- Research article
- Open Access
Subcutaneous administration of TC007 reduces disease severity in an animal model of SMA
BMC Neuroscience volume 10, Article number: 142 (2009)
Spinal Muscular Atrophy (SMA) is the leading genetic cause of infantile death. It is caused by the loss of functional Survival Motor Neuron 1 (SMN1). There is a nearly identical copy gene, SMN2, but it is unable to rescue from disease due to an alternative splicing event that excises a necessary exon (exon 7) from the majority of SMN2-derived transcripts. While SMNΔ7 protein has severely reduced functionality, the exon 7 sequences may not be specifically required for all activities. Therefore, aminoglycoside antibiotics previously shown to suppress stop codon recognition and promote translation read-through have been examined to increase the length of the SMNΔ7 C-terminus.
Here we demonstrate that subcutaneous-administration of a read-through inducing compound (TC007) to an intermediate SMA model (Smn-/-; SMN2+/+; SMNΔ7) had beneficial effects on muscle fiber size and gross motor function.
Delivery of the read-through inducing compound TC007 reduces the disease-associated phenotype in SMA mice, however, does not significantly extend survival.
Spinal Muscular Atrophy (SMA) is the leading genetic cause of infantile death. The clinical categorization of SMA is based upon disease severity and age of onset . SMA results from the lack of a functional copy of the Survival Motor Neuron 1 (SMN1) gene . There is a nearly identical copy gene, SMN2, found only in humans . SMN2 does not fully compensate for the loss of SMN1, due to an alternative splicing event induced by a non-polymorphic C to T transition within exon 7 [4, 5]. Alternative pre-mRNA splicing, therefore, results in the majority of SMN2 transcripts excluding exon 7 (SMNΔ7), encoding a less stable protein product compared to full-length SMN [6, 7]. Loss of full-length SMN protein leads to the death of α-motor neurons, however, it is unclear why motor neurons are particularly susceptible to low levels of this ubiquitously expressed protein. However, two hypotheses suggest that axonal RNA transport and/or snRNP biogenesis underlie the SMA-associated activity .
Since the lack of SMN exon 7 leads to SMA development, this sequence is clearly important. There is a cytoplasmic localization signal within SMN exon 7 (QNQKE) that can transport SMN exons 1-6 and other heterologous nuclear proteins to the cytoplasm . However, heterologous sequences can mediate proper SMN localization in several cellular contexts in vitro. In addition, heterologous sequences can also partially restore functionality in cell-based assays, such as protein stability, snRNP assembly and neurite extension assays [10–13]. For these reasons, aminoglycosides have been examined in SMA for their ability to induce translational "read-through." These compounds are presumed to inhibit the recognition of the endogenous SMNΔ7 translational stop codon, located four amino acids into exon 8. "Read-through" of the stop codon would thereby allow the incorporation of a C-terminal extension of an additional five amino acids [10–13]. Treating Type I primary SMA patient fibroblasts (3813s) or SMA iPS-derived neuronal cultures with aminoglycosides was shown to increase SMN protein [10, 13, 14]. When delivered via intra-peritoneal injection, treatment with the aminoglycoside G418 in a SMA mouse model increased gross motor function at select time points . Additionally, direct injection of TC007, a novel aminoglycoside, into the central nervous system extends life span approximately 30% and elevates SMN protein in the brain and spinal cord . To begin to examine a less invasive means of delivery, we have examined alternative routes of delivery for TC007. Here we demonstrate that subcutaneous administration of TC007, while not extending survival, results in improved molecular and cellular aspects of the SMA phenotype, as well as benefits in gross motor function in a SMA mouse model.
Results and discussion
Subcutaneous dosing of SMA mice with TC007 significantly increases gross motor function, but not lifespan
Based on previous in vivo examinations of aminoglycosides and stop codon readthrough , we administered subcutaneous doses of TC007  at 30 mg/kg daily from post-natal day (p) 2 to 15 to the well-characterized Δ7 SMA model (Smn-/-; SMN2+/+; SMNΔ7) . TC007 treated mice (n = 16) lived approximately 16% longer (from an average of 15.75 ± 1.315 to 18.25 ± 0.7555 days) than vehicle treated mice (n = 16), although this difference did not reach statistical significance (Figure 1). The aminoglycosides appeared to prevent the death at a younger age, resulting in larger numbers of mice dying later (median lifespan of vehicle-treated mice 17.5 days versus a median of 19 days for TC007-treated). However, the longest life spans were similar in the vehicle and TC007-treated mice. Moreover not all aminoglycosides that increase SMN levels confer the same survival effect. For example, administration of Neo002 (n = 8) , a compound containing the same chemical backbone as TC007, significantly elevated SMN levels in vitro (data not shown), but only marginally affected lifespan (Figure 1). Total body weight was unaffected in TC007 and Neo002 treated animals compared to vehicle treated SMA animals (data not shown). Since SMN read-through therapies are proposed to function in part through a stabilization of SMNΔ7 protein, various tissues were examined for an increase in steady-state levels of SMN protein. Therefore brain, spinal cord and muscle of p10-treated mice were isolated. Under these experimental conditions, we could not detect a significant increase of SMN (Figure 2), which may also explain the modest extension in lifespan.
TC007-treated mice, however, did exhibit increased gross motor function. A previously quantifiable measure of gross motor function in these SMA mice is determining the time it takes for a pup to right itself from a prone position, or time-to-right . Not only did TC007-treated pups right faster, but they were also able to right significantly more often than their untreated counterparts at mid- to end-stage of disease (Figure 3A and 3B). When the gastrocnemius of p10 mice were examined, the fibers were significantly larger in the TC007-treated group (Figure 4), showing an anatomical correlation with our observed increase in overall gross motor function.
To determine if with the increase in fiber size, an increased survival of motor neurons was also observed, ventral horn cells (VHCs) were examined of p10 TC007-treated and vehicle-treated mice. While there was no increase in VHC cell body size, there was a slight trend towards an increased number of VHCs in treated tissues (Figure 5), although statistical significance was not achieved. This time point was chosen for histological examination due to its correlation with the most prominent display of an increase in gross motor function by the TC007-treated group. The increased fiber size along with the increase VHC numbers does provide a cellular corroboration to the improved gross motor phenotype seen upon subcutaneous administration of TC007. However, more pronounced improvements were likely not observed if TC007 failed to cross the blood-brain-barrier or if the compound exhibits a short half life. As no medicinal chemistry has been performed on TC007 to improve its drug-like qualities, it is not surprising that at this early stage the compound lacks properties typically associated with drugs for CNS disorders. To date, properties such as blood-brain-barrier permeability and pharmacokinetics have not been examined for TC007 but will be important to analyze in the event that TC007 or similar scaffolds move forward toward clinical application. While it is possible that TC007 is functioning as a general neuroprotectant, it is more likely that SMN levels were the basis for the cellular and gross motor activity increases. Unfortunately, the in vivo examination of this compound did not correlate with the in vitro activity when administered under these experimental conditions , however, direct administration of TC007 into the CNS by intraventricular injection did significantly elevate SMN levels and extend life by approximately 30% . Clearly, moving this compound forward and making it more amenable for central nervous system diseases will require an in depth analysis of its pharmacokinetics and the development of medicinal chemistry beyond these proof-of-concept experiments.
SMNΔ7 read-through benefits SMA mouse models
Translation stop codon read-through occurs at a relatively low frequency in the presence of aminoglycosides and this is likely true for the SMNΔ7 exon 8 stop codon based upon its specific stop codon and the proximal sequences flanking the stop signal [10, 14]. Aminoglycoside treatment likely generates a low level of SMN read-through protein that enters into an SMN complexes with the existing full-length protein. This theory is supported by previously published data, demonstrating a small increase in SMN-FL protein after treatment, without increasing SMN2-transcription or altering exon 7 splicing . In vitro studies have indicated that this possible hetero-oligomerization leads to an increase in the functionality of the SMN protein . While it is still possible that read-through SMN is not as active in SMA-specific activities, experiments such as the development of a read-through SMA mouse would be an important step towards determining the extent of SMN read-through functionality and whether read-through based therapeutic strategies hold promise for SMA.
In conclusion, similar benefits have been reported here for TC007 regarding a SMNΔ7 read-through therapy compared to previously published work using a FDA-approved aminoglycosides, G418 . While TC007 treatment does not result in a statistically significant extension in median lifespan, there were significant increases in gross motor function and muscle integrity at mid-stage of disease (p10). Extension in life span was demonstrated when TC007 was administered directly to the central nervous system via intracerebral ventricular injection, suggesting that the importance in delivery strategies as well as likely target tissues for SMA therapeutics . Taken together, these results demonstrate the proof-of-concept utility of read-through compounds in SMA cell and animal models.
Animals and drug treatment
All animal experiments were carried out in accordance with protocols approved by the Animal Care and Use Committee of the University of Missouri. Mice were genotyped and litters excluded as previously described . TC007 was initially resuspended in dH20, further diluted in PBS, and administered by subcutaneous injection (10 μl/gram of body weight) on post-natal days 2 through 15. PBS (vehicle) was injected as a negative control. To assess gross motor function, righting reflex (as described in ) was measured starting at post-natal day 5.
Western blot analysis
Tissues were harvested at indicated times and analysis was performed as previously described . Mouse anti-SMN (BD) was used for western at 1:1,000 and rabbit anti-actin (Sigma) was used at 1:250.
Histology and morphometry
Spinal cords were harvested on post-natal day (p) 10 and analysis of VHCs were performed as previously described . Gastrocnemius muscle was also harvested on p10, dissected, fixed in 4% paraformaldehyde, embedded in paraffin, sectioned and stained with hematoxylin and eosin stain. 200 fiber diameters were measured per section, 15 sections per muscle.
Analysis was performed as previously described . Briefly, error bars on graphs represent Standard Error of the Mean (S.E.M.). Significance of lifespan between TC007- and vehicle-treated mice was determined by Mantel-Cox test. All other indicated statistical significance was calculated by either Student's T Test or two-way ANOVA with a Bonferonni post hoc test of p < 0.05 or greater, as indicated in figure legend.
Survival Motor Neuron
Spinal Muscular Atrophy
ventral horn cell.
Munsat TL, Davies KE: International SMA consortium meeting. (26-28 June 1992, Bonn, Germany). Neuromuscul Disord. 1992, 2 (5-6): 423-428. 10.1016/S0960-8966(06)80015-5.
Lefebvre S, Burglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M, et al.: Identification and characterization of a spinal muscular atrophy-determining gene. Cell. 1995, 80 (1): 155-165. 10.1016/0092-8674(95)90460-3.
Rochette CF, Gilbert N, Simard LR: SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens. Hum Genet. 2001, 108 (3): 255-266. 10.1007/s004390100473.
Lorson CL, Hahnen E, Androphy EJ, Wirth B: A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy. Proc Natl Acad Sci USA. 1999, 96 (11): 6307-6311. 10.1073/pnas.96.11.6307.
Monani UR, Lorson CL, Parsons DW, Prior TW, Androphy EJ, Burghes AH, McPherson JD: A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2. Hum Mol Genet. 1999, 8 (7): 1177-1183. 10.1093/hmg/8.7.1177.
Burnett BG, Munoz E, Tandon A, Kwon DY, Sumner CJ, Fischbeck KH: Regulation of SMN protein stability. Mol Cell Biol. 2009, 29 (5): 1107-1115. 10.1128/MCB.01262-08.
Lorson CL, Androphy EJ: An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN. Hum Mol Genet. 2000, 9 (2): 259-265. 10.1093/hmg/9.2.259.
Burghes AH, Beattie CE: Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?. Nat Rev Neurosci. 2009, 10 (8): 597-609. 10.1038/nrn2670.
Zhang HL, Pan F, Hong D, Shenoy SM, Singer RH, Bassell GJ: Active transport of the survival motor neuron protein and the role of exon-7 in cytoplasmic localization. J Neurosci. 2003, 23 (16): 6627-6637.
Heier CR, DiDonato CJ: Translational readthrough by the aminoglycoside geneticin (G418) modulates SMN stability in vitro and improves motor function in SMA mice in vivo. Hum Mol Genet. 2009, 18 (7): 1310-1322. 10.1093/hmg/ddp030.
Hua Y, Zhou J: Modulation of SMN nuclear foci and cytoplasmic localization by its C-terminus. Cell Mol Life Sci. 2004, 61 (19-20): 2658-2663. 10.1007/s00018-004-4300-z.
Mattis VB, Bowerman M, Kothary R, Lorson CL: A SMNDelta7 read-through product confers functionality to the SMNDelta7 protein. Neurosci Lett. 2008, 442 (1): 54-58. 10.1016/j.neulet.2008.06.059.
Wolstencroft EC, Mattis V, Bajer AA, Young PJ, Lorson CL: A non-sequence-specific requirement for SMN protein activity: the role of aminoglycosides in inducing elevated SMN protein levels. Hum Mol Genet. 2005, 14 (9): 1199-1210. 10.1093/hmg/ddi131.
Mattis VB, Rai R, Wang J, Chang CW, Coady T, Lorson CL: Novel aminoglycosides increase SMN levels in spinal muscular atrophy fibroblasts. Hum Genet. 2006, 120 (4): 589-601. 10.1007/s00439-006-0245-7.
Mattis VB, Ebert AD, Fosso MY, Chang CW, Lorson CL: Delivery of a read-through inducing compound, TC007, lessens the severity of a spinal muscular atrophy animal model. Hum Mol Genet. 2009, 18 (20): 3906-13. 10.1093/hmg/ddp333.
Yang C, Feng J, Song W, Wang J, Tsai B, Zhang Y, Scaringe WA, Hill KA, Margaritis P, High KA, et al.: A mouse model for nonsense mutation bypass therapy shows a dramatic multiday response to geneticin. Proc Natl Acad Sci USA. 2007, 104 (39): 15394-15399. 10.1073/pnas.0610878104.
Chang CW, Hui Y, Elchert B, Wang J, Li J, Rai R: Pyranmycins, a novel class of aminoglycosides with improved acid stability: the SAR of D-pyranoses on ring III of pyranmycin. Org Lett. 2002, 4 (26): 4603-4606. 10.1021/ol0269042.
Le TT, Pham LT, Butchbach ME, Zhang HL, Monani UR, Coovert DD, Gavrilina TO, Xing L, Bassell GJ, Burghes AH: SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN. Hum Mol Genet. 2005, 14 (6): 845-857. 10.1093/hmg/ddi078.
Zhang J, Chiang FI, Wu L, Czyryca PG, Li D, Chang CW: Surprising alteration of antibacterial activity of 5"-modified neomycin against resistant bacteria. J Med Chem. 2008, 51 (23): 7563-7573. 10.1021/jm800997s.
Butchbach ME, Edwards JD, Burghes AH: Abnormal motor phenotype in the SMNDelta7 mouse model of spinal muscular atrophy. Neurobiol Dis. 2007, 27 (2): 207-19. 10.1016/j.nbd.2007.04.009.
Rose FF, Mattis VB, Rindt H, Lorson CL: Delivery of recombinant follistatin lessens disease severity in a mouse model of spinal muscular atrophy. Hum Mol Genet. 2009, 18 (6): 997-1005. 10.1093/hmg/ddn426.
We would like to thank John Marston for assistance with the mouse colony. This work was supported by grants from FightSMA [C.L.L.]; and the National Institutes of Health [C.L.L, R01 NS41584; R01 HD054413] and [C.W.C., AI053138].
VBM carried out all mouse and molecular studies, participated in the design of the study and drafted the manuscript. C-WC and MF manufactured compounds TC007 and Neo002. CLL conceived of the study, and participated in its design and coordination and drafted the manuscript. All authors read and approved the final manuscript.
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Mattis, V.B., Fosso, M.Y., Chang, C. et al. Subcutaneous administration of TC007 reduces disease severity in an animal model of SMA. BMC Neurosci 10, 142 (2009). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2202-10-142
- Spinal Muscular Atrophy
- Spinal Muscular Atrophy Patient
- Spinal Muscular Atrophy Mouse
- Spinal Muscular Atrophy Mouse Model
- Stop Codon Readthrough