Influence of low-level laser irradiation on osteocalcin protein and gene expression in bone tissue¹

Abstract

Purpose:

To evaluate osteocalcin gene and protein expression in vitro and in an in vivo model of ostectomy.

Methods:

Twenty Wistar rats were assigned into two groups A (n=10, laser) and B (n=10, control). Ostectomy was performed in the femur diaphysis; the twenty fragments removed, composed in vitro groups named as in vivo (A and B) and cultivated in CO₂ atmosphere for thirteen days. Low-level laser irradiation was performed in groups A (in vivo and in vitro) by an GaAlAs device (λ=808 nm, dose of 2J/cm², power of 200mW, power density of 0.2W/cm², total energy of 1.25J, spot diameter of 0.02mm) for 5 seconds, at one point, daily. It was performed immunocytochemistry assays in vivo and in vitro groups. In vitro groups were also submitted to RNA extraction, cDNA synthesis and gene expression by quantitative PCR. Statistical analysis was realized with p<0.05.

Results:

Immunocytochemistry scores showed no significant differences between control and laser groups either in vivo and in vitro. Gene expression also showed no statistical differences.

Conclusion:

Low-level laser irradiation did not alter osteocalcin protein and gene expression in vivo and in vitro in the studied period but it may have been expressed them in an earlier period.

Key words:
Low-Level Light Therapy; Osteocalcin; Bone; Rats

Introduction

According to the World Health Organization, there are more than 150 diseases and syndromes related to skeletal and joint problems. Approximately six million long-bone fractures are reported annually in the USA. Although progress has been made in treatment methods over the past decades, approximately 5-10% of fractures still result in delayed union or non-union. Moreover, 600.000 individuals experience prolonged pain and discomfort associated with fracture non-union. This data reports that bone fractures are related to functional disease, disability and burden in world^1-3.

Several treatments were described to bone fractures as internal fixation of fractures that preserve anatomy and early function, although reconstruction and absolute stability of fixation were essential preconditions for success. Besides, shock wave treatment can be used to promote bone healing because produce bone micro fractures, which can stimulate osteoblast synthesis, neovascularization and bone callus. However, non-invasive treatments need to be considered to bone formation as low-level laser (LLL) irradiation^4-7.

Low-level laser irradiation can increase bone formation through osteoblasts mitosis and higher protein deposition and consequently promoting new bone formation. LLL parameters and wavelength are important to regulate bone function. It also was showed that infrared low-level laser increases bone density and gene expression in bone formation^7,8. Osteoblasts are specialized mesenchymal cells that are primarily responsible for the synthesis and deposition of the mineralized collagen-rich matrix that composes bone tissue. They are effector cells for bone formation with the widely known ability to form bone tissue by secretion of alkaline phosphatase, type I collagen, proteoglycan, bone sialoprotein, and osteocalcin (OC)⁸.

Osteocalcin has routinely been used as a serum marker of osteoblastic bone formation and believed to act in the bone matrix to regulate mineralization⁹. A novel function of the skeleton in the regulation of energy metabolism and fat mass has been suggested. Even if it is not possible to exclude the involvement of other bone proteins in the regulation of energy metabolism, OC seems exert not only skeletal effects but also plays a role in the regulation of angiogenesis, male reproduction and energy metabolism. A better understanding of OC functions, mainly the identification of OC receptors and the signaling pathway activated by OC, could also offer exciting opportunities for new therapeutic strategies in bone diseases and metabolic disturbances^9,10.

The aim of this study was to evaluate protein and gene expression of osteocalcin, in vitro and in an in vivo model of ostectomy after low-level laser irradiation.

Methods

All experimental procedures were conducted under Ethical guidelines of COBEA-CONCEA and submitted to approval of Animal Research Ethical Committee of Universidade Federal de São Paulo (UNIFESP), protocol number 0279/2012.

Animals and surgical procedure

Twenty male Wistar rats (12 weeks, proximally 300 g) were provided with regular standard rat food and water ad libitum throughout the experiment and were housed one animal per cage in a room with a 12-h light-dark cycle. Animals were assigned into two groups: A - ostectomy and laser therapy (n=10) and B - ostectomy (n=10). Surgery procedure was performed in all animals of both groups as described by Sella et al.¹¹.

Low-level laser irradiation

Group A (in vitro) received daily, after 70% of confluence, low-level laser irradiation by a Gallium-Aluminum-Arsenide laser (GaAlAs - DMC Equipment, Sao Carlos, Brazil), model Magnus Plus, λ=808 nm, power of 200mW, power density of 0.2 W/cm², fluency of 37 J/cm² per site, nominal dose of 2 J, spot size of 0.02 mm², energy per point=1.25 J, total energy of 1.25J and exposure time of 5 s per application for 13 days. Group B was submitted to the same procedure, however with the instrument in off position. Group A of in vivo received low-level laser irradiation in a single dose, one day after surgery with the same parameters and group B with the laser device off. All laser parameters were described before by Sella et al.¹¹.

Euthanasia and sample collection

After an experimental period of 13 days all animals were euthanized by an overdose of Ketamin 10% (3mL/kg) and heart’s blood exsanguination to perform femurs excision. Femurs were submitted to standard histological procedures (decalcification, dehydration, histological slices - 5µm) in silanized slices to immunohistochemistry assays. Cell culture were tripsinazed by tripsin-EDTA 25% (Sigma Chemical Co., St. Louis, MO, USA) for 10 minutes under 5% of CO₂ atmosphere for cells` liberation. Part of these cells, 10³, were fixed in formalin 10% solution and an aliquot of cells (10³) were kept in RNAlater (Sigma Chemical Co., St. Louis, MO, USA) to gene expression analysis and to preserve RNA sample.

In vitro experiments - cell culture

Twenty femur fragments that were excised by surgical procedure from the in vivo experimental groups composed the in vitro groups following the same division of in vivo groups (A and B). Cell culture was performed with femur fragments with proximally 5mm to obtainment of osteoblasts cells according to Binderman et al.¹². The fragments were placed into PBS buffer solution (pH 7,4; 1 X, sterile) and maintained for 15 minutes, then removed and washed in PBS buffer (pH 7,4; 1 X, sterile) and maintained in DMEM culture medium (Modified Eagle Medium - Dubelcco Nutricell, Campinas, SO, Brazil) with the addition of gentamicin (10 mg/mL - Sigma Chemical Co., St. Louis, MO, USA) and Amphotericin B (250 μg/mL - Sigma Chemical Co., St. Louis, MO, USA) in sterile environment. They were subsequently submitted to mechanical and enzymatic digestion with DMEM to cell extraction, by addition of 2% of collagenase type II (2 mg/mL - Sigma Chemical Co. St. Louis, MO, USA) for 30 minutes at 37°C under constant agitation. The supernatant was stored and the procedure repeated two times. The supernatants were stored and centrifuged at 3000g for 10 minutes. The precipitate was resuspended in 2ml of DMEM containing 10% of fetal bovine serum (Invitrogen - Life Technologies, USA), gentamicin, Amphotericin B, ascorbic acid (5 mg/mL - Sigma Chemical Co. St. Louis, MO, USA), dexamethasone (5 mg/mL - Sigma Chemical Co. St. Louis, MO, USA) and β-glycerophosphate (10 mM - Sigma Chemical Co. St. Louis, MO, USA). After this process, the quantification of cell viability was performed by vital dye trypan blue (Sigma Chemical Co., St. Louis, MO, USA) at Neubauer’s chamber. The cells were seeded in plastic Petri dishes with 2x10⁴cells per plate supplemented with 2 mL of DMEM maintained at 37°C and 5% CO₂, the culture medium was changed every 2 days.

RNA extraction, RNA quantitation and cDNA Synthesis

After 13 days total RNA was extracted from all in vitro samples with a commercial kit AxyPrep Multisource Total RNA (Axygen, Tewksbury, MA, USA) according to manufacturer instructions. For quantification of RNA was used 1μL of RNA and its analyzed by spectrophotometry at 260 nm absorbance (NanoDrop 1000 Spectrophotometer, Thermo Fisher Scientific, Wilmington, DE, USA). cDNA was synthesized from 20 ng of total RNA, 1μL of reverse sequence of each primer, β-actin and Osteocalcin (Table 1) and 1μL of Superscript III^® (2000U/μL, Invitrogen Techonologies).

Table 1
Primers sequences and annealing temperatures (AT) of β-actin and osteocalcin used for gene expression by real time PCR.

Gene	Sequence	AT (ºC)
β-actin	F- 5’AACCGCGAGAAGATGACCCAGATCATGTTT 3’ R- 5’AGCAGCCGTGGCCATCTCTTGCTCGAAGTC 3’	60
Osteocalcin	F- 5’ AGGACCCTCTCTCTGCTCAC 3’ R- 5’ AACGGTGGTGCCATAGATGC 3’	60

Gene expression analysis

Gene expression was performed by real time polymerase chain reaction technique after reverse transcription (qPCR) for β-actin and Osteocalcin genes, following the primers sequences describe in Table 1, using 2μL of cDNA and 8μL of Master Mix (Syber Green PCR Master Mix 1X; β-actin primers 0.075mM; Osteocalcin primers 0.03mM and Milli-Q water to volume adjust). It was set an annealing temperature of 60°C and 50 cycles of denaturation, annealing and extension. All experiments were performed by ™System StepOnePlus (Applied Biosystems^®, Life Technologies Corporation) and software AB Prism Step One. Gene expression was analyzed by Cycle threshold (Ct) comparative technique (2^-ΔΔCt) after normalization between gene of interest and the housekeeping (β-actin). The experiments were performed in triplicate.

Immunohistochemistry (in vivo) and citochemistry (in vitro)

Briefly, histological slices and fixed cells were incubated in sodium citrate buffer 0.01M pH 6.0 with Tween-20 0.05%, at 100°C for 20 minutes for antigenic recuperation. Methanol (0.3%) with hydrogen peroxide (10V) were used for endogenous peroxidase block. All samples were washed in PBS (1X) and incubated with primary antibody, anti-osteocalcin (1:500, Santa Cruz Technologies) overnight at 4ºC. Samples were washed and incubated with secondary antibody DAKO LSAB (DAKO, Glostrup, Denmark) plus System, HRP, for 20 minutes at room temperature with posterior incubation with DAB of Substrate Chromogen Solution (DAKO LSAB, Glostrup, Denmark), for five minutes at room temperature. Slices and cells were stained with metil green solution. Immunoreaction was analyzed by Image J (NIH, free program) evaluating the color formed by the antibody reaction as describes before¹¹.

Statistical analysis

Graph Prism 5.0^® was used to calculate the arithmetic mean and standard deviation. The values of 2^-ΔΔCt, immunohistochemistry and cytochesmitry were statistically analyzed using Wilcoxon-Mann-Whitney test for nonparametric independent samples. It was set significance level of 5% (p <0.05).

Results

After normalization between osteocalcin and β-actin (housekeeping) was produced ΔCt values and showed no significant differences. The expression, median ± standard deviation, of groups A 4.06±3.814 and group B 3.45 ± 4.447 with p=0.756 (Figure 1B). Immunohistochemistry (in vivo) and cytochemistry (in vitro) scores’ values were, respectively, in groups A (median 2.0±0.67) and B (2.5±0.89) (p=1) (Figure 2 A,B) and A (1.6±1.51) and B (0.3±0.82) (p=0.100) (Figure 1A) showed no statistical differences.

Figure 1
Osteocalcin protein expression of in vitro groups (A) and osteocalcin gene expression of in vitro groups (B).

Figure 2
Immunohistochemistry section of groups A (laser) and B (no laser). Figure shows in arrows the scores obtained by reaction and presence of osteocalcin (DAB stain, x100). Osteocalcin is produced and secreted by osteoblasts to extracellular space.

Discussion

Several studies have used osteoblastic cell cultures in the most diverse areas such as light interaction with cells, cytotoxicity, calcium flux and transport, molecular analyzes, growth factors and cell death, but most studies involve cells from young rats from 3 to 21 days and until newborns^12-15. These cells have a high degree of differentiation and proliferation, especially by the high number of fibroblasts and mesenchymal cells.

In this study, unlike the literature, we worked with adult osteoblastic cells from rat femurs that naturally have a difficulty in their handling by the tissue structure itself, besides the difficulty in extracting the cells and specific phenotypic characteristic¹⁵. In addition to the cited points, adult cells are indistinguishable somatic cells, which divide only if there is a need for tissue, as well as in bone fractures, which brings our research closer to the clinical.

The choice to use adult cells is based precisely on the difficulty of this tissue and the resolution of bone fractures. The applicability of this study is related to the same difficulties that the bone tissue would find for the reestablishment of its normal activity. When observing the behavior of adult cells in vitro, it is extrapolated to the environment in which the adult and elderly patient is, since this population has greater difficulty in the process of tissue repair when compared to the pediatric patient.

Earlier studies of our group have shown the applicability of adult cells to cell culture through cytochemical, immunocytochemical and molecular evaluations. These studies aimed at aspects related to the process of bone mineralization and cellular mechanisms in the increase and/or reduction of proteins and ions involved in this process due to the use of low-level laser^16,17.

Low-laser laser has photobiomodulatory properties and in previous studies evaluating the effects in vivo and in vitro, an increase in osteoblastic proliferation and growth factors and cofactors was observed for the bone mineralization process¹⁸. Light, like low-level laser, can be absorbed and stimulate photoreceptors acting on mitochondrial respiratory chain. These photoreceptors stimulate the internal and external mitochondrial membrane, altering the respective membrane potential and leading to an increase in mitochondrial metabolism and consequent increase in ATP production and oxygen consumption.

These stimulations can activate DNA, RNA and the synthesis of cell cycle regulatory proteins, increasing the speed of the mitotic cycle by intensifying the DNA synthesis, as the irradiated cells pass more quickly from the G1 phase to the S phase of the cell cycle increasing cell division¹⁹.

The stimulation of RNA and DNA synthesis is associated with the ability of porphyrins and flavoproteins, components of the respiratory chain, to generate reactive oxygen species, such as singlet oxygen (O^-). Small amounts of these species have beneficial effects by activating the mechanism of cellular mitosis, however, high doses may induce apoptosis and/or necrosis of cells irradiated with low-level laser²⁰.

Some studies have shown the effects of LBI irradiation on osteoblasts in the gene expression of bone morphogenic protein 2 (BMP-2), osteocalcin, transforming growth factor β1 (TGF-β1)²¹, stimulation of bone proliferation and mineralization²². However, these same studies differ on LBI parameters, which may vary in wavelength, energy density and power^23,24.

In our study we used the same parameters for LLL used previously by our group¹¹, however an unused power was chosen in clinical practice so that a larger dose of energy could be provided with a shorter application time^25,26.

Corroborating our findings of osteocalcin, in a study by Wu et al.²⁷using LLL with λ=660nm, 4J/cm², 70mW and Bouvet-Gerbettaz et al.²⁸using GaAlAr LLL with λ=808nm, 4J/cm², 520mW was not observed increase of osteocalcin expression, suggesting that, as the energy density is inside the therapeutic window, the laser power can be responsible to influence the gene expression process in our study, since it was used a 200mW of power.

This leads to the possibility that the gene expression occurs in the initial periods of the cell culture leaving only the protein formed between the 13th and the 20th day. We must consider that the end of the expression must be associated with the presence of a mineralized bone matrix, since this is formed from the expression of the osteocalcin protein associated with calcium deposition. It is suggested that the potency used in this study had a photo inhibitory effect whereas other studies have shown an increase in osteocalcin expression either in vivo or in vitro^29,30.

It should be kept in mind that in the clinic the laser is applied on the skin, while in the cell culture it is applied directly on the cells. This was why our study focused on the in vivo model that analyzed the gene and protein expression through immunohistochemical analysis of the femurs of the animals, however, no differences were observed between the irradiated and non-irradiated groups.

Conclusion

Low-level laser irradiation with these parameters showed no up or down regulation of osteocalcin gene and protein in vivo and in vitro in the studied period and showed just a constant expression between irradiated and control. Our results suggest that low-level laser parameters influence gene and protein expression.

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• Financial sources:

  FAPESP, CAPES and CNPq

• 1
  Research performed at Operative Technique and Experimental Surgery Division, Department of Surgery, Universidade Federal de São Paulo (UNIFESP), and Laboratory of Molecular Biology of FHO-UNIARARAS, Brazil. Part of PhD degree thesis, Postgraduate Program in Interdisciplinary Surgical Science. Tutor: Prof. Dr. Hélio Plapler.

Publication Dates

• Publication in this collection
  Sept 2018

History

• Received
  10 May 2018
• Reviewed
  12 July 2018
• Accepted
  10 Aug 2018