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This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Integrins are required for normal muscle differentiation and disruptions in integrin signaling result in human muscle disease. The intracellular components that regulate integrin function during myogenesis are poorly understood. Unc-112 is an integrin-associated protein required for muscle development in C. elegans. To better understand the intracellular effectors of integrin signaling in muscle, we examined the mammalian homolog of Unc-112, kindlin-2.
Kindlin-2 expression is upregulated during differentiation and highly enriched at sites of integrin localization. RNAi knockdown of kindlin-2 in C2C12 cells results in significant abnormalities during the early stages of myogenesis. Specifically, differentiating myocytes lacking kindlin-2 are unable to elongate and fail to fuse into multinucleated myotubes. These changes are correlated with decreased cell substratum adhesion and increased cell motility. They are also associated with redistribution of a known kindlin-2 binding partner, integrin linked kinase (ILK), to the membrane insoluble subcellular fraction.
In all, our study reveals kindlin-2 as a novel integrin adaptor protein important for muscle differentiation, and identifies it particularly as a critical regulator of myocyte elongation.
Skeletal muscle is a highly specialized tissue composed of multinucleated myotubes. The formation of myotubes from mononucleated precursor myoblasts via myogenesis is a complex, highly regulated process requiring both genetic and morphologic changes[1,2]. Understanding the molecular components of myogenesis is of high biologic and clinical importance, as the differentiation program is employed not only during development but also in the muscle regeneration response to injury. In addition, several myopathies in humans are the result of aberrant muscle differentiation.
Integrin receptor mediated adhesion and signaling is required for proper myogenesis. Specifically, integrin function has been demonstrated both in vitro and in vivo to be required for myoblast fusion and for sarcomerogenesis[6,7]. In addition, integrins are implicated in many other aspects of myogenesis, especially those related to the morphologic changes that accompany the differentiation process. The importance of integrins in skeletal muscle is underscored by the association between integrin abnormalities (both direct and indirect) and the pathogenesis of muscular dystrophy[8,9].
Numerous cytosolic effector molecules localize to integrin junctions and are associated with fundamental integrin-regulated processes like cell adhesion and cell migration. However, the specific effectors that are responsible during myogenesis for transducing integrin signals, and thus for regulating integrin function in muscle, are not well established. Exceptions are integrin-linked kinase (ILK), which likely has multiple important roles[11,12], filamin-C, which is important for myoblast fusion, and focal adhesion kinase (FAK), which participates in the regulation of costamerogenesis.
We are interested in identifying other integrin-associated cytoplasmic adaptors important for myogenesis. One interesting potential candidate is kindlin-2/mig-2, a FERM and PH domain-containing protein that localizes to focal contacts and directly binds to the tail domain of β1 integrin[15,16]. Kindlin-2 is a member of the kindlin family of proteins. These proteins are so named because of the association between kindlin-1 mutations and Kindler Syndrome, an epidermal blistering/skin fragility syndrome. The kindlin family represents the vertebrate homologs of unc-112, a C. elegans protein implicated in integrin signal transduction during myogenesis. Unc-112 specifically functions in the establishment of the linkage between the nematode integrins and the sarcomeric protein complex. Loss of unc-112 results in severe abnormalities in the organization and stability of the C. elegans body wall musculature.
Because of the important role of unc-112 in regulating integrin dependent aspects of muscle development in C. elegans, it is likely that kindlins are critical for vertebrate myogenesis. Kindlin-2 function is of particular interest as it is the only unc-112 homolog appreciably expressed in muscle in vivo[17,20]. Our previous work has revealed an essential role for kindlin-2 in vertebrate development. Gene targeting in the mouse results in early embryonic lethality, and gene knockdown in the zebrafish causes abnormalities in multiple organ systems. Kindlin-2 loss in the zebrafish produces a severe cardiac and skeletal myopathy, and demonstrates a specific requirement for kindlin-2 in mediating the attachment of myofibrils to the sarcolemmal membrane.
In the present study, we focused on the role of kindlin-2 during the early stages of myogenesis. To test kindlin-2's function, we utilized the well-characterized C2C12 cell culture model system. C2C12 cells, when induced by serum withdrawal, go through a series of developmental stages that eventually produce a multinucleated myotube capable of spontaneous contraction. We first defined kindlin-2 expression during C2C12 myogenesis, and found it upregulated during the differentiation stage just prior to myoblast fusion and characterized by myocyte elongation. At these time points the protein is localized to sites of integrin expression. Using RNAi mediated gene knockdown, we then examined the function of kindlin-2. Kindlin-2 was required for differentiation to proceed through the stage of myoblast fusion. In particular, cells with reduced levels of kindlin-2 failed to spread and expand during the developmental phase of myocyte elongation. The myocytes exhibit decreased adhesion to fibronectin and instead had an increased capacity for migration. They were also characterized by an abnormal distribution of integrins and integrin associated proteins. In particular, the integrin associated protein, integrin linked kinase (ILK) was redistributed to the membrane insoluble fraction. In all, our study reveals that the integrin associated cytoplasmic effector molecule kindlin-2 is a critical regulator of myogenesis, and implicates kindlin-2 and integrin junctions in the regulation of myocyte elongation. Further, we propose that kindlin-2 functions by stabilizing and promoting cell-cell adhesion over cell migration.
To study the expression and function of kindlin-2 during myogenesis, we utilized the well-characterized C2C12 cell culture model system. Proliferating C2C12 cells resemble fibroblasts, but upon serum removal they withdraw from the cell cycle, elongate, and fuse to form multinucleated myotubes. These stages of differentiation are accomplished within the first four days after serum withdrawal, with myoblast fusion usually beginning by day 3 or 4.
We examined kindlin-2 expression using Western blot analysis in confluent, proliferating C2C12 cells and during the first four days after serum withdrawal-induced myogenesis (Figure (Figure1).1). In undifferentiated cells (GM), kindlin-2 is present at low levels. Upon induction of differentiation (DM), kindlin-2 levels rise, peaking at day 3. At DM3, kindlin-2 expression is approximately 5-fold higher than in undifferentiated cells. We compared kindlin-2 levels with those of the differentiation markers myogenin (myog) and myosin heavy chain (MHC). Myogenin is induced upon cell cycle withdrawal, while MHC is expressed coincident with the onset of myoblast fusion. Kindlin-2 levels rise after myogenin but before MHC, at time points consistent with the myocyte elongation stage of differentiation.
We next determined the subcellular localization of kindlin-2 during myogenesis using immunohistochemistry. In undifferentiated C2C12 cells, kindlin-2 expression is faint but detectable at membrane protrusions and cell-matrix contacts (Figure (Figure2A;2A; arrowheads). It co-localizes with β1 integrin in a pattern consistent with expression at focal contacts. The staining in undifferentiated cells is similar to that reported for kindlin-2 in non-myogenic cell lines.
Upon differentiation, kindlin-2 immunofluorescence noticeably increases, in agreement with our Western blot data. In two day differentiated C2C12 cells, kindlin-2 is highly enriched in puncta along the plasma membrane (arrowheads, Figure Figure2B).2B). These puncta also contain β1 integrin, and likely represent areas of cell-cell and cell-matrix adhesion. In addition, staining is observed along linear structures within the cell (*). In four day differentiated cells, kindlin-2 is primarily expressed in this linear staining pattern (Figure (Figure2C).2C). At this structure, it co-localizes with β1 integrin and focal adhesion kinase (FAK) (Figure 2B–C and data not shown). As corroborated by previously published reports of β1 integrin and FAK expression patterns, this kindlin-2 staining corresponds to the developing costamere. Costameres are integrin-containing junctions that link sarcomeres to the plasma membrane. They are believed to represent the differentiated muscle equivalent of the focal contact. One additional site of kindlin-2 localization is along the plasma membrane between adjacent cells (Figure (Figure2D).2D). As with its expression at other subcellular compartments, it colocalizes with β1 integrin at these cell-cell contacts.
To support the relevance of the abundant staining of kindlin-2 in C2C12 cells, we examined expression in mouse skeletal muscle (Figure (Figure2E).2E). As with cell culture, anti-kindlin-2 strongly stains the sarcolemmal membrane in muscle cross sections and overlaps with the expression of β1 integrin. Kindlin-2 also appears enriched in the perinuclear area (**), an organelle rich domain that is enriched with neuromuscular junctions.
To study the function of kindlin-2 during myogenesis, we designed synthetic RNAi to the murine kindlin-2 gene. The extent of knockdown was determined using quantitative RT-PCR (qPCR) (Figure (Figure3A),3A), Western blot analysis (Figure (Figure3B),3B), and immunohistochemistry (see Figure Figure6B).6B). Based on the qPCR data, we consistently observed 70–80% knockdown 24 hours after RNAi transfection. This effect was maintained at 3 days after transfection (differentiation day 2), but diminished to approximately 50% by 5 days (differentiation day 4). The specificity of the RNAi for kindlin-2 knockdown and the observed phenotypic changes were verified using an independent RNAi designed to a second part of the gene. Information for each RNAi is listed in the materials and methods. Of note is that the homologous gene products kindlin-1 and kindlin-3, as determined by RT-PCR, are not expressed in C2C12 cells under control conditions and are not upregulated with kindlin-2 knockdown.
We began our analysis of kindlin-2 function by determining the ability of C2C12s with reduced kindlin-2 levels to differentiate through the stage of myoblast fusion. We chose this differentiation end point because it typically occurs 3–4 days after serum withdrawal, and kindlin-2 levels are highest in the days just prior to it. To measure myoblast fusion, we calculated the myoblast fusion index (MFI). The MFI is determined by immunostaining day 4 differentiated cells (DM4) with myosin heavy chain (MHC), counting the number of nuclei in each MHC positive cell, and then comparing the number of multinucleated cells to the overall number of MHC positive cells. Myotubes were considered partially fused if they contained 2–3 nuclei, and fully fused if they contained 4 or more nuclei. In C2C12 cells transfected with a scrambled RNAi, 25.5% were partially fused and 23.4% were fully fused (Figure 4A, B). These data are consistent with previously published reports on myotube fusion at DM4. In contrast, in C2C12 cells transfected with kindlin-2 RNAi, only 15.4% were partially fused (vs. 25.5%, p = 0.0036) and only 8.9% fully fused (vs. 23.4%, p < 0.0001) (Figure 4A, B). Overall, while approximately half of all control/scrambled cells fused, only 25% of cells from kindlin-2 RNAi transfections were able to differentiate to the point of even partial fusion, suggesting a delay or arrest in differentiation prior to or at the stage of myoblast fusion.
To confirm that kindlin-2 RNAi significantly hindered myogenesis, we measured the levels of various markers of differentiation using both qPCR and Western blot analysis. We examined myosin heavy chain isoform 8 (myh8) and myotilin RNA levels at differentiation day 4 using qPCR. Both genes are expressed starting at the stage of myoblast fusion. As expected from our myotube fusion data, both myh8 and myotilin levels were substantially lower in kindlin-2 RNAi transfected cells as compared to scrambled RNAi transfected cells (Figure (Figure5A).5A). We utilized Western analysis of myosin heavy chain to substantiate our RNA data. As shown in Figure Figure5B,5B, MHC protein levels are also diminished at differentiation day 4. Myogenin protein levels were also examined, and were undistinguishable between scrambled and kindlin-2 RNAi samples. This suggests that differentiation proceeds through the point of myogenin induction, but is altered prior to later events like fusion.
To address if differentiation is simply delayed as opposed to arrested, we examined cultures incubated for 6 days in differentiation media. At this time point, because our RNAi is delivered via transient transfection, kindlin-2 levels are recovered to greater than 50% of normal (data not shown). Despite this, there continues to be a reduction in the number of fused myotubes (Figure (Figure5C).5C). In addition, as determined by Western blot analysis, there are reduced levels of the late differentiation marker β1D integrin (Figure (Figure5D).5D). These data suggest an arrest of myogenesis prior to the stage of myoblast fusion.
A key event during in vitro differentiation is myocyte elongation. Elongation directly precedes myoblast fusion. Given that integrin adhesion is implicated in the elongation process, we next examined the extent to which RNAi transfected cells increased in cellular volume after differentiation. We accomplished this by measuring the two-dimensional attached area of cells just prior to differentiation and then two days after induction of differentiation. Undifferentiated C2C12 cells transfected with kindlin-2 RNAi, while phenotypically normal in appearance, had slightly less attached area than controls (7,000 pixels vs. 8,000 pixels; Figure Figure6A).6A). Upon differentiation, however, there was a dramatic difference in calculated areas. Cells transfected with scrambled RNAi increased to 14,000 pixels by differentiation day 2, while kindlin-2 RNAi treated cells only increased to 8,000 pixels (Figure (Figure6A).6A). This statistical difference was also apparent by visual inspection and on cells immunostained with various antibodies. One example is depicted in Figure Figure6B,6B, which shows D2 differentiated cells stained with anti-kindlin-2. As compared to cells transfected with scrambled siRNA (left panel), the cells with reduced levels of kindlin-2 were clearly smaller and had a non-extended morphology (right panel). In all, these data indicated that reduction of kindlin-2 levels resulted in a failure of myocyte elongation.
To better understand the reason myocytes with reduced kindlin-2 levels do not properly elongate, we measured their ability to spread/adhere to different extracellular matrices and also to migrate through transwell chambers. Cells were transfected with RNAi, differentiated for 2 days by serum withdrawal, and then trypsinized in preparation for the relevant assays.
To study cell adhesion, cells were replated onto plastic, fibronectin, laminin-1 and collagen IV. After replating for one hour onto plastic dishes, 75% of control cells adhered and spread. Conversely, only 42% of kindlin-2 RNAi cells spread (Figure (Figure7A,7A, p < 0.0001, n = 5 trials). A similar decrease in spreading was observed with laminin and collagen IV coated dishes (data not shown). Replating on fibronectin, however, produced a much more dramatic difference. At one hour, 94% of control cells spread on fibronectin dishes, an expected increase over plastic dishes given that α5β1, a fibronectin receptor, is the predominant integrin heterodimer expressed at differentiation day 2[23,24] (Figure (Figure7A).7A). On the other hand, only 47% of kindlin-2 RNAi transfectants spread on this surface, a value only marginally higher than that recorded for plastic dishes (Figure (Figure7A,7A, p < 0.0001, n = 5 trials). Representative RNAi transfected cells replated onto fibronectin are shown in Figure Figure7B7B.
We then examined whether cell motility was also affected by kindlin-2 knockdown. To test migration, siRNA transfected cells were replated onto the upper surface of transwell chambers. Using crystal violet staining as an indicator of cell number, we measured the number of cells which migrated through to the bottom of the transwell after 24 hours. We observed a substantial difference between conditions, with significantly more cell migration detected in chambers with cells exposed to kindlin-2 RNAi (Figure (Figure7C).7C). This finding demonstrates that loss of kindlin-2 has a pro-migratory effect on C2C12 cells. When considered with our observation that kindlin-2 deficient myoblasts fail to properly elongate and have altered substratum adhesion, it suggests that kindlin-2 is critical for the transition of C2C12 cells from a motile state to a strongly adhered, elongated state.
Given these changes in cell adhesion and cell motility, and in particular the changes observed with spreading on fibronectin, we examined the possibility that kindlin-2 knockdown affected extracellular matrix protein or integrin receptor expression. Using a combination of RT-PCR, real time PCR, and Western blot analysis, we detected no difference in the RNA or protein levels of fibronectin, laminin and merosin, and no alteration of RNA levels of α5 or α7 integrins (data not shown).
In C. elegans, unc-112, the worm homolog of kindlin-2, binds to and modulates the function of Pat-4, the worm homolog of ILK. Because ILK is required for mammalian myogenesis both in vivo and in vitro, we wanted to establish the effect of kindlin-2 knockdown on ILK expression and localization. At differentiation days 2 and 4, the overall levels of ILK were unchanged between conditions (Figure (Figure8A),8A), yet the localization of ILK was significantly altered. As determined using subcellular fractionation, essentially all ILK in control transfected cells was present in the cytosolic fraction at differentiation day 2 (Figure (Figure8B).8B). This is consistent with previously published reports on ILK localization in C2C12 cells. In contrast, ILK was found only in the membrane/insoluble fraction in the kindlin-2 knockdown myocytes (Figure (Figure8B).8B). Thus, in the absence of kindlin-2, ILK fails to redistribute to its proper cytosolic localization during myogenesis.
We next examined other focal contact components for similar changes in subcellular localization. In control transfected cells at differentiation day 2, we observed the expected pattern of expression for β1 integrin and paxillin both in discrete points along the membrane as well as in linear structures throughout the cells (Figure (Figure9A).9A). In kindlin-2 RNAi transfected cells, we detected a relative shift in this distribution, with concentration of the staining in punctate at the sarcolemmal membrane. Of note is that we did not see obvious changes in the subcellular localization of FAK or migfilin (data not shown).
We also measured F-actin staining using Oregon Green conjugated phalloidin. We again observed a qualitative redistribution of F-actin from a linear pattern in control myocytes to concentration along the sarcolemmal membrane in kindlin-2 RNAi myocytes (Figure (Figure9B).9B). Taken together with our ILK results, these data suggest that integrin based, ILK-containing adherens junctions are inappropriately distributed in differentiating myocytes. We hypothesize that, in the absence of kindlin-2, ILK enriched focal adhesions fail to redistribute into an extensive linear pattern during myogenesis, and that this in turn results in defective myocyte elongation (Figure (Figure1010).
C2C12 cells undergo a well-documented series of steps after induction of differentiation by serum withdrawal. Within 24 hours, cells exit the cell cycle and begin expressing muscle specific transcription factors. The next stage is myocyte elongation, where dramatic changes in cell morphology occur between 1 and 3 days after induction. Elongation is followed by myoblast fusion, which begins at differentiation day 3. In this study, we describe for the first time the role of kindlin-2 in these early stages of differentiation. In particular, we identify kindlin-2 as a novel integrin associated cytoplasmic adaptor protein important for the process of myocyte elongation.
Myocyte elongation, while a well-described morphologic phenomenon, is not well characterized at the molecular level. As revealed by two published studies, integrin signaling has been previously implicated in the process. In the first, alteration of integrin binding to the extracellular matrix by manipulation of matrix metalloprotease function in C2C12 cells causes abnormalities in myocyte elongation. In the second study, overexpression of the focal contact associated protein FHL1/SLIM induces hyper-elongation, with the hyper-elongation dependent on integrin-ligand binding. Our study clearly supports and advances this association between integrin junctions and myocyte elongation. Furthermore, it introduces kindlin-2 as one of the key molecular regulators of the process.
How might kindlin-2 regulate elongation? Our hypothesis is that kindlin-2 promotes and stabilizes cell adhesions. This hypothesis is supported by several observations. The first is differentiating myocytes with reduced kindlin-2 expression have impaired spreading on all extracellular matrix surfaces and in particular on fibronectin. The second is that kindlin-2 expression appears to reduce the motile behavior of myocytes. This effect of cell migration has been previously demonstrated for kindlin-2 in a series of non-myogenic tumor cell lines. Specifically, Wu and colleagues showed an inverse correlation between tumor cell motility and kindlin-2 levels, and additionally showed that expression of kindlin-2 in motile cell lines decreased their migration and strengthened their attachments. The third, as described in our previous study, is that loss of kindlin-2 in zebrafish muscle leads to less elaborate cell-cell junctions which, by ultrastructural analysis, do not have their typical associations with the underlying cytoskeleton. In addition, we reported that both cardiac muscle and skeletal muscle in the fish are smaller in the absence of kindlin-2. The data from the present study suggest that this may be on the basis of failed myocyte elongation.
Understanding how precisely kindlin-2 stabilizes adhesion and promotes myocyte elongation is an open question deserving further study. Our data support a potential role for ILK in this process. Previous work on ILK, while clearly showing a requirement for the gene for both cardiac and skeletal myogenesis[11,12,27], has not specifically implicated the protein in myocyte elongation. However, ILK is associated both with the stabilization of adhesion and with the promotion of migration[28,29]. Participation in these seemingly paradoxical activities depends on ILK kinase activity, ILK localization and differential association with ILK binding partners. As known binding partners, kindlin-2 and ILK are logical candidates to share functions. Similar to observations from C. elegans, we describe here altered localization of ILK with the reduction of kindlin-2 expression. Because ILK localization is a significant factor in whether it functions to promote adhesion or migration, a plausible mechanism for kindlin-2 function is that it localizes to integrin junctions in the differentiating myocyte and it in turn stabilizes ILK association with these junctions. This interaction then promotes adhesion and stimulates elongation, likely via actin cytoskeletal remodeling. Loss of kindlin-2 would then be expected to cause improper localization of ILK, potentially to sites that promote migration.
Regardless of the exact mechanism, the suggestion from our data that kindlin-2 is involved with ILK regulation is important in reference to human muscle disease. ILK has been both directly and indirectly implicated in cardiac hypertrophy, cardiomyopathy[31,32] and muscular dystrophy. An association of kindlin-2 with ILK thus strengthens the hypothesis that kindlin-2 is likely to be important for human muscle diseases.
It is quite likely, however, that kindlin-2 function is transmitted in part by additional regulatory proteins. One intriguing molecule is FHL1, a LIM domain containing protein. Currently, other than β1 integrin, the only well-established binding partner for kindlin-2 is migfilin, which is also a LIM domain protein. We did not observe alterations in migfilin expression, and migfilin has yet to be associated with skeletal myogenesis. Thus one possibility may be that kindlin-2 regulates elongation by recruiting FHL1 to integrin junctions. This hypothesis is of clinical relevance, as FHL1 mutations have been detected in patients with an X-linked muscle disease called Scapulo-Peroneal Syndrome[33,34]. Another possibility is that kindlin-2 facilitates and stabilizes the association between integrin junctions and the underlying actin cytoskeleton. Such a role is supported by the function of its C. elegans homolog unc-112 and by our previous published data from the zebrafish[19,20].
An additional event in myogenesis that may require kindlin-2 function is myoblast fusion. Integrin junctions have a well established association with fusion, and kindlin-2 is expressed at the correct development time (3–4 days after induction of differentiation) and in the correct location (co-localized with integrin at sites of cell-cell attachment). We clearly observe a defect in the ability of kindlin-2 RNAi transfected cells to proceed through the stage of myoblast fusion. Alternatively, this observation may be explained by the fact that these myocytes have defective elongation, and elongation may be required for fusion to proceed. Further experimentation is thus necessary to resolve this potential function.
In summary, we have demonstrated that kindlin-2 is a critical regulator of early myogenesis in vitro. Its specific functions in myocyte elongation suggest it is a novel regulator of integrin signaling during myogenesis. Based on its expression and function, kindlin-2 represents a potentially important factor in integrin-related human muscle pathologies, especially the muscular dystrophies.
C2C12 cells were obtained from ATCC. They were maintained in growth media (GM; DMEM (Gibco) + 10% FBS (HyClone)) and differentiated in differentiation media (DM; DMEM + 2% Horse Serum (HyClone)). Cells were grown on 60 mm plastic ware (Falcon) or on 22 mm coverglass coated with Fibronectin (BD Biosciences). All transfections were done with Lipofectamine 2000 (Invitrogen). RNAi specific for mouse Kindlin-2 was obtained from Invitrogen (oligo IDs MSS211904/5). Stealth Negative Control Medium was used as the scrambled control (Invitrogen). Transfection efficiency of the RNAi was > 90%, as determined by co-transfection with the BLOCK-iT reagent (FITC conjugated; Invitrogen).
Immunofluorescence microscopy was performed on C2C12 cells and cryosections from fresh frozen adult mouse quadriceps using standard methodology. Cells were fixed for 10 minutes at 4°C in 1:1 methanol:acetone or at room temperature in 4% paraformaldehyde and tissue sections were fixed for 5 minutes at room temperature in acetone. The following primary antibodies were used: goat anti-Kindlin-2 (1:25; Santa Cruz); mouse anti-kindlin-2 (1:30; Abnova); mouse anti-paxillin (1:300; Transduction Laboratories); anti-β1 integrin-FITC (1:100; Santa Cruz); rat anti-β1 integrin (1:25; Chemicon); mouse anti-myosin heavy chain (MF20; 1:30; Developmental Hybridoma Bank), and Oregon Green phalloidin (1:200; Invitrogen). Alexafluor-conjugated secondary antibodies were used at 1:250 (Invitrogen). Nuclei were counterstained with ProLong Gold plus DAPI (Invitrogen). Analysis was performed with an Olympus FluoView 500 laser scanning confocal microscope. Samples were scanned on an Olympus IX-71 inverted confocal microscope using either a 60× or 100× oil immersion objective and captured using the FluoView v4.3 software.
Protein was extracted from C2C12 cell cultures using RIPA buffer with Complete Protease Inhibitors (Roche). Samples were quantitated using the Bradford assay (Pierce). 40 μg or 70 μg (for kindlin-2) of extract was resolved by SDS-PAGE, transferred to Immobilon (Millipore), and subjected to immunoblotting. Membranes were blocked for 1 hour with 5% milk in PBS containing 0.1% Tween. Membranes were incubated in primary and secondary antibodies for 1 hour at room temperature. Primary antibodies used were: mouse anti-kindlin-2 (1:250); mouse anti-GAPDH (1:1000); rabbit anti-myogenin (1:1000; abcam); mouse anti-MHC (1:1000); rabbit anti-ILK (1:1000; Millipore); rabbit anti-FAK (1:2000; Santa Cruz); rabbit anti-laminin (1:2000; Sigma); rabbit anti-fibronectin (1:200; Santa Cruz); β1D integrin (1:1000; Chemicon). Secondary antibodies were from Santa Cruz Biotechnology and used at 1:2000. Blots were developed using Lumiglo (Cell Signalling) and exposed to Hyperfilm (GE Biosciences). Protein extracts for cell fractionation studies were obtained using the Qproteome Cell Compartment kit (Qiagen). Successful fractionation was verified using the following antibodies: nuclei and membrane (insoluble)- emerin (1:1000; Abcam), cytoplasmic- GAPDH, cytoskeletal- actin (1:200, Santa Cruz).
RNA was extracted from C2C12 cell cultures using the Trizol reagent (Invitrogen). First strand cDNA was synthesized from 1 μg RNA using the Promega Reverse Transcription System with the Random Hexamer Primer. cDNA was diluted 1:10, and then 2 μL was used for Real Time PCR. Real Time PCR was performed using the QuantiTect SYBR-Green reagent and iCycler iQ PCR machine (Qiagen). Real Time primers were obtained from Qiagen. GAPDH was used as the amplification control.
Immunofluorescence using anti-β1 integrin FITC was performed on RNAi transfected C2C12 cells incubated in either growth media or differentiation media. Fluorescence was visualized at 20× using a Nikon Microphot Microscope. Digital images were obtained in MetaMorph using SPOT camera. Cell size was determined for mononuclear cells in MetaMorph with the free hand tool and area determination calculator. Cell areas were then analyzed and histograms generated using Prism. Single-tailed Student's t-test was used to determine statistical significance.
Immunofluorescence using anti-MHC was performed on C2C12 cells at 4 days after differentiation. Nuclei were counterstained with DAPI. Digital images were captured at 20× as done above for cell size determination. The Myoblast Fusion Index was calculated as follows: MHC-positive cells were scored as having 1, 2–3, or >3 nuclei. Values were expressed as a percentage of the total number of MHC-positive cells counted. At least 250 cells were counted for each condition, and 4 separate trials were performed. Values were analyzed and histograms generated using Prism, and statistical significance determined using a single-tailed t-test.
RNAi transfected C2C12 cells at differentiation day 2 were dissociated with trypsin and then replated onto 60 mM culture dishes. Dishes either had no coating or were precoated with laminin-1, collagen IV, or fibronectin (Bectin Dickinson). Cells were allowed to adhere for 60 minutes at 37°C in differentiation media, and then were fixed for 10 minutes at room temperature in 4% paraformaldehyde. Cells were examined with an inverted microscope at 20× magnification and scored as adhered if they assumed a spread morphology and non adhered/spread if they had a rounded morphology with no processes. 5 counts of at least 25 cells were performed for each condition.
RNAi transfected C2C12 cells were dissociated with Dissociation solution (Sigma), counted with a hemocytometer, and plated on top of transwells (1 × 105 cells/well). Cells were incubated for 12 hours in DMEM/2%HS. Transwells (Costar) were then processed as follows: Cells were removed from inner wells with Q-tips. Outer wells were stained with crystal violet for 20 minutes, eluted with 10% acetic acid, and then measured on a plate reader at 590 nm.
JJD carried out or supervised all experiments and drafted the manuscript. AV and SK performed certain experimentation. JJD, JG and ELF conceived of the study, participated in its design and edited the manuscript.
The authors thank Elizabeth Gibbs for critical reading of the manuscript, and Mary Soules and Carey Backus for technical assistance. JJD is supported by a Muscular Dystrophy Association Career Development Award and an NICHD K12 award (K12HD028820-16). ELF is supported by the National Institutes of Health (NS38849, and DK60994) and the Program for Neurology Research and Discovery.