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Acta Cirurgica Brasileira

Print version ISSN 0102-8650On-line version ISSN 1678-2674

Acta Cir. Bras. vol.23 no.6 São Paulo Nov./Dec. 2008

http://dx.doi.org/10.1590/S0102-86502008000600014 

14 - ORIGINAL ARTICLE
EXPERIMENTAL NEUROLOGY

 

S100ß and fibroblast growth factor-2 are present in cultured Schwann cells and may exert paracrine actions on the peripheral nerve injury1

 

S100ß e fator de crescimento de fibroblasto-2 estão presentes nas células de Schwann cultivadas e exercem ações parácrinas na lesão do nervo

 

 

Tatiana DuoblesI; Thais de Sousa LimaI; Beatriz de Freitas Azevedo LevyII; Gerson ChadiIII

IFellow of Department of Neurology, University of São Paulo School of Medicine, São Paulo, Brazil
IIFellow Master degree of Neuroscience and Behavior, Psychology Institute, University of São Paulo, São Paulo, Brazil
IIIMD, PhD, Full Professor, Experimental Neurology, Department of Neurology, University of São Paulo School of Medicine, São Paulo, Brazil

Correspondence

 

 


ABSTRACT

PURPOSE: The neurotrophic factor fibroblast growth factor-2 (FGF-2, bFGF) and Ca++ binding protein S100ß are expressed by the Schwann cells of the peripheral nerves and by the satellite cells of the dorsal root ganglia (DRG). Recent studies have pointed out the importance of the molecules in the paracrine mechanisms related to neuronal maintenance and plasticity of lesioned motor and sensory peripheral neurons. Moreover, cultured Schwann cells have been employed experimentally in the treatment of central nervous system lesions, in special the spinal cord injury, a procedure that triggers an enhanced sensorymotor function. Those cells have been proposed to repair long gap nerve injury.
METHODS: Here we used double labeling immunohistochemistry and Western blot to better characterize in vitro and in vivo the presence of the proteins in the Schwann cells and in the satellite cells of the DRG as well as their regulation in those cells after a crush of the rat sciatic nerve.
RESULTS:
FGF-2 and S100ß are present in the Schwann cells of the sciatic nerve and in the satellite cells of the DRG. S100ß positive satellite cells showed increased size of the axotomized DRG and possessed elevated amount of FGF-2 immunoreactivity. Reactive satellite cells with increased FGF-2 labeling formed a ring-like structure surrounding DRG neuronal cell bodies.Reactive S100ß positive Schwann cells of proximal stump of axotomized sciatic nerve also expressed higher amounts of FGF-2.
CONCLUSION: Reactive peripheral glial cells synthesizing FGF-2 and S100ß may be important in wound repair and restorative events in the lesioned peripheral nerves.

Key words: Dorsal root ganglia. FGF-2. S-100ß. Paracrine action. Satellite cells. Sciatic nerve axotomy.


RESUMO

OBJETIVO: O fator neurotrófico fator de crescimento de fibroblastos-2 (FGF-2, bFGF) e a proteína ligante de Ca++ S100ß são expressos pelas células de Schwann dos nervos e por células satélites do gânglio da raiz dorsal (GRD). Estudos recentes indicam a importância das moléculas nos mecanismos parácrinos relacionados à manutenção neuronal e à plasticidade de neurônios periféricos motores e sensoriais. Além disso, células de Schwann cultivadas têm sido empregadas experimentalmente no tratamento de lesões no sistema nervo central, especialmente na lesão da medula espinal, a qual mostrou uma melhora da função sensoriomotora. Estas células são ainda propostas no reparo do nervo lesado com perda de tecido.
MÉTODOS:
Usamos a dupla marcação imunohistoquímica e o Western blot para caracterizar melhor in vitro e in vivo a presença das proteínas nas células de Schwann e nas células satélites do GRD assim como sua regulação nessas células após a compressão do nervo ciático de ratos.
RESULTADOS:
FGF-2 e S100ß estão presentes nas células de Schwann do nervo ciático e nas células satélites do GRD. Células satélites do GRD axotomizado positivas para S100ß possuíam quantidade aumentada de imurreatividade da FGF-2. Células satélites reativas apresentando maior quantidade de FGF-2 formaram um anel ao redor dos corpos neuronais do GRD. Células de Schwann do coto proximal à axotomia do nervo ciático e positivas para S100ß também expressaram quantidades aumentadas de FGF-2.
CONCLUSÃO: As células gliais periféricas ao sintetizar FGF-2 e S100ß podem ser importantes no reparo de cicatrização e em eventos restaurativos nas lesões do nervo.

Descritores: Gânglio da raiz dorsal. FGF-2. S-100ß. Ação parácrina. Células satélites. Axotomia do nervo ciático.


 

 

Introduction

Satellite and Schwann cells, type of peripheral glia, surround neuronal cell bodies (sensory ganglia) and fibers (sensory and motor neurons) in the peripheral nervous system, providing physical and chemical supports for neurons. Those cells react after axotomy indicating their importance in the wound repair and regeneration1. In fact, interactions of sensory neurons and satellite cells as well as motor neurons and Schwann cells have been described during the development, and in the events of neuroplasticity related to nerve regeneration2.

Fibroblast growth factor-2 (FGF-2, bFGF), a neurotrophic factor member of heparin-binding growth factor family, and the S100ß, a Ca+2 binding protein3,4, seem to exert neurotrophic effects to peripheral sensory and motor neurons5 and can be up-regulated in dorsal root ganglia (DRG) after axotomy6,7.

The actions of glial neurotrophic factors such as FGF-2 and S100ß have been described to central neurons and also investigated recently in the peripheral nervous system8-10. Despite the presence of S100ß in the satellite glial cells of the DRG and in the Schwann cells of the sciatic nerves, the cellular change the S100ß in those cells of axotomized sensory ganglia is still a material of a detailed investigation.

The ability of Schwann cells to trigger neuronal regeneration in the peripheral nervous system has been recently applied to promote neuronal restoration in the central nervous system11. In fact, cultured Schwann cells from sciatic nerve has been employed in the spinal cord regeneration experimentally12, rising the necessity of a more detailed analysis on the presence of neurotrophic molecules in those cells in vitro and in vivo.

In the present study, the presence of FGF-2 and S100ß has been analyzed in cultured Schwann cells as well as in the normal and axotomized DRG and sciatic nerve of the rat, by means of Western blot and immunocytochemical analyses.

 

Methods

Specific pathogen-free adult male Wistar rats [body weight (b.w.) 200g, n=8] from the University of São Paulo were kept under controlled temperature and humidity conditions with a standardized light-dark cycle (lights on at 7.00 a.m. and off at 7.00 p.m.) and free access to food pellets and tap water. The study was conducted under protocols approved by the Animal Care and Use Ethic Committee at University of São Paulo and in accordance with the Guide for the Care and Use of Laboratory Animals.

Schwann cell culture

Pure cultures of Schwann cells were obtained from sciatic nerves explants of adult Wistar rats as described previously13. Briefly, animals were deeply anaesthetized with sodium pentobarbital 3% (100mg/kg, ip) and sciatic nerves were dissected under sterile conditions, placed in 60 mm dishes containing Leibovitz-15 medium (L-15; Gibco, Grand Island, NY), and divested of their epineurial sheaths. Nerves were chopped into 1 mm2 pieces and transferred to 35mm dishes containing DMEM (Gibco) supplemented with 10% fetal bovine serum (FBS; Hyclone Laboratories, Logan, UT), 50 mg/ml gentamycin (DMEM-10; Gibco, NY). Nerve pieces were transferred to another 35 mm dish every week for 5 weeks and were fed twice a week. After five transfers, explants were devoid of fibroblasts and contained only Schwann cells. Explants were replated onto 35 mm dishes with 1.25 U/ml dispase (Boehringer Mannheim, Mannheim, Germany), 0.05% collagenase (Worthington, Freehold, NJ), and 15% FBS in DMEM and were incubated at 37°C in 6% CO2 overnight. After incubation, explants were washed with DMEM-10 and dissociated, and the SC were seeded onto poly-L-lysine-coated 100 mm dishes at a density of 2-3x106 cells/dish. After 24 hours, the culture medium was changed to DMEM-10 supplemented with 2 mM forskolin (Sigma, St.Louis, MO) and 20 mg/ml pituitary extract (Gibco). Cells, fed twice a week with that medium, were allowed to expand until confluence. The purified SC were suspended in culture medium to yield a final density of 106 cells/ml.

Immunocytochemistry

Schwann cell cultures were rinsed 2 times with phosphate buffered saline (PBS), and then fixed in paraformaldeyde (30min, at 4ºC). Sequential incubation of the fixed cells then took place at room temperature in: (1) wash in PBS for 5min in agitation; (2) wash in PBS with 1% Triton for 10min; (3) wash in PBS with 0.02% Tween 20 (BioRad) for 5min; (4) wash in PBS with 0.02% Tween 20 and 1% BSA (Sigma) for 5min; (5) block in PBS with 2% normal goat serum (NGS), 4% BSA, 0.2% Triton (Sigma) for 30min; (6) primary antibody incubation: using policlonal S-100 (Dako) or FGF-2 (Sigma) at 1:100 dilution in 2% NGS, 4% BSA, 0.2% Triton in PBS overnight. (7) Wash 3 times with PBS; (8) secondary antibody incubation with biotinylated anti-rabbit IgG (Vector Laboratories) at 1:250 dilution in PBS with 0.2% Triton, 1% NGS, 2% BSA for 2 hours; (9) wash 3 times with cold PBS; (10) Incubation with Avidin-Biotin at 1:125 dilution in PBS; (11) wash again 3 times with PBS; (12) DAB reaction until color observation. The reaction was made in 0.01% H2O2, 0.5mg DAB/ml. DAB labeled cultures were washed 3 times with distillated water, and the reaction was interrupted with Trizma.

Western blot analysis of cultured Schwann cells

Schwann cell FGF-2 and S100ß proteins were assessed by Western blot analysis14. The Schwann cells cultures were homogenized in PBS, pH 7.4, containing 1% NP40, 0.5% sodium deoxycholate, 1% sodium dodecyl sulfate, 1 mM ethylenediamine-tetraacetic acid, 1 mM ethylene glycol tetraacetic acid, and 1% protease inhibitor cocktail (Sigma). After centrifugation at 14,000 rpm for 20 min, the supernatants were transferred into new tubes and stored at -70º C until use. Protein concentrations were determined. The samples were separated on a sodium dodecyl sulfate-polyacrylamide gel electrophoresis (30µg of protein/lane) using a 12% Tris-HCl ready gel (Bio-Rad, California, USA) at 100V for 1h. Proteins were transferred to nitrocellulose membrane for 1h at 100V. After 1h blocking with 5% milk in Tris-buffered saline 0.05% Tween 20 (TBS-T). Membranes were incubated overnight with rabbit polyclonal antibodies to bovine FGF-2 (residues 1-24) (1:1,000, Sigma, USA) or to S100ß protein (1:250, Dako, Denmark). The antisera were diluted in 3% milk/TBS-T. Membranes were washed 2 times for 10 minutes in TBS-T and incubated at room temperature for 1h with anti-rabbit (1:10,000, Amersham, USA, diluted as described above) IgG-ECL conjugated secondary antibody. Blots were washed two times with TBS-T and once in TBS. After final washes, the membrane was incubated with Western Lightning Chemiluminescence Reagent Plus (PerkinElmer Life Science, USA) for 1 minute. The membranes were exposed to an X-ray film for imaging (HyperfilmTM ECL, Amersham Biosciences, USA) to visualize protein bands.

Animals treatment

Rats (n=5) were anaesthetized with sodium pentobarbital 3% (38 mg/kg, ip) and submitted to an unilateral crush (Figure 1) of the sciatic nerve as described elsewhere15. The proximal stump of the sciatic nerve was studied and contralateral unoperated side was used as control. Seven days after surgery, the rats were deeply anesthetized and killed by a transcardiac perfusion through a cannula inserted in the ascending aorta with 50 ml of isotonic saline at room temperature followed by 350 ml (rats) of fixation fluid (4ºC) over 6 min. The fixative consisted of 4% (w/v) paraformaldehyde and 0.2% (v/v) picric acid in 0.1M phosphate buffer (pH 6.9). The tissues were then rinsed in 10% sucrose (Merck, Germany) in 0.1M phosphate buffered saline, pH 7.4 (PBS) for 48 h, frozen in dry ice-cooled (-40ºC) isopentane (Sigma, U.S.A) and stored at -70ºC freezer until use for immunohistochemical experiments as described bellow.

 

 

Immunohistochemical procedures of the sciatic nerve and DRG

Adjacent serial thaw-mounted 14 µm sections were obtained with a cryostat (Leica, CM 3000, Germany) from the entire DRG and sciatic nerve fragments, bilaterally, of the rats. The sections were sampled systematically during sectioning. Seven series were obtained, including every seventh section. Immunoreactivity was detected by the avidin-biotin peroxidase technique16-18. Sections were washed for 2x10 min in PBS and incubated with 5% normal goat serum (Sigma) for 30 min at room temperature with shaking. In the one-color immunoperoxidase experiments sections were then incubated for 48 h at 4ºC with rabbit polyclonal antisera against the residues 1-24 of the bovine FGF-2 (Sigma), or also against a cow S100ß (Dakopatts, Denmark).

The antibodies were diluted (1:1500) in PBS containing 0.5% Triton X-100 (Sigma) and 1% bovine serum albumin (Sigma). The sections were washed again in PBS (2x10 min) and incubated with biotinylated goat anti-rabbit immunoglobulins diluted 1:250 (Vector, U.S.A.) for 2 h. After rinsing in PBS, they were incubated with an avidin-biotin peroxidase complex (both diluted 1:100, Vectastain, Vector) for 90 min. Immunoreactivity was visualized using 3-3'-diaminobenzidine tetrahydrocloride (DAB, Sigma) as a chromogen and H2O2 (0.05%, v/v, Sigma) for 8 min. The anti-cow S100 was a purified immunoglobulin fraction from rabbit antiserum; it reacts with S100α and S100ß in many species including rat (Dakopatts).

Furthermore, two-color immunoperoxidase was used for further evaluation of the simultaneous detection of the FGF-2 and S100ß immunoreactivities. Briefly, FGF-2 immunostaining of the polyclonal bovine and rat FGF-2 antisera was performed as described above. Following the DAB reaction, the sections were rinsed several times in PBS and incubated over 48 h at 4°C with the rabbit polyclonal S100ß antiserum (diluted 1:400). After several more rinses in PBS, they were incubated with biotinylated goat anti-rabbit immunoglobulin (diluted 1:200, Vector) for 1 h at room temperature, rinsed again in PBS, incubated with the avidin-biotin solution (both diluted 1:100, Vectastain, Vector) for 45 min at room temperature, and stained for 10 min using 0.05% 4-chloro-naphthol (Sigma) as a chromogen and 0.05% (v/v) H2O2 (Sigma). The sections were rinsed in PBS and cover-slipped in a glycerol phosphate buffered medium. This procedure gave a brownish color to the FGF-2 immunoreactivities and a bluish color to the S100ß immunoreactivity. The sections were analyzed and photographed with an AX70 Olympus photomicroscope (U.S.A).

As controls, adjacent sections were incubated in the absence of either the primary or secondary antibodies in the one- and two-color immunohistochemical procedures. Some sections were also incubated with the solvent of the avidin-biotin solution.

 

Results

FGF-2 and S100ß in the cultured Schwann cells

Immunocytochemistry demonstrated the presence of a strong labeling of S100ß in the cytoplasm of the cultured Schwann cells (Figure 2A). All Schwann cells in the culture stained for S100ß. Cultured cells were confluent and occupied the majority of the spaces in the plate surface as seen in the picture of phase contrast microscopy (Figure 2A,C). Confluent Schwann cells possessed a round to elliptic shape with 2 long well visible processes (Figure 2A). Moreover, FGF-2 immunoreactivity was also found in the majority of confluent cultured Schwann cells (Fig 2B).

 

 

Moreover, the Western blot technique revealed the band of the FGF-2 protein in the homogenized cultured Schwann cells (Figure 3). The analysis of the position of the band of the FGF-2 signal revealed a molecular weight of 18kDA. Furthermore, the Western blot method also showed the band of the S100ß protein in the homogenized cultured Schwann cells (Figure 3). The analysis of the position of the band of the S100ß signal revealed a molecular weight of 10kDA.

 

 

FGF-2 and S100ß in the satellite cells and Schwann cells in vivo and the effects of the sciatic nerve axotomy

Two-color immunoperoxidase method for simultaneous detection of FGF-2 and S100ß demonstrated the presence of a brownish color FGF-2 labeling in the bluish color S100ß immunostained satellite cells of the DRG and also in the bluish color S100ß immunostained Schwann cells of the sciatic nerve of the rat (Figure 4A,D).

 

The S100ß immunoreactive satellite cells of the axotomized DRG showed larger cytoplasm and accumulated increased amount of the FGF-2 immunoreactivity when compared to the contralateral unoperated side (Figure 4C,D). Moreover, the larger reactive satellite cells of the axotomized DRG formed ring like structures around the DRG neurons particularly those of larger size. Furthermore, the S100ß immunoreactive Schwann cells of the proximal stump of the axotomized sciatic nerve also accumulated increased amount of the FGF-2 immunoreaction product when compared to the contralateral unoperated side (Figure 4A,B).

Control sections of the DRG and nerves incubated with FGF-2 pre-adsorbed antibody showed no immunoreaction (not shown). Sections incubated with the solvent for the primary FGF-2 and S100ß antibodies, secondary antibody, or for avidin-biotin also showed no reaction.

 

Discussion

S100ß immunoreactive satellite cells surrounding the sensory neurons of the DRG indicate a functional interactive relationship. Sensory neurons of DRG are surrounded by satellite cell cytoplasmic expansions linked by gap junctional communications19. This morphological aspect further emphasizes the existence of a paracrine regulation, involving satellite glia and sensory neuron in the DRG. Moreover, sciatic nerve Schwann cells are also stained for S100ß immunoreactivity thus being an important histological marker to identify those cells. As described for the satellite cells/neuronal cell bodies of rat DRG, the Schwann cells also surround motor and sensory peripheral fibers forming the myelin sheath. Besides the functional importance of the myelin to neurons regarding the conduction of the action potential, the Schwann cells likely the satellite cells function as an important paracrine regulator of peripheral neurons at axonal level20,21.

Regardless the common embryonic origin of the DRG satellite cells and the Schwann cells, it seems possible that those cells share the ability to monitor and to trigger physiological functions of their neighbor neurons. The paracrine trophic actions of satellite cells and the Schwann cells have been described during development of peripheral neurons7,19, and in the pos natal life regarding the maintenance and protection from injury-induced cell death5.

The above consideration might explain the fact that satellite and Schwann cells may express similar types of molecules particularly in lesioned situations as described in the present analysis. The Schwann cells expressing FGF-2 and S100ß proteins were confirmed in the present analysis by means of immunocytochemistry and Western blot techniques.

The paracrine regulation among the satellite glia/Schwann cells and the lesioned peripheral neurons have been postulated because the neuronal disappearance coincides with the death of the up-regulated satellite cells after axotomy22. Moreover, axotomy also induces the hyperplasia of perineuronal satellite cells and triggers an incremented coupling in the lesioned DRG23. Likewise, Schwann cells react after axotomy both distally and proximally to the site of nerve injury. It seems possible that a trophic interaction of reactive satellite glia/Schwann cells and peripheral neurons is related to neuronal protection and/or nerve regeneration after axotomy2. It is likely that the satellite glia is also related to a continuous regulation of function and plasticity in peripheral sensory neurons as described for astrocytes in the lesioned central nervous system20,24-26.

Neurotrophic factors produced by satellite cells and Schwann cells are the key molecules in the mechanisms of peripheral neuronal development, maintenance, function and regeneration7,15.

S100ß immunoreactivity has been used as a marker for Schwann cells in vivo and in vitro27,28 and also for the satellite cells in vivo7. Moreover, the localization of S100ß protein in satellite cells of the DRG has been implicated in the maturation and trophic mechanisms of DRG neurons during development29.

It is known that FGF-2 is able to protect adult DRG neurons from lesion-induced sensory nerve cell death5. Moreover, FGF-2 immunoreactivity was demonstrated in cultured neuronal cells derived from DRG of chick and rat embryos, and also in developing rat DRG in vivo30,31.

We demonstrated here FGF-2 immunoreactivity in the satellite cells labeled by S100ß immunoreactivity respectively in the rat DRG and sciatic nerve by means of two-color immunohistochemistry. Our results are in line with previous descriptions that have identified FGF-2 mRNA signal in putative satellite cells of the rat DRG and Schwann cells by means of in situ hybridization6. Moreover, we have described in a previous publication7 increases of FGF-2 immunoreactivity in lumbar DRG and sciatic nerve of adult rat after axotomy. We have also showed increases of S100ß immunoreactivity in satellite cells of axotomized DRG by means of microdensitometric image analysis7. Two-color immunoperoxidase for FGF-2 detection in the S100ß positive satellite cells confirmed the increases of the FGF-2 product in reactive satellite glia of the axotomized DRG and also in the Schwann cells of proximal stump of axotomy of the sciatic nerve. An elevated number of Schwann cells expressing higher amounts of the FGF-2 immunoreactivity was also found in the proximal stump of the lesioned sciatic nerve. These observations confirmed and extended our previous analysis7.

Moreover, our results are in line and extend previous publications that have demonstrated increases of FGF-2 mRNA signal in putative satellite cells of DRG and in putative Schwann cells after axotomy of sciatic nerve32. Furthermore, increased FGF-2 mRNA signal was detected in macrophages and Schwann cells at the lesion site of axotomized sciatic nerve, as revealed by the cellular analysis of consecutive section33.

By means of S100ß immunohistochemistry, we identified increased amount of FGF-2 in activated DRG satellite cells and sciatic nerve Schwann cells after axotomy, cells that also expressed increased amount of S100ß protein, suggesting a possible interaction between those two molecules. Moreover, the increased S100ß and FGF-2 in reactive satellite cells of axotomized DRG and lesioned sciatic nerve may also be associated with local neovascularization, gliogenesis and repair34 as well as to paracrine neuronal trophism and plasticity in remaining DRG peripheral motor neurons.

 

Conclusion

The changes of FGF-2 and S100ß in activated satellite cells and Schwann cells of axotomized DRG and sciatic nerve respectively, open up the possibility for interactions between those molecules, a possible mechanism that should be investigated in the trophic/repair regulation of lesioned peripheral nervous system, thus important in the restoration of the lesioned nerves.

 

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Correspondence:
Gerson Chadi, M.D., Full Professor
Department of Neurology
University of São Paulo
Av. Dr. Arnaldo, 455 2nd floor, room 2119
01246-903 - São Paulo.Brazil
Phone: 55 11 3061-7460
gerchadi@usp.br

Received: August 16, 2008
Review: September 14, 2008
Accepted:October 21, 2008
Conflict of interest: none
Financial source: FAPESP and CNPq

 

 

How to cite this article
Duobles T, Lima TS, Levy BF, Chadi G. S100ß and fibroblast growth factor-2 are present in cultured Schwann cells and may exert paracrine actions on the peripheral nerve injury Acta Cir Bras. [serial on the Internet] 2008 Nov-Dec; 23(6). Available from URL: http://www.scielo.br/acb
1 Research performed at Neuroregeneration Center (LIM 45), Department of Neurology, University of São Paulo School of Medicine, University of São Paulo, São Paulo, Brazil

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