Changes in cell shape and desmin intermediate filament distribution are associated with down-regulation of desmin expression in C2C12 myoblasts grown in the absence of extracellular Ca2+

Braz J Med Biol Res, July 2005, Volume 38(7) 1025-1032

Changes in cell shape and desmin intermediate filament distribution are associated with down-regulation of desmin expression in C2C12 myoblasts grown in the absence of extracellular Ca ²⁺

C.S. Mermelstein, L.M. Amaral, M.I.L. Rebello, J.S.N. Reis, R. Borojevic and M.L. Costa

Departamento de Histologia e Embriologia, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil

References

^{Correspondence and Footnotes}

Abstract

Desmin is the main intermediate filament (IF) protein of muscle cells. In skeletal muscle, desmin IFs form a scaffold that interconnects the entire contractile apparatus with the subsarcolemmal cytoskeleton and cytoplasmic organelles. The interaction between desmin and the sarcolemma is mediated by a number of membrane proteins, many of which are Ca²⁺-sensitive. In the present study, we analyzed the effects of the Ca²⁺ chelator EGTA (1.75 mM) on the expression and distribution of desmin in C2C12 myoblasts grown in culture. We used indirect immunofluorescence microscopy and reverse transcription polymerase chain reaction (RT-PCR) to analyze desmin distribution and expression in C2C12 cells grown in the presence or absence of EGTA. Control C2C12 myoblasts showed a well-spread morphology after a few hours in culture and became bipolar when grown for 24 h in the presence of EGTA. Control C2C12 cells showed a dense network of desmin from the perinuclear region to the cell periphery, whereas EGTA-treated cells showed desmin aggregates in the cytoplasm. RT-PCR analysis revealed a down-regulation of desmin expression in EGTA-treated C2C12 cells compared to untreated cells. The present results suggest that extracellular Ca²⁺ availability plays a role in the regulation of desmin expression and in the spatial distribution of desmin IFs in myoblasts, and is involved in the generation and maintenance of myoblast cell shape.

Key words: Extracellular Ca^2+, EGTA, Myoblasts, Desmin, Intermediate filaments, RT-PCR

Introduction

Desmin (53 kDa) is the main intermediate filament protein of striated muscle cells. This abundant protein polymerizes to form an extensive network of 10-nm intermediate filaments that span the nuclear envelope to the sarcolemma and link myofibrils together in a three-dimensional scaffold around Z discs, forming an extrasarcomeric component of the muscle cytoskeleton (1). Therefore, desmin has structural domains that direct or indirectly link this protein to the nuclear membrane, Z-disk components and the sarcolemma. It has been shown that desmin is present in subsarcolemmal costameres in association with membrane and membrane-associated proteins such as the dystrophin protein complex (2), spectrin, ankyrin, integrins, vinculin, and a-actinin (3). Mutational analysis indicates that it is the head domain of desmin that is specialized for its association with the sarcolemma (4). The association of desmin with the sarcolemma is supposed to be dependent on the versatile cytoskeletal linker protein plectin (5), which is a very large size polypeptide (>500 kDa) abundant in the subsarcolemmal region. Many transmembrane components of these complexes are Ca²⁺-sensitive in their intra- and extracellular domains. Variations in extracellular Ca²⁺ concentration are one of the regulatory mechanisms involved in the activation of these membrane complexes through conformational changes (6,7). One of the evolutionary advantages of Ca²⁺ ions as regulators of protein structure and function is the possibility of rapid changes in their concentration (8).

To investigate the function of desmin in all muscle types in vivo, desmin null mice were generated by homologous recombination (9). Although a considerable number of these mice are viable and fertile, they present a multisystem disorder involving cardiac, skeletal and smooth muscle that begins early during postnatal life. Histological and electron microscopic analysis of both heart and skeletal muscle tissues reveals severe disruption of muscle architecture and degeneration, including perturbation of myofibril anchorage to the sarcolemma. The study of desmin is especially relevant because a number of desmin-related pathologies have been described (10). Desmin-myopathies consist of alterations in the distribution of desmin, particularly the presence of desmin aggregates and inclusions in the cytoplasm of myogenic cells (11).

Previous work from our group suggested a role for extracellular Ca²⁺ in the regulation of the spatial distribution of microfilaments, microtubules, intermediate filaments, and adhesion sites in myoblasts (12). The present investigation was undertaken to study the effects of extracellular Ca²⁺ withdrawal on cell shape and on the expression and distribution of desmin in myoblasts grown in culture.

Material and Methods

Antibodies and fluorescent probes

Rabbit polyclonal anti-desmin antibody was purchased from Sigma (St. Louis, MO, USA) and fluorescein isothiocyanate-goat anti-rabbit IgG antibody was purchased from Jackson Immunoresearch Laboratories (West Grove, PA, USA). The nuclear dye DAPI (4'6-diamino-2-phenylindole dihydrochloride) was purchased from Molecular Probes Inc. (Eugene, OR, USA).

Cell cultures

The mouse skeletal muscle cell line C2C12 was obtained from the Rio de Janeiro Cell Bank (PABCAM, Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil). Cells were routinely grown in Dulbecco's modified Eagle's medium containing 20% fetal calf serum, 1% L-glutamine and 1% penicillin-streptomycin (all from Sigma), in a humidified 5% CO₂ atmosphere at 37ºC. Cells were grown at a low density of 5 x 10⁵ cells/35-mm culture dishs (Nunc, Roskilde, Denmark) onto aclar plastic coverslips (Pro-Plastics Inc., Linden, NJ, USA) coated with rat collagen. EGTA (Sigma) at a concentration of 1.75 mM (12,13) was added to the medium of subconfluent cultures. Both control and EGTA-treated cultures were fed daily with fresh medium containing or not EGTA. After 24 h of EGTA exposure, live cultures were observed by phase contrast microscopy, or cells were submitted to fluorescence microscopy or to semi-quantitative polymerase chain reaction (RT-PCR).

Immunofluorescence and phase contrast microscopy

For immunofluorescence microscopy, cultures were rinsed with phosphate-buffered saline (PBS) and fixed with 2% formaldehyde in PBS for 3 min at room temperature (14). They were then permeabilized with 0.5% Triton-X 100 (Sigma) in PBS three times for 10 min. The same solution was used for all subsequent washing steps. Cells were incubated with anti-desmin polyclonal antibody at 1:100 dilution for 1 h at 37ºC in a humid chamber. After incubation, cells were washed for 30 min and incubated with secondary antibody for 1 h at 37ºC in a humid chamber, and then washed for 30 min. After a 30-min wash with PBS, the nuclear dye DAPI was added at 0.1 µg/ml in 0.9% NaCl for 5 min. Cells were washed for 5 min with 0.9% NaCl and specimens were mounted in glycerol containing, by weight, 5% n-propyl gallate, 0.25% 1,4-diazabicyclo[2.2.2]octane and 0.0025% para-phenylenediamine (all from Sigma). Cells were examined with an Axiovert 100 epifluorescence inverted light microscope (Carl Zeiss, Oberkochen, Germany) using filter sets that were selective for fluorescein or blue wavelength channel. Images were acquired with a C2400i integrated CCD camera (Hamamatsu Photonics, Shizuoka, Japan) using an Argus 20 image processor (Hamamatsu Photonics). Digitalized images were transferred to a Dell OptiPlex GL 575 computer (Dell Corporate, Round Rock, TX, USA) and plates were mounted using Adobe Photoshop software (Adobe Systems Incorporated, San Jose, CA, USA).

Control experiments with no primary antibody showed only a faint background staining (data not shown).

Live C2C12 cells grown on collagen-coated aclar coverslips were examined and images were acquired by phase contrast microscopy using the same microscope and digital system described above.

Digital image processing and analysis

Phase contrast images were analyzed using the public domain NIH Image program (developed at the US National Institutes of Health and available on the Internet at http://rsb.info.nih.gov/nih-image). Pixels with a gray-level over 125 were set to black, and cells were initially isolated with 4 series of erosions and dilations. Cells were then manually separated from their neighbors for proper identification as objects. The parameters area, perimeter, major axis, minor axis, angle, and axis ratio (ratio between the major and the minor axis of cells) were measured. Only cells over 200 pixels in area were considered in order to avoid computing parts of cells. Images were calibrated at 1.02 pixels/µm using a slide with a grating. After automatically measuring all the cells/objects, data were exported to Excel (Microsoft Corporation, Redmond, WA, USA) and to Statistic for Windows (StatSoft Inc., Tulsa, OK, USA) for statistical analysis.

RNA extraction, reverse transcription, amplification and RT-PCR

Total cellular RNA from control and 24-h EGTA-treated C2C12 cells was isolated using TRIzol^® reagent. The RNA and the cDNA were quantified by spectrophotometry (Spectronic, Genesys 2PC, Rochester, NY, USA). cDNA was synthesized from 3 µg total RNA. RNA was primed with 0.5 µg oligo-(dT)_12-18 primer (reaction volume: 20 µl). After RNA was denatured (10 min at 70ºC) and cooled on ice, the following reagents were mixed and then added: 10 mM of each deoxynucleoside triphosphate (dNTP), 6 µl 5x reverse transcription (RT) buffer, 0.1 mM DTT, and 200 U superscript RT (reaction volume: 30 µl). The reaction was performed by incubation for 1 h at 42ºC.

Amplification reactions consisted of a 0.2 µM primer for desmin (5' primer sequence: TCTCCCGTGTTCCCT/3' primer sequence: ATACGAGCTAGAGTGGCA; size of PCR product: 571 base pairs), 10 mM of each dNTP, PCR buffer, 5 µl of the cDNA reaction, and 0.5 U Taq DNA polymerase. The primer sequence for glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was ATCA CCATCTTCCAGGAGCG (sense) and CCTG CTTCACCACCTTCTTG (antisense). cDNAs from control and EGTA-treated cells were subjected to PCR amplifications with serial dilutions at 0.1, 0.01, and 0.001 µg. GAPDH expression was used to standardize cDNA under non-saturating conditions at 28 cycles. Amplification was carried out during 33 PCR cycles for desmin, each cycle consisting of a denaturation step at 94ºC for 1 min, another denaturing step at 94ºC for 30 s, an annealing step at 60ºC for 30 s, and an extension step at 72ºC for 30 s. After the last cycle, incubation for another 5 min at 72ºC was performed. The PCR products (10 µl) were analyzed by electrophoresis in 1% agarose gels with Tris-borate-EDTA buffer, stained with 1 µg/ml ethidium bromide for 10 min and analyzed with the thermal imaging system FTI-500 (Pharmacia, Uppsala, Sweden). Gels were scanned with a Silver Scanner II (LaCie Limited, Hillsboro, OR, USA), at 400 dpi, and densitometric profiles were obtained using the public domain NIH Image program (developed at the US National Institutes of Health and available on the Internet at http://rsb.info.nih.gov/nih-image). Areas corresponding to the GAPDH and desmin gel bands from each profile were selected and the number of pixels in each peak was measured. For normalization, desmin expression (number of pixels in the gel band) was divided by GAPDH expression (for 0.1 and 0.01 µg cDNA dilution) for both control and EGTA-treated samples, and then plotted on a column chart. Data related to 0.001 µg cDNA were not submitted to normalization and analysis since they were considered to be below the minimum level of expression and visualization in the gels.

Results

To better understand the role of extracellular Ca²⁺ in the expression and distribution of the muscle-specific protein desmin, skeletal muscle C2C12 cells were grown in the presence or in the absence of the Ca²⁺-chelator EGTA (1.75 mM) and then observed by phase contrast microscopy. C2C12 cells grown in normal medium without EGTA (control cells) were well spread (Figure 1A), whereas the majority of C2C12 cells grown in medium with EGTA for 24 h drastically changed to a bipolar morphology (Figure 1B).

Since there were major observable changes in the overall shape of cells treated with EGTA for 24 h, we decided to quantify these changes using digital processing of phase contrast microscopy images. Figures 1C and 1D show the digitally processed images from control C2C12 cells and EGTA-treated C2C12 cells. The parameters area, perimeter, major axis, minor axis, angle, and axis ratio (ratio between the major and the minor axis of cells) were computed for the isolated objects from both processed images. The major significant (P < 0.001) differences between control and EGTA-treated cells concerned the area, minor axis and axis ratio. Area measurements were 29.79 ± 19.78 µm² for control cells and 18.30 ± 9.70 µm² for EGTA-treated cells. Minor axis measurements were 3.04 ± 1.41 µm for control cells and 1.39 ± 0.36 µm for EGTA-treated cells. Axis ratio measurements were 5.03 ± 3.47 for control cells and 12.78 ± 6.98 for EGTA-treated cells. The other parameters (perimeter, major axis and angle) were not significantly different between control and EGTA-treated cells (data not shown).

It is possible to see that the areas of control C2C12 cells were larger than those of EGTA-treated cells (Figure 2A). Not only were the EGTA-treated cells smaller, but they also varied less in shape, as shown in the histogram in Figure 2A and by comparing the standard deviation (SD) of the cell areas described above.

The elongation of the cells can be quantified by the axis ratio (the ratio between the major and the minor axis of cells). The axis ratio of EGTA-treated C2C12 cells was more than two-fold greater than that of control cells (Figure 2B), showing that treated cells were more elongated than control cells.

To investigate whether the observed cell shape changes in EGTA-treated C2C12 were related to the distribution of the cytoskeleton, we analyzed the organization of the intermediate filament desmin in these cells, since it has been postulated that desmin has a major structural role in maintaining the shape of myogenic cells (1,15). Indirect immunofluorescence microscopy using a polyclonal antibody against desmin revealed a characteristic desmin filament organization spanning the distance from a highly concentrated area around the nuclear envelope to the plasma membrane (Figure 3A), while EGTA-treated cells showed a less intense desmin staining, which was visible mainly as dots and short filaments (Figure 3C). The nuclear staining with DAPI showed a normal nuclear pattern in both control cells (Figure 3B) and in cells treated with EGTA for 24 h (Figure 3D), confirming that EGTA-treated cells were viable.

Since in the immunofluorescence images of EGTA-treated cells desmin appeared to have a less intense staining, we decided to further analyze desmin expression by RT-PCR. In agreement with the immunofluorescence analysis, we confirmed that desmin expression was down-regulated in C2C12 cells treated with EGTA for 24 h (Figure 4B) when compared to untreated C2C12 cells (control) that showed a comparatively higher expression of desmin (Figure 4A). These results can be better visualized in the normalized data obtained by densitometric analysis of the agarose gels shown in Figure 4C.

Figure 1.
Phase contrast microscopy of C2C12 grown in the absence of EGTA (control cells, A) or in the presence of 1.75 mM EGTA for 24 h (B). Digitally processed images of C2C12 cells in the absence of EGTA (control cells, C) and in the presence of 1.75 mM EGTA (D) (from images A and B, respectively). Bar = 50 µm.

Figure 2.
Histogram and best-fit plot of control and EGTA-treated cell area (A), and major/minor axis ratio of control and EGTA-treated cells (B). Axis ratio data from control and EGTA-treated groups were compared statistically (*P < 0.0001, t-test for independent samples). Both histograms were obtained from data described in the Results section.

Figure 3.
Fluorescence microscopy of C2C12 cells grown in the absence of EGTA (control cells, A and B) or in the presence of 1.75 mM EGTA for 24 h (C and D). Cells were stained with anti-desmin antibody (A and C) and with the nuclear probe DAPI (B and D). Desmin is present as a dense network of filaments in control cells (A), as opposed to fragmented filaments and dots observed in EGTA-treated cells (C). Bar in B corresponds to 10 µm and bar in D corresponds to 5 µm.

Figure 4.
RT-PCR analysis of the expression of desmin in control (A) and in 24-h EGTA-treated C2C12 cells (B). Lanes 1-3 of both agarose gels (A and B) correspond to GAPDH expression (0.1 µg, 0.01 µg, and 0.001 µg cDNA, respectively). Lanes 4-6 of both agarose gels correspond to desmin expression (0.1 µg, 0.01 µg and 0.001 µg cDNA, respectively). C, Comparative expression of desmin in control and EGTA-treated cells after normalization of PCR data (for details, see Material and Methods). GAPDH = glyceraldehyde-3-phosphate dehydrogenase.

Discussion

The present study analyzed the involvement of extracellular Ca²⁺ in the generation and maintenance of cell shape and its relation with the expression and distribution of the intermediate filament desmin in the mouse skeletal muscle cell line C2C12.

Well-spread control C2C12 cells (grown without EGTA) changed to a bipolar morphology after 24 h of EGTA treatment. The quantification of these changes showed substantial modifications in area and in the ratio between the major and the minor axis of cells. The cell area of control cells was larger than that of EGTA-treated cells, and the axis ratio of EGTA-treated cells was more than two-fold larger than that of control myoblasts. The lack of differences in perimeter between control and treated cells was due to the elongation of EGTA-treated cells, which is clearly demonstrated by the axis ratio showing that treated cells were thinner and longer than control cells.

Ca²⁺ depletion from the medium by EGTA influences a number of Ca²⁺-sensitive membrane proteins. One major Ca²⁺-dependent transmembrane protein found in the sarcolemma of myoblasts is integrin. Previous work from our group showed a change in the distribution of a5-integrin adhesion sites in C2C12 cells after EGTA treatment (12). Using indirect immunofluorescence, a5-integrin was detected in fibrillar adhesions at the terminations of stress fibers in both control and 24-h EGTA-treated C2C12 cells. Besides, a dense a5-integrin labeling was seen inside most treated cells, indicating a possible internalization of integrin after EGTA exposure (12). The effects of calcium depletion on desmin distribution observed in the present study may have been initiated by various cell surface components that require extracellular Ca²⁺, such as a5-integrin, which in turn can influence intracellular signaling pathways. It has been shown that desmin is present in the subsarcolemmal region in association with membrane and membrane-associated proteins, such as integrins (3).

In the present work, we found desmin aggregates in the cytoplasm of EGTA-treated C2C12 cells. Similar desmin dots and aggregates have been described as the major structural alteration in several desminopathies (10). Desmin-related myopathies are characterized by the accumulation of desmin in certain inclusions, sarcoplasmic bodies, cytoplasmic bodies, and granulofilamentous material (11). The mechanisms that control the formation and aggregation of desmin filaments in desminopathies are still unclear. A chaperone protein, aB-crystalline, is involved in the correct assembly of desmin filaments and an impaired chaperone function could promote the increase in desmin aggregation (11).

The relation between changes in extracellular Ca²⁺ concentration and the expression and distribution of cytoskeletal proteins (such as desmin) could be directly mediated by changes in Ca²⁺-binding membrane molecules (such as integrins). Another possibility is that changes in extracellular Ca²⁺ concentration could indirectly change the intracellular Ca²⁺ concentration, which in turn could have an effect on the cytoskeletal components. One consequence of changes in intracellular Ca²⁺ concentration is the activation of Ca²⁺-activated enzymes, such as calpains, which are major proteolytic systems in skeletal muscle (16). Calpains are proteases that can selectively cleave cytoskeletal proteins, and desmin has been shown to be one of their major and first substrates both in vivo and in vitro; and calpains are found in association with the sarcolemma (17). We speculate that in the present study Ca²⁺ depletion might have induced a calpain-dependent cytoskeletal remodeling including desmin cleavage, resulting in the presence of desmin dots and aggregates in the cytoplasm.

The results presented in this paper suggest the requirement of extracellular Ca²⁺ for the regulation of cell shape and for the expression and distribution of desmin in skeletal muscle cells grown in culture.

Address for correspondence: C.S. Mermelstein, Departamento de Histologia e Embriologia, ICB, UFRJ, 21941-590, Rio de Janeiro, RJ,Brasil. Fax: [phone]. E-mail: [e-mail]

Research supported by CNPq, FAPERJ, FUJB-UFRJ, and PRONEX-Brasil. Presented at the XI Congresso Brasileiro de Biologia Celular, Campinas, SP, Brazil, July 15-18, 2004. Received July 7, 2004. Accepted March 2, 2005.

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Correspondence and Footnotes

Publication Dates

• Publication in this collection
  04 July 2005
• Date of issue
  July 2005

History

• Accepted
  02 Mar 2005
• Received
  07 July 2004