1. Department of Spinal Surgery, Nanfang Hospital, Southern Medical University, China
2. Department of Spinal Surgery, Provincial Hospital affiliated to Shandong University, China
3. Department of Spinal and Orthopedic Surgery, the First Affiliated Hospital of Fujian Medical University, China
4. Department of Anaesthesia, Nanfang Hospital, Southern Medical University, China
* Zhao-Ming Zhong and Tao Li contributed equally to this work.
Purpose: Abnormal growth of vertebral body growth plate (VBGP) is considered as one of the etiologic factors in the adolescent idiopathic scoliosis (AIS). It was well-known that melatonin was correlated with the emergence and development of AIS. This study aimed to investigate the effect of melatonin on rat VBGP chondrocytes in vitro.
Methods: Chondrocytes were isolated from rat VBGP, and treated with or without melatonin. Cell proliferation was measured by the Alamar Blue assay. Gene expression of collagen type II and aggrecan were evaluated by real-time PCR. Expression of the melatonin receptors (MT1, MT2), proliferating cell nuclear antigen (PCNA, a cell proliferation marker), Sox9 (a chondrocytic differentiation marker) and Smad4 (a common mediator in regulating the proliferation and differentiation of chondrocytes) were detected by Western blotting.
Results: Expression of melatonin receptors (MT1, MT2) were detected in the rat VBGP chondrocytes. Melatonin, at 10 and 100 µg/mL concentration, significantly inhibited the proliferation of VBGP-chondrocytes and the gene expression of collagen type II and aggrecan, and down-regulated the protein expression of PCNA, Sox9 and Smad4. In addition, the inhibitory effect of melatonin was reversed by luzindole, a melatonin receptor antagonist.
Conclusions: These results suggest that melatonin at high concentrations can inhibit the proliferation and differentiation of VBGP chondrocytes, which might give some new insight into the pathogenic mechanism of AIS.
Keywords: melatonin, vertebral body growth plate, adolescent idiopathic scoliosis, proliferating cell nuclear antigen, Sox9, Smad4.
Adolescent idiopathic scoliosis (AIS) is a three-dimensional structural deformity of the spine which is more commonly seen in girls [1-3]. The longitudinal growth of the human vertebral body is through the growth and development of the growth plate . The proliferation and differentiation of growth plate chondrocytes during the growth period plays a key role in regulation of the development of vertebral growth plate . Growing evidence suggested that the growth kinetics indexes of vertebral body growth plate (VBGP) were higher in AIS patients [6-9]. However, the mechanism of regulating the proliferation and differentiation of VBGP chondrocytes in the AIS patients is largely unknown.
Melatonin, or N-acetyl-5-methoxytryptamin, is a hormone mainly synthesized and secreted by the pineal gland . Melatonin exhibits potential multifunctional bioactivities, such as antioxidative defense, anti-inflammatory, endocrinologic and behavioral effects [10-12]. Melatonin deficiency experimentally induced the development of scoliosis in the pinealectomised chicken model [13-15]. The serum level of melatonin in the patients who had progressive curve was significantly lower than the level in the patients who had a stable curve or in the control subjects . Dysfunction of melatonin signaling pathway occurs in osteoblasts derived from AIS patients [17, 18]. These previous studies support the hypothesis that melatonin deficiency might be correlated with the pathogenesis of AIS. Melatonin was found to play an important role in modulating osteoblastic differentiation and bone formation [19-21]. Recently, melatonin has also been reported to enhance cartilage matrix synthesis of porcine articular chondrocytes . However, the effect of melatonin on the proliferation and differentiation of VBGP chondrocytes remains unclear.
The present study was designed to investigate whether melatonin regulates the proliferation and differentiation of VBGP chondrocytes. Chondrocytes from rat VBGP were isolated and cultures in vitro, and treated with melatonin. Cell proliferation was analyzed. Gene expression of collagen type II and aggrecan, and protein expression of the melatonin receptors, proliferating cell nuclear antigen (PCNA, which reflecting the proliferation potentiality of cells), Sox9 (a core transcription factor in controlling chondrocytic differentiation) and Smad4 (a common mediator in regulating the proliferation and differentiation of chondrocytes) were also measured.
VBGP chondrocytes were isolated and cultured in vitro with improved trypsin-collagenase type II digestion method . Briefly, the spine samples were obtained from four 1-week-old Sprague-Dawley rats and the VBGP cartilage tissue was carefully separated under a microscope. After washed by sterile phosphate-buffered saline (PBS), the intact VBGP samples were digested in 0.25% trypsin (Sigma-Aldrich Co., St. Louis, MO, USA) for 30 minutes and then in 0.2% collagenase type Ⅱ (Sigma) for 1 hour. After that, the attached connective tissue and muscle were removed. The VBGP samples were then minced into small pieces and digested in 0.2% collagenase type Ⅱ for 5 hours. After removing tissue debris by a cribble, chondrocytes were collected in DMEM (Gibco BRL, Melbourne, Victoria, Australia) supplemented with 10% fetal bovine serum (Gibco) and incubated in humidified 5% CO2 atmosphere at 37 ℃. The medium was replaced every other day and the cells were subcultured by trypsinization with 0.25% trypsin when reaching a subconfluent state. The chondrocytes were identified by inverted phase contrast microscope. Chondrocytes were identified by inverted phase contrast microscope and staining with toluidine blue as previously described . The first to third passage cells were used in the following studies .
Melatonin (Sigma) was dissolved in absolute ethanol (vehicle) according to the manufacturer's instructions. VBGP chondrocytes were seeded into 96-well culture plates at the rate of 1000 cells/well and were cultured with DMEM containing 10% FBS for 5 days. The medium was then replaced with serum-free DMEM containing various concentrations of melatonin (0.1, 1, 10 and 100 µg/mL), and the cells were incubated for 24 hours.
In order to further investigate the effect of melatonin on proliferation and differentiation of VBGP chondrocytes, luzindole (Sigma), a melatonin receptors antagonist, was also used in this study. Cells were pretreated for 60 minutes with luzindole at a concentration of 100 µg/mL before the melatonin treatment as previously described [26, 27].
The effect of melatonin on proliferation of VBGP chondrocytes was determined by Alamar Blue assay as previously described [28, 29]. Briefly, after cells were cultured with melatonin-containing medium for 24 hours, Alamar Blue (Invitrogen Co., Carlsbad, CA, USA) was added directly to the medium at 10% of the medium volume and was incubated in the incubator for 5 hours. Fluorescence intensity (excitation wavelength: 530 nm, emission wavelength: 590 nm) was measured using a SpectraMax M5 spectrophotometer (Molecular Devices Co., Sunnyvale, CA, USA).
Gene expressions of collagen type II and aggrecan were examined by real-time quantitative polymerase chain reaction (real-time PCR). Briefly, total RNA was extracted using the TRI Reagent ® according to the manufacturer's instructions. 0.5 μg of each RNA sample was converted to cDNA using PrimeScript® RT reagent Kit With gDNA Eraser (Takara, Dalian, China). Real-time PCR was performed using the Mx3005P device (Stratagene, CA, USA.) with SYBR Premix Ex Taq (Takara.) according to the manufacturer's instructions. Sequences of the sense and antisense primers were 5′- AAG GAT GGC TGC ACG AAA CA-3´ and 5′- TGT CCA TGG GTG CAA TGT CA-3´ for detecting rat collagen type II mRNA, 5′- GAG TCA ACC GCT GCA GAC AT -3´ and 5′- CAC ATT GCT CCT GGT CGA TCT-3´ for detecting rat aggrecan mRNA. Rat glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was amplified as an endogenous control with the primer pair of sense 5′-AGA CAG CCG CAT CTT CTT GT-3′ and antisense 5′-CCA CAG TCT TCT GAG TGG CA-3′. Relative gene expressions of collagen type II and aggrecan were calculated by the 2-∆∆CT method and normalized against the expression of GAPDH.
VBGP chondrocytes treated with melatonin at different concentrations were washed 3 times with cold PBS, then lysed with RIPA lysis buffer (Beyotime Bio., Haimen, China). The protein-containing supernatants were obtained by centrifuged at 4°C, 12,000 rpm for 15 minutes. The protein contents were measured according to Bradford's method . Equal amounts of proteins (40μg) were loaded per lane onto 10% SDS-PAGE gels for β-actin (43 kDa), PCNA (36 kDa), Sox9 (56 kDa), Smad4 (65 kDa), MT1/ MT2 (60/39 kDa), and transferred subsequently onto PVDF membranes. After blocking with 5% skim milk in TBST, the membranes were probed with mouse anti-β-actin (1:1000; Zhongshan Goldenbridge Biotechnology Co., Beijing, China), mouse anti-PCNA (1:800; Santa Cruz Biotechnology, Santa Cruz, CA, USA), rabbit anti-Sox9 (1:100; Abcam, Temecula, CA, USA), rabbit anti-Smad4 (1:1000; Abcam) and rabbit anti-MEL-1A/B-R (namely MT1/2, 1:200; Santa Cruz) overnight at 4°C. The membranes were washed 3 times with TBST and incubated with horseradish peroxidase conjugated goat anti-mouse or anti-rabbit IgG (1:5000; Santa Cruz) at room temperature for 1 hour. The immunoreactive bands were visualized by enhanced chemiluminescent kit (Pierce, Rockford,IL, USA).
Results are expressed as mean ± standard deviation (SD). The data from different groups were evaluated using one-way ANOVA, following by Dunnett's post hoc analysis. Multiple comparisons were performed using the LSD method or Dunnett's T3 method. Differences were considered statistically significant at P < 0.05. Statistical analyses were performed using SPSS 13.0 software.
The cultured VBGP chondrocytes were mainly polygonal in shape, and few in irregular shape, their nuclei were mainly round or oval in shape (Fig.1A). Toluidine blue staining also showed that the cells varied somewhat in shape, the nuclei were stained intensely, and the cytoplasm were stained faintly and contained some fine granules (Fig.1B). In order to investigate whether VBGP chondrocyte is a target cell of melatonin, we measured the protein of melatonin receptors in primary cultured rat VBGP chondrocytes. As shown in Fig.1C, melatonin receptors (MT1, MT2) were detected in VBGP chondrocytes.
Melatonin significantly inhibited the proliferation of primary cultured rat VBGP chondrocytes by 13.07% at 10 µg/mL (P< 0.05) and by 38.76% at 100 µg/mL (P< 0.01), but not at 0, 0.1 and 1µg/mL (P> 0.05). There was no significant effect of vehicle (alcohol) on the proliferation of the cells (Fig.2A). Luzindole, a melatonin receptors antagonist, reversed the proliferation inhibition effect of melatonin on rat VBGP chondrocytes (Fig.2B). Furthermore, Melatonin treatment at 10 and 100 µg/mL concentrations also inhibited the protein expression of PCNA, which reflects the proliferation potentiality of cells (Fig.4).
Collagen type II and aggrecan are two typical markers of chondrogenic differentiation. There was no obvious difference in mRNA levels of the chondrogenic marker genes between control groups and melatonin-treated groups at melatonin dosages of 0.1 and 1µg/mL(P> 0.05), but the high concentration of melatonin (10 µg/mL and 100 µg/mL) was shown to down-regulate gene expression of collagen type II and aggrecan of rat VBGP chondrocytes (Fig.3A). However, this inhibited effect was reversed with luzindole treatment at a concentration of 100 µg/mL (Fig.3B).
To further gain insight into the effect of melatonin on the differentiation of VBGP chondrocytes, we investigated the effect of melatonin on expression of Sox9, a transcription factor regulating chondrocyte differentiation, and Smad4, which is a common mediator in regulating the proliferation and differentiation of chondrocytes. As shown in Fig.4, the protein expression of Sox9 and Smad4 were detected in VBGP chondrocytes, which were significantly down-regulated by melatonin treatment at the concentrations of 10 and 100 µg/mL.
Characterization of the cultured VBGP chondrocytes. The cell morphology was evaluated by inverted phase contrast microscope (A) and Toluidine blue staining (B). The cultured VBGP chondrocytes exhibited the mainly polygonal morphology with round or oval nuclei. Melatonin receptors (MT1, MT2) were detected in VBGP chondrocytes(C).
Effects of melatonin on the proliferation of the cultured VBGP chondrocytes. VBGP chondrocytes were incubated for 24 hours with medium containing melatonin at different concentration or vehicle (0.2% ethanol). Cell proliferation was evaluated using Alamar Blue assay. Date from three independent experiments are presented as mean ± SD. *P < 0.05 and #P < 0.01 vs the control (the 0 µg/ml melatonin group) (A). Cells were cultured for 24 hours in the presence or absence of melatonin combined with or without luzindole pretreatment at 100 µg/ml. The date showed that luzindole pretreatment could reverse the proliferation inhibition (B).
Effects of melatonin on the gene expressions of collagen types II and aggrecan in cultured VBGP chondrocytes. VBGP chondrocytes were incubated for 24 hours with medium containing melatonin at different concentration or vehicle (0.2% ethanol). Gene expressions of collagen types II and aggrecan were evaluated by real-time PCR. Date from three independent experiments are presented as mean ± SD. #P < 0.01 vs the control (the 0 µg/ml melatonin group) (A). The melatonin at high concentrations inhibited the gene expressions of collagen types II and aggrecan, but this inhibited effect was reversed with luzindole pretreatment at 100 µg/ml(B).
Effect of melatonin on the protein expression of PCNA, Sox9 and Smad4 in cultured VBGP chondrocytes. VBGP-chondrocytes were treated with melatonin at different concentrations for 24 hours. The effect of melatonin on PCNA, Sox9 and Smad4 expression were assessed by western blotting. Picture and data are representative of three independent experiments. All values are shown as mean ± SD. *P < 0.05 and #P < 0.01 vs the control (the 0 µg/ml melatonin group).
AIS is the single most common form of spinal deformity seen in orthopedic practice. Abnormal high growth indexes of the VBGP were well documented in AIS patients [6-9]. Because scoliosis developed in pinealectomized chickens, melatonin deficiency has been implicated as a possible cause for scoliosis [13-17]. In our study, the existence of melatonin receptors were demonstrated in the rat VBGP chondrocytes, which reveals that VBGP chondrocytes may be the target cells of melatonin. Therefore, there is an urgent need to understand the effects of melatonin on the proliferation and differentiation of VBGP chondrocytes.
The longitudinal growth of spine is through the growth and development of the spinal growth plate [4, 31]. The longitudinal bone growth attributes to endochondral ossification, during which the cartilage transformed into bone . Endochondral ossification depends on the numbers of proliferative zone chondrocytes and their rate of proliferation, the volume of hypertrophic chondrocytes and the cartilage matrix turnover . Therefore, the chondrocytic proliferation events are very important in the development of vertebral growth plate. Here, we provided three lines of evidence for deciding the effects of melatonin on the proliferation of VBGP chondrocytes. First, the presence of melatonin significantly inhibited the proliferation of primary cultured rat VBGP chondrocytes at high concentrations (10 and 100 µg/ml), but not at low concentrations (0, 0.1 and 1µg/ml). Second, melatonin treatment at 10 and 100 µg/mL concentrations also inhibited the protein expression of PCNA, which is a cell proliferation marker . Third, melatonin inhibition of VBGP chondrocyte proliferation is attenuated by luzindole, a melatonin receptor antagonist. These findings suggested that melatonin at high concentrations can inhibit the proliferation of VBGP chondrocytes in vitro.
Chondrocyte differentiation is another key event in the process of endochondral bone formation . Collagen type II and aggrecan are the typical markers of chondrogenic differentiation. Sox9, an early chondrogenic transcription factor, is mainly required in regulating in successive steps of chondrocyte differentiation [36, 37]. Smad4, a central intracellular mediator of transforming growth factor-beta signaling, was reported to play crucial roles in the proliferation and differentiation of chondrocytes [38-40]. We found that melatonin at high concentration (10 and 100 µg/ml) suppressed the process of chondrogenic differentiation, as assessed by the decrease in the mRNA expression of collagen type II and aggrecan. Those melatonin-induced perturbations in chondrogenic gene expression can be prevented by luzindole treatment at a concentration of 100 µg/mL. Furthermore, high concentration of melatonin decreases the protein expression of Sox9 ans Smad4 in VBGP chondrocytes. The results hint that melatonin at high concentration may suppress the process of VBGP chondrocyte differentiation in vitro.
Melatonin deficiency secondary to pinealectomy experimentally induced scoliosis in bipedal animal models, which has similar anatomical features to those of human idiopathic scoliosis [13-17, 41]. However, the published clinical data has addressed the controversy over the role of melatonin deficiency in AIS [16, 42-45]. Serum melatonin concentrations vary considerably according to age: infants younger than 3 months of age secrete very little melatonin, the secretion of melatonin peaks from age 1 to 3 (325 pg/mL) and then declines gradually with age (10 to 60 pg/ mL for adults) . Relative anterior spinal overgrowth in AIS is believed to be a contributing cause of the lordosis and the hypokyphosis . Our results cannot clearly elucidate whether melatonin deficiency is involved into the anterior spinal overgrowth. Uncertainties still surround the role of melatonin at lower concentration on VBGP chondrocytes and future research is needed.
In conclusion, the present study demonstrates for the first time that that melatonin at high doses can inhibit the proliferation and differentiation of VBGP chondrocytes in vitro. These findings give some new insight into the pathogenic mechanism of the AIS.
This work was supported in part by the National Natural Science Foundation of China (No.81000785), and the Natural Science Foundation of Guangdong Province (No. S2012040006830).
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Corresponding author: Jian-Ting Chen. Department of Spinal Surgery, Nanfang Hospital, Southern Medical University, 1838 North Guangzhou Avenue, Guangzhou 510515, China. E-mail: chenjt99com.