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SKELETAL MUSCLE AND EXERCISE |
Departments of
1 Physiological Science
2 Pathology and Laboratory Medicine, University of California, Los Angeles, CA, USA
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Abstract |
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(Received 28 July 2006;
accepted after revision 5 October 2006;
first published online 12 October 2006)
Corresponding author J. G. Tidball: Department of Physiological Science, 5833 Life Science Building, University of California, Los Angeles, CA 90095, USA. Email: jtidball{at}physci.ucla.edu
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Introduction |
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Macrophages are also able to promote muscle growth and repair. In vitro findings show that conditioned media from peritoneal macrophages or macrophage cell lines can increase proliferation of myoblasts in culture and elevate the proportion of myoblasts that express MyoD (Cantini & Carraro, 1995; Cantini et al. 2002), which indicates a role for macrophage-derived factors in muscle growth and differentiation. In vivo observations may also support a positive role for macrophages in muscle growth and repair. Muscle repair by transplanted whole-muscle grafts is diminished if the graft recipients are irradiated before transplantation (Lescaudron et al. 1999), which reflects a role for proliferative cells, such a macrophages, in muscle regeneration. More recent findings have shown that null mutation of cyclooxygenase-2 (COX-2) or administration of COX-2 inhibitors can slow muscle regeneration and reduce myoblast proliferation after acute injury of muscle (Bondesen et al. 2004). COX-2 null mutants also showed less macrophage invasion of injured muscle during regeneration (Bondesen et al. 2004), which may indicate that macrophages normally promote muscle cell proliferation and muscle regeneration following injury. Alternatively, COX-2 may have a direct effect on muscle cells to affect proliferation and repair.
The apparently conflicting roles of macrophages in promoting muscle injury and repair may reflect the functions of distinct macrophage subpopulations in muscle. Several investigations have supported the potentially dichotomous role of macrophage subpopulations by examining the time courses of macrophage invasion, muscle fibre damage and muscle repair following modified muscle use. During periods of increased muscle use that are sufficient to cause muscle membrane lysis and muscle inflammation, muscle is initially invaded by a phagocytic population of macrophages that can enter and degrade the contents of injured muscle fibres (Krippendorf & Riley, 1993; St Pierre & Tidball, 1994; Tidball et al. 1999). These macrophages reach peak concentrations in the muscle at 2 days following increased muscle loading, and then rapidly decline in numbers (St Pierre & Tidball, 1994). Most lesions of the muscle membrane that are caused by muscle reloading occur during this first 2 day period (Tidball et al. 1999). A second, non-phagocytic population (McLennan, 1993) invades the muscle and reaches peak concentration at 4 days following increased loading, but remains elevated for at least several days after muscle loading is increased (Krippendorf & Riley, 1993. St Pierre & Tidball, 1994; Tidball et al. 1999). This second, non-phagocytic population is mostly distributed near regenerative fibres (St Pierre & Tidball, 1994), suggesting their potential role in muscle regeneration. Furthermore, peritoneal macrophages that are phenotypically similar to the non-phagocytic population in injured muscle have been shown to release in vitro unknown factors that can promote myoblast proliferation (Massimino et al. 1997).
In the present investigation, we have tested whether the late invading population of macrophages affects muscle membrane lysis, membrane repair, satellite cell activation, muscle regeneration or muscle fibre growth during a period of increased muscle loading that is imposed after a 10 day period of muscle unloading. We have developed a protocol for antibody depletion of macrophages that reduces the concentration of macrophages after 2–4 days of increased loading, but does not affect macrophage numbers during earlier stages of increased muscle loading. Our findings show that the selective depletion of macrophages at the 2–4 day time point prevents repair of the muscle cell membrane that normally occurs at this time and prevents muscle fibre growth and regeneration, which usually occur between 2 and 4 days of increased muscle use. These findings show that the late-invading macrophage population can contribute significantly to muscle repair, growth and regeneration in vivo.
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Methods |
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All experiments involving animals were conducted according to the National Institutes of Health Guide for the Care and Use of Laboratory Animals and were approved by the University of California, Los Angeles Institutional Animal Care and Use Committee. C57BL/6J mice were obtained from the Jackson Laboratories (Bar Harbour, ME, USA) and were 5 months of age at the time of experimentation. Mice were maintained in an accredited animal care facility and examined daily for signs of distress, injury or disease. At the end of experimentation, mice were killed by intraperitoneal injection with an overdose of sodium pentobarbital, according to the Panel on Euthanasia of the American Veterinary Medical Association.
Hindlimb muscle unloading and reloading
Muscle injury and inflammation were induced by subjecting mice to 10 days of muscle unloading of both hindlimbs, followed by reloading for 2 days or 4 days by normal weight bearing. An apparatus that was a modification of that described by Morey-Holton & Globus (2002) was used for hindlimb unloading. Muscle unloading by this technique produces approximately a 40% mass loss of the soleus muscle in a 10 day period (Thomason & Booth, 1990) and approximately a 30% reduction in fibre cross-sectional area. Muscle reloading when returned to normal ambulation causes muscle inflammation, fibre injury and membrane lesions in soleus muscle fibres (Krippendorf & Riley, 1993; St Pierre & Tidball, 1994; Kasper, 1995; Tidball et al. 1999). Mice received either anti-F4/80 injections or injections of isotype control antibody followed by either 0, 2 or 4 days of reloading after hindlimb unloading. There were five mice in each anti-F4/80 or isotype control IgG group at each time point. The ‘unloaded only’ groups consisted of mice injected with anti-F4/80 or isotype control antibody that were subjected to hindimb unloading for 10 days and then immediately killed for tissue collection, without experiencing reloading. The ‘ambulatory control’ group consisted of five control mice that experienced normal cage activity until killed for tissue collection. After the animal was killed, soleus muscles were rapidly dissected. One soleus muscle from each animal was rapidly frozen in isopentane, and used for immunohistochemical analysis and Western blot analysis. The second soleus from each animal was used for assessment of muscle membrane damage.
Macrophage depletion protocol
Anti-F4/80 was prepared by ammonium sulphate precipitation of immunoglobulins from F4/80 hybridoma cultures (ATCC). The precipitated immunoglobulins were resuspended in 50 mM sodium phosphate buffer pH 7.2 containing 150 mM sodium chloride (PBS), sterile filtered and then the IgG concentration was assayed by enzyme-linked immunosorbent assay. Mice received intraperitoneal injections of 100 µg anti-F4/80 IgG or isotype control IgG (rat IgG2b; BD Pharmingen, San Diego, CA, USA) every 24 h, beginning on day 7 of hindlimb unloading until the day the animal was killed.
Immunohistochemistry
Frozen, cross-sections were taken from the midbelly of one soleus muscle from each animal and used for immunohistochemical analysis. The 10 µm thick sections were fixed in acetone and then immunolabelled for macrophages using using rat anti-mouse F4/80, or for satellite cells using mouse anti-MyoD (clone 5.8A; RDI, Flanders NJ, USA), or mouse anti-Pax-7 (clone P3U1; Developmental Studies Hybridoma Bank, Iowa City IA, USA). Sections probed with anti-F4/80 were processed as previously described (Wehling et al. 2001) and immunoreactive cells were identified using a biotinylated mouse anti-rat IgG second antibody and horseradish peroxidase conjugated avidin before reaction with aminoethylcarbonyl (Vector). Sections treated with antibodies generated by mouse hybridomas were processed similarly, although endogenous IgGs were blocked using a MOM kit (Vector) and the second antibody was a rat anti-mouse IgG. The total volume of each section was determined by measuring the area of each section using a stereological, point-counting technique (Spencer et al. 2001), and then multiplying that value by the section thickness. The concentrations of immunolabelled cells were expressed as the number of cells per volume of each section. One-way analysis of variance was used to test whether variation between groups was significant at P < 0.05. Bartlett's test for homogeneity of variances was used to test whether all experimental groups came from populations with equal standard deviations. The Bonferonni multiple comparisons test was used to test for differences between pairs of experimental groups with P < 0.05.
Assays of muscle membrane injury
Injuries to soleus muscle fibre membranes were assayed by measuring the relative concentration of the fluorescent, extracellular tracer dye, procion orange, in the cytoplasm of muscle fibres. Procion orange dye solutions remain in the extracellular space unless membrane lesions are present. One soleus from each experimental or control mouse was incubated in 0.5% procion orange dye solution in Krebs-Ringer solution for 1 h followed by washes with Krebs-Ringer solution. The soleus muscles were then frozen in isopentane and serial cross-sections for each muscle were cut at 10 µm thickness. Fibre membrane injury was assessed using two assays. In the first, the number of brightly fluorescent, injured fibres in each section taken from the midbelly of each muscle was expressed as a percentage of the total fibres that were present in the section. The size of the lesions in these brightly fluorescent fibres was also determined by following each fibre through serial sections of the muscle. In the second assay, the fluorescence intensity of each, individual fibre in each muscle cross-section was measured in an 8 µm diameter, circular area that was sampled at the centre of each fibre using a digital imaging system (Bioquant, Nashville, TN, USA). Fluorescence intensity values for each fibre were attained below signal saturation levels and were corrected for background levels, by measuring the signal from an area of the slide that contained no tissue, and subtracting that background value from the cytosolic fluorescence measurements.
Assay for muscle membrane remodelling
Muscle membrane remodelling was assessed by comparing the relative concentrations of dysferlin in extracts of experimental and control soleus muscles by Western blot analysis. Previous investigations have established that dysferlin participates in the repair of muscle fibre membranes following acute, muscle injury (Lennon et al. 2003), as well as muscle membrane remodelling during muscle atrophy (Chopard et al. 2005). Samples were homogenized in a Dounce homogenizer in reducing sample buffer (80 mM Tris, pH 6.8, containing 0.1 M dithiothreitol and 70 mM SDS), and then boiled for 1 min and centrifuged to remove particulate material. The protein concentration of the supernatant fraction was measured (Minamide & Bamburg, 1990) and 30 mg each sample was loaded on 10% polyacrylamide gels (Laemmli, 1970), and then transferred electrophoretically to nitrocellulose (Burnette, 1981). Protein blots were incubated with a mouse anti-dysferlin (clone Ham3/17B2; Novocastra, Newcastle-upon-Tyne, UK) diluted 1 : 20 in 50 mM Tris, pH 7.6, containing 150 mM NaCl, 0.1% NaN3, 0.05% Tween 20, and 3% bovine serum albumin. After washing with buffer, the blots were incubated with a second antibody conjugated to horseradish peroxidase and the bound antibody was detected by enhanced chemiluminescence (Amersham). After digitally recording the chemiluminescent signal, the blots were stripped of antibody by incubating in them 62.5 mM Tris at pH 6.7 containing 2% SDS and 100 mM
-mercaptoethanol and then reprobed with rabbit anti-chicken desmin (Sigma) followed by similar processing and incubation with a second antibody to rabbit IgG that was conjugated to horseradish peroxidase and then assayed by enhanced chemiluminescence. The desmin labelling was used to assess uniformity of loading, and to normalize the dysferlin data relative to muscle protein.
Assay for muscle fibre regeneration
Myonuclei that are distributed along the longitudinal, central axes of muscle fibres, called central nuclei, are morphological markers of fibres undergoing regeneration (Bigard et al. 1975). The number of muscle fibres in complete cross-sections of soleus muscles from experimental and control animals was counted and expressed as a percentage of the total number of fibres in the muscle cross-section to provide an index of muscle regeneration. Each value is expressed as the mean ± S.E.M.
Measurement of muscle fibre cross-sectional area
Muscle fibre cross-sectional area was measured for every fibre in complete cross-sections of each soleus muscle using a digital imaging system (Bioquant). Muscle atrophy or growth was assessed by measuring changes in fibre cross-sectional area (Nguyen & Tidball, 2003b).
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Results |
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Immunohistochemical analysis of the concentration of F4/80-expressing macrophages in soleus muscles at the end of a 10 day period of muscle unloading, and then at 2 or 4 days of reloading confirms that muscle reloading causes macrophage invasion of soleus muscles. As previously reported (Krippendorf & Riley, 1993; St Pierre & Tidball, 1994), macrophages that invaded at early stages of reloading tended to be most concentrated near damaged fibres, and occasionally were observed to have infiltrated fibres. Macrophages that invaded at later stages, such as after 4 days of reloading, were distributed more homogeneously within the perimysium, and did not invade muscle fibres. Macrophage concentrations in soleus muscle of control mice are relatively low after 10 days of unloading (817 ± 142 cells mm–3, n = 5), but after 2 days of reloading they increase significantly (8590 ± 2212 cells mm–3, n = 5), and remain elevated after 4 days of reloading (10224 ± 3619 cells mm–3) (Fig. 1). Our anti-F4/80 treatment protocol did not cause a significant reduction in macrophage concentrations in soleus muscles after 10 days of unloading (721 ± 212 cells mm–3, n = 5) or at 2 days of reloading (7470 ± 2675 cells mm–3, n = 5), compared to isotype control IgG-treated mice. However, anti-F4/80 treatments caused an 86% reduction in macrophages in soleus muscles at the 4 day reloading time point (1462 ± 503 cells mm–3, n = 5) (Fig. 1).
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We identified muscle fibres with membrane lesions by the presence of the extracellular marker dye procion orange in the cytoplasm of the reloaded muscle fibres. The proportion of injured fibres that contained high concentrations of procion orange in the fibres, as indicated by bright cytosolic fluorescence observed by epifluorescence microscopy, did not differ significantly between anti-F4/80-treated mice and isotype control IgG-treated mice after 2 days of muscle reloading (non-depleted, 1.8 ± 0.2% injured, n = 5; F4/80 depleted, 1.4 ± 0.35% injured, n = 5) (Fig. 2). Inspection of the distribution of injured fibres in serial cross-sections of muscles that were reloaded for 2 days revealed no preferential distribution of lesions relative to the site at which the section was taken. Serial sections also showed that lesions were focal, and the high concentration of procion orange at lesion sites did not cause bright fluorescence along the entire length of injured fibres. The size of lesions was determined in a total of 46 fibres identified in six soleus muscles that experienced 2 days of reloading, which showed that foci of injury are 126 ± 76.0 µm in length. The typical, individual lesion formed 4.2 ± 2.5% of the total fibre length.
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Because measuring cell damage by determining the proportion of fibres that are brightly fluorescent after incubation in procion orange solution provides a large underestimate of the number of fibres with membrane damage (Nguyen & Tidball, 2003b), we also assayed the intracellular fluorescence of all fibres in soleus muscle cross-sections. These data were then expressed as a frequency distribution of fluorescence intensity for all soleus muscle fibres in anti-F4/80-treated and isotype control IgG-treated muscles (Fig. 2B). The mean fluorescence intensity did not differ between the anti-F4/80- or isotype IgG-treated groups after either 10 days of hindlimb unloading or after 2 days of reloading. However, after 4 days of reloading, the mean fluorescence intensity in the isotype control IgG group was significantly less than the anti-F4/80 group. These findings show that macrophage depletion prevented the repair of membrane damage that normally occurs between 2 and 4 days of muscle reloading.
We further tested whether macrophages may play a role in membrane remodelling during reloading by assaying for dysferlin, a membrane-associated protein that has been implicated in muscle membrane turnover and repair (Bansal et al. 2003). Western blots show that soleus muscles from mice that were not treated with anti-F4/80 contained higher concentrations of dysferlin after 10 days of muscle unloading compared with levels in ambulatory control muscles (Fig. 3). No further increase in dysferlin in the isotype control-treated soleus muscles was evident during the reloading period. Anti-F4/80-treated mice showed a similar increase in dysferlin in soleus muscles during unloading. However, further increases in dysferlin concentration occurred in soleus muscles of macrophage-depleted mice at 4 days of reloading (Fig. 3), which suggests that in the absence of macrophages, muscle membrane turn-over and repair persist.
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Centronucleation of muscle fibres was used as an index of muscle regeneration during muscle reloading. Isotype control IgG-treated animals showed more than a five-fold increase in the percentage of central-nucleated fibres in muscle cross-sections of 4 day reloaded muscle than in 2 day reloaded muscle (Fig. 4). However, anti-F4/80 treatments greatly reduced the occurrence of centronucleation, so that at 4 days of reloading the level of centronucleation in macrophage-depleted muscle was 77% less than in non-depleted muscles. This finding indicates that macrophages promote muscle regeneration during the period between 2 and 4 days of reloading.
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Macrophage depletion between day 2 and day 4 of muscle reloading reduces muscle growth
Changes in soleus muscle fibre cross-sectional area were used as an index of muscle atrophy or growth during muscle unloading and reloading. Similar to previous reports on rodents experiencing hindlimb muscle unloading, our results on animals receiving isotype antibody control injections showed 38% atrophy during 10 days of muscle unloading, followed by rapid recovery of size during reloading (return to 80% of original fibre cross-sectional area by 2 days of reloading and 95% of original cross-sectional area by 4 days of reloading). For much of the experimental time course the results were identical for anti-F4/80-treated mice. There was a 37% reduction in fibre cross-sectional area after 10 days of reloading, which returned to 79% of the original cross-sectional area after 2 days of reloading (Fig. 6). However, there was no further, significant increase in soleus fibre diameter in the anti-F4/80-treated mice between 2 days and 4 days of reloading.
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Discussion |
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Other studies of injured muscle may indicate a role for macrophages in promoting muscle growth or repair in vivo. An earlier and thought-provoking investigation showed that expression of a lacZ reporter transgene under the control of the muscle-specific, desmin promoter was reduced in muscle fragments that were transplanted into a recipient mouse that had experienced whole-body irradiation, compared to a non-irradiated recipient (Lescaudron et al. 1999). Transgene expression in the non-irradiated recipient corresponded to the time and location of invasion of the transplant by CD11b-expressing leucocytes. Because macrophages can express CD11b, the observation suggested that macrophages may play a significant role in muscle repair or regeneration. More recently, null mutation of COX-2 or COX-2 inhibition was shown to cause a reduction in muscle fibre size in areas of muscle repair following injury, and decreases in MyoD mRNA in muscle (Bondesen et al. 2004). Because COX-2 inhibition or null mutation also reduced the numbers of CD11b-positive cells at sites of muscle repair, these findings may also reflect a role for muscle macrophages in muscle growth and repair.
The findings of the present investigation show that macrophages can play an important role in affecting remodelling of muscle membrane damage during modified muscle use. However, the present investigation and previous work (Tidball et al. 1999) provide no evidence for macrophage-mediated damage to muscle cell membranes during muscle reloading after periods of unloading. As the data in the present investigation show, membrane lesions that were indicated by procion orange dye influx were normally repaired between 2 and 4 days of muscle reloading, but the specific depletions of late-invading populations of macrophages prevented this repair. The elevated expression of dysferlin in muscle that is undergoing atrophy or in which there is increased muscle membrane damage indicates that membrane remodelling during modified muscle use may be mediated by dysferlin. Deficiency in dysferlin underlies the pathology of limb-girdle muscular dystrophy 2B (LGMD2B) and Miyoshi myopathy (Liu et al. 1998; Bashir et al. 1998), which are progressive muscle wasting diseases. Patients with LGMD2B and Miyoshi myopathy experience elevated muscle creatine kinase in the serum, suggesting that muscle membrane damage is a feature of the pathologies (Prelle et al. 2003). However, current evidence indicates that dysferlin plays a role in membrane repair, not membrane stability, because dysferlin-deficient mice show no increased membrane damage with increased muscle loading (Bansal et al. 2003). Instead, dysferlin-deficient mice show an accumulation of membrane vesicles subjacent to the cell membrane (Cenacchi et al. 2005), and more slowly repair membrane damage caused by injuring myotubes with a scalpel in vitro (Lennon et al. 2003) or intense irradiation of isolated fibres (Bansal et al. 2003). The current findings show that elevated dysferlin levels persist in muscle fibres during periods of muscle membrane damage caused by modified muscle use, and that membrane repair and normalization of dysferlin levels is positively influenced by macrophages.
The failure of macrophage-depleted muscles to regenerate or grow during days 2–4 of muscle reloading could potentially be caused by a defect in membrane repair that may be a prerequisite for growth or regeneration. However, previous studies using the same model of modified muscle use have shown that null mutation of gp91phox prevented muscle membrane lysis during reloading, but did not affect muscle fibre growth during reloading (Nguyen & Tidball, 2003c). This observation indicated that membrane damage is not required for subsequent fibre growth, suggesting that the mechanism through which macrophages promote muscle fibre growth during muscle reloading does not involve a role in membrane repair.
An alternative explanation for the negative effect of macrophage depletion on fibre growth or regeneration would be that depleted muscles may experience defects in satellite cell activation leading to impaired growth and regeneration during increased loading. This latter alternative has been supported by findings which showed that macrophages increase muscle cell proliferation and MyoD expression in vitro (Massimino et al. 1997), although the reductions of phagocytic macrophages in vivo did not cause a significant change in the number of MyoD-expressing cells in muscle following injury (Summan et al. 2006). However, our results are not completely consistent with these previous findings and the differences in the findings may be attributable to differences in the model systems studied or the phenotype of the macrophages that mediate the response. At 2 days of reloading when there was no depletion of macrophages in our treatment, we observed no significant difference in the concentration of MyoD-positive cells in muscles from anti-F4/80-treated or control mice. At 4 days of reloading, the number of MyoD-positive cells in the control muscle decreased significantly, although total satellite cell numbers (indicated by Pax7 labelling) were unchanged. This indicates that there was no further net increase of satellite cells between days 2 and 4 of reloading and that MyoD-positive cells may have differentiated to MyoD-negative cells during this interval. Differentiation beyond the stage at which MyoD was expressed would render the cells fusion-competent and able to contribute to fibre growth (Smith et al. 1994; Friday et al. 2003). However, there was no change in the numbers of MyoD-positive cells in macrophage-depleted muscles between 2 and 4 days of reloading, which may reflect their failure to differentiate so that fusion with fibres and fibre growth could occur.
The mechanisms that regulate the accumulation of two distinct populations of macrophages at different stages of muscle reloading are not known, although potential mechanisms have been suggested in previous investigations. Although early studies proved that a large proportion of leucocytes that accumulate in injured muscle invade from the vasculature in response to muscle injury (Bintliff & Walker, 1960), there is a small population of resident macrophages in healthy muscle that is phenotypically similar to the non-phagocytic subpopulation examined in the present investigation (Honda et al. 1990). Thus, part of the accumulation of the non-phagocytic macrophages may reflect proliferation of resident macrophages rather than chemoattraction from the vasculature. However, our previous experience has shown us that antibody depletion of resident populations of cells within the muscle parenchyma is very inefficient, and we anticipate that the reduction of non-phagocytic macrophages in reloaded muscle is a consequence of depletion of a precursor population of monocytes in circulation. Other observations show that the mechanisms that increase the numbers of phagocytic and non-phagocytic macrophages in muscle differ. Inhibition of complement activation by intraperitoneal injections of soluble complement receptor sCR1 significantly reduced the concentration of early invading, phagocytic macrophages in muscle but caused a small, transient increase in the numbers of non-phagocytic macrophages in a rat model of hindlimb suspension (Frenette et al. 2000). More recently, studies have also shown that activated satellite cells release factors that are chemoattractive to monocytes and macrophages in vitro (Chazaud et al. 2003). Nearly 80% of the chemoattraction of monocytes/macrophages to activated satellite cells was blocked by neutralizing antibodies to monocyte chemoattractant protein-1 (MCP-1), macrophage-derived chemokine, fractalkine, vascular endothelial growth factor, urokinase type plasminogen-activator receptor (µPAR) and urokinase. Because injured muscle tissue expresses elevated levels of mRNA for MCP-1 receptor and µPAR-1 (Barash et al. 2004), the chemokines that bind these receptors may be particularly likely candidates for chemoattraction to injured muscle. Although there are no data to address whether these chemokines selectively attract phagocytic or non-phagocytic macrophages, the observation that µPA-null mice have less leucocyte invasion into injured muscle that accompanies defects in muscle regeneration (Lluis et al. 2001) could feasibly reflect a defect in µPA chemoattraction of non-phagocytic macrophages.
Our findings suggest that macrophages that invade muscle 2–4 days following increased muscle use or injury can contribute to muscle repair, growth and regeneration by affecting muscle fibre membrane repair and satellite cell differentiation. These results are consistent with the model in which the macrophage subpopulation that first invades injured muscle serves to remove cellular debris, after which the subsequent invasive population participates in repair, regeneration and growth. This model has received other experimental support in a recent investigation in which the early invading, phagocytic macrophages were depleted prior to muscle injury by intravenous injections of liposomes that contained clodronate (Summan et al. 2006). Phagocytic cells such as macrophages internalize and degrade the liposomes, thereby releasing the clodronate that induces apoptosis. Clodronate treatment produced a large, significant reduction in muscle macrophages at 3 days after injury. However, the depletion of macrophages at this time point caused an increase in muscle macrophages at 9 days after injury. Unlike the findings of the present investigation in which the late-invading macrophages were targeted, depletion of the early invading population produced a slowing of the removal of cellular debris, but had no effect on muscle regeneration, on the effect of muscle fibre growth following injury, or on satellite cell differentiation that was reflected as levels of MyoD expression. Thus, in vivo observations now provide functional data for two populations of macrophages involved in distinct roles in the response of muscle to injury. These findings highlight the potential value of targeting macrophages for modulating the repair and growth of skeletal muscle, but also emphasize the likely importance of selectively manipulating the numbers or activities of specific subpopulations of macrophages for designing therapeutic strategies.
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