Overproduction or poor clearance of amyloids lead to amyloid aggregation and even amyloidosis development. Different amyloids may interact synergistically to promote their aggregation and accelerate pathology in amyloidoses. Amyloid oligomers assembled from different amyloids share common structures and epitopes, and are considered the most toxic species in the pathologic processes of amyloidoses, which suggests that an agent targeting the common epitope of toxic oligomers could provide benefit to several amyloidoses. In this study, we firstly showed that an oligomer-specific single-chain variable fragment antibody, W20 simultaneously improved motor and cognitive function in Parkinson’s disease and Huntington’s disease mouse models, and attenuated a number of neuropathological features by reducing α-synuclein and mutant huntingtin protein aggregate load and preventing synaptic degeneration. Neuroinflammation and oxidative stress in vivo were also markedly inhibited. The proposed strategy targeting the common epitopes of amyloid oligomers presents promising potential for treating Parkinson’s disease, Huntington’s disease, Alzheimer’s disease, and other amyloidoses.
Amyloid protein misfolding and pathological aggregation are considered common hallmarks of amyloidoses1,2. More than 40 different diseases, such as Alzheimer’s disease (AD), Parkinson’s disease (PD), and Huntington’s disease (HD), have been associated with amyloid aggregation, and some of these diseases cause great social and economic burdens because of their extensive prevalence and lack of effective therapy3,4. Amyloid aggregation processes can be initiated by overproduction or poor clearance of disease-related proteins. Amyloid monomers undergo conformational changes, resulting in misfolding, aggregating into small oligomers and protofibrils, or finally stabilizing as mature fibrils4. Numerous clinical observations have confirmed that the severity of amyloid-associated neurodegenerative diseases was not correlated with the amount of amyloid deposit in the brain of patients, but was correlated with elevated levels of toxic oligomers5,6. Various studies have revealed that amyloid oligomers, rather than monomers or insoluble fibrils, are the primary toxic species in the pathological processes of amyloidoses7,8. The mechanisms of toxicity of the oligomers are they interact with the lipid bilayer of the cell membranes, leading to membrane disruption or even pore formation, inducing oxidative stress by generation of reactive oxygen species (ROS), in turn causing lipid and protein oxidation, mitochondrial dysfunction, disturbance of autophagy and changes in ion homeostasis, and cell death eventually9,10.
Different amyloids have distinct amino acid sequences, but their oligomers contain common structures with rich cross-β-sheets and share universal mechanisms of toxicity11,12. Thus, amyloid oligomers can be considered perfect therapeutic targets. During one amyloid aggregation and amyloidosis development, other amyloids may be induced to aggregate and participate in the pathological processes of amyloidoses. Emerging evidence showed that Aβ, tau, and α-synuclein may interact synergistically to promote their aggregation and accumulation and accelerate neuropathology and cognitive dysfunction13,14. Moreover, amylin was found to co-precipitate with Aβ to form complex amylin/Aβ plaques in the brains of AD patients15, and mature amylin fibrils promoted the robust growth of mixed amylin/Aβ amyloids16. Furthermore, oligomers of α-synuclein, prion protein, TDP-43, tau, and Aβ, were detected in the brains of AD patients17,18,19,20, suggesting that direct treatment of one amyloid protein may not be sufficient to cure the disease21. Thus, developing agents that target common structures of oligomers assembled from different amyloids could be a promising strategy to treat one amyloidosis or several amyloidoses.
PD is the second most frequent neurodegenerative disease in humans, which is characterized pathologically by the formation of intraneuronal inclusions called Lewy bodies. α-synuclein aggregates are the main components of Lewy bodies, and they induce the progressive death of dopamine-producing neurons in the substantia nigra of the midbrain, leading to motor and cognitive deficits22. HD is another fatal neurodegenerative disorder characterized by progressive motor, cognitive, and psychiatric deficits, which is due to the aggregates of mutant huntingtin protein (mHTT) composed of an extended polyglutamine (polyQ) tract23. mHTT oligomers are the main neurotoxic factors that induce the death of striatal and cortical neurons8. Thus, inhibiting the aggregation and cytotoxicity of α-synuclein and mHTT is a potential approach for treating PD and HD.
Some anti-oligomer antibodies, such as A11, NU4, and F11G3, have significantly improved cognitive impairment in AD transgenic mice24,25, but few agents have been reported to simultaneously exert beneficial effects on AD, PD, and HD animal models. We previously reported a conformation-dependent oligomer-specific single-chain variable fragment (scFv) antibody W20, which was isolated from a naïve human scFv library via phage display, recognized various oligomers assembled from Aβ, α-synuclein, amylin, insulin, prion protein, lysozyme and polyQ. W20 also inhibited the fibrillation of numerous amyloids and attenuated amyloid oligomer-induced cytotoxicity in vitro26,27. In another work, W20 ameliorated memory deficits and brain amyloid burden in AD transgenic mice28. Considering the pathological processes of one amyloidosis may be simultaneously associated with several types of amyloids, and W20 is a pan-amyloid oligomer specific antibody, in the present study, we separately investigated the effect of W20 on the behavior, cognition, and neuropathology in both PD and HD transgenic mouse models to explore whether W20 is suitable for treating different amyloidoses.
W20 improved motor performance in A53T α-synuclein mice
To assess the effect of W20 on locomotion and reaction to a novel environment in PD animal model, we performed open field test on transgenic A53T α-synuclein mice, which overexpressed A53T mutant human α-synuclein under the mouse prion promoter and developed severe motor impairment and cognitive deficits by accumulation of A53T α-synuclein at 9–16 months of age29. The results showed that A53T α-synuclein mice treated with the vehicle or non-specific (ns) - scFv travelled a longer distance (Fig. 1a), exhibited higher movement velocity (Fig. 1b), and reared more frequently (Fig. 1c) than wild-type (WT) mice. These findings demonstrated that A53T α-synuclein mice were hyperactive, which was consistent with the previous reports30,31. By contrast, W20-treated A53T α-synuclein mice exhibited decreased locomotion, velocity, and rearing compared with vehicle-treated mice (Fig. 1a–c).
In addition to the alterations in locomotion, A53T α-synuclein mice also displayed progressive motor function impairment by falling off the rotarod sooner than WT mice treated with either the vehicle or W20 in all trials, whereas W20-treated A53T α-synuclein mice stayed on the accelerating rotarod longer than vehicle- or ns-scFv-treated controls and showed significant improvement in rotarod latency (Fig. 1d).
Hindlimb clasping has been observed in various neurodegenerative mouse models. A53T α-synuclein mice exhibited severe hindlimb clasping behavior compared with the WT littermates. W20 treatment improved this behavior as illustrated by the remarkable decrease in hindlimb severity score (Fig. 1e).
The pole test was utilized to measure motor coordination and balance in mouse models of PD. A53T α-synuclein mice treated with the vehicle or ns-scFv took a longer time to turn (Fig. 1f) and descend from the pole (Fig. 1g) compared with the WT littermates. By contrast, W20 substantially improved the deficits in motor coordination of A53T α-synuclein mice by reducing movement initiation and descending time in the pole test. These results suggested that W20 significantly restored motor behavior in A53T α-synuclein mice.
W20 attenuated cognitive deficits in A53T α-synuclein mice
The Morris water maze (MWM) test was conducted to assess spatial learning and memory in A53T α-synuclein mice. During the acquisition period, both WT and W20-treated A53T α-synuclein mice required shorter time to reach the platform after training compared with vehicle-treated A53T α-synuclein mice (Fig. 2a). During the memory retention test in the probe trials, W20-treated mice exhibited spatially oriented swimming behavior and shorter escape latencies than vehicle-treated mice (Fig. 2b). Moreover, W20-treated A53T α-synuclein mice showed higher frequency of platform crossings (Fig. 2c) and spent more time in the target quadrant (Fig. 2d) compared with vehicle-treated mice. These results suggested that A53T α-synuclein mice exhibited impaired spatial learning and memory, whereas W20 treatment significantly improved the cognitive impairment of the PD mouse model. The spatial memory of the mice was further evaluated with the object recognition test. WT mice preferred to investigate the target object and exhibited a significant increase in the percentage of investigations to the target object during training and test session (Fig. 2e,f). A53T α-synuclein mice did not show a preference for the target object. However, W20-treated A53T α-synuclein mice displayed improved object recognition by showing remarkable preference to investigate both a novel object (Fig. 2e) or a known object at a novel location (Fig. 2f). These results further indicated that W20 treatment reversed the memory deficits in A53T α-synuclein mice.
W20 reduced α-synuclein levels in A53T α-synuclein mouse brains
The amount of α-synuclein in the brains of A53T α-synuclein mice are correlated with disease onset and mouse survival29. To determine whether the motor and memory improvements by W20 treatment were associated with the reduction of α-synuclein levels, we performed western blot using mice brain lysates. Levels of α-synuclein in the brain lysates of A53T α-synuclein mice were obviously higher compared with those of the WT littermates (Fig. 3a). However, W20 treatment significantly decreased levels of total α-synuclein (Fig. 3a,c) and overexpressed human A53T α-synuclein (Fig. 3a,d) levels, as detected by Syn-1 and LB509 antibody, respectively. It is notable that ns-scFv, unlike W20, did not affect the levels of α-synuclein in the brains of A53T α-synuclein mice. Moreover, both PBS and W20 did not affect the levels of α-synuclein in WT mice, suggesting that W20, but not ns-scFv had specific therapeutic function on PD mice (Supplementary Fig. 1). Soluble α-synuclein oligomers are considered the most neurotoxic forms in PD. We determined the levels of α-synuclein oligomers in the brain lysates by dot-blot using oligomer-specific antibodies OC and A11 (Fig. 3b). W20-treated mice showed 13.6% (Fig. 3e) and 32.1% (Fig. 3f) reductions in levels of α-synuclein oligomers, as detected by OC and A11 antibodies, respectively, compared with vehicle-treated A53T α-synuclein mice.
W20 attenuated neuropathology in A53T α-synuclein mice
To further explore the effects of W20 on the different neurodegenerative phenotype, we assessed the extent of neuropathology of A53T α-synuclein mice by immunohistochemistry analysis. Human α-synuclein levels in the brainstem of A53T α-synuclein mice were further detected by immunostaining with an antibody to detect phospho-Ser129-α-synuclein, which is a specific pathological form of human α-synuclein. The results showed that phospho-Ser129-α-synuclein positive staining was clearly detected throughout the brainstem of A53T α-synuclein mice rather than WT mice. By contrast, W20, but not ns-scFv, significantly reduced α-synuclein levels (Fig. 4a, Supplementary Fig. 2a).
Levels of tyrosine hydroxylase (TH) and dopamine transporter (DAT) were quantified to evaluate the effect of W20 on the dopaminergic (DA) signaling pathway. TH is the limiting enzyme in DA synthesis32, whereas DAT is a plasma membrane glycoprotein expressed in DA cells, responsible for DA uptake through a Na+/Cl− coupled cotransport mechanism33. Both of them are pivotal players in DA signaling. A significant negative correlation was found between TH and DAT expression and motor impairment31,32. TH and DAT levels were significantly decreased in the brainstem of A53T α-synuclein mice compared with those of the WT littermates, whereas W20, not PBS or ns-scFv, remarkably increased TH and DAT levels in PD transgenic mice (Fig. 4b,c, and Supplementary Fig. 2b,c). These results indicated that W20 substantially attenuated neuropathology in A53T α-synuclein mice.
W20 attenuated gliosis in the brains of A53T α-synuclein mice
Increased inflammation in the brains of A53T α-synuclein mice is strongly correlated with motor and memory impairment34,35. We detected the effects of W20 on astrocytosis and microgliosis in the brainstem of A53T α-synuclein mice. The results showed that astrocytosis in PD transgenic mice significantly increased compared with that in WT mice, and W20, rather than ns-scFv, remarkably reduced astrocytosis (Fig. 4d, Supplementary Fig. 2d). Similarly, A53T α-synuclein mice exhibited increased activation of microglia, whereas W20, but not ns-scFv, markedly decreased microgliosis (Fig. 4e, Supplementary Fig. 2e).
W20 ameliorated motor and memory impairments in BACHD mice
BACHD mouse is a conditional human genomic transgenic mouse model for HD, which expresses human full-length mHTT with a polyQ repeat of 97 glutamines36. Model mice exhibit progressive motor and psychiatric-like behavioral deficits, as well as selective cortical and striatal atrophy37, and are thus considered suitable for HD preclinical studies. The open field test is a reliable assay for evaluating locomotion and anxiety in BACHD mice. During the 30-minute open field exploration, vehicle-treated or ns-scFv-treated BACHD mice displayed hypoactivity and anxiety by covering a low total distance (Fig. 5a), showing limited rearing (Fig. 5b), entering the center of the field infrequently (Fig. 5c), and spending a limited amount of time at the center of the field (Fig. 5d). By contrast, W20 treatment significantly decreased hypoactivity and anxiety-like behavior by increased locomotion (Fig. 5a) and rearing (Fig. 5b), higher frequency of entering the center (Fig. 5c) and more time spent in the center (Fig. 5d). In addition, all mice, regardless of genotype or treatment, traveled at similar average velocities (Fig. 5e). These results demonstrated that W20 could markedly improve locomotion and attenuate exploration deficits in BACHD mice.
Progressive motor deficit is an important clinical feature of HD36. The accelerating rotarod test was performed to evaluate the therapeutic efficacy of W20 on motor performance in BACHD mice. At 12 months of age, BACHD mice showed robust rotarod impairment compared with the WT littermates in all trials. However, W20-treated BACHD mice stayed on the accelerating rotarod longer during each individual testing session than vehicle-treated BACHD mice (Fig. 5f). These findings indicated that W20 rescued motor impairment in BACHD mice.
Cognitive impairment, in addition to motor abnormalities, is another important clinical characteristic of HD patients38. We performed the object recognition test to verify whether W20 treatment could improve the cognitive function in BACHD mice. BACHD mice treated with vehicle or ns-scFv exhibited cognitive deficits in novel object recollection, whereas W20 treatment significantly prevented the cognitive impairment in BACHD mice (Fig. 5g,h).
W20 reduced mHTT levels in BACHD mouse brains
To further address the mechanism by which W20 exerted protective effect, we performed western blot to evaluate the relative levels of mHTT in both RIPA-soluble fraction and 10% SDS-soluble fraction, the latter contained the mHTT aggregates from the mouse brain lysates and were termed as insoluble fraction. Levels of soluble and insoluble mHTT were significantly higher in the BACHD mouse control than in the WT littermates (Fig. 6a,c,d,f,g). Treating BACHD mice with W20 markedly decreased both soluble and insoluble mHTT levels in the BACHD mice brains. While neither ns-scFv affected the mHTT levels in the brains of BACHD mice nor W20 had any effects in WT mice, suggesting W20 had specific therapeutic function on HD mice (Supplementary Fig. 3).
We also determined the levels of mHTT oligomers in the mouse brain lysates by dot-blot using oligomer-specific antibodies OC and A11 (Fig. 6b). W20-treated mice showed 36.5% (Fig. 6e) and 31.1% (Fig. 6h) reductions in the levels of mHTT oligomers, as detected by OC and A11 antibodies, respectively, compared with vehicle-treated BACHD mice.
W20 reduced neuropathology in BACHD mice
Progressive aggregation of mHTT in the brain is another pathological hallmark of HD. The BACHD mouse model may reproduce a mHTT aggregation pattern similar to that in adult-onset HD and exhibits robust high levels of mHTT aggregates at 12 months of age36. Here we examined the effects of W20 on mHTT aggregates in the cortex and striatum of BACHD mice by EM48 immunostaining. The results showed that mHTT aggregates dramatically decreased in the cortex and striatum of W20-treated BACHD mice compared with those in the vehicle-treated BACHD control by 26% (Fig. 7a, Supplementary Fig. 4a) and 49.5% (Fig. 7b, Supplementary Fig. 4b), respectively.
Levels of synaptophysin, a presynaptic marker, in mouse brains were measured by immunostaining to further explore the mechanism by which W20 attenuated motor and memory deficits in BACHD mice. Vehicle- or ns-scFv-treated BACHD mice exhibited obvious loss of synaptophysin in the cortex and striatum, whereas W20 significantly increased synaptophysin levels in BACHD mice, but not WT mice (Fig. 7c,d, Supplementary Figs 4c,d and 5), thereby indicating that W20 treatment may rescue neurodegeneration by inhibiting synapse loss in the brains of BACHD mice.
Neuron death is an important pathological hallmark in HD. We performed TUNEL analysis on the brain sections of BACHD mice to assess the neuronal protective effect of W20. The number of apoptotic cells in the brains of vehicle-treated BACHD mice was significantly higher than that in the WT littermates (Fig. 7e,f). W20 treatment decreased the apoptotic cells by 69.6% (Supplementary Fig. 4e) in the cortex and 73.3% (Supplementary Fig. 4f) in the striatum of BACHD mice.
W20 attenuated the neuroinflammation in BACHD mice
Increasing evidence reveals that reactive gliosis occurs in vulnerable regions of HD brains and strongly associated with HD pathogenesis39. In this study, we evaluated the effects of W20 on astrocytosis and microgliosis in BACHD mouse brains by immunostaining for GFAP and Iba-1. The brains of BACHD mice showed substantial astrocytosis and microgliosis at 12 months of age, whereas W20 significantly inhibited this neuroinflammation (Fig. 7g–j). Immunostaining area analysis demonstrated that W20 decreased the astrocytosis in the cortex and striatum by 55.7% (Supplementary Fig. 4g) and 72.7% (Supplementary Fig. 4h), respectively, and reduced microgliosis by 15.2% (Supplementary Fig. 4i) and 28.1% (Supplementary Fig. 4j), respectively. Additionally, ns-scFv, unlike W20, did not affect the astrocytosis and microgliosis in the BACHD mice, W20 also did not affect the levels of GFAP and Iba-1 in WT mice (Supplementary Fig. 5), confirming the therapeutic specificity of W20 on HD mice.
W20 decreased TNF-α and IL-1β production in BACHD mice
Proinflammatory cytokines contribute to the neurodegeneration in HD patients and mouse models40. To investigate the effect of W20 on cytokine production, we determined TNF-α and IL-1β levels in the brain lysates of BACHD mice treated with or without W20. TNF-α and IL-1β levels were significantly reduced in W20-treated BACHD mice compared with those in vehicle-treated mouse controls by 13.1% (Supplementary Fig. 6a) and 16.8% (Supplementary Fig. 6b), respectively. These results suggest that W20 may exert anti-neuroinflammatory effect by downregulating cytokine production.
W20 prevented ROS generation and increased SOD activity in the brains of BACHD mice
Oxidative stress is a fundamental aspect of HD pathogenesis41. We determined ROS levels in the brain lysates of BACHD mice to evaluate the effects of W20 on ROS production. ROS levels were markedly increased in the brains of vehicle-treated BACHD mice compared with those in the WT littermate controls. However, W20 treatment prevented this increase by 27.4% (Supplementary Fig. 6c). We then determined the SOD activities in the brain lysates to examine whether W20 affected the antioxidant activities in the brains of BACHD mice. A significant increase in total SOD (Supplementary Fig. 6d) and Mn-SOD (Supplementary Fig. 6e) activity was observed in W20-treated BACHD mice relative to the vehicle-treated BACHD controls.
W20 penetrated neurons and dissociated performed amyloid deposits
We previously reported that W20 disrupted the equilibrium between oligomers and fibrils, and disassociated preformed amyloid fibrils in vitro26. To validate whether W20 penetrated the neurons, mouse hippocampal neuronal cells (HT22) were incubated with W20 for 2 h, and then the distribution patterns of W20 were visualized by confocal laser-scanning microscopy. The results showed that W20 was internalized and located in the cytoplasm, but not in the nuclear region of HT22 cells (Supplementary Fig. 7). To investigate the potential mechanism for W20 to reduce intracellular amyloid deposits, the brain slides of A53T α-synuclein mice and BACHD mice were incubated with W20 (2 mg/ml) overnight at 37 °C, and then the aggregates of human α-synuclein and mHTT were detected by phospho-Ser129-α-synuclein and EM48 immunostaining, respectively. The results showed that both α-synuclein and mHTT aggregates were significantly decreased in the brain slides, suggesting W20 may decrease intracellular amyloid deposits in transgenic mouse models by penetrating neurons and disassociating preformed amyloid aggregates (Supplementary Fig. 8).
Binding of W20 to α-synuclein
Previous report indicated that oligomer-specific scFv antibody W20 recognized α-synuclein oligomers26. To determine which residues in α-synuclein dimer contribute to the binding to W20, we performed molecular dynamics analysis. The results showed that W20 predominately binds to Val 71 and Val 77 of α-synuclein dimer through hydrophobic interaction with the residues in its CDR3 region (Fig. 8a,b).
Passive immunization has emerged as the main immunotherapy strategy against neurodegenerative diseases because of the side effects and poor responses of elderly patients to vaccination42. To the best of our knowledge, our study is the first to evaluate the implications of passive immunotherapy with oligomer-specific antibody in both PD and HD transgenic mouse models simultaneously.
Amyloid aggregation is a molecular pathogenic mechanism for numerous age-dependent neurodegenerative disorders, such as AD, PD, and HD. Although the symptoms, pathology, and related amyloids of different amyloidoses are very diverse, amyloid aggregates share common features such as cross-β-sheet structures, common epitopes, and neurotoxicity. As well, amyloid aggregates have oligomer-specific or fibril-specific epitopes8. Amyloid oligomers play a key role in the pathological processes of amyloidoses7. Oligomers formed from α-synuclein, mHTT, and Aβ may induce oxidative stress, gliosis, synapse loss, and neuron death9. Targeting these oligomers could be a direct and efficient approach for treating amyloidoses. Different amyloids, such as Aβ, PrP, α-synuclein, polyQ, and amylin, not only aggregate into oligomers with common epitopes, but also promote the aggregation of other amyloids, mutually enhance the cytotoxicity of amyloid aggregates, and facilitate the progression of amyloidoses13,14,43. Thus, strategies targeting common oligomeric conformation would be an appealing approach to circumvent oligomer-mediated cytotoxicity by various amyloids, such strategies are widely believed to be a more efficient treatment method for amyloidoses than agents targeting a single type of amyloid. Moreover, the approach may have a broader spectrum to treat different amyloidoses regardless of the different sequences of disease-associated amyloids. We previously reported an oligomer-specific scFv antibody, W20, recognized the common epitope of oligomers assembled from Aβ, α-synuclein, insulin, lysozyme, and amylin, and inhibited their cytotoxicity26. When applied to the AD transgenic animal model, W20 prevented memory deficits and attenuated pathologies in APP/PS1 transgenic mice28. In the present study, we tested the effects of W20 on PD and HD transgenic mouse models, and our results indicated that W20 ameliorated motor deficits in PD and HD transgenic mouse models by improving motor cooperation. Moreover, the spatial memory deficits of PD and HD transgenic mice were significantly improved, as detected by the object recognition test and MWM test.
Soluble oligomer species are typically transient and structurally heterogeneous. Several types of α-synuclein oligomers are found in the brains of PD patients and transgenic mice, which may be classified as OC-positive fibrillar oligomers (FOs) or A11-positive prefibrillar oligomers (PFOs)12. W20 not only significantly reduced the levels of both types of α-synuclein oligomers, but also decreased α-synuclein deposits in the brainstem of A53T α-synuclein mice. This finding is consistent with a previous report that W20 disrupts the equilibrium between oligomers and fibrils, and disassociates preformed fibrils26. Similarly, our findings showed that W20 treatment significantly reduced levels of soluble and insoluble mHTT, mHTT oligomers as well as EM48-positive mHTT aggregate accumulation in the brains of BACHD mice. Numerous processes, such as aberrant cleavage of amyloid proteins, protein misfolding, and reduced protein degradation because of disruption of autophagy and/or the ubiquitin-proteasome system, contribute to amyloid aggregate formation44, W20 may block α-synuclein and mHTT fibrillation, reduce their cytotoxicity, and accelerate amyloid oligomer clearance from transgenic mouse brains, resulting in improved motor and cognition performances.
α-Synuclein plays a role in synaptic transmission, axonal transport, and regulation of DA homeostasis45. TH is a rate-limiting enzyme involved in DA generation, while DAT is expressed in striatal presynaptic terminals and is a major determinant of DA homeostasis. TH and DAT levels are inversely correlated with the total α-synuclein burden in the substantia nigra of PD patients or animal models32,46. W20 increased levels of TH and DAT in the brainstem of A53T α-synuclein mice by decreasing α-synuclein levels, protecting neuronal cells from degeneration, thus leading the improvement of motor and cognition performances. Synaptic deficiencies likely contribute to the clinical symptoms in HD patients, such as chorea, dystonia, and cognitive decline23. Moreover, mHTT oligomers play a key role in causing neuronal cell death in HD by activating apoptotic pathways47. W20 decreased neuronal apoptosis, resulting in increased synaptophysin levels in the cortex and striatum of BACHD mice.
α-Synuclein and mHTT aggregates induced neuroinflammatory reactions, especially astrocytosis and microgliosis in the brains of PD and HD patients and corresponding mouse models, which contribute significantly to the progression of PD and HD48,49. We observed a positive correlation between levels of α-synuclein or mHTT accumulation and levels of GFAP and Iba-1 in the brains of A53T α-synuclein and BACHD mice, indicating that pathogenic amyloid aggregates could be correlated with the degree of neuroinflammation. W20 treatment markedly attenuated astrocytic and microglial activation by decreasing levels of α-synuclein and mHTT aggregates. As immunotherapy for CNS disorders is likely to induce severe adverse neuroinflammatory responses50, which is important for the development of neurodegenerative diseases, thus, an immuno-agent for treating CNS disorders should not promote neuroinflammation. In this study, W20 exhibited its beneficial neuro-protective effects by alleviating astrocytosis and microgliosis.
Proinflammatory cytokines, such as TNF-α and IL-1β, are elevated in HD brains and may augment inflammatory signals51, contributing directly to neuronal dysfunction. Treating BACHD mice with W20 significantly reduced the production of proinflammatory factors by neutralizing toxic mHTT oligomers. In addition, oxidative stress in cells occurs under excess ROS levels or deficient antioxidant capacity, causing morphological abnormalities and death in neurons52. The brains of HD patients and mouse models have been reported to show signs of oxidative stress and DNA damage41,53. W20 markedly decreased ROS production and normalized SOD activity, thus suggesting that W20 could protect the brains of BACHD mice from oxidative stress through blocking mHTT oligomer-induced neuronal cytotoxicity.
In conclusion, a therapeutic approach using W20 against a common epitope of various toxic oligomeric structures assembled from different amyloids significantly improved motor and cognitive deficits in PD and HD transgenic mice. Moreover, levels of pathogenic α-synuclein and mHTT species were reduced and neuroinflammation in the mouse brains was attenuated as well. In our recent study, 3F, the matured form of W20, exhibited remarkably increased affinity to pathogens, longer half-life period in vivo, better penetration across the blood brain barrier, and beneficial effects on cognitive improvement in AD mice by intranasal delivery, further showing the promising potential of a disease mechanism-directed clinical therapy against PD, HD, AD, and other amyloidoses.
Animals and W20 treatment
9-month-old male A53T α-synuclein mice, 12-month-old male BACHD mice, and their WT littermates were purchased from Jackson Laboratory (Stock numbers are 006823 and 008197, respectively). A53T α-synuclein mice overexpress human A53T α-synuclein using the mouse prion protein promoter. BACHD mice are bacterial artificial chromosome-mediated transgenic models that express full-length human mHTT with 97 CAG repeats36. All mice for experiments were group-housed (five mice/cage), provided food and water ad libitum, and kept in a colony room at 22 ± 2 °C and 45% ± 10% humidity on a reverse 12 h light/dark cycle. W20 was developed and prepared in our laboratory as previously described27. An ns-scFv antibody was obtained from a phage library and showed no affinity to α-synuclein or mHTT. All of the mice were anesthetized intraperitoneally with avertin (300 mg/kg) and placed in a stereotaxic apparatus. Intracerebroventricular (icv) administration was conducted according to a previously described method with minor modifications54. An incision was made in the scalp of each mice. The skull was exposed, and burr holes were drilled in the skull over the injection site. The injection coordinates were 1.8 mm caudal to bregma, 1.8 mm lateral to midline, and 2.5 mm ventral to the brain surface of the skull. A Hamilton microsyringe fitted with a 30-gauge needle was used for icv infusion of W20 (5 μL, 4 mg/mL), ns-scFv (5 μL, 4 mg/mL), or PBS (5 μL) as the vehicle control, injections were administered at a rate of 0.2 μL/min. After injection, the needle was retained for 5 min to ensure adequate diffusion of agents and then was slowly retracted. Another icv injection was conducted after 7 d. Mice were randomly treated in cohorts (n = 8) to render behavior testing more manageable. No mice were excluded from behavioral studies due to fever, weight loss, infection or behavioral alterations as a result of W20 treatment. All experiments were performed in accordance with the China Public Health Service Guide for the Care and Use of Laboratory Animals. Experiments involving mice and protocols were approved by the Institutional Animal Care and Use Committee of Tsinghua University.
Open field exploration
A53T α-synuclein and BACHD mice were placed in the center of the chamber (27 × 27 × 20.3 cm3), and their behavior was recorded for 15 and 30 min, respectively. Five measures, namely, total locomotion, total rearing frequency, center entries, center duration and velocity were quantitatively analyzed. Chambers were cleaned with 70% ethanol before each use.
Motor coordination was assessed with a rotarod apparatus (TSE Systems). Daily sessions included a 5-minute training trial at 4 rpm. After 1 h, the animals were tested over three consecutive accelerating trials with the speed changing from 0 rpm to 40 rpm over 300 s. The inter-trial interval was 30 min. The latency to fall from the rod was recorded, and results were averaged. Mice remaining on the rod for more than 300 s were removed, and their time was scored as 300 s. Mice were tested over three consecutive days.
Hindlimb clasping was evaluated in A53T α-synuclein mice according to a previously described method55. Mice were suspended by the base of the tail and videotaped for 15 s. Hindlimb clasping was rated from 0 to 3 based on severity: 0 = hindlimbs splayed outward and away from the abdomen; 1 = one hindlimb retracted inward toward the abdomen for at least 50% of the observation period; 2 = both hindlimbs partially retracted inward toward the abdomen for at least 50% of the observation period; and 3 = both hindlimbs completely retracted inward toward the abdomen for at least 50% of the observation period. Scores of 0.5 were utilized when appropriate. Hindlimb clasping severity scores were averaged for the three separate trials over three consecutive days.
The pole test was utilized to measure motor coordination and balance in A53T α-synuclein mouse model. Mice were initially habituated and trained 1 d prior to testing. Then they were placed on the top of a rough-surfaced wooden pole (50 cm in length and 1 cm in diameter) and allowed to descend to the base of the pole. During the test, mice were placed with their heads oriented toward the top of the pole. The time required by the mouse to turn its head downward and descend the entire length of the pole was measured. The best performance of each mouse over five consecutive trials was recorded.
The effect of W20 on the spatial cognitive performance of transgenic mice were investigated through the MWM test according to a previously described method56. The mice were allowed to habituate for 1 day and then tested in a water maze (1.1 m in diameter). The maze filled with water was drained daily. The temperature of the water was maintained at 22 ± 1 °C. The platform (10 cm in diameter) was fixed 1 cm beneath the water surface throughout the training period, and the starting positions were counter balanced. All mice were initially assessed in the water maze to identify inherent quadrant preferences, and mice exhibiting some preferences were eliminated from subsequent testing. The mice were allowed to swim for 60 s to find the platform, on which they were allowed to stay for 10 s. Mice unable to locate the platform were guided to it. The mice were trained twice per day over five consecutive days, with an inter-trial interval of 3–4 h. The swimming activity of each mouse was monitored using a video camera (Sony, Tokyo, Japan) mounted over the maze and automatically recorded via a video tracking system. About 24 h after the last learning trial, the mice were tested for memory retention in a probe trial without the platform.
The object recognition test was performed according to the previously described method with slight modifications57. In the novel location task, mice were first presented with two different novel objects placed in the upper two corners of a box (50 cm × 50 cm × 25 cm) for 5 min. Then, the mice were removed from the box for a 1 h retention period, and the upper right object was moved to the lower right corner. Afterward, the mice were reintroduced to the box, and their behavior was recorded for 5 min. The percentages of investigations to the target object in the new and original locations were recorded. Preference for a novel object was assessed on the subsequent day with the exception that the retention period was 24 h. The right object was replaced with a completely novel object in the original location.
Brain lysate preparation and Western blot
The brain tissues of A53T α-synuclein mice were homogenized in TNE buffer (10 mM Tris-HCl, pH 7.4, 150 mM NaCl, 5 mM EDTA) containing complete protease inhibitor mixture tablets (Roche Diagnostics) and detergents (0.5% Nonidet P-40). The homogenate was centrifuged (5 min at 100,000× g), and the supernatants were collected for α-synuclein detection.
BACHD mouse brain lysates were prepared by homogenizing brain tissues in a modified RIPA buffer supplemented with complete protease inhibitor mixture tablets (Roche Diagnostics), then followed by centrifugation at 4 °C for 15 min at 16,000× g. The supernatants were obtained for soluble huntingtin protein (HTT) detection. The pellets were dissolved in 10% SDS, heated to 70 °C for 10 min, and then spun at 2000× g for 30 s. The new supernatants were considered to be the insoluble fraction.
The protein concentrations of soluble and insoluble fractions were determined using the BCA protein assay (Pierce) according to the manufacturer’s instructions. Proteins were separated by SDS-PAGE and transferred onto a nitrocellulose membrane (Bio-RAD). α-synuclein immunoblot analysis was performed using primary antibodies including Syn-1 (BD Biosciences, 610787, 1:1000) against both human and mouse α-synuclein, and LB509 (Abcam, ab27766, 1:1000) against human-specific α-synuclein. For HTT immunoblot analysis, the membranes were blotted with primary antibodies including 2166 (Merck Millipore, MAB2166, 1:1000) against both mHTT and endogenous WT-HTT, and 1574 (Merck Millipore, MAB1574, 1:1500) against polyQ-expanded HTT. α-tubulin (Sigma, T9026, 1:1000) was used as a loading control. Blots were washed thrice in TBST before incubation with IR secondary antibodies (Li-Cor, #926-3211 and #926-68020, 1:5000) for 1 h at room temperature. Then blots were washed thrice again and imaged in a Li-Cor Odyssey IR detection system. Densitometry was performed using the integrated intensity value for each band, and the results were analyzed as the ratio of protein to α-tubulin.
The soluble fraction of brain homogenates was applied to nitrocellulose membranes (Merck Millipore), which were then blocked with 5% milk in PBST for 1 h and incubated with OC (Merck Millipore, SPC-507D, 1:1000), A11 (Invitrogen, AHB0052, 1:1000), or anti-GAPDH antibodies (CST, 2118S, 1:1000) at room temperature for 1 h. Next, the bound antibodies were probed with the corresponding HRP-conjugated secondary antibody. Immuno-reactive blots were visualized with an ECL chemiluminescence kit.
Mice were deeply anesthetized with avertin, transcardially perfused with ice-cold PBS containing heparin (10 U/mL), and finally sacrificed. Their brains were immediately removed and divided along the sagittal plane. One brain hemisphere was fixed in 4% paraformaldehyde in PBS at 4 °C overnight and processed for either frozen or paraffin-embedded sections. For A53T α-synuclein mice, 6 μm sagittal paraffin-embedded sections were immunostained with anti-TH antibody (Abcam, ab152, 1:100), anti-DAT antibody (Merck Millipore, MAB369, 1:100), anti-phospho-Ser129-α-synuclein antibody (Abcam, ab59264, 1:50), anti-Iba-1 antibody (GeneTex, GTX100042, 1:100), or anti-GFAP antibody (Abcam, ab53554, 1:100), respectively. For BACHD mice, 20 μm coronal frozen sections were immunostained with anti-EM48 antibody (Merck Millipore, MAB5374, 1:50), anti-Iba-1 antibody (GeneTex, GTX100042, 1:100) or anti-GFAP antibody (Abcam, ab53554, 1:100), respectively. All aforementioned primary antibodies were followed by appropriate HRP-labeled secondary antibodies and visualized with diaminobenzidine (DAB). For synaptophysin staining, sections were immunostained with anti-synaptophysin antibody (Abcam, ab32127, 1:1000) followed by goat anti-rabbit secondary antibody conjugated to Alexa Fluor 488 (Santa Cruz, I1112, 1:1000).
All images were acquired with an Olympus IX73 inverted microscope with DP80 camera, and all analyses were performed blind to the genotype and treatment of the mice. We selected sections with similar neuroanatomical regions of the brainstem for A53T α-synuclein mice and similar neuroanatomical regions of the cortex or striatum for BACHD mice for all histological analyses. At least three sections were analyzed per mouse, and three fields of view for each section were imaged. Immunofluorescence intensities or immunostaining regions were quantified using Image J software (National Institutes of Health, USA).
For quantitative analysis of astrocytosis and microgliosis, we quantified the positively stained area in brainstem sections of PD mouse model, and cortex and striatum sections of HD mouse model. At least three sections were analyzed per mouse, and three fields for each section were imaged and quantified. GFAP or Iba-1 immunostaining regions were quantified using Image J software.
Cell death was detected with an in situ cell death detection kit (Roche Diagnostics) according to the manufacturer’s protocol. Briefly, the brain sections were fixed, permeabilized, and incubated with 50 μLof TUNEL reaction mixture for 60 min at 37 °C in the dark. The sections were then rinsed by PBS thrice and incubated with 50 μL of converter-POD for 30 min. Sections were stained with DAB, counterstained with hematoxylin, and then imaged using an Olympus IX73 inverted microscope. Images were analyzed by Image J software.
Molecular dynamics simulation
Molecular dynamics stimulation was calculated as previously described58,59. Initially, an unfolded and fully extended structure was generated by PROTEIN program in Tinker software60 (backbone torsion ϕ, ψ = −135, 135) using OPLS-AA force field parameters to assign the atom types. The structure was subsequently optimized by Truncated Newton Conjugate Gradient method using GB/SA continuum solvation model. Afterward, 1 ns molecular dynamics stimulation was carried out at a time step of 2.0 fs, and the system thermostat temperature was targeted to 298 K. The result of molecular dynamics stimulation was further rendered with POV-RAY program. ScFv antibody structure was modeled by customized program through homology modeling and protein-peptide docking was performed using AutoDock.
All quantitative analysis was performed under blinded conditions. Statistical significance was tested using Student’s t-test or one-way ANOVA analysis of variance followed by Tukey’s post hoc test (GraphPad Prism 6.0). Results are expressed as group mean ± SD, and P < 0.05 was considered statistically significant.
How to cite this article: Zha, J. et al. A scFv antibody targeting common oligomeric epitope has potential for treating several amyloidoses. Sci. Rep. 6, 36631; doi: 10.1038/srep36631 (2016).
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Zerovnik, E. Protein conformational pathology in Alzheimer’s and other neurodegenerative diseases; new targets for therapy. Current Alzheimer research 7, 74–83 (2010).
Jucker, M. & Walker, L. C. Pathogenic protein seeding in Alzheimer disease and other neurodegenerative disorders. Annals of neurology 70, 532–540 (2011).
Montine, T. J. & Montine, K. S. Precision medicine: Clarity for the clinical and biological complexity of Alzheimer’s and Parkinson’s diseases. The Journal of experimental medicine 212, 601–605 (2015).
Chiti, F. & Dobson, C. M. Protein misfolding, functional amyloid, and human disease. Annual review of biochemistry 75, 333–366 (2006).
Paleologou, K. E. et al. Detection of elevated levels of soluble alpha-synuclein oligomers in post-mortem brain extracts from patients with dementia with Lewy bodies. Brain: a journal of neurology 132, 1093–1101 (2009).
Tokuda, T. et al. Detection of elevated levels of alpha-synuclein oligomers in CSF from patients with Parkinson disease. Neurology 75, 1766–1772 (2010).
Kayed, R. & Lasagna-Reeves, C. A. Molecular mechanisms of amyloid oligomers toxicity. Journal of Alzheimer’s disease: JAD 33 Suppl 1, S67–S78 (2013).
Guerrero-Munoz, M. J., Castillo-Carranza, D. L. & Kayed, R. Therapeutic approaches against common structural features of toxic oligomers shared by multiple amyloidogenic proteins. Biochemical pharmacology 88, 468–478 (2014).
Andreasen, M., Lorenzen, N. & Otzen, D. Interactions between misfolded protein oligomers and membranes: A central topic in neurodegenerative diseases? Biochimica et biophysica acta 1848, 1897–1907 (2015).
Fandrich, M. Oligomeric intermediates in amyloid formation: structure determination and mechanisms of toxicity. Journal of molecular biology 421, 427–440 (2012).
Kayed, R. et al. Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis. Science 300, 486–489 (2003).
Kayed, R. et al. Fibril specific, conformation dependent antibodies recognize a generic epitope common to amyloid fibrils and fibrillar oligomers that is absent in prefibrillar oligomers. Molecular neurodegeneration 2, 18 (2007).
Jellinger, K. A. Interaction between pathogenic proteins in neurodegenerative disorders. Journal of cellular and molecular medicine 16, 1166–1183 (2012).
Clinton, L. K., Blurton-Jones, M., Myczek, K., Trojanowski, J. Q. & LaFerla, F. M. Synergistic Interactions between Abeta, tau, and alpha-synuclein: acceleration of neuropathology and cognitive decline. The Journal of neuroscience: the official journal of the Society for Neuroscience 30, 7281–7289 (2010).
Jackson, K., Barisone, G. A., Diaz, E., Jin, L. W., DeCarli, C. & Despa, F. Amylin deposition in the brain: A second amyloid in Alzheimer disease? Annals of neurology 74, 517–526 (2013).
O’Nuallain, B., Williams, A. D., Westermark, P. & Wetzel, R. Seeding specificity in amyloid growth induced by heterologous fibrils. The Journal of biological chemistry 279, 17490–17499 (2004).
Hamilton, R. L. Lewy bodies in Alzheimer’s disease: a neuropathological review of 145 cases using alpha-synuclein immunohistochemistry. Brain pathology 10, 378–384 (2000).
Ferrer, I. et al. Prion protein expression in senile plaques in Alzheimer’s disease. Acta neuropathologica 101, 49–56 (2001).
Wilson, A. C., Dugger, B. N., Dickson, D. W. & Wang, D. S. TDP-43 in aging and Alzheimer’s disease - a review. International journal of clinical and experimental pathology 4, 147–155 (2011).
Lasagna-Reeves, C. A. et al. Identification of oligomers at early stages of tau aggregation in Alzheimer’s disease. FASEB journal: official publication of the Federation of American Societies for Experimental Biology 26, 1946–1959 (2012).
Kovacs, G. G. et al. Non-Alzheimer neurodegenerative pathologies and their combinations are more frequent than commonly believed in the elderly brain: a community-based autopsy series. Acta neuropathologica 126, 365–384 (2013).
Savitt, J. M., Dawson, V. L. & Dawson, T. M. Diagnosis and treatment of Parkinson disease: molecules to medicine. The Journal of clinical investigation 116, 1744–1754 (2006).
Wang, N. et al. Neuronal targets for reducing mutant huntingtin expression to ameliorate disease in a mouse model of Huntington’s disease. Nature medicine 20, 536–541 (2014).
Rasool, S., Martinez-Coria, H., Wu, J. W., LaFerla, F. & Glabe, C. G. Systemic vaccination with anti-oligomeric monoclonal antibodies improves cognitive function by reducing Abeta deposition and tau pathology in 3xTg-AD mice. Journal of neurochemistry 126, 473–482 (2013).
Xiao, C. et al. Brain transit and ameliorative effects of intranasally delivered anti-amyloid-beta oligomer antibody in 5XFAD mice. Journal of Alzheimer’s disease: JAD 35, 777–788 (2013).
Zhang, X. et al. Conformation-dependent scFv antibodies specifically recognize the oligomers assembled from various amyloids and show colocalization of amyloid fibrils with oligomers in patients with amyloidoses. Biochimica et biophysica acta 1814, 1703–1712 (2011).
Wang, X. P. et al. Conformation-dependent single-chain variable fragment antibodies specifically recognize beta-amyloid oligomers. FEBS letters 583, 579–584 (2009).
Zhao, M. et al. Pan-amyloid oligomer specific scFv antibody attenuates memory deficits and brain amyloid burden in mice with Alzheimer’s disease. Current Alzheimer research 11, 69–78 (2014).
Lee, M. K. et al. Human alpha-synuclein-harboring familial Parkinson’s disease-linked Ala-53 –> Thr mutation causes neurodegenerative disease with alpha-synuclein aggregation in transgenic mice. Proceedings of the National Academy of Sciences of the United States of America 99, 8968–8973 (2002).
Unger, E. L. et al. Locomotor hyperactivity and alterations in dopamine neurotransmission are associated with overexpression of A53T mutant human alpha-synuclein in mice. Neurobiology of disease 21, 431–443 (2006).
Graham, D. R. & Sidhu, A. Mice expressing the A53T mutant form of human alpha-synuclein exhibit hyperactivity and reduced anxiety-like behavior. Journal of neuroscience research 88, 1777–1783 (2010).
Arawaka, S. et al. Zonisamide attenuates alpha-synuclein neurotoxicity by an aggregation-independent mechanism in a rat model of familial Parkinson’s disease. PloS one 9, e89076 (2014).
Giros, B. & Caron, M. G. Molecular characterization of the dopamine transporter. Trends in pharmacological sciences 14, 43–49 (1993).
Smith, W. W. et al. Synphilin-1 attenuates neuronal degeneration in the A53T alpha-synuclein transgenic mouse model. Human molecular genetics 19, 2087–2098 (2010).
Wilms, H. et al. Suppression of MAP kinases inhibits microglial activation and attenuates neuronal cell death induced by alpha-synuclein protofibrils. International journal of immunopathology and pharmacology 22, 897–909 (2009).
Gray, M. et al. Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice. The Journal of neuroscience: the official journal of the Society for Neuroscience 28, 6182–6195 (2008).
Pouladi, M. A. et al. Marked differences in neurochemistry and aggregates despite similar behavioural and neuropathological features of Huntington disease in the full-length BACHD and YAC128 mice. Human molecular genetics 21, 2219–2232 (2012).
Doria, J. G. et al. The mGluR5 positive allosteric modulator, CDPPB, ameliorates pathology and phenotypic signs of a mouse model of Huntington’s disease. Neurobiology of disease 73, 163–173 (2015).
Simmons, D. A. et al. A small molecule TrkB ligand reduces motor impairment and neuropathology in R6/2 and BACHD mouse models of Huntington’s disease. The Journal of neuroscience: the official journal of the Society for Neuroscience 33, 18712–18727 (2013).
Bouchard, J. et al. Cannabinoid receptor 2 signaling in peripheral immune cells modulates disease onset and severity in mouse models of Huntington’s disease. The Journal of neuroscience: the official journal of the Society for Neuroscience 32, 18259–18268 (2012).
Boussicault, L. et al. Impaired brain energy metabolism in the BACHD mouse model of Huntington’s disease: critical role of astrocyte-neuron interactions. Journal of cerebral blood flow and metabolism: official journal of the International Society of Cerebral Blood Flow and Metabolism 34, 1500–1510 (2014).
Lindstrom, V. et al. Immunotherapy targeting alpha-synuclein, with relevance for future treatment of Parkinson’s disease and other Lewy body disorders. Immunotherapy 6, 141–153 (2014).
Larson, M. E. et al. Soluble alpha-synuclein is a novel modulator of Alzheimer’s disease pathophysiology. The Journal of neuroscience: the official journal of the Society for Neuroscience 32, 10253–10266 (2012).
Zuccato, C., Valenza, M. & Cattaneo, E. Molecular mechanisms and potential therapeutical targets in Huntington’s disease. Physiological reviews 90, 905–981 (2010).
Surguchov, A. Molecular and cellular biology of synucleins. International review of cell and molecular biology 270, 225–317 (2008).
Kovacs, G. G., Milenkovic, I. J., Preusser, M. & Budka, H. Nigral burden of alpha-synuclein correlates with striatal dopamine deficit. Movement disorders: official journal of the Movement Disorder Society 23, 1608–1612 (2008).
Williams, A. et al. Aggregate-prone proteins are cleared from the cytosol by autophagy: therapeutic implications. Current topics in developmental biology 76, 89–101 (2006).
Tai, Y. F. et al. Imaging microglial activation in Huntington’s disease. Brain research bulletin 72, 148–151 (2007).
Hsiao, H. Y., Chen, Y. C., Chen, H. M., Tu, P. H. & Chern, Y. A critical role of astrocyte-mediated nuclear factor-kappaB-dependent inflammation in Huntington’s disease. Human molecular genetics 22, 1826–1842 (2013).
Gilman, S. et al. Clinical effects of Abeta immunization (AN1792) in patients with AD in an interrupted trial. Neurology 64, 1553–1562 (2005).
Kwan, W. et al. Mutant huntingtin impairs immune cell migration in Huntington disease. The Journal of clinical investigation 122, 4737–4747 (2012).
Valencia, A. et al. Elevated NADPH oxidase activity contributes to oxidative stress and cell death in Huntington’s disease. Human molecular genetics 22, 1112–1131 (2013).
Illuzzi, J., Yerkes, S., Parekh-Olmedo, H. & Kmiec, E. B. DNA breakage and induction of DNA damage response proteins precede the appearance of visible mutant huntingtin aggregates. Journal of neuroscience research 87, 733–747 (2009).
Xue, D. et al. A multifunctional peptide rescues memory deficits in Alzheimer’s disease transgenic mice by inhibiting Abeta42-induced cytotoxicity and increasing microglial phagocytosis. Neurobiology of disease 46, 701–709 (2012).
Lieu, C. A., Chinta, S. J., Rane, A. & Andersen, J. K. Age-related behavioral phenotype of an astrocytic monoamine oxidase-B transgenic mouse model of Parkinson’s disease. PloS one 8, e54200 (2013).
Xu, P. X. et al. Rutin improves spatial memory in Alzheimer’s disease transgenic mice by reducing Abeta oligomer level and attenuating oxidative stress and neuroinflammation. Behav Brain Res 264, 173–180 (2014).
Southwell, A. L. et al. A fully humanized transgenic mouse model of Huntington disease. Human molecular genetics 22, 18–34 (2013).
Lu, S. et al. Targeting of embryonic stem cells by peptide-conjugated quantum dots. PloS one 5, e12075 (2010).
Zhou, W. W. et al. Decreasing oxidative stress and neuroinflammation with a multifunctional peptide rescues memory deficits in mice with Alzheimer disease. Free radical biology & medicine 74, 50–63 (2014).
Ponder, J. W. & Case, D. A. Force fields for protein simulations. Advances in protein chemistry 66, 27–85 (2003).
This work was supported by grants from the National Natural Science Foundation of China (81371208 and 81402837) and the National Science and Technology Major Projects of New Drugs (2014ZX09102045-005 and 2014ZX09102041-007).
The authors declare no competing financial interests.
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Zha, J., Liu, Xm., Zhu, J. et al. A scFv antibody targeting common oligomeric epitope has potential for treating several amyloidoses. Sci Rep 6, 36631 (2016). https://doi.org/10.1038/srep36631
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