Immortalization of mouse myogenic cells can occur without loss of p16 INK4a , p19 ARF , or p53 and is accelerated by inactivation of Bax
© Nowak et al; licensee BioMed Central Ltd. 2004
Received: 16 September 2003
Accepted: 08 January 2004
Published: 08 January 2004
Upon serial passaging of mouse skeletal muscle cells, a small number of cells will spontaneously develop the ability to proliferate indefinitely while retaining the ability to differentiate into multinucleate myotubes. Possible gene changes that could underlie myogenic cell immortalization and their possible effects on myogenesis had not been examined.
We found that immortalization occurred earlier and more frequently when the myogenic cells lacked the pro-apoptotic protein Bax. Furthermore, myogenesis was altered by Bax inactivation as Bax-null cells produced muscle colonies with more nuclei than wild-type cells, though a lower percentage of the Bax-null nuclei were incorporated into multinucleate myotubes. In vivo, both the fast and slow myofibers in Bax-null muscles had smaller cross-sectional areas than those in wild-type muscles. After immortalization, both Bax-null and Bax-positive myogenic cells expressed desmin, retained the capacity to form multinucleate myotubes, expressed p19 ARF protein, and retained p53 functions. Expression of p16 INK4a , however, was found in only about half of the immortalized myogenic cell lines.
Mouse myogenic cells can undergo spontaneous immortalization via a mechanism that can include, but does not require, loss of p16 INK4a , and also does not require inactivation of p19 ARF or p53. Furthermore, loss of Bax, which appears to be a downstream effector of p53, accelerates immortalization of myogenic cells and alters myogenesis.
Keywordsapoptosis Bax myoblast muscle fiber p16 INK4a p19 ARF p53
Under cell culture conditions in which almost all primary mouse cells cease proliferation after 10 – 30 population doublings in serial subcultures, a small number of cells escape this proliferation block, spontaneously immortalize, and continue to proliferate indefinitely. Many types of mouse cells undergo this spontaneous immortalization, including fibroblasts obtained from mouse embryos and myogenic cells obtained from skeletal muscles [1–3]. In the case of myogenic cells, immortalization does not impair the ability of the cells to respond to differentiation signals by ceasing to proliferate and fusing to form multinucleate myotubes [1, 3]. Such immortalized myogenic cell lines have been very valuable in studies of myogenesis, but the molecular alterations underlying myogenic cell immortalization have not been examined. In this study, we examine the mechanisms of myogenic cell immortalization and differentiation with a focus on apoptosis regulators. We focused on apoptosis regulators because we have found that myogenic cells express several members of the Bcl-2 family of apoptosis regulators and that Bcl-2 is required for normal fast myofiber development [4, 5]. Furthermore, muscle cell apoptosis is found in diseased and injured muscle [6, 7]. Finally, inactivation of apoptosis pathways, including inactivation of members of the p53 and pRb pathways, is one possible route to cell immortalization .
The molecular and cellular mechanisms which allow some types of mouse cells to circumvent proliferation limits in vitro have begun to be identified. For example, improved culture conditions allow some types of rodent cells to circumvent this usual replication limit and continue to proliferate indefinitely [9–11]. Inadequate culture conditions may produce stress-related changes in rodent cells that rapidly lead to cessation of growth, a mechanism distinct from the cessation of growth due to telomere shortening seen with cultured human cells [8, 12, 13].
Even under culture conditions that do not support long-term growth of most cells, however, immortalization of mouse cells can occur upon inactivation of one or more cell cycle regulators including p19 ARF , p53, or the Cyclin D regulator p16 INK4a . For example, mouse embryo fibroblasts and pre-B cells escape proliferation limits and grow indefinitely upon inactivation of either p19 ARF or p53 [2, 14–16]. Some cell types, such as mouse bone marrow macrophages, immortalize upon inactivation of p16 INK4a rather than p19 ARF or p53 . Inactivation of p16 INK4a also accelerates immortalization of mouse embryo fibroblasts . On the other hand, mouse cells that are deficient in DNA repair due to mutation of ATM, Brca2, Ku80, XPG, or Ligase IV cease replicating even sooner than wild-type cells in culture . These results have raised the possibility that spontaneous immortalization of rodent cells under inadequate culture conditions may require inactivation of either the p16 INK4a -regulated Cyclin D/Rb pathway or the p19 ARF /p53 pathway that responds to DNA damage by inducing apoptosis .
Though immortalized myogenic cells will proliferate indefinitely under high serum conditions or at low density, these cells retain the ability of non-immortalized myoblasts to respond to low serum or high density by ceasing proliferation and fusing to form multinucleate myotubes in which the myonuclei are post-mitotic. Thus, myogenic cell immortalization must occur via molecular alterations that promote continued proliferation without impairing differentiation. With respect to the p53 and pRb pathways, myogenesis is known to proceed normally in p53-null mice in vivo and with a moderately lowered fusion index in p53-null myoblasts in vitro [18, 19], whereas myogenesis is highly impaired in pRb-null mice in vivo and by pRb-null myoblasts in vitro [20, 21]. Though loss of p53 pathway function thus appears compatible with immortalization of myogenic cells, at least one mouse myogenic cell line, C2C12, has previously been shown to have normal p53 function .
Several lines of evidence suggest that the response of rodent cells to culture conditions may be under control of apoptosis regulators that are downstream of p19 ARF /p53, particularly the pro-apoptotic protein Bax. First, cells that lose the capacity to proliferate in culture often undergo apoptosis, a process that is regulated in many cases by members of the Bcl-2 family, including Bax which promotes apoptosis [8, 23]. Second, Bax appears to act downstream of p53 in the apoptotic pathway. For example, p53 and Bax undergo nuclear translocation upon chemotherapy-induced apoptosis in human melanoma cells ; and inactivation of p53 prevents Bax translocation upon apoptosis induction in embryonic neurons . Studies of tumorigenesis in double knock-out mice also suggest that Bax acts downstream of p53 , and inactivation of Bax alters the tumor type and number, though not age of tumor appearance, in p19 ARF -null mice .
In this study, we found that, unlike mouse embryo fibroblasts, mouse myogenic cells undergo spontaneous immortalization via a mechanism that does not require inactivation of p19 ARF or loss of p53 functions. In some, but not all cases, immortalization of muscle lines was accompanied by loss of p16 INK4a . Furthermore, we identified a new mechanism, inactivation of Bax, that accelerates the immortalization of mouse myogenic cells. We also found that Bax functions in myogenesis, because Bax-null myogenic cells produced relatively more mononucleate cells and fewer multinucleate myotubes than wild-type myogenic cells in culture, and the myofibers in Bax-null muscles in vivo were smaller than those in wild-type muscles. Thus, we find that mouse postnatal myogenic cells can spontaneously immortalize by a different mechanism than mouse embryo fibroblasts; that inactivation of Bax accelerates immortalization of myogenic cells, and that Bax functions in regulation of myogenesis.
In Figure 1, we show results from three separate experiments in which we started four independent cultures of Bax-null myogenic cells. Each of these cultures produced immortalized Bax-null cells at no later than 30 days after the beginning of the experiment (Fig. 1, Expts. 1 – 3). In contrast, only one of the three wild-type, and neither of the two heterozygote, cultures produced immortalized cells; and the one line of immortalized wild-type cells that did arise was not produced until ~40 days after the beginning of the experiment (Fig. 1, Expt. 3). The Bax-null, heterozygous, and wild-type myogenic cells all showed an early period of rapid growth lasting about ten days (3 – 4 passages), which was followed by a plateau period of slower or no growth in the wild-type and heterozygous cultures. In Bax-null cultures, the early period of fast growth was followed by either a similar, though shorter, plateau period of slower or no growth (Fig. 1; Expts. 2 and 3) or by little change in growth rate (Fig. 1; Expt. 1). We found immortalized cells by day 50 of culture in 7 of 7 Bax-null cultures, but in only 3 of 9 Bax-positive cultures which included 1 of 4 Bax (+/-) cultures and 2 of 5 Bax (+/+) cultures (P = 0.011 by Fisher's exact test comparing Bax-null to Bax-positive results). As noted before , loss of Bax is not required for immortalization, because spontaneously immortalized wild-type and Bax (+/-) heterozygous myogenic cells, as well as NIH3T3 cells, retained Bax protein expression (Fig. 5 and not shown).
Because p53-null mouse embryo fibroblasts immortalize very efficiently , we also examined proliferation of p53-null myogenic cells. The p53-null myogenic cells, similar to the p53-null mouse embryonic fibroblasts , showed rapid growth without the period of slower growth seen in the Bax-null and wild-type cells (Fig. 1, Expt. 3). The proliferation rate of the immortalized myogenic cells appeared to be independent of genotype, because the immortalized Bax-null, p53-null, and wild-type cells all had a proliferation rate at 60 days of culture of approximately one doubling per day.
Immortalized Bax-null, p53-null, and wild-type muscle cells taken from rapidly growing, late passage cultures grew in clonal cultures at high efficiency, with >50% of single cells forming colonies after cloning. Starting with muscle-derived cells from long-term (>20 passages) cultures, we used two rounds of cloning to obtain multiple independent cell lines of different genotypes (Bax-null, p53-null, wild-type). These lines of immortalized cells were further characterized and compared to cells in primary, non-clonal cultures at early passage (<4 passages).
Immortalized and cloned Bax-null cells retained many molecular and functional properties of satellite cell myoblasts. In particular, when proliferating at low density, the immortalized Bax-null cells expressed desmin and had the typical bipolar morphology of myoblasts (not shown). In the clonal lines, all of the cells expressed desmin, whereas some cells in the primary cultures, which were not cloned and thus contained a mixture of myogenic and non-myogenic cells, did not express desmin. Upon reaching confluence, Bax-null cells of the clonal lines fused and formed myosin-expressing, multinucleate myotubes (not shown). The clonal lines derived from p53-null and wild-type cells similarly showed desmin expression and the ability to form multinucleate myotubes. Multinucleate myotubes formed by Bax-null, wild-type, and p53-null cells appeared to have identical morphologies.
The immortalized and cloned Bax-null myogenic cells failed to grow in soft agar, suggesting that they were not tumorigenic, and they did not express SA-β-Gal, suggesting that they were not senescent and/or "stressed" . In addition, the immortalized and cloned Bax-null cells did not express either Sca-1 or Bcl-2, two proteins that appear to mark muscle-derived cells that are at an early stage of myogenesis or have stem cell-like properties [4, 5, 28–32]. In contrast, a small proportion (~1–5%) of the desmin-positive cells in uncloned primary cultures did express the Sca-1 and Bcl-2 proteins (not shown), just as in previous work [4, 5].
Effect of Bax genotype on properties of muscle colonies formed by the progeny of individual myogenic cells in vitro.
Bax-positive ave ± SE (n)
Bax-null ave ± SE (n)
Number of nuclei per colony
428 ± 17 (341)
486 ± 22 (303)
P < 0.05
Number of mononucleate cells per colony
131 ± 7.0 (341)
191 ± 8.6 (306)
P < 0.0001
Percentage of nuclei in multinucleate cells
65.1 ± 0.9 (341)
55.5 ± 1.1 (306)
P < 0.0001
Number of nuclei per multinucleate cell
3.9 ± 0.1 (341)
3.9 ± 0.1 (305)
P > 0.5
This difference in fusion index appeared to be due to a higher number of mononucleate cells, rather than a lower number of nuclei in myotubes, in the Bax-null cultures. For example, muscle colonies formed by the progeny of individual Bax-null cells contained both significantly more total nuclei and significantly more mononucleate cells than those formed by Bax-positive cells (Table 1). In contrast, neither the average number of nuclei per multinucleate myotube (Table 1) nor the average number of myotubes per colony (not shown) differed between Bax-positive and Bax-null colonies.
Effect of Bax genotype on properties of myofibers in vivo.
Bax-positive ave ± SE (n)
Bax-null ave ± SE (n)
Cross-sectional area (μm2) of fast‡ myofibers
1045 ± 17.0 (451)
785 ± 11.9 (500)
P < 0.0001
873 ± 7.7 (1364)
717 ± 6.9 (1570)
P < 0.0001
Cross-sectional area (μm2) of slow‡ myofibers
1399 ± 33.7 (193)
1096 ± 16.6 (270)
P < 0.0001
640 ± 15.0 (136)
547 ± 12.8 (150)
P < 0.0001
Percentage of fast myofibers
70.2 ± 1.8 (3)
70.8 ± 0.1 (3)
P > 0.7
90.7 ± 0.7 (5)
91.2 ± 0.8 (5)
P > 0.7
Cross-sectional area (mm2) of whole muscle
1.54 ± 0.12 (4)
1.18 ± 0.06 (5)
P = 0.024
Total number of myofibers
1081 ± 36 (4)
1102 ± 17 (5)
P > 0.5
Thus, immortalized wild-type and Bax-null myogenic cells had normal p53 function as assayed by maintenance of normal karyotype, promoter activation, and induction by actinomycin.
In addition to normal p53 function, immortalized myogenic cells continued to express p19 ARF protein (Fig. 5). For p19 ARF assays, we examined expression in primary cultures (not immortalized) of myogenic cells obtained from postnatal skeletal muscle, and in cultures of spontaneously immortalized mouse embryonic fibroblasts (NIH3T3), wild-type postnatal myogenic cells, and Bax-null postnatal myogenic cells. Immunoblotting showed that, as expected , NIH3T3 cells did not express detectable amounts of p19 ARF ; however, p19 ARF was present in all Bax-null and wild-type myogenic cells, including both early passage primary cells and late passage immortalized cells (Fig. 5). The amount of p19 ARF protein appeared to be increased in both Bax-null and wild-type immortalized myogenic cells, a result also seen in late passage, wild-type mouse embryo fibroblasts .
In contrast to p53 and p19 ARF , which were found in all tested myogenic lines, p16 INK4a was deleted in two of the four Bax-null myogenic lines that were examined (Fig. 5). As found previously in mouse embryo fibroblasts , we found that p16 INK4a protein was undetectable in rapidly growing cultures of early passage (not immortalized) mouse myogenic cells (Fig. 5), but became highly expressed when the cultures reached the slow growing "crisis" stage after 4–5 passages (not shown). After immortalization, we found that p16 INK4a was expressed by two independently-derived Bax-null myogenic lines and one Bax-positive line but was not expressed in two additional Bax-null lines (Fig. 5 and not shown). Thus, immortalization was accompanied by lack of p16 INK4a expression in some, but not all, myogenic cell lines.
We found that mouse myogenic cells can undergo spontaneous immortalization via a mechanism that can include, but does not require, loss of p16 INK4a protein expression, and also does not require loss of p19 ARF protein or p53 function. Furthermore, we identified a new mechanism, inactivation of Bax, that accelerates the immortalization of mouse myogenic cells. We also found that Bax-null myogenic cells produced relatively more mononucleate cells than wild-type myogenic cells in culture and that the myofibers in Bax-null muscles in vivo were smaller than those in wild-type muscles. We discuss these findings below.
Mouse embryo fibroblasts and some immune cells are highly dependent on either mutations of p53 or deletions of p19 ARF to escape replicative limits in culture [2, 14–16]. In contrast, we did not find such alterations in immortalized myogenic cells, whether Bax-positive or Bax-null, suggesting that immortalization of postnatal myogenic cells and embryonic fibroblasts can occur by different mechanisms. As shown previously, spontaneously immortalized myogenic cell lines that are derived from wild-type mouse cells typically retain p53 function [19, 22, 33, 35] and Bax protein expression . Here we showed that immortalized Bax-null myogenic cells also retained p53 functions, as well as p19 ARF protein. Cell cycle checkpoints required for ceasing mitosis and differentiation were also normal in immortalized myogenic cells, because both Bax-positive and Bax-null cells were able to cease dividing and form multinucleate myotubes that contained post-mitotic myonuclei.
Inactivation of p16 INK4a , which occurred in some myogenic cell lines, also leads to immortalization of macrophages  and accelerated immortalization of mouse embryo fibroblasts . Inactivation of p16 INK4a is also associated with establishment of immortalized cell lines from mouse liver and lung epithelial tissues [36, 37]. Though deletion of their overlapping reading frames often leads to simultaneous inactivation of p16 INK4a and p19 ARF in cells such as mouse embryo fibroblasts , we did not observe such double inactivation in immortalized mouse myogenic cells. Promoter-specific hypermethylation is one mechanism that can inactivate p16 INK4a but not p19 ARF expression [e. g., ]. Our results show that myogenic cell immortalization can sometimes occur without loss of the three proteins – p16 INK4a , p19 ARF , and p53 – that are typically found to be inactivated upon immortalization of mouse cells of many non-myogenic lineages. Thus, though loss of p16 INK4a protein expression is likely to be one of the mechanisms underlying myogenic cell immortalization, further work is needed to identify the additional mechanisms that appear to exist in mouse myogenic cells. Though p16 INK4a is an indirect regulator of pRb function, it is unlikely that loss of pRb function itself can underlie myogenic cell immortalization, because loss of pRb function causes a drastic loss of muscle differentiation capacity [20, 21].
How might the absence of Bax increase the speed and frequency of myogenic cell immortalization? A likely explanation is that many potentially immortal Bax-null cells can arise and replicate instead of being destroyed by Bax-dependent cell death. Bax is a pro-apoptotic member of the Bcl-2 family, and inactivation of Bax can render cells more resistant to apoptosis, as shown previously for several cell types [38, 39] and here for myogenic cells (Fig. 2). Spontaneous immortalization of myogenic cells under usual (perhaps sub-optimum) culture conditions is a rare event . Primary cultures of myogenic cells, as well as other cell types [11, 12, 15], typically undergo a "crisis" during which most cells cease replicating, followed by emergence of the progeny of rare immortalized cells (cf. Fig. 1, Expt. 3).The mouse C2 myogenic cell line, for example, was initially derived from such rare spontaneously immortalized cells . It may be that many cultured cells which carry potential immortalizing alterations are normally subject to apoptosis. Disabling the apoptosis mechanism, such as by Bax inactivation, would increase the number of such potentially immortal cells that survive. Further work is needed to determine if other mutations that inactivate apoptosis will also increase myogenic cell immortalization in culture.
Bax inactivation appeared to affect the balance between myoblast proliferation, survival, and fusion to form multinucleate myotubes. Differentiated cultures of Bax-null myogenic cells contained relatively more mononucleate cells, but had a lower fusion rate, than parallel wild-type cultures. These differences could also arise due to increased resistance of Bax-null myogenic cells to apoptosis. As muscle cell differentiation begins in culture, some myoblasts typically undergo apoptosis rather than fusing to form myotubes or surviving in a quiescent state [40–42]. If myoblasts normally destined for apoptosis at the beginning of differentiation instead survive but do not fuse when Bax is inactivated, then Bax-null cultures would have more mononucleate cells, and relatively fewer multinucleate myotubes, than wild-type cultures. A role for inhibition of apoptosis in myoblast survival is supported by the finding that apoptosis of myoblasts is prevented by the heat shock protein, alpha B-crystallin, which also inhibits activation of caspase-3 .
Though a small percentage of the desmin-positive, myogenic cells in Bax-null cultures expressed Sca-1, this protein was not expressed by immortalized Bax-null myogenic cells. Expression of the cell surface protein Sca-1, at least on some muscle-derived cells, appears to identify rare cells that are at a very early stage of the myogenic pathway and may have stem cell properties [4, 28, 30–32, 44]. Because none of the immortalized Bax-null myogenic cells expressed Sca-1, it is likely that they were derived by immortalization of Sca-1-negative myoblast precursors.
The smaller myofibers in the Bax-null soleus might have been due to indirect, rather than direct, effects on muscle development. Unlike Bcl-2 inactivation which leads to a specific loss of fast myofibers , Bax inactivation affects both fast and slow myofibers equally. Bax (-/-) mice have normal viability, but have abnormalities in reproductive cells, lymphoid hyperplasia, and decreased apoptosis during development [45, 46]. No difference in the growth rates of Bax-null and Bax-positive mice has been reported, and skeletal muscles had not previously been examined in Bax-null mice. In skeletal muscles, the size of myofibers is regulated by a number of factors, including motor neuron activity and exercise patterns; protein growth factors such as growth hormone, IGF1, and myostatin; steroid hormones; availability of muscle precursor cells (myoblasts); and food intake . Myofiber size in Bax-null muscles would likely be affected if any of these regulatory factors is altered by Bax-deficiency. As one possibility, for example, excess motor neurons which are eliminated during neuromuscular development in Bax-positive mice survive in Bax-null mice , which could perhaps lead to inappropriate nerve activity and decreased myofiber size. Further studies are necessary to determine if Bax inactivation leads to alterations in factors that indirectly regulate myofiber size.
A direct, muscle cell autonomous, effect of Bax inactivation that would produce smaller myofibers is perhaps less likely. Increased resistance to apoptosis in muscle precursor cells would seem to be consistent with the production of more myogenic cells and larger myofibers. If, however, Bax-null myoblasts are less likely to fuse in vivo as in vitro, smaller myofibers could result. In this case, however, one would then expect to see higher numbers of myoblasts in Bax-null muscles, but we did not observe an increased density of nuclei outside of myofibers in Bax-null muscles (not shown). Studies of mice with muscle-specific inactivation of Bax, or with muscle-specific expression of Bax in Bax-null mice could determine whether Bax inactivation affects myofiber size directly or indirectly.
We found that mouse myogenic cells can undergo spontaneous immortalization via a mechanism that can include, but does not require, loss of p16 INK4a , and also does not require inactivation of p19 ARF or p53. Furthermore, we identified a new mechanism, inactivation of Bax, that accelerates the immortalization of mouse myogenic cells. We also found that Bax-null myogenic cells produced relatively more mononucleate cells and fewer multinucleate myotubes than wild-type myogenic cells in culture and that the myofibers in Bax-null muscles in vivo were smaller than those in wild-type muscles. These results, as well as our earlier work with Bcl-2 [4, 5], implicate Bcl-2 family-mediated processes in controlling the proliferation and differentiation of myogenic cells. In addition, this study emphasizes that mouse cells of different lineages take different routes to immortalization.
Mice and cell culture
Breeding pairs of heterozygous B6.129X1-Bax tm1Sjk mice  were obtained from the Jackson Laboratory and mated in our laboratory. Progeny were genotyped , and muscle tissue or cells for primary cultures were obtained from tissues of the resulting wild-type, heterozygous, and Bax-null littermates at 4–6 weeks of age. At this age, there was no difference in body weights between Bax-null and Bax-positive mice. To obtain myogenic cells for culture, hindlimb muscles were isolated and treated with pronase to release mononucleate cells as described . To obtain highly enriched myogenic cell populations, each mononucleate muscle cell preparation was fractionated by 2-step (35%, 70% Percoll) gradients, and cells were collected from the 35–70% interface as described [4, 49]. Unless otherwise noted, cells were cultured on ECL Matrix (Upstate Biotechnology) in proliferation medium (PM) which consisted of DMEM with 15% horse serum, 4% chicken embryo extract, 2 mM L-glutamine, 10 mM HEPES pH 7.4, 100 U/ml penicillin, and 1 mM pyruvate. Myoblasts were induced to differentiate by transfer to differentiation medium (DM) which consisted of DMEM without chicken embryo extract and with only 2% horse serum.
Cell proliferation and clonal assays
To measure proliferation of cells obtained from adult tissues, myogenic cell cultures were initiated at ~100 cells per cm2. Growth medium was used at ~0.1 ml per cm2 and medium was replaced each day with fresh medium. Myogenic cells were passaged and reseeded at the initial density after 3 – 6 days of culture, at which time the cells had not reached confluence and fusion to form multinucleate myotubes had not begun. For all proliferation assays, cells were released from the culture dish by treatment with trypsin, and cell numbers were determined using a hemocytometer to enumerate viable cells that excluded Trypan Blue (GIBCO-Invitrogen). Cell growth was also assessed by counting cells per unit area in culture using an inverted microscope with results equivalent to those obtained with a hemocytometer.
To determine the properties of clonally-derived muscle colonies, cultures of myogenic cells that were initiated at clonal density (~1–10 cells/cm2) were fixed with paraformaldehyde (see below) after 8 days of growth, immunostained for the muscle-specific intermediate filament protein desmin (typically >80% of the colonies were composed of cells that were desmin-positive), and examined to determine the number of nuclei per colony and the percentage of nuclei contained within multinucleate myotubes (fusion index). Measurements of muscle colonies were carried out by observers unaware of the genotypes of the cells. Clonal cell lines were derived by 2 consecutive rounds of subcloning carried out using limiting dilution. Statistical analysis was done using the InStat program (v. 2.0, Graphpad Software, San Diego CA).
Immunostaining, immunoblotting, and β-Galactosidase assays
Antibodies included rabbit anti-desmin (ICN/Cappel, Costa Mesa CA) used at a dilution of 1:500; rabbit anti-p16 INK4a (sc-1207, Santa Cruz Biotechnology, Santa Cruz CA) used at 2 μg/ml, rabbit anti-p19 ARF (Novus Biologicals, Littleton CO) used at 0.5 μg/mL, and mouse anti-glyceraldehyde 3-phosphate dehydrogenase (GAPDH) used at 2 μg/ml (Research Diagnostics, Flanders NJ). Antibody binding was visualized using a horseradish peroxidase-based detection system (Vectastain Elite kit; Vector Laboratories) with diaminobenzidine substrate. Detection of Sca-1 and Bcl-2 was performed as previously described , except only a single mAb (clone E13-161.7; Pharmingen Laboratories, San Diego CA) was used to detect Sca-1.
Protein extraction from cultured cells and immunoblotting was carried out as described .
To detect senescence- (or stress-) associated β-galactosidase activity (SA-βGal) [10, 11, 13], cells were washed in PBS, fixed for five minutes in 4% paraformaldehyde, washed two times with PBS and incubated overnight at 37°C in fresh staining solution consisting of 1 mg of 5-bromo-4-chloro-3-indolyl β-D-galactoside (X-Gal; stored as a 20 mg/ml stock in DMSO) per ml / 40 mM citric acid/sodium phosphate, pH 6.0 / 5 mM potassium ferrocyanide /5 mM potassium ferricyanide /150 mM NaCl /2 mM MgCl2.
p53, karyotyping, soft agar growth
To analyze p53 transcriptional activity, target cells were transfected with the PG13-GFP reporter plasmid from which expression of Green Fluorescent Protein (GFP) is under control of a p53-dependent promoter consisting of thirteen copies of the p53 consensus binding sequence . As a control for transfection efficiency, target cells were simultaneously transfected with a plasmid on which β-galactosidase is under control of a constitutively active fragment of CMV promoter (BD Biosciences, San Diego CA). FuGENE 6-mediated transfection was carried out using supplier-provided protocols (Roche Applied Sciences, Indianapolis IN), using 2 μg of the PG13-GFP reporter plasmid and 0.5 μg of the control plasmid per 35 mm culture dish. At 72 hours after transfection, cultures were switched into differentiation medium, and, after an additional 48 hours, cells were examined for expression of GFP by fluorescence microscopy. Finally, cells were paraformaldehyde-fixed and immunostained for β-galactosidase using a specific primary antibody (Molecular Probes, Eugene OR) and a rhodamine F(ab)-conjugated secondary antibody (ICN/Cappel, Costa Mesa CA).
Induction of p53 by Actinomycin D was determined by treating cells with 60 ng/ml of Actinomycin D for 8 hours. Cells were collected for immunoblot analysis 16 hours after the Actinomycin D had been removed and replaced with fresh medium.
Karyotypes of colcemid-treated and fixed cells were determined essentially as in previous work [14, 50], except that chromosomes were not eosin-stained. Chromosomes of 20 – 30 cells of each genotype were counted in metaphase spreads.
Soft agar assays to test for anchorage-independent growth were performed as described . For each assay, 2 × 104 cells were cultured per 6 cm dish in proliferation medium.
Induced cell death assays
Cultures of cloned, immortalized Bax-null and wild-type myogenic cells were grown to near confluence in growth medium, at which time fresh growth medium containing adriamycin (doxorubicin, 1.7 μM), staurosporine (50 nM), or no addition as a control was added. After 24 h, the number of viable cells in each culture was determined as above. Untreated Bax-null and Bax-positive cultures had statistically identical numbers of cells, and the number of cells in the adriamycin- and staurosporine-treated cultures was converted to percentage of the untreated control cell number.
Sections (10 μm) were prepared [4, 51] from frozen soleus muscles dissected from Bax-null and Bax-positive littermates at seven weeks of age. Muscles were examined from three pairs of gender- and age-matched littermates. ATPase staining of muscle sections at pH 10.2 and 4.3 was used to identify fast and slow myofibers . The cross-sectional area of every fast and slow myofiber within a 0.3 mm2 area of each soleus was determined by computer-assisted morphometry (NIH Image program, http://rsb.info.nih.gov/nih-image/), with average cross-sectional areas, average density of myofibers, and statistical comparisons determined with the InStat program.
We thank Dr. Silvia Soddu (Regina Elena Cancer Institute, Rome, Italy) for providing the PG13-GFP plasmid. This work was supported by a grant to Janice A. Dominov from the NIH (AR049306) and by grants to Jeffrey B. Miller from USDA (NRICGP), NIH (AR049496, ES011384, HL064641) and the Muscular Dystrophy Association.
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