts and HMVECs for lysis. The concentration of protein in each synovial tissue and cell lysate was determined using a bicinchoninic acid assay (Pierce, Rockford, IL, USA), using BSA as the standard. Protein extracts (25 μg) were mixed with an equal volume of 2× Laemmli's sample buffer. Equal amounts of each sample were loaded and run on a 10% SDS-PAGE gel and transferred to nitrocellulose membranes using a semi-dry transblotting apparatus (Bio-Rad, Richmond, CA, USA). Nitrocellulose membranes were blocked with 5% nonfat milk in Tris-buffered saline Tween (20 mM Tris, 137 mM NaCl, pH7.6, with 0.1% Tween 20) for 60 minutes at room temperature. Blots were incubated overnight with anti-Tie1 and anti-Tie2 antibodies (R&D Systems) at 1:5000, in Tris-buffered saline Tween containing 5% nonfat milk. Blots were washed three times and then incubated in horseradish-peroxidase-conjugated antibody (1:10,000 dilution) for one hour at room temperature. All blots were developed using the enhanced chemiluminesence reagents (Amersham, Piscataway, NJ, USA) as per the manufacturer's instructions.
bovine serum albumin
fetal bovine serum
human microvascular endothelial cell
polymerase chain reaction
reverse transcription polymerase chain reaction
receptor tyrosine kinase
vascular endothelial growth factor.
This work was supported by NIH Grants HL58695, AI40987, the Gallagher Professorship for Arthritis Research, and funds from the Veteran's Administration Research Service.