Many growth factors are intimately bound to the extracellular matrix, with regulated processing and release leading to cellular stimulation. Myostatin and GDF11 are closely related members of the TGFβ family whose activation requires two proteolytic cleavages to release the growth factor from the prodomain. Specific modulation of myostatin and GDF11 activity by targeting growth factor-receptor interactions has traditionally been challenging. Here we demonstrate that a novel strategy for blocking myostatin and GDF11, inhibition of growth factor release, specifically and potently inhibits signaling both in vitro and in vivo. We developed human monoclonal antibodies that selectively bind the myostatin and GDF11 precursor forms, including a subset that inhibit myostatin proteolytic activation and prevent muscle atrophy in vivo. The most potent myostatin activation-blocking antibodies promoted robust muscle growth and resulted in significant gains in muscle performance in healthy mice. Altogether, we show that blocking the extracellular activation of growth factors is a potent method for preventing signaling, serving as proof of concept for a novel therapeutic strategy that can be applied to other members of the TGFβ family of growth factors.
Muscle atrophy is associated with a variety of clinical conditions, including diseases of denervation, genetic disorders, cachexia syndromes, and disuse. In these patients, reduced muscle strength and function are highly disabling and lack adequate treatments, often undermining successful management of the primary condition. Loss of muscle strength and mass also occurs as a natural process of aging and in severe cases is categorized as sarcopenia. While varied in their cause, these indications lead to significant disability, lengthy physical rehabilitation and recovery times, and quality of life impairment.
Despite intense interest, pharmacological interventions for preventing or reversing muscle atrophy remain an unmet medical need. Therapeutics for muscle atrophy currently in preclinical or clinical development include inhibitors of myostatin (also known as Growth and Differentiation Factor 8 or GDF8), a secreted growth factor that negatively regulates muscle mass. Myostatin’s expression is mainly restricted to skeletal muscle, with low levels of mRNA reported in adipose1 and cardiac2 tissues. Naturally occurring and engineered mutations that reduce myostatin signaling lead to a hypermuscular phenotype1,3,4,5,6,7,8. Conversely, myostatin overexpression in rodents induces a cachexia-like syndrome with muscle wasting and fat loss9. Because of the well-established impact of myostatin signaling on muscle mass, a number of agents that target the myostatin signaling pathway have entered the clinic for indications involving muscle atrophy.
Myostatin signals by binding a cell surface receptor complex consisting of a type I receptor (ALK4/5) and a type II receptor (ACTRIIa/b)1. To date, all of the anti-myostatin drug candidates in early-stage clinical studies block the interaction between mature myostatin and its receptors through antibodies, ligand traps, or overexpression of natural inhibitors such as Follistatin10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26. However, because the receptor recognition surfaces of mature myostatin and other Transforming Growth Factor β (TGFβ) family members share a high degree of similarity27,28,29, many of these myostatin-targeted biologics cross-react with other members of the TGFβ family (most commonly GDF11 or Activin A). In all of these cases, while promising results have been reported, it is too early to fully appreciate both their efficacy in patients and potential clinical toxicities associated with their lack of target specificity.
Here we demonstrate the efficacy of a novel alternative therapeutic approach to preventing growth factor engagement with cell surface receptors: blocking growth factor maturation from its autoinhibited precursor forms. Like other TGFβ family members, myostatin and its close homolog GDF11 are synthesized as inactive precursor polypeptides (here termed proMyostatin and proGDF11). Mature growth factor release from the unprocessed precursor is regulated through two discrete protease cleavage events (Fig. 1a). ProMyostatin and proGDF11 are cleaved by proprotein convertases, such as Furin or Proprotein Convertase Subtilisin/Kexin type 5 (PCSK5), that recognize a conserved RXXR site between the prodomain and mature growth factor9,30,31,32. This cleavage produces an inactive latent complex, here termed latent myostatin or latent GDF11, with two prodomains remaining associated with the growth factor dimer, preventing receptor binding.
Release of the active growth factor is accomplished through a separate prodomain cleavage by a protease from the BMP/tolloid family, such as Tolloid-like Protein 2 (TLL-2) or Bone Morphogenetic Protein 1 (BMP1)30,33 (Fig. 1a). This additional cleavage releases the mature growth factor from the latent complex, allowing it to bind to its receptor and activate signaling via the SMAD2/3 pathway. In muscle, this ActRIIb-induced signaling inhibits protein synthesis and enhances protein degradation pathways leading to muscle atrophy34,35.
In vivo, myostatin is detected both in circulation, where it exists predominantly in its latent form9,36,37,38, and in muscle where it resides primarily as unprocessed proMyostatin39. Notably, myostatin precursor forms are significantly more abundant in these compartments than the active mature growth factor9,36,37,39,40. Here we show that pro- and latent myostatin reside predominantly in the extracellular space within the muscle fiber, in close proximity to the cell surface. In addition, we show that myostatin precursors alter their distribution during glucocorticoid-induced atrophy, suggesting that myostatin processing plays a biologically important role in muscle atrophy.
We also demonstrate that highly specific TGFβ family growth factor regulation can be achieved by modulating extracellular activation, a fundamentally distinct approach from blocking receptor/growth factor interactions. We developed fully human monoclonal anti-proMyostatin and anti-proGDF11 antibodies that potently inhibit their target by blocking growth factor release from the prodomain and, consequently, signaling. Because the prodomains share a much lower degree of conservation (47% identity between myostatin and GDF11 prodomains vs. 90% in the mature domains), this approach allows greater control of antibody specificity. These precursor-directed antibodies were specific for their intended targets in vitro. In vivo, myostatin-specific activation-blocking antibodies were able to prevent atrophy in a corticosteroid atrophy model, and also increased muscle mass and function in healthy animals. Taken together, these data suggest that inhibition of extracellular activation is a potent and highly selective method for inhibiting TGFβ family signaling.
Specific modulation of the activation of myostatin and GDF11
Most growth factor-targeted therapeutic antibodies block the growth factor-receptor interaction. However, release of mature growth factor from the prodomain is tightly regulated in many TGFβ family members, offering an alternative strategy to modulate signaling. We therefore developed a novel phage display approach, using recombinant proMyostatin, latent myostatin and proGDF11 as antigens to screen for antibodies against the pro- and latent forms of myostatin and GDF11. Antibodies were then counterscreened against the mature growth factors to identify fully human monoclonal antibodies that specifically recognize the pro- and latent forms of myostatin or GDF11 without recognizing the mature growth factors. Table 1 summarizes data for six of the monoclonal antibodies identified in our screen: three with specificity for myostatin precursors and three with specificity for GDF11 precursors.
To evaluate whether the antibodies inhibit proMyostatin or proGDF11 activation, we developed an assay in which recombinant proMyostatin or proGDF11 were incubated with a tolloid protease (mTLL2 or BMP-1) and a proprotein convertase (Furin or PCSK5) (Fig. 1a.). Following proteolysis the activity of released growth factor was measured on 293 T cells expressing a SMAD2/3-dependent luciferase reporter. Because uncleaved recombinant proMyostatin and proGDF11 cannot induce signaling, antibodies that inhibit protease activation and growth factor release will result in reduced luciferase expression from the reporter cell line.
We identified multiple antibodies that specifically blocked proteolytic activation of either proMyostatin or proGDF11 (Fig. 1b,c, Table 1). None of the antibodies cross-reacted between myostatin and GDF11 in binding or inhibition of signaling, indicating the high specificity of this targeting strategy. It should be noted that a high concentration of precursor (proMyostatin in particular) is needed to drive the proteolysis reaction to completion in this assay, leading to artificially high EC50 values, even with the high affinity antibodies described here. Overall, these data demonstrate selective inhibition of myostatin and GDF11 signaling by antibodies that target precursor proteins rather than the mature growth factor domains.
We employed an expanded panel of myostatin precursor-specific antibodies (identified in our screen) to ask whether inhibition of myostatin activation is necessary and sufficient to inhibit myostatin signaling in vitro and in vivo. We chose ten antibodies with a wide range of binding profiles for this experiment as assessed by epitope binning and affinity measurements towards murine GDF8 proteins (Table 2 and Supplementary Fig. S1). These antibodies exhibited binding to 1) all three myostatin forms, (GDF8-013); 2) pro- and latent- myostatin (SRK-015, GDF8-030, GDF8-086, GDF8-040, GDF8-008, GDF8-062); 3) only proMyostatin (GDF8-021, GDF8-020); and 4) latent and mature myostatin (GDF8-083). Importantly, none of these antibodies recognized GDF11 and all displayed high affinity to their targets. This panel included SRK-015, an optimized version of the best myostatin selective antibody identified in our screen (SRK-015P, P stands for “parental”). SRK-015 was engineered by replacing five resides in the variable domain of SRK-015P outside of the complementarity-determining region (the residues which contact the myostatin precursors). SRK-015 showed a slight increase in affinity for myostatin precursors (compare Tables S1 and S2).
Three antibodies in the panel (SRK-015, GDF8_086, and GDF8_030 dose-dependently inhibited myostatin release in the myostatin activation assay, with calculated EC50 values ranging from 174–555 nM, close to the concentration of proMyostatin in the assay (200 nM) (Fig. 2a and Table 2). Two others, GDF8_021 and GDF8_040, weakly inhibited proMyostatin activation with EC50 values greater than 1 μM. The remainder of the precursor-binding antibodies in the panel failed to demonstrate inhibitory activity in this assay. These data demonstrate that high affinity binding alone to myostatin precursors is insufficient to block activation in vitro.
To compare direct receptor blockade to inhibition of activation, we assessed the ability of SRK-015, GDF8_021, and GDF8-C541,42 to inhibit signaling of mature myostatin. GDF8-C541,42 binds to the latent and mature species of both myostatin and GDF11 and directly inhibits mature growth factor signaling on reporter cells (see Supplementary Fig. S2 and Table 2). This control antibody (along with two others used throughout this manuscript) was produced based on publically available sequences of monoclonal antibodies which target the mature myostatin growth factor and are, or have been, in clinical development. While GDF8-C5 potently inhibited the ability of mature myostatin to signal in the cell based assay, neither SRK-015 nor GDF8_021 inhibited signaling of the mature growth factor (see Supplementary Fig. S2 and Table 2).
Blockade of myostatin activation prevents dexamethasone-induced muscle atrophy
The panel of antibodies described above allowed us to evaluate the significance of blocking extracellular activation in vivo, as each blocking antibody in the panel has a partner antibody with a similar binding profile that lacks the capacity to inhibit myostatin activation (all supporting data summarized in Table 2). Such experimental design allows us to establish whether inhibition of activation is necessary for blocking myostatin signaling, or if binding to precursor forms is sufficient to block myostatin signaling in vivo.
For this experiment we chose a dexamethasone-induced muscle atrophy model due to its relevance to myostatin signaling and human disease. Elevated circulating glucocorticoids are associated with a number of muscle wasting diseases43,44,45,46. In addition, therapeutic use of corticosteroids can lead to induction of muscle atrophy, which was recently explored in rodent models47. A number of glucocorticoid receptor target genes have been described to mediate catabolic responses in muscle such as DNA damage-inducible transcript 4 protein (DDIT4/REDD1), Krueppl-like factor 15 (KLF15), and the E3 ubiquitin ligases Murf1/TRIM63 and F-box only protein 32 (FBXO32/Mafbx/atrogin-1)48,49. Importantly, myostatin is thought to be a key mediator of catabolic effects of steroid hormones through glucocorticoid responsive elements in its promoter50,51,52,53.
Muscle atrophy in male C57BL/6 mice was induced by two weeks of dexamethasone treatment. Starting on day 1 of the study, mice were given either normal drinking water (vehicle) or water containing dexamethasone. Concurrent with dexamethasone treatment, mice were administered anti-Myostatin antibodies (Fig. 2) and a negative control antibody (IgG) once weekly (20 mg/kg) by intraperitoneal (IP) injection. Muscle atrophy was monitored during the study by measurement of changes in lean mass from baseline, measured by QNMR at baseline, 1 week and 2 weeks post start of dexamethasone treatment (see Supplementary Fig. S3a) and by measurement of muscle weights at the end of the 2 week study (Fig. 2 and Supplementary Fig. S3b).
Dexamethasone treated animals that received IgG control antibody showed significant atrophy in gastrocnemius muscles (~20%) compared to controls that did not receive dexamethasone (No Dex) (Fig. 2b, black squares, all calculated P values are reported in Table S4). In contrast, both the GDF8-C5 positive control antibody and two of the five myostatin activation-blocking antibodies (SRK-015 and GDF8_086) showed statistically significant protection against gastrocnemius muscle atrophy (vs. IgG control, P = 0.0012, 0.0019 and 0.0427 respectively) with no difference in muscle weights as compared to the healthy control (vs. No Dex) (Fig. 2b). Two additional activation-blocking antibodies (GDF8_030 and GDF8_040) showed trends towards protection but no significant difference from the IgG control. One antibody in a unique epitope class with weak blocking activity in vitro, GDF8_021, showed no significant effect on atrophy. Similar results were observed with rectus femoris muscle weights and total body lean mass (see Supplementary Fig. S3). Overall, antibodies that bind pro/latent myostatin (but do not inhibit its activation) all failed to protect against atrophy.
These data confirm that pro- and latent myostatin-specific antibodies that prevent growth factor release can inhibit myostatin signaling in vivo. Furthermore, the equivalent potency of SRK-015 and GDF8-C5 suggest that blocking myostatin proteolytic cleavage is as effective as conventional blockade of myostatin receptor/ligand binding.
SRK-015 uniquely targets the proteolysis of the pro- and latent forms of myostatin
As shown in Table 3, our most potent myostatin precursor-specific antibody, SRK-015, and its parental version, SRK-015P bound robustly to proMyostatin and latent myostatin, and no binding could be detected against the TGFβ family members GDF11, Activin A, BMP9 and 10, or TGFβ1. This binding profile is unique when compared to two antibodies that bind and directly inhibit the growth factor domain (see Supplementary Fig. S2 and Table 3 produced based on publically available sequences from clinical-stage antibodies). One, GDF8-C154, recognized the latent and mature forms of myostatin. The second control antibody, GDF8-C355, displayed a broader recognition profile, binding to not only GDF11 and myostatin, but also to Activin A and BMP10, demonstrating the lack of specificity which arises from targeting the mature growth factor.
We next explored the mechanism of SRK-015 and SRK-015P action in more detail. Importantly, SRK-015P inhibited activation of both latent myostatin and proMyostatin, suggesting that the furin cleavage step is not significantly affected by antibody binding (Figs 1b, 2a and 3a). To test whether SRK-015/SRK-015P blocks tolloid protease cleavage, latent myostatin proteolysis was analyzed by tracking a myostatin prodomain fragment (white box, Fig. 3b) that is generated by TLL-2 cleavage. SRK-015P (and SRK-015, data not shown) dose-dependently inhibited generation of this fragment, corresponding with signaling inhibition in the activation assay (Fig. 3a,b). These data suggest that SRK-015P and SRK-015 block myostatin activation by inhibiting prodomain cleavage by tolloid family proteases.
proMyostatin, the major form of myostatin in the muscle, is stored in the extracellular space
As SRK-015 binds both the pro and latent forms of myostatin, we investigated the abundance of these proforms in mouse serum and skeletal muscle. Our goal was to establish whether these forms of myostatin are present in compartments where they can be bound and inhibited by the antibody. First we confirmed by western blot that the predominant form of myostatin in serum is latent, while proMyostatin is the primary form in muscle (see Supplementary Fig. S4), consistent with previous reports9,36,37,39. We next performed immunoprecipitation experiments using non-reducing SDS-PAGE to separate precursor myostatin forms. Figure 3c demonstrates that SRK-015 bound proMyostatin, latent myostatin and other partially processed forms of myostatin in serum and proMyostatin in muscle (for raw data see Supplementary Fig. S5a).
The control antibody GDF8-C1, chosen specifically for this experiment because it bound to latent and mature myostatin in vitro (Table 2), also immunoprecipitated partially processed myostatin precursors in serum, but no interactions with proMyostatin homodimers were detected in either muscle or serum. We note that an antibody with the same sequence as GDF8-C1 was previously reported to immunoprecipitate proMyostatin from serum10, and, consistent with this, we detected a prominent ~90 kDa band that was immunoprecipitated from serum by both antibodies (double asterisk, Fig. 3c). This band, however, was smaller than proMyostatin found in skeletal muscle (marked by the arrow, detailed blow-up in Fig. 3c), and may therefore be a partially processed precursor found in serum but, notably, not in muscle.
The above data suggest that the majority of myostatin found in the muscle is stored as proMyostatin, but this data cannot discriminate between intracellular and secreted stores of proMyostatin. To address this, we performed immunofluorescence on tibialis anterior muscle from healthy mice using GDF8_086, which specifically detects pro- and latent myostatin (Tables 1 and 2, see Supplementary Fig. S6a). Co-staining with laminin, an extracellular matrix marker, demonstrated that the majority of myostatin precursors detected in muscle are interstitial and around interstitial nuclei, with little signal detected intracellularly (Fig. 3d). Co-staining with the vascular marker CD-31 (see Supplementary Fig. S6b) suggested that pools of extracellular myostatin precursors are in close proximity to the circulatory system. Taken together, our data strongly suggest that proMyostatin lies dormant in the extracellular space in healthy muscle and that SRK-015 uniquely recognizes the major forms of myostatin found in both muscle (pro) and serum (latent).
Myostatin precursor redistribution during atrophy
Western blot analysis of animals treated for 15 days with dexamethasone (Fig. 4a) suggested significant alteration of pro- and latent myostatin in the muscles of dexamethasone-administered mice. To further explore the effects of inhibition of myostatin activation in muscle atrophy, we again employed the dexamethasone-induced muscle atrophy model (described above). In this experiment, however, mice were given either normal water (Vehicle) or dexamethasone-spiked water (Dex) and administered a single 20 mg/kg injection of IgG control antibody or SRK-015. Cohorts of animals were then sacrificed on days 4, 6, 8, and 15 and muscle weights determined.
By day 8, gastrocnemius weights of IgG control mice administered dexamethasone were significantly smaller than mice given normal water (P = 0.0021), signifying that these mice had undergone muscle atrophy, an effect that was even more pronounced at day 15 (P < 0.0001, Fig. 4b). In contrast, animals treated with a single injection of SRK-015 were completely protected from dexamethasone-induced muscle loss, with no difference in muscle weight compared to IgG control mice given normal water (Fig. 4b). In addition to preventing atrophy in dexamethasone treated mice SRK-015 induced a significant increase in muscle mass in healthy (non-dexamethasone treated) animals (17.5% increase, Fig. 4b) 15 days after a single dose of antibody. Furthermore, in accordance with the above data, SRK-015 treatment significantly blunted the upregulation of atrogenes caused by dexamethasone treatment on day 4 (see Supplementary Fig. S7). Interestingly, SRK-015 had no effect on myostatin gene expression (see Supplementary Fig. S7).
In order to understand whether the distribution of myostatin precursor forms is altered during atrophy, we examined myostatin precursors in muscle and serum from the above study using a quantitative fluorescent western blot assay. We confirmed the specificity of the assay in both muscle and serum using samples from mice in which the myostatin prodomain was deleted (see Supplementary Fig. S4). Due to a lack of specific reagents, we were not able to quantify the levels of mature myostatin, though ours and others’ data suggest that mature myostatin levels (outside of the latent complexes) are very low36,39,40.
Levels of proMyostatin and latent myostatin were quantified relative to untreated controls (n = 3 per group, Fig. 4c–e), with similar results observed in four independent studies (original western blot images from this experiment are shown in see Supplementary Fig. S5b,c). Following 14 days of dexamethasone treatment, we observed an increase in proMyostatin (1.77 × no dex controls) in the muscle and a decrease in latent myostatin (0.34 × no dex controls) in the serum compared to vehicle treated animals (P < 0.001 and <0.002, respectively, Fig. 4c–e). The altered biodistribution of the myostatin precursors suggests an alteration in the myostatin activation pathway. We also observed dexamethasone-induced changes in myostatin precursors occurring prior to or concomitant with statistically significant decreases in muscle weights (between days 4 and 6), suggesting that redistribution of myostatin precursors may be an important driver of reduced muscle mass. Thus, these data reveal an increase in proMyostatin levels at the site of myostatin signaling during muscle atrophy.
We also confirmed target engagement by SRK-015, showing that levels of both pro- and latent myostatin rose significantly in muscle and serum following antibody treatment (see Supplementary Fig. S5b–f). These data indicate significant SRK-015 target engagement by day 4 and that engagement is sustained until at least two weeks post dose. These findings are also consistent with the unique mechanism of SRK-015, which binds the most abundant form of myostatin (proMyostatin) at the site of signaling. This is in contrast to other monoclonal antibodies that bind the mature growth factor domain without recognizing proMyostatin (such as GDF8-C1, Fig. 3c). Thus, to our knowledge, SRK-015 remains the only monoclonal antibody that specifically binds pro- and latent myostatin in the muscle, blocking activation.
Blockade of myostatin activation enhances muscle function in healthy animals
To test whether inhibition of myostatin activation affects muscle performance, we carried out a four-week study in C57BL/6 mice, dosing at 20 mg/kg weekly. We used muSRK-015P, a functionally equivalent, murine constant region chimeric version of SRK-015P (Table S3) to limit the potential immune response that can occur from long term dosing of a human antibody in mice. In vivo, animals treated with muSRK-015P generated an 16–18% increase in isometric torque in the plantarflexor group (gastrocnemius, soleus and plantaris muscles, normalized to limb length) at frequencies greater than 60 Hz (main effect P = 0.003) (Fig. 5a). While there was a trend towards increased rate of contraction, this effect was not significant. In addition, no changes were observed in the relaxation rate (see Supplementary Fig. S8a). Because the increase in force was mirrored by a 19% increase in the gastrocnemius weight (P = 0.024, Fig. 5b), there are no differences between groups when force is normalized to muscle weight (Fig. 5c), suggesting that muSRK-015P-induced hypertrophy did not adversely affect muscle quality or excitability.
We next isolated the EDL muscle and measured force in vitro to confirm direct effects of myostatin blockade on muscle, independent of nerve function and blood supply. muSRK-015P treatment resulted in a 20–29% increase in maximal force at frequencies greater than 60 hz (main effect P = 0.0003, Fig. 5d) with no alteration in rates of contraction and relaxation (see Supplementary Fig. S8b). Myostatin blockade resulted in a 34% increase in the EDL weight (P = 0.0086, Fig. 5e), such that, again, there were no differences between groups when force was normalized to muscle weight (Fig. 5f).
Histological evaluation of the plantarflexor muscle group revealed a 27% increase in total muscle cross sectional area (P = 0.019, see Supplementary Fig. S8c) and a 14% increase in mean fiber cross sectional area (P = 0.027, see Supplementary Fig. S8d). As expected for a myostatin-specific inhibitor10, this increase was underpinned by a 20% increase in Type IIB fiber cross-sectional area (P = 0.011)(Fig. 5g,h), which was independent of any change to relative distribution of fiber types (Fig. 5i) or cross sectional area (CSA) of Type I, IIA, or IIx fibers (see Supplementary Fig. S8e–g). To our knowledge, these data are comparable to or even surpass effects on muscle function reported for other myostatin inhibiting agents10,56. Altogether, these data show that inhibition of extracellular myostatin activation promotes a robust anabolic response in the muscle, accompanied by enhanced function with no detrimental side effects.
The data in this manuscript demonstrate a fundamentally novel approach to growth factor inhibition: targeting the prodomain to modulate the activation of the mature growth factor rather than by blocking receptor-ligand interactions. This is important, as the high homology of the mature ligands has confounded discovery of truly selective antibodies. Indeed, selective pharmacological modulation of highly related mature myostatin and GDF11 growth factors has proven to be technically challenging. Divergent results have been reported regarding the biological functions of GDF11, with much of the controversy stemming from a lack of reagent specificity57,58,59,60. We show in this manuscript that by targeting precursor forms of myostatin and GDF11 we were able to generate several highly specific and pharmacologically effective antibodies towards these two homologs. Encouragingly, SRK-015 limited dexamethasone-induced muscle atrophy as effectively as a clinically vetted mature myostatin-targeting antibody (Fig. 2b, compare SRK-015 to GDF8_C5).
Lack of therapeutic specificity extends more broadly within the TGFβ superfamily. Several clinical-stage “anti-myostatins” exhibit cross-reactivity to Activin A, BMPs 9 and 10, and GDF11 (as shown in Tables 2 and 3, for example). Side effects from blocking these growth factors could limit the utility of candidate therapeutics. For example, an early clinical trial of the ActRIIb ligand trap, ACE-031, in Duchenne muscular dystrophy was terminated prematurely due to epistaxis and telangiectasis26 attributed to BMP9 or BMP10 reactivity26,61. TGFβ family prodomains universally share much less sequence conservation than the mature ligands29 and we are currently applying this approach to other members of the family.
Our data confirms and extends previous findings9,36,37,39 showing that myostatin is stored extracellularly in its pro- and latent forms in vivo. We show that pro- and latent myostatin are the predominant myostatin forms in muscle and serum, respectively. While Anderson et al. also demonstrated that some fraction of the proMyostatin pool resides extracellularly, where it can be regulated by extracellular furin cleavage39, the relative abundance of intracellular vs. extracellular proMyostatin in muscle tissue remained unclear. By immunofluorescence with a pro/latent-specific antibody, we show here that the bulk of proMyostatin is stored in the sarcolemma-associated extracellular matrix (Fig. 3d). ProMyostatin distribution overlapped with laminin, but was more focal, often detected near junctions between three sarcolemma, suggesting that additional factors may influence proMyostatin extracellular distribution. Indeed the extracellular matrix proteins latent TGFβ binding protein 3 (LTBP3), latent TGFβ binding protein 4 (LTBP4), and perlecan, have been reported to interact with myostatin and/or myostatin precursors39,62,63, though the role of these anchoring proteins in modulating signaling is, as yet, unknown.
Our finding that most proMyostatin resides extracellularly in its primary target tissue, muscle, suggests that extracellular activation is a critical step in myostatin signaling. While the follistatins and GASPs (growth and differentiation factor-associated serum proteins 1 and 2) are naturally occurring inhibitors of myostatin and GDF11, these appear to bind a small fraction of mature myostatin in circulation36,37,39. Consistent with this hypothesis, we observed changes in the balance of myostatin precursors in a model of muscle atrophy. We found that proMyostatin protein levels were upregulated in muscle by day 4 of glucocorticoid-induced atrophy, while decreased circulating latent myostatin was evident in the same timeframe. Given that changes in proMyostatin levels occurred prior to significant loss of muscle mass, we believe that reduced circulating latent myostatin was not due to decreased muscle mass. We hypothesize instead that changes in serum latent myostatin reflect enhanced myostatin processing in atrophying muscle, underscoring the importance of proteolytic processing in controlling the myostatin signaling pathway.
While circulating myostatin has been examined as a biomarker of muscle atrophy and dysfunction38,40,58, our data highlight the importance of understanding myostatin processing and signaling in the muscle as well as in serum, as circulating myostatin levels may not adequately reflect the extent of myostatin signaling in the muscle itself. Quantitation of myostatin by ELISA or immunoaffinity mass spectrometry has been reported38,40, but these measurements do not distinguish between free mature myostatin and mature myostatin in latent complexes (bound to the propeptide or other inhibitory proteins). Reagents with specificity for the various forms of myostatin, such as the antibodies described in this study, could be useful in developing truly specific quantitative assays. This, coupled with additional studies to understand myostatin forms in patient samples and preclinical models, will help elucidate the broader role of extracellular processing in myostatin regulation and help to identify patient populations responsive to anti-myostatin therapy.
While our results highlight the therapeutic potential of inhibiting myostatin activation in muscle wasting diseases, an important step towards clinical development is identification of patient populations that would benefit the most from such a therapy. Evaluation in additional disease models, as well as more detailed analysis of the pharmacokinetic and pharmacodynamic properties of SRK-015 is ongoing. In addition, the panel of antibodies that we have developed also affords the opportunity to measure the distribution and dynamics of myostatin precursor forms in healthy and diseased serum and muscle. Such translational insights, complemented by biomarker data previously generated using other assay systems, can further inform the selection of clinical indications in which blockade of extracellular myostatin activation may bring greatest benefit to patients. Based on the highly regulated release of these growth factors in tissue, the novel mechanism of SRK-015 may afford improved safety and/or efficacy profiles compared to antibodies targeting the mature growth factor domain.
Finally, the finding that prodomain-targeted antibodies can modulate signaling of two independent growth factors, myostatin and GDF11, suggests the broader applicability of our approach. We note that these proteins are closely related, and additional investigation is necessary to understand whether our approach can be extended to other TGFβ family members or, more broadly, to prodomains of other signaling molecules. Nevertheless, the data presented here clearly demonstrate the efficacy of our novel approach to inhibit signaling by blocking maturation of a proprotein to its active form, and suggest a potential to selectively modulate a range of growth factor signaling pathways by targeting extracellular activation.
Materials and Methods
Full-length human and murine Myostatin and GDF11 proteins were stably integrated into FLP-INTM T-REXTM 293 cells (Life Technologies, Carlsbad, CA) and expressed according to manufacturer’s instructions (Uniprot reference numbers: O14793, O08689, O95390, Q9Z1W4). Fully human anti-myostatin and anti-GDF11 antibodies were identified using a phage library displaying scFvs (single chain variable fragments)64. Separate antibody discovery campaigns were run using recombinant human proMyostatin, latent Myostatin, and proGDF11 for both positive and negative selection as appropriate to obtain antibodies with the desired binding profile. Antibodies were cloned and expressed using standard techniques, and binding profiles assessed on a FortéBio Octet QKe in various formats according to manufacturers directions (Supplementary methods). To potentially reduce immunogenicity, SRK-015 was generated from its parental version, SRK-015P, by introduction of five mutations in the variable domain. These antibodies are identical in the complementarity determining regions (CDRs) and have similar affinities and functional activity both in vitro and in vivo. muSRK-015P is identical to SRK-015P but contains a murine IgG1 constant region instead of a human IgG4 constant region.
Reporter cell assays
Fully matured growth factors were purchased from R&D systems. Samples of human or murine proMyostatin (200 or 500 nM, as indicated) or human/murine proGDF11 (50 nM) were incubated with supernatants (either singly or in combination as appropriate) collected from stably integrated 293 cells overexpressing a pro-protein convertase (either Furin/PACE3 or PCSK5) and/or a Tolloid protease (either BMP-1 or mTLL2) at 37 °C for 16 hrs. After the proteolysis reaction, Myostatin or GDF11 activity was assessed by adding samples to 293 T cells containing a stably integrated pGL4 plasmid (Promega, Madison, WI) with a promoter comprising SMAD- responsive CAGA sequences. Cells were incubated at 37 °C for 6 hours before detection of luciferase expression using BRIGHT-GLOTM reagent (Promega, Madison, WI) according to manufacturer’s instructions.
Results were used to calculate the percent inhibition for each condition (% inhibition = 100 × ((Reading with test antibody but in the presence of protease – reading without tolloid protease)/(reading without antibody but in the presence of protease-reading without tolloid protease)). EC50 values were calculated in GraphPad Prism 7.0.1 from a four parameter logistic curve. Activation assay data are representative of at least 3 independent experiments, and means and standard deviations of three technical replicates are shown.
In vivo dexamethasone studies were conducted at the Covance Laboratories Inc. Greenfield, Indiana. The Institutional Animal care and Use Committee approved experiments and procedures conformed to their guidelines. Animals were randomly assigned to treatment groups based on body weight at study initiation. Sample sizes (n = 8–10) are standard for detecting statistically different changes in muscle weights of the muscles examined. All data from animals that perished due to dexamethasone toxicity prior to study completion were removed from the analysis. Dexamethasone data are representative of four separate studies for SRK-015 and two studies for SRK-015P. All other antibodies were evaluated once in this model.
Ten male mice (per group, C57BL/6) were enrolled in the studies at 13–14 weeks of age. Starting on day 1 of the study, mice were given either normal drinking water (vehicle) or water containing dexamethasone (Dex, 17.5 mg/L)(Sigma Aldrich, Dexamethasone 21-phosphate disodium salt) treatment for two weeks. In studies with antibody treatments, test articles were administered by intraperitoneal (IP) injection (20 mg/kg) once per week (Fig. 2b) or once (Fig. 4, and see Supplementary Fig. S3) starting at the time of dexamethasone administration. Echo MRI (QNMR) measured body mass composition parameters (fat mass, lean mass and water content) on the indicated days. At necropsy, (on days 4, 6, 8, or 15), animals were sacrificed via CO2 overdose and blood was collected via cardiac puncture for serum preparation. Additionally, upon study termination, gastrocnemius and rectus femoris muscles were dissected from both the right and left legs of study mice. All tissues were weighed and then snap frozen for storage at −80 C.
For analysis, weights of the individual muscles from both legs were combined and the average muscle weight in grams was calculated, the average weights were normalized by initial body weight and the percent difference in muscle weight was calculated relative to the mean of the IgG vehicle control group (no Dex). In all experiments, outliers were identified and removed in GraphPad Prism 7.0.1 using the robust regression and outlier removal (ROUT) method (Q = 1%).
Immunoprecipitation and western blot from homogenized murine muscle and serum
Using standard procedures, clarified supernatants from homogenized muscle tissues or murine serum were analyzed by SDS-PAGE followed by western blot with the following primary antibodies: anti-myostatin prodomain AF1539 (R&D Systems); anti-mature Myostatin ab124621 (Abcam). Immunoprecipitations with SRK-015, IgG control, or GDF8-C1 antibodies from homogenized clarified muscle lysate and murine serum were carried out using the Thermo Scientific Pierce™ Co-Immunoprecipitation Kit according to the manufacturer’s specifications.
For quantitative fluorescent western blots, samples were loaded onto Any kD Mini-PROTEAN TGX Stain-Free Gels (Bio-Rad) and signal was detected by near-IR imaging (Azure c600, Azure Biosystems) and quantified using the western blot analysis tool in AzureSpot software (Azure Biosystems). Band intensity (number of positive pixels per unit area) from pro and latent Myostatin was measured and normalized to total loaded protein per lane. For all data presented, a minimum of three biological replicates were measured to generate the presented average values, and error bars on all graphs represent standard deviations. Statistical significance was determined by t-test (two-tailed, homoscedastic).
Muscle performance study
The Institutional Animal Care and Use Committee of the Office of Animal Welfare Assurance at the University of Maryland School of Medicine approved muscle performance studies. Experiments conformed to all Association for Assessment and Accreditation of Laboratory Animal Care guidelines. Muscle physiology experiments were conducted once.
Nine-week old male and female C57BL/6 J mice (n = 10) were acclimated for one week and randomized based on body weight, then assigned to treatment groups with approximately equal body weights across all groups. The treatment or controls were administered I.P. via tuberculin syringe weekly. Following 4 weeks of treatment, plantarflexor function was tested in vivo, followed by in vitro functional testing of the extensor digitorum longus (EDL).
Muscle performance was measured in vivo with a 305 C muscle lever system (Aurora Scientific Inc., Aurora, CAN). Anesthesia was accomplished via inhalation (~5% isoflurane, or to effect), and maintained via nose-cone (~2% isoflurane, or to effect). The knee was isolated using a pin partially inserted into the tibial head and the foot firmly fixed to a footplate on the motor shaft. Contractions were elicited by percutaneous electrical stimulation of the sciatic nerve. Optimal isometric twitch torque was determined by increasing the current with a minimum of 30 seconds between each contraction to avoid fatigue. A series of stimulations were then performed at increasing frequency of stimulation (0.2 ms pulse, 500 ms train duration): 1, 10, 20, 40, 60, 80, 100, 150 Hz, followed by a final stimulation at 1 Hz. Following the measurements, the foot was released and the pin removed and the mouse allowed to recover in a separate clean cage prior to returning to its living chamber.
EDL muscle performance was measured in vitro with the 305 C muscle lever system adapted with a horizontal perfusion bath. Briefly, the skin on the lower limb was degloved half-length to the knee and the tibialis anterior muscle carefully dissected free from the underlying EDL. A silk suture (4-0) was tied to the distal tendon of the EDL and the tendon severed. The muscle was then carefully dissected free from the tibia and adjacent muscles, the proximal tendon visualized and severed. The muscle was placed in an ice-cold physiological buffered solution and a silk suture tied to the proximal tendon. The muscle was placed in the horizontal bath of the 305 C muscle lever system and perfused with physiological buffer oxygenated with 95% O2/5% CO2 and kept at 37 °C. The sutures were tied to a fixed post on one side, and the lever arm on the other. A series of 1 Hz and 100 Hz field stimulations (0.2 ms pulse, 100 ms duration) at 0.01 Hz frequency were delivered via platinum electrodes flanking the muscle to ensure that the sutures are tight and that the maximal developed force was stable. Once stable, a series of stimulations were performed at increasing frequency of stimulation (1 ms pulse, 250 ms train duration): 1, 10, 20, 40, 60, 80, 100, 150 Hz, followed by a final stimulation at 1 Hz.
Data were analyzed using Aurora Scientific 615 A Dynamic Muscle Analysis Software Suite in high-throughput mode. Each data file was manually inspected to ensure that cursors and fits were assigned properly and corrected when necessary. Data were then grouped and means and standard errors calculated. Force was normalized to limb length defined as the distance from the knee to the bottom of the ankle. Data were compared over time by calculating the % change using standard equations. Statistical analysis was performed using SigmaPlot v11. Data were analyzed using either a Student’s t-test with Mann-Whitney test, a One-way ANOVA or Two-way ANOVA with Holm-Sidak post-hoc when appropriate with an α = 0.05.
The plantarflexor muscle group, soleus, gastrocnemius and tibialis anterior muscles frozen for histology were sectioned and stained according to standard protocols. For quantization using fluorescence microscopy, sections were stained with wheat germ agglutinin to determine cross sectional area or antibodies against MyHC-I, MyHC-IIa, or MyHC-IIb (1:20 dilution; Developmental Studies Hybridoma Database) for fiber-type determination. For proMyostatin localization studies, sections were stained with rabbit anti-laminin (Abcam) and GDF8_086 (Scholar Rock). H&E staining was performed according to Treat-NMD protocol MDC1a_M1.2.004.
Correspondence and requests for reagents described in this manuscript (available via MTA) can be directed at Adriana Donovan, email@example.com.
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For the kind gift of muscle and serum from myostatin knockout mice, we thank Dr. Thomas Braun (Max Planck Institute for Heart and Lung Research, Bad Nauheim). We would like to thank Shude Yan and his team at Chempartner for their contribution to the antibody discovery campaigns. We also thank Covance for conducting the muscle atrophy studies and acknowledge Ramzi Khairallah and the team at Myologica for conducting the muscle performance study. We thank Dong-Yun Lee, Jared Sheehan, Caroline Hill and William David Church for their early contributions to the project. Lastly, we thank Leonard Zon and Timothy Springer for advice and critical reading of the manuscript.
All authors were employees at Scholar Rock, Inc., at the time of work completion.
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Pirruccello-Straub, M., Jackson, J., Wawersik, S. et al. Blocking extracellular activation of myostatin as a strategy for treating muscle wasting. Sci Rep 8, 2292 (2018). https://doi.org/10.1038/s41598-018-20524-9
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