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Int J Med Sci 2013; 10(8):1053-1060. doi:10.7150/ijms.6223

Research Paper

FasL Expression on Human Nucleus Pulposus Cells Contributes to the Immune Privilege of Intervertebral Disc by Interacting with Immunocytes

Zhi-Heng Liu1,*, Zhen Sun1,*, Hai-Qiang Wang1,*, Jun Ge1, Ting-Shuai Jiang2, Yu-Fei Chen1, Ying Ma3, Chen Wang4, Sheng Hu4, Dino Samartzis5, Zhuo-Jing Luo1, Corresponding address

1. Department of Orthopaedics, Xijing Hospital, Fourth Military Medical University, 127 Changle Western Road, Xi'an, P. R. China.
2. Department of Ophthalmology, Xijing Hospital, Fourth Military Medical University, 127 Changle Western Road, Xi'an, P. R. China.
3. Department of Immunology, Fourth Military Medical University, 127 Changle Western Road, Xi'an, P. R. China.
4. Department of Anesthesiology, Fourth Military Medical University, 127 Changle Western Road, Xi'an, P. R. China
5. Department of Orthopaedics and Traumatology, University of Hong Kong, Pokfulam, Hong Kong, SAR China.
* These authors contribute equally to this work.

This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) License. See http://ivyspring.com/terms for full terms and conditions.
How to cite this article:
Liu ZH, Sun Z, Wang HQ, Ge J, Jiang TS, Chen YF, Ma Y, Wang C, Hu S, Samartzis D, Luo ZJ. FasL Expression on Human Nucleus Pulposus Cells Contributes to the Immune Privilege of Intervertebral Disc by Interacting with Immunocytes. Int J Med Sci 2013; 10(8):1053-1060. doi:10.7150/ijms.6223. Available from http://www.medsci.org/v10p1053.htm

Abstract

The mechanisms of immune privilege in human nucleus pulposus (NP) remain unclear. Accumulating evidence indicates that Fas ligand (FasL) might play an important role in the immune privilege of the disc. We aimed for addressing the role of FasL expression in human intervertebral disc degeneration (IDD) and immune privilege in terms of the interaction between NP cells and immunocytes via the FasL-Fas machinery. We collected NP specimens from 20 patients with IDD as degenerative group and 8 normal cadaveric donors as control. FasL expression was detected by qRT-PCR, western blotting and flow cytometry (FCM). We also collected macrophages and CD8+ T cells from the peripheral blood of patients with IDD for co-cultures with NP cells. And macrophages and CD8+ T cells were harvested for apoptosis analysis by FCM after 2 days of co-cultures. We found that FasL expression in mRNA, protein and cellular resolutions demonstrated a significant decrease in degenerative group compared with normal control (p<0.05). FCM analysis found that human NP cells with increased FasL expression resulted in significantly increased apoptosis ratio of macrophages and CD8+ T cells. Our study demonstrated that FasL expression tends to decrease in degenerated discs and FasL plays an important role in human disc immune privilege, which might provide a novel target for the treatment strategies for IDD.

Keywords: intervertebral disc degeneration, FasL, immune privilege, macrophage, CD8+ T cell.

Introduction

Intervertebral disc degeneration (IDD) is a major cause of many spinal disorders [1, 2]. Over the past decade, the underlying mechanisms of IDD have been well documented in terms of biomechanics [3], cell apoptosis [4, 5], deregulated genes and microRNAs (miRNAs) [6, 7]. Moreover, studies with human disc cells, especially focusing on nucleus pulposus (NP) cells, are seldom found in the literature. Despite intensive basic and clinical pieces of studies aiming for addressing the issues, the physiopathological mechanisms of IDD remain yet speculative with particular reference to the maintenance of immune privilege. The immune privilege of tissues is ascribed not only to the physiological blood-tissue barrier, but the local expression of Fas ligand (FasL).

As the largest avascular organ in the human body, the intervertebral disc is isolated from the host immune system [8]. Many pieces of evidence indicate the immune privilege of the disc, the chief of which is NP [9-11]. As an important death receptor of immune privilege, FasL is expressed on activated T cells, NK cells, and in immune privileged sites [12], i.e., eyes, ovary, placenta[13-15], transplantation organs [16-20]. Various levels of the expression of FasL have been noted in both degenerative and non-degenerative NP [21-23]. It has been consequently hypothesized that the Fas-FasL death complex may play a role upon maintaining the immune privilege of the disc.

Cross-linking of FasL with Fas leads to apoptosis via a complex signaling pathway [24]. In immune privileged sites, activated cytotoxic T lymphocytes (CTLs) and macrophages can recognize target cells and subsequently become activated. The FasL in these cells binds to Fas on the surface of the target cells and induces apoptosis. Alternatively, when the target cells express FasL, CTLs or macrophages might die of apoptosis via the same pathway. This mechanism protects the disc from auto-immune attack [13].

The FasL expression of the disc samples from patients with IDD and cadavers was seldom reported due to the paucity of human samples. It has been noted that FasL exists in human intervertebral disc cells, especially in NP cells [22, 25]. Furthermore, we found that deregulated miR-155 promotes Fas-mediated apoptosis in human intervertebral disc degeneration by targeting FADD and CASP3. However, the FasL derivation remains largely unknown. Nevertheless, the difference of FasL expression between degenerative and normal NP tissues is still unclear. Accordingly, the purpose of this study was to address the role of FasL expression in human intervertebral disc degeneration (IDD) and immune privilege in terms of the interaction between NP cells and immunocytes via the FasL-Fas machinery.

Materials and Methods

Sample collection

The NP samples and peripheral blood mononuclear cells (PBMCs) collection for experimental application was approved by our institutional Ethics Review Board of Xijing hospital (No. 20090611-3, No. 20111103-7). Moreover, we obtained written informed consents from each patient. For cadaveric donors, we obtained the same style of written informed consents from their relatives. Human NP specimens were collected from patients with IDD undergoing discectomy as degenerative NP samples [n=20; average age 43.4±5.4 (range 35-52)] and normal cadaveric donors as control [n=8; average age 41.8±3.6 (range 37-47)] (Table 1). The cadavers and patients included in control and experimental groups are matched for age, with no smoking, diabetes, hypertension and radicular symptoms, etc. All the the patients with disc degeneration were strictly selected by MRI and intraoperative findings to exclude NP samples that had herniated outside the annulus. The degeneration degree was graded by magnetic resonance imaging (MRI) according to the Pfirrmann's grading system [26]. As for the cadavers, MRI data in records were collected. All the samples were dissected carefully under magnification and subsequently managed under various schemes according to the corresponding procedures.

 Table 1 

Demographic data of cadaveric donors and patients.

NO.AgeGenderLevelDegree*
Normal control
144ML4/5I
238ML4/5I
337FL4/5I
445ML4/5I
547ML4/5I
639FL4/5I
745ML4/5I
839ML4/5I
IDD Group
947FL4/5IV
1052ML4/5IV
1143FL4/5V
1236FL4/5IV
1342ML4/5V
1450FL5/S1IV
1545FL5/S1IV
1641ML4/5IV
1738ML4/5IV
1835FL5/S1V
1939ML4/5IV
2042FL5/S1IV
2152ML4/5IV
2242ML4/5IV
2346ML4/5IV
2438FL4/5IV
2549FL4/5IV
2636ML5/S1IV
2743FL4/5IV
2851ML4/5IV

* Pfirrmann's grading system.

NP cell cultures

Human NP cells were isolated from intervertebral disc tissues during surgical procedures for patients and dissection for cadaveric donors. After carefully washed, annulus fibrosus and cartilaginous endplate were removed under the microscope. The remain tissues were then minced and digested for 40 min at 37°C in PBS with 0.25% pronase (Gibco-BRL, Carlsbad, CA, USA). Then solution was removed, remaining tissue washed, and digested for 4 h in PBS with 0.025% collagenase type II (Invitrogen). The digest was then washed three times and filtered through a 45-µm pore-size nylon mesh. Cells were plated and expanded for 3 weeks in DMEM/F12-based culture medium, containing 15% fetal bovine serum (FBS; Gibco-BRL) and 1% penicillin/streptomycin (Invitrogen) in a 5% CO2 incubator. The culture medium was changed every three days. NP cells of Passage 1 or 2 were used for our experiments.

Western blotting analysis

To determine the FasL expression level of NP cells in IDD patients and cadaveric donors, the cultured NP cells were trypsinized. Prepare total cell lysates by solubilizing cells in 2X SDS sample buffer. Following electrophoresized in 10% gel, proteins were transfered to PVDF membrane. The membranes were incubated for 1 h at room temperature with rabbit polyclonal antibody specific to FasL (Santa Cruz Biotechnology, CA, USA), and mouse monoclonal antibody specific to β-actin (Sigma, Saint Louis, USA) as control. Antibody labeling was identified using IRDye 800 anti-rabbit or anti-mouse IgG antibody (LI-COR Biosciences, Nebraska, USA). Expression levels were analyzed by LI-COR Odyssey Imaging System.

RNA isolation and qRT-PCR

NP cells from cadavers and patients with IDD were harvested, and total RNA was isolated using the Trizol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions.

Reverse transcription to cDNA was performed using a High-Capacity cDNA Archive Kit (ABI, Foster City, CA, USA). Predesigned primers for human FasL and human GAPDH as control were purchased from Sangon (Sangon, Shanghai, China). RNA concentrations were measured using a NanoDrop instrument ( NanoDrop, Wilmington, DE, USA). The levels of FasL mRNA were normalized to GAPDH mRNA controls. All RT reactions, including GAPDH controls, were run in triplicate in a GeneAmp PCR 9700 Thermocycler (ABI). The relative amounts of FasL mRNA were calculated using the comparative Ct (2-ΔΔCt) method. The primers used in the study included: FasL forward: 5'- TTGCCTTGGTAGGATTGG-3', reverse: 5'-ATGGACCTTGAGTTGGACTT-3'; GAPDH forward: 5'-GCACCGTCAAGGCTGAGAAC-3', reverse: 5'- TGGTGAAGACGCCAGTGGA-3').

PBMCs collection

PBMCs were isolated from whole blood by Ficoll-Hypaque density gradient centrifugation as reported previously. Briefly, the peripheral blood was obtained in heparinized vacutainer collection tubes from IDD patients and diluted 1:3 in RPMI-1640 (Gibco, Grand Island, NY, USA).Then 30 mL diluted blood was slowly layered over 15 mL Ficoll-Paque (GE Healthcare, Piscataway, NJ, USA), and centrifuged at 800×g for 30 min at room temperature. The PBMCs were subsequently collected for macrophage separation.

Isolation and cultures of macrophages from patients with IDD

The PBMCs collected from the patients with IDD were washed three times with RPMI-1640, and plated in tissue culture dishes (BD Bioscience, San Diego, CA, USA) at 3×106 cells/mL in RPMI-1640 supplemented with 2 mM L-glutamine (Gibco), 100 U/mL penicillin (Gibco), 100 μg/mL streptomycin (Gibco), 0.1 mM sodium pyruvate (Gibco), 1% non-essential amino acids (Gibco), 50μM 2-mercaptoethanol (Gibco), and 10% fetal bovine serum (Gibco). After 24 h, the PBMCs in tissue culture dishes were washed gently with RPMI-1640 to remove a majority of the non-adherent cells. The monocytes which had been adherent in the dishes were cultured for an additional five days supplemented with 18 ng/ mL GM-CSF (PeproTech, Rocky Hill, NJ, USA) and 20 ng/mL M-CSF (PeproTech). Thereafter, the cells were washed with RPMI-1640 to remove the non-adherent or dead cells. The remaining adherent cells that had been induced to differentiate into macrophages were scraped from the plate and stained with the monoclonal antibody CD68-PE (eBioscience, San Diego, CA, USA) in FCM analysis to confirm the purity of the cells prior to the next steps.

Isolation of CD8+ T cells

CD8+ T cells were positively isolated from the whole blood of IDD patients using the CD8+ T-cell Positive Isolation Kit (Invitrogen Dynal AS, Norway) according to the manufacturer's instructions. Over 90% of the CD8+ T-cell isolation was confirmed by FCM analysis with monoclonal antibody CD8a-APC (eBioscience, San Diego, CA, USA).

Up-regulation of FasL with lentiviral vector

The lentiviral vector labeled with green fluorescent protein (GFP) encoding FasL and a scrambled sequence as control were purchased from Genechem. Human NP cells were plated at a density of 1.5×105 cells/well in a 24-well plate in a final volume of 250 µl complete medium. Viral solutions at a multiplicity of infection (MOI) of 10 were added to NP cells. Following 10 h of incubation at 37°C, the cells were allowed to recover over the ensuing 96h in culture medium. Culture flasks were detected by fluorescent microscopy to verify cell transfection.

Indirect co-cultures of NP cells and immunocytes

Transwell inserts (0.4μm pore-size) were utilized for non-contacting co-culture in six-well plates. The co-culture ratio is 50:50, consisted of NP cells with CD8+T cells or macrophages from the same patient. NP cells were plated into six-well plate (1.5×106 per well) with 10% DMEM/F12 culture medium mentioned above, macrophages or CD8+T cells (1.5×106 per well) were plated into Transwell inserts respectively with same culture medium, respectively. Eight groups with different combinations of cell types were defined in this study (Table 2). Macrophage and CD8+T cell were harvested after 2 days of culture for FCM apoptpsis analysis.

 Table 2 

Groups for co-cultures of human NP cells and immunocytes

GroupNP cellsImmunocytes
IDDUp-regulated FasLLentiviral controlmacrophagesCD8+ T cells
1++
2++
3++
4+
5++
6++
7++
8+

+: Cell types in each group.

IDD: intervertebral disc degeneration.

NP cells: nucleus pulposus cells.

Flow cytometry (FCM) analysis

To address apoptosis in macrophages and CD8+ T cells after co-cultures, we performed FCM with Annexin V-FITC/PI (BD Biosciences, San Diego, CA, USA) staining upon the aforementioned treated cells, In brief, after washing twice with PBS, 1×106 cells were re-suspended in binding buffer. Annexin V-FITC and PI were added and then incubated at room temperature for 15 min. The samples were then analyzed by FCM. Each experiment was repeated for at least three times.

Statistical analysis

Analysis of two-group parameters was performed with Student's t-test. Comparisons of multiple group data were performed with ANOVA test. The threshold of significance was set as P-value<0.05. The statistical analysis was performed with the SPSS 12.0 statistical package (SPSS, Chicago, IL, USA).

Results

FasL expressed in human degenerative and normal NP cells with different resolutions

The levels of mRNA expression of FasL in NP cells of non-degenerative group were significantly higher than those of the degenerative group (Figure 1A). Western blotting analysis further showed that the intensity of FasL in non-degenerated group was higher than that in the degenerated group (Figure 1B). Quantitative analysis revealed that the average FasL ratio in the degenerated group was 56%±0.09, whereas the average FasL ratio in the non-degenerated group was 89%±0.12 (p<0.05).

To compare FasL expression in degenerated and non-degenerated tissues, we also performed FCM analysis to identify the level of FasL in NP cells quantitatively. As shown in Figure 1C, the average ratio of FasL positive cells (68.8%±0.072) in non-degenerative NP cells is significantly higher than in degenerative NP cells (35.4%±0.053) (p<0.05).

Up-regulated FasL of NP cells resulted in increased immunocyte apoptosis after co-cultures

The cultured NP cells from patients with IDD in our study were in good growing condition (Figure 2A). Macrophages were successfully isolated and cultured (Figure 2B). The purity of macrophages and CD8+T cells was detected by FCM. The GFP-expressing lentiviral vector transfection at a MOI of 10 encoding FasL resulted in high-level GFP expression in NP cells (Figure 2C). FCM detection revealed the apoptosis of immunocytes in different groups (Figure 3A). As for macrophages without co-cultures, the apoptosis rate was 4.8%±0.007. Approximately 6.5%±0.0075 macrophages were apoptotic when cultured with IDD NP cells. It was noteworthy that NP cells with up-regulated FasL resulted in about 17.5%±0.012 apoptosis rate of macrophages (p<0.05). In the lentiviral-control group with scrambled sequence, the apoptosis rate of macrophages was 6%±0.008 (Figure 3B). Similar findings were observed in CD8+ T cells co-cultured with NP cells (Figure 3C).

Discussion

IVD degeneration is the major cause in neck or low back pain and disc herniation, which are the most common disorders leading to morbidity [27]. Apoptosis in IVD was initially reported by Gruber in 1998. And more and more evidences indicating that apoptosis plays an important role in human degenerative diseases. As one of the most important pathways of apoptosis, cell surface death receptor pathway is crucial in IVD process. In death receptor pathway, ligation of Fas ligand to the Fas receptor on the cell membrane leads to the recruitment and activation of caspase-8, which will activates downstream caspases and results in apoptosis [27]. This mechanism also works in some autoimmune diseases, helps to maintain the balance of self-antigen and immune system.

We found that FasL expression in non-degenerated NP was significantly higher than in degenerated discs. So far, the study is the first in successfully establishing an in vitro model addressing the interaction of human NP cells and immunocytes. By modulating the FasL expression in degenerative NP cells co-cultured with immunocytes, we found that the degenerative NP cells with up-regulated FasL resolution would induce the apoptosis of invaded macrophages and CD+8 T cells, which contributes to the immune privilege of NP. Furthermore, this study is the first clarifying the underlying mechanisms of immune privilege of human intervertebral disc via FasL-Fas network.

The immune privilege of NP is not only due to the simple physiological barrier, but FasL expression as molecular mechanisms. Most immune privileged organs express FasL [13, 28-30]. Previously studies on the expression of FasL in NP cells from normal intervertebral disc of mature Sprague-Dawley rats and humans suggested that the Fas-FasL system may play a key role as the underlying mechanisms for maintaining the immune privilege of the disc [22]. FasL expression levels alter in NP during intervertebral disc formation [31]. The apoptosis in human NP is closely linked with autocrine or paracrine FasL mechanisms [10, 25]. However, most studies used NP samples from herniated lumbar disc, animals, and patients with scoliosis [23], which might not well represent the degeneration process in the body.

 Fig 1 

FasL expression of NP cells in different levels from degenerative and normal NP. A. qRT-PCR analysis of FasL expression. B. Western blotting detection of FasL expression. C. Flow cytometry detection of FasL positive cells. Data are representative of six independent experiments. Error bars represent SEM. *p<0.05.

Int J Med Sci Image (Click on the image to enlarge.)
 Fig 2 

NP cells, macrophages and CD8+T cells from patients with intervertebral disc degeneration were detected. A. Cultured NP cells for 14 days. Scale bars = 500 µm. B. Cultured macrophages for 7 days from peripheral blood of patients with disc degeneration. Scale bars = 50 µm. C. Brightfield (left) and fluorescent (right) microscopy of human NP cells 96 h following transfection with lentivirus labeled with green fluorescent protein. Scale bars = 20 µm.

Int J Med Sci Image (Click on the image to enlarge.)

In this study, we collected non-degenerative cadaveric disc specimens as normal control. Moreover, we performed comprehensive analysis on FasL expression by qRT-PCR, western blotting and FCM. We carefully removed annulus fibrosus and cartilaginous endplate under the microscope in aseptic conditions due to the high degree of sensitivity of NP tissues. Our results based upon the multiple lines of evidence indicate a significant decrease of FasL expression in degenerative NP compared with normal discs in humans.

Our study clarified the mechanisms of the role of FasL-Fas network in human NP and shed light on the derivation of FasL in human disc. NP has been suggested to trigger an autoimmune response if exposed to the immune system in animal experiments as well as in patients with disc herniation [27, 32-35]. Both FasL and Fas are expressed by human T lymphocytes [36] and NP cells [21, 22, 25]. FasL is one of the major effectors of CTLs to destroy target cells [37, 38]. As in most immune privileged organs, the FasL-Fas network is involved in the apoptotic pathways and immune privilege [12]. It is well established that eyes, as a typical immune privileged site, constitutively expresses FasL to control the spread of inflammation by killing Fas positive lymphoid cells that invade the tissue [13]. As well, FasL plays key roles in CTL-mediated tissue destruction under pathological conditions such as graft-versus-host disease (GVHD) [39] and experimental autoimmune diseases [40, 41]. Soluble and membrane-bound FasL can activate a cascade of caspases that culminates in apoptosis via binds to cell surface Fas [42, 43]. However, the role of FasL-Fas network in human NP cells has not been clarified until now. We found that FasL expression in non-degenerative cadaveric NP samples is higher than in that in degenerative NP (grade IV and V). In normal NP, the expression of FasL could induce the apoptosis of immune cells. However, in the scenario of degenerated NP, FasL expression decreases, which was further confirmed by our preliminary study since we tried to down-regulate FasL expression via RNAi but failed. The apoptosis rate between immune cell group and immune cells co-cultured with NP cell group is not statistically different because of the low level expression of FasL in degenerated NP. Our findings indicate that the combination of FasL of normal NP cells to Fas positive T cell triggers the apoptosis of CTLs, which help keep the immune privileged condition of NP. Co-cultures of human NP cells with up-regulated FasL with auto-CD8+T cells and macrophages, the apoptosis ratio of immunocytes significantly increased. These results suggest that FasL plays an important role in the immune privilege of human NP.

Despite our de novo in vitro model, we acknowledge that several shortcomings exist in our study. First, we didn't compare living patient degenerative NP cells with living patient normal NP cells because of clinical and ethical reasons. Secondly, we only up-regulated the FasL expression of NP cells by lentiviral vector without down-regulating the expression. This is partly due to the low expression level of FasL in NP tissue in our preliminary study (data not shown). Furthermore, we selected macrophages and CD8+ T lymphocytes as representatives of immunocytes despite we are fully aware of the complicated interaction within the body, such as NK cells, CD4+ T lymphocytes. However, the impact of NK cells and CD4+ T lymphocytes in human IDD remains unknown. Further studies are needed to address these issues.

 Fig 3 

Flow cytometry apoptosis analysis of immunocytes after co-cultures. A. Contour diagram of Annexin V-FITC/PI FCM of human NP cells. The graphs stand for typical results of cell apoptosis; values represent the means for three experiments. B. Comparison of apoptotic cells in various macrophages groups (*p<0.05). Data are representative of three experiments. Error bars represent SEM. C. Comparison of apoptotic cells in various CD8+T cell groups (*p<0.05). Data are representative of three experiments. Error bars represent SEM.

Int J Med Sci Image (Click on the image to enlarge.)

Conclusions

The study is the first in successfully establishing an in vitro model addressing the interaction of human NP cells and immunocytes. Our study clarifies the mechanisms of the role of FasL-Fas network in human NP and shed light on the derivation of FasL in human disc.

Acknowledgements

This work was supported by Chinese National Natural Science Foundation Grants (No.30901509, No.81270028, No.81171747, No.81271342, and No.30972883). We thank Jin-Tao Hu for her assistance in FCM analysis; Dan Li for helping obtain cadaveric specimens.

Competing Interests

The authors have declared that no competing interest exists.

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Author contact

Corresponding address Corresponding author: Zhuo-Jing Luo. zjluoedu.cn.


Received 2013-3-10
Accepted 2013-6-17
Published 2013-6-21