Neuroprotection by rAAV-mediated gene transfer of bone morphogenic protein 7
- Ann-Marie Heinonen1,
- Mahbubur Rahman2,
- Godwin Dogbevia1, 2,
- Hannah Jakobi1,
- Stefan Wölfl3,
- Rolf Sprengel†1Email author and
- Markus Schwaninger†2
© Heinonen et al.; licensee BioMed Central Ltd. 2014
Received: 18 July 2013
Accepted: 5 March 2014
Published: 11 March 2014
Bone morphogenic proteins (BMPs) promote the survival of neurons, suggesting a therapeutic application of BMPs in the treatment of acute and chronic neurodegenerative disorders. However, the application of recombinant BMPs in vivo is limited by their short half-life. To provide a continuous supply for functionally active BMPs, we expressed BMP7, BMP2 and the BMP inhibitor Noggin under the control of rAAV vectors in vivo. For visual control of rAAV-mediated BMP (v-BMP) expression we fused the secreted morphogenic polypeptides and the fluorescent reporter protein Venus via the ‘ribosomal skip’ promoting 2A peptide-bridge.
In primary cortical neurons, the rAAV-expressed morphogenic polypeptides were efficiently released from the 2A-Venus fusion precursors, were secreted, correctly processed and functionally active as shown by their effects on Smad phosphorylation in HeLa cells and in primary neurons, by the protection of v-BMP7-transduced primary cortical neurons against oxidative stress, and by the activation of BMP responsive GFP in v-BMP2 transduced reporter mice. In the stroke model of middle cerebral artery occlusion rAAV-transduced v-BMP7 reduced the infarct size in mice.
Polycistronic rAAV vectors encoding secreted polypeptides and 2A-linked reporter proteins are potential novel therapeutic tools for the treatment of neurological and neurodegenerative diseases. Using this technique we documented that rAAV delivery of BMP7 reduced ischemic cell death in mice.
KeywordsStroke Apoptosis BMP7 BMP2 Noggin 2A peptide Ribosomal skip
Bone morphogenic proteins (BMP) are members of the transforming growth factor-β (TGFβ) family. Mammalians encode and express more than a dozen BMPs. Two members, BMP2 and BMP7, are in clinical use for the treatment of bone fractures providing evidence for the therapeutic application of BMPs to regulate the viability and differentiation of osteoblasts , which might be of strong interest for other human cell types; in particular for those in the nervous system. BMPs play an important role during development of the nervous system . In adults, they stimulate adult neurogenesis, exert a neuroprotective effect, and stimulate the regeneration of neurons [3–5]. In models of ischemic stroke BMP7 reduced the infarct size [4, 6, 7] and improved functional recovery at delayed time points after stroke [3, 4, 7–9]. BMP7 also exerted neuroprotective effects in models of Parkinson’s disease, spinal cord injury [10, 11]. In addition, BMP2 had neuroprotective properties in vitro[12, 13] and stimulated angiogenesis, neuronal differentiation, and neurite outgrowth [14–16]. Although BMP2 is upregulated after cerebral ischemia , its function as an endogenous neuroprotectant is controversial since recombinant soluble Noggin, an antagonist of BMP2, BMP4 and BMP7, demonstrates neuroprotective effects in models of stroke [18–20].
A major obstacle for the therapeutic use of BMPs is the short half-life of the peptides; in the case of BMP7 about 30 min , precluding intravenous administration for chronic conditions. Transplanted cells secreting BMPs or Noggin can be one option to solve this issue [22, 23] but viral gene therapy using lentiviruses or recombinant adeno-associated viruses (AAVs) might open an attractive, well-defined alternative option for providing constant supply of recombinant BMP [24, 25].
In this study we used rAAVs to express BMP2, BMP7, and Noggin in the brain of mice since rAAVs enable efficient gene delivery in the CNS without inducing toxic or inflammatory responses . For visual inspection of rAAV encoded gene transduction we expressed BMP2, BMP7, and Noggin as fusion with a fluorescent protein (FP) using the ribosomal skipping 2A peptide bridge from Thosea asigna virus . In contrast to conventional techniques, such as the internal ribosomal entry site (IRES), bidirectional and dual promoters, or co-infection of several viruses, the ribosomal skipping leads to nearly equimolar ratios of the 2A-linked proteins [28–31].
In this study we demonstrate that BMP2, BMP7, or the inhibitor Noggin can be functionally expressed by rAAV encoded, 2A fused open reading frames together with fluorescent reporter proteins. When released from the 2A linked reporter proteins during protein translation, BMP2, BMP7, and Noggin are secreted and are functionally active. We found that rAAV-delivered BMP7 exerted neuroprotective properties in vitro and in vivo suggesting that this might represent a new approach for long-term administration of BMP7 in neurological diseases.
Expression of secreted morphogenic proteins and 2A-linked Venus
For the functional analysis of the rAAV vectors in neurons we first infected primary neurons by rAAVs encoding the viral BMPs (v-BMP2 and v-BMP7) and viral Noggin (v-Noggin) (Figure 1A). Seven days post infection (DPI 7) cell culture medium (supernatant, S) contained a major amount of mature v-BMP7, v-BMP2, and v-Noggin as revealed by immunoblots using an anti-2A antibody selective for 18 amino acids of 2A-peptides that remained at the C-terminus of v-BMP2, v-BMP7 and v-Noggin after successful ribosomal skipping (Figure 1B). For Noggin, three bands were visualized in immunoblots of cell lysates corresponding to the unmodified protein (26 kDa), the glycosylated protein (30 kDa), and the mature protein (32 kDa). In addition, in cell lysates the anti-2A antibody detected the BMP7 and BMP2 precursors, in the range of the predicted molecular weight (MW) of 48 kDa and 45 kDa, respectively. The anti-2A antibody also detected a Noggin-immunosignal at about 53 kDa, which might indicate residual Noggin-2A-Venus fusion proteins that escaped the ribosomal skip. However, the anti-GFP antibody revealed only minor amounts (about 6%) of BMP7-2A-Venus and BMP2-2A-Venus full-length proteins but no Noggin-2A-Venus fusion. This suggests that the 53-kDa immunosignal for Noggin in the supernatant represents Noggin dimers that can be detected under low stringent reducing conditions during electrophoresis . Thus, the ribosomal skipping and the secretion of the target proteins encoded by the rAAVs were very efficient. The minor amount of mature factors that can be detected in the lysates of neurons is most likely due to the crude, one-step separation procedure of supernatants and lysates. In contrast to the almost complete secretion of BMPs and Noggin, the secreted Venus (sVenus) which contains the N-terminal signal sequence of Noggin (Figure 1C) was only partially secreted and equal amounts of sVenus were found in the supernatant and cell lysate using the Venus cross reactive anti-GFP antibody (Figure 1D).
The immunocytology of rAAV-infected primary cortical neurons on DPI 7 was in accordance with the concept that 2A-tagged v-BMP7, v-BMP2 and v-Noggin entered the secretory pathway in rAAV transduced cells, since the 2A immunoreactivity for all three factors showed nuclear exclusion (Figure 1E). The immunofluorescence was associated with cell membranes, whereas the signal in v-Venus transduced neurons was localized mainly in the cytosol indicating that low expression of the virally transduced factors is not the reason for nuclear exclusion of their 2A immunoreactivity. A similar change in the distribution of the Venus fluorescence was found when the fluorescence patterns of virally delivered sVenus and Venus (v-sVenus; v-Venus) were compared (Figure 1E). Therefore, we conclude that the subcellular immunosignal distributions of 2A-linked secreted and cytosolic proteins indicate an efficient secretion of the secreted proteins in 2A based polycistrons.
Efficient expression of 2A-linked secretory proteins in vivo
In crude hippocampal extracts mature v-BMP2, v-BMP7 and v-Noggin could be detected together with their v-BMP2 and v-BMP7 precursors and Noggin dimer of v-Nogin (Figure 2C). As already noticed in virally transduced primary neurons (Figure 1B), the electrophoretic mobility of the v-BMP2 precursor (at 49 kDa) is slower than expected (45 kDa). Since this slower mobility of the v-BMP2 45-kDa precursor was consistently observed in different expression systems this might be an intrinsic property of the v-BMP2 precursor in our electrophoretic system.
2A-released secretory proteins are biologically active
To analyze whether 2A-tagged v-BMP2, v-BMP7 and v-Noggin expressed in brain cells are bioactive we analyzed v-BMP2, v-BMP7 and v-Noggin induced Smad1/5/8 phosphorylation, the neuroprotection afforded by v-BMP7 against H2O2 toxicity and the v-BMP2 activation of the BMP2 BRE:GFP reporter gene in the BMP reporter mouse brains .
We treated PCN with conditioned supernatants of PCN cultures (Figure 3A, B) since it was documented that BMP2 and BMP7 stimulate the phosphorylation of Smad1/5/8 (pSmad1/5/8) whereas Noggin inhibits the formation of pSmad . As controls we applied recombinant r-BMP7, r-BMP2, r-Noggin (100 ng/ml) and supernatant from non-transfected PCN. The Smad1/5/8 specific immunoblots showed that r-BMPs and v-BMPs increased the level of pSmad 4 h after stimulation whereas supernatants from v-Noggin or v-Venus expressing cells and uninfected cells did not increase pSmad1/5/8 levels (Figure 3C; upper panel). The identical treatment of HeLa cells provided a similar result (Figure 3C; lower panel). In HeLa cells the v- and r-BMP7 stimulation induced higher pSmad1/5/8 levels than v- and r-BMP2. The v- and r-Noggin treated HeLa cells showed lower pSmad1/5/8 levels than HeLa cells stimulated with conditioned supernatants harvested from Venus expressing or uninfected PCN (Figure 3C; lower panel). Thus, the efficient stimulation of pSmad1/5/8 by v-BMP2 and v-BMP7 strongly suggested that the 2A-tagged v-BMP2 and v-BMP7 are secreted as bioactive proteins from rAAV infected PCN.
Since our goal was the application of the virally delivered BMPs for neuroprotection and since reactive oxygen species are known to be involved in the pathophysiology of several brain disorders, including stroke, we exposed primary cortical neurons to H2O2 investigating the protective activity of rAAV-delivered BMP7. On day in vitro (DIV) 11 we treated PCN with H2O2 and 24 h later we measured the cell toxicity indicator lactate dehydrogenase (LDH) in the supernatant of PCN cultures. As shown in Figure 3D H2O2 exposure induced neuronal toxicity in a H2O2 concentration-dependent manner. For the subsequent experiments we used 0.2 mM H2O2 that induced about 30 % of the global toxicity obtained by 1 M H2O2 exposure. Treatment with r-BMP7 itself (1.2 nM to 12.5 nM) did not affect LDH release (Figure 3D, right panel). However, treatment of DIV 11 neurons with r-BMP7 (1.2 nM) 30 min before H2O2 exposure significantly reduced H2O2-induced LDH levels in the medium (Figure 3E). Interestingly, infection of PCN with rAAV-BMP7-2A-Venus at DIV 4 also protected PCN from H2O2-induced exposure at DIV 11 (Figure 3E). These results indicate that, given shortly before the noxious stimulus or chronically administered by rAAV delivery several days before H2O2 treatment, v-BMP7 has protective properties in primary neurons.
To provide additional evidence for the bioactive expression of v-BMPs in the adult brain we injected rAAV-BMP2-2A-tdTomato into the hippocampus and cortex of BRE:GFP reporter mice . Two weeks after rAAV delivery we detected the majority of GFP positive cells in the granular cell layer of the dentate gyrus (DG) in addition to some sparse GFP immunopositive neurons and glia in the cortex at the injection site (Figure 3F). The presence of the GFP immunopositive cells could not be observed in PBS-infected BRE:GFP mice (Figure 3F) suggesting that the virally delivered v-BMP2 is functionally active. The poor GFP expression by rAAV transduced v-BMP2 might reflect the low sensitivity of the BRE:GFP reporter in brain tissue, since injection of r-BMP2 did lead to GFP positive cells 24 or 48 h after injection of rBMP2 (not shown). Thus, in summary, our results collectively show that BMP2, BMP7 and can be expressed and secreted as native peptides in neuronal cultures and in adult brains as rAAV encoded 2A fusions.
Virally expressed BMP7 has a neuroprotective effect in MCAO
In a second cohort of eight-week-old mice injected at P0 with rAAV-BMP7-2A-Venus, rAAV-BMP2-2A-Venus, rAAV-Noggin-2A-Venus and rAAV-Venus MCAO was performed. In this model of ischemic strokes, infarcts are mainly limited to the cortex. When cortical infarct volumes were quantified 48 h after MCAO, rAAV-mediated overexpression of v-BMP7 (Figure 4B, (i)v-BMP7), significantly reduced infarct volumes, whereas the rAAV mediated expression of v-Venus, v-BMP2 and v-Noggin did not alter infarct volumes (Figure 4B). In another independent experimental group, we confirmed the protective effect of v-BMP7 in MCAO (Figure 4B, (ii)v-BMP7) and showed in these mice that v-BMP7 did not affect the cerebral blood flow (Figure 4C). To further investigate the protective properties of v-BMP7 in vivo, we analyzed neuronal apoptosis after MCAO in eight-week-old P0 rAAV-BMP7-2A-Venus injected animals. Apoptosis was evaluated in the periphery of the ischemic area by TUNEL staining on coronal sections at the level of the anterior commissure. We detected significantly fewer TUNEL-positive cells in mice expressing v-BMP7 compared to rAAV-Venus infected or naïve mice (Figure 4D).
Our results indicate that rAAV-induced neuronal overexpression of BMP7 is protective in MCAO and that rAAV-mediated polycistronic gene transfer can be applied to study cerebral ischemia in vivo.
The morphogenic protein BMP7 has neuroprotective properties in vitro. However, in vivo administration is limited by the short half-life and the large amounts of biologically active BMP7 that need to be administered (at least 10 mg/kg body weight) , which might explain why recombinant BMP7 reduced the infarct volume in some, but not all experimental stroke studies [4, 7–9]. Using rAAV expressed BMP7 we observed a 2-fold reduction in the infarct size, suggesting that rAAV vectors represent a superior mode for the delivery of biological active BMP7. Previous work has revealed an anti-apoptotic effect of BMP7 in neurons in vitro[38, 39]. Our work extends this finding, demonstrating that BMP7 reduces apoptotic cell death in vivo as rAAV expression of BMP7 significantly decreased the number of TUNEL-positive cells in the periphery of the ischemia.
In contrast to a previous study , the viral expression of Noggin, an extracellular inhibitor of BMP2, BMP4 and BMP7, had no effect on the infarct size although we verified that the rAAV expressed Noggin was bioactive by decreasing the level of Smad phosphorpylation of HeLa cells. Besides the different time points for the analysis after MCAO (2 days in this study versus 14 days in ) a lower expression level of biological active Noggin in our system cannot be excluded. Similarly, low expression levels of v-BMP2 might be responsible for the lack of neuroprotection in our MCAO experiments.
Our study was not designed to analyze long-term effects of BMP2, BMP7 and Noggin, but rather was designed to propose a convenient, reliable route for prolonged delivery of short-lived peptide hormones. Future work will be required to explore the potential of BMPs and BMP inhibitors in regenerative treatment of stroke and other neurodegenerative diseases. Similarly, a paracrine or autocrine neuroprotective activity of the v-BMP7 needs to be investigated in future studies, using neuron specific rAAV vectors.
Our study illustrates that 2A-tagged BMP2, BMP7 and Noggin can be co-expressed in 2A-linked fusions with a reporter protein in neurons using rAAVs as gene transfer vectors. In cells of adult mouse brains the 2A induced ribosomal skip  was very efficient and no full-length 2A-fusion protein composed of the secretory polypeptides, the 2A peptide linker and Venus could be detected in adult mouse brains. After or during translation the N-terminal secretory protein precursors and the C-terminal reporter protein were differentially sorted as separated proteins into the cytosol or functionally assembled in secretory pathways indicating that the C-terminally attached 2A peptide did not inhibit the BMP2, BMP7 and Noggin bioactivity and that v-BMP7 is similar active as r-BMP7 in vitro.
Polycistronic expression of 2A-linked peptide hormones and a reporter gene using rAAVs provide a convenient and promising gene therapeutic tool for the genetic delivery of neuroprotective factors.
Molecular, biochemical experiments and genetic manipulations of mice were licensed by the regional council in Karlsruhe, Germany, under project licenses 35–9185.81/G171-10. Animal experiments and were performed according to the animal welfare guidelines of the Max Planck Society. Efforts were made to minimize numbers of animals used.
Cloning strategies of specific rAAV vectors
The plasmid pAAV-CAG-Noggin-2A-Venus was generated by PCR-isolating the CMV enhancer chicken β-actin (CAG) promoter from plasmid pAAV-CMV-Rluc2A-Venus, GenbankID: KC152484 , with KpnI and EcoRI restriction sites and subcloning it between XbaI and EcoRI in pAAV-Syn-Noggin-2A-Venus  by 5′ blunt and EcoRI ligation to replace the synapsin promoter. The human BMP2 and human BMP7 genes were amplified by PCR from the pcDNA3.1-BMP2 and pcDNA5-BMP7 template DNA using specific primers to replace Noggin in pAAV-CAG-Noggin-2A-Venus using EcoRI and XhoI restriction sites to construct pAAV-CAG-BMP2-2A-Venus and pAAV-CAG-BMP7-2A-Venus. The plasmids pAAV-CAG-BMP7-2A-Tomato, pAAV-CAG-BMP2-2A-Tomato and pAAV-CAG-Noggin-2A-Tomato were generated by replacing Venus by tdTomato from pAAV-Syn-iCre-2A-Tomato using BamHI and BsrGI restriction sites. To generate pAAV-CAG-Venus, Noggin-2A was deleted in pAAV-CAG-Noggin-2A-Venus by EcoRI and BamHI restriction digest and subsequent religation of the vector.
Generation of rAAV vectors
Recombinant AAV gene transfer vectors were generated by molecular cloning of specific gene cassettes into rAAV2-based expression vectors , containing viral cis-acting elements required for genome replication and packaging, a woodchuck posttranscriptional regulatory element (WPRE), a bovine growth hormone polyadenylation site (bGHpA), two flanking inverted terminal repeats (ITRs) of serotype 2 (S2) and the cytomegalovirus enhanced chicken beta-actin promoter (CAG) for efficient expression in cells of the brain. All constructs were confirmed by sequencing.
Preparation and delivery of rAAV vectors
Recombinant AAVs of serotype 1 and 2 were generated as described  and purified by AVB Sepharose affinity chromatography . For each virus the genomic titer was determined by real-time PCR using primers and a probe against WPRE: WPRE forward primer: 5′-TGCCCGCTGCTGGAC-3′; WPRE reverse primer: 5′-CCGACAACACCACGGAATTG-3′; and WPRE probe: 5′-CAGTGCCCAACAGCC-3′ (1.0–6.0 × 1012 viral genomes (vg)/ml, TaqMan Assay, Applied Biosystems). In addition, the filling rate of the rAAV preparation was determined by electron microscopy. Purified virus samples were applied to carbon-coated electron microscopy grids, negatively stained with 1% uranyl acetate and rinsed with ultrapure water. Representative images of selected areas were taken using transmission electron microscopy at 6,3000x magnification (Zeiss 912 Omega Transmission Electron Microscope). The filling rate was determined by manually counting filled and empty particles using ImageJ (NIH). Empty capsids were distinguished from filled capsids, resulting from the uptake of uranyl acetate in the capsid core or from collapse staining of the particle. The genomic titers (genome copies (gc)/ml) and the filling rate (%) were as follows: rAAV-BMP7-2A-Venus, 1.69 × 1012, 88%; rAAV-BMP2-2A-Venus, 1.86 × 1012, 92%; rAAV-Noggin-2A-VENUS, 1.02 × 1012, 49%; rAAV-Venus, 2.90 × 1012, 64%; and for rAAV-sVenus, 5.96 × 1012, 98%. The infectivity was determined in primary neurons. Primary cortical neurons were infected with rAAVs on DIV 4 at multiplicities of infection (MOI) of 2 × 103 gc/cell. The expression of rAAV-transduced proteins in rat primary neurons was evaluated on DPI 7 by Venus fluorescence, immunoblots, immunoassay, or immunostainings [27, 44].
BMP stimulation of HeLa cells
HeLa cells were incubated at 37°C and 5% CO2 in a humidified atmosphere. For stimulation experiments HeLa cells were plated in 12-well plates in MEM containing 5% FCS (Invitrogen) at a density of 1.5 × 105 in 1 ml/well. The following day medium was changed to serum-free MEM. On the third day medium was replaced by 1 ml conditioned medium taken from infected primary cortical neurons or 1 ml DMEM containing 100 ng/μl recombinant proteins (r-BMP7, r-BMP2 and r-Noggin, R&D Systems) to stimulate HeLa cells.
Primary cortical neuron culture
Cultures of primary cortical neurons were prepared from cerebral cortices of E16 NMRI mice as described previously . Briefly, cortices were dissected in ice-cold PBS supplemented with Hepes (7.38 g/l) and glucose (6 g/l). Pooled cortical tissues were dissociated by incubation with trypsin-EDTA for 8 min at 37°C, followed by mechanical trituration using a fire-polished Pasteur pipette. After resuspension in Neurobasal (NB) medium containing 1 × B27, 0.5 mM L-glutamine, 100 U/ml penicillin, and 100 μg/ml streptomycin, 2 × 105 cells per well were plated in 24-well plates precoated with poly-D-lysine (50 μg/ml). On DIV 1 half of the medium was exchanged by fresh NB medium containing 5% fetal bovine serum. Then, on DIV 4 and DIV 8 half of the medium was exchanged with fresh NB until DIV 10–12 when cells were used for experiments. On DIV 11 half of the medium was exchanged with fresh medium containing r-BMP7 (R&D Systems). Thirty minutes later, H2O2 was added to the medium for 24 hours. Culture media were collected to measure levels of lactate dehydrogenase (LDH) using the cytotoxicity detection kit (Roche). Here, six wells were analyzed per condition and the assays were performed in duplicate. Per well, 75 μl of supernatant was added to 75 μl of assay reagent and incubated for 30 min at room temperature. LDH activity was determined by colorimetry according to the LDH assay kit’s instructions and expressed as percentage of LDH activity of untreated cells (LDH %Control).
Constitutive release of v- BMP7, v-BMP2 and v-Noggin in PCN
Primary cortical neurons (PCN) were cultured as described above. On DIV 4 PCN were infected with rAAV-BMP7-2A-Venus, rAAV-BMP2-2A-Venus or rAAV-Noggin-2A-Venus at a MOI of 1 × 103 gc/cell. Lysates (L, 4 μl) and supernatants (S, 12 μl) were collected and analyzed in immunoblots or by ELISA.
Characterization of rAAV in immunoblots
Infected primary cortical neurons were harvested with RIPA lysis buffer (50 mM Tris–HCl, pH 7.6; 150 mM NaCl; 1% NP-40; 0.5% sodium deoxycholate; 0.1% SDS) containing protease inhibitor cocktail (Complete, Roche) 7 days after rAAV infection. Brain tissue (cortex and hippocampus) was collected 8 weeks after virus injection and homogenized in 25 mM Hepes buffer containing a protease inhibitor cocktail on ice. Proteins were separated by SDS-PAGE (10% separating and 4% stacking gels) and transferred onto nitrocellulose membranes. Immunoblots were probed with monoclonal mouse anti-GFP (1:8000, Clontech), polyclonal rabbit anti-2A (1:2000, Millipore), polyclonal rabbit anti-phospho-Smad1/5/8 (1:1000, Cell Signaling Technology), polyclonal rabbit anti-BMP7 (1:1000, Abcam), and monoclonal mouse anti-β-actin (1:5000) antibodies. Horseradish peroxidase-linked anti-rabbit or anti-mouse was used as secondary antibodies (1:15,000, Vector Laboratories), and blots were visualized by enhanced chemiluminescence (ECL kit, GE Healthcare). Immunoblots were quantified using ImageJ (NIH).
Characterization of rAAV expression by immunostaining
Cultured primary cortical neurons on DPI 7 or brains from virus-injected mice on DPI 56 were fixed with 4% paraformaldehyde (PFA), and 100-μm sagittal sections were obtained from brains. Immunostaining was performed with polyclonal rabbit anti-2A (1:1000) or polyclonal chicken anti-GFP (1:5000, Abcam) and Cy3-coupled anti-rabbit or FITC-coupled anti-chicken secondary antibodies (1:400, Jackson ImmunoResearch).
Stereotaxic rAAV delivery into brains of adult mice
Stereotaxic rAAV injection into adult C57BL6/N mice was performed according to a protocol described previously . The following coordinates relative to bregma were used for injection: anteroposterior −2 mm; mediolateral ±1.5 mm; dorsoventral from pial surface −1.55 mm for DG, −1.05 mm for CA1, −0.35 for CTX. In brief, animals were anesthetized with an intraperitoneal injection of a mixture of ketamine hydrochloride (Inresa Arzneimittel; 100 mg per kilogram body weight) and xylazine (Inresa Arzneimittel; 10 mg per kilogram body weight) in PBS. After loss of reflexes the animal was fixed in a small animal stereotaxic frame (David Kopf instruments) and eyes were covered with bepanthene. The skull was exposed and levels were adjusted using the Kopf digital display console (David Kopf instruments). Coordinates were set and a small craniotomy was made at the defined position into the skull using an OS-40 drilling device (Osada Electronic). Virus solution was sucked into a glass micropipette with an inner diameter of 9 μm by applying back-pressure and a total volume of 264 nl was injected into the three different injection sites at a rate of 50 nl/min. After injection, the micropipette was kept in place for 5 min to avoid backflow of the injected virus during micropipette retraction. The scalp was sutured, and the animal was placed on a heating pad until recovery from surgery and then returned to its home cage.
BRE: GFP mice
Adult BRE: GFP reporter mice  were analyzed on DPI 10 after rAAV or PBS injection in the cortex and hippocampus. Coronal sections were immunostained as described above using mouse anti-GFP (1:1000, Clontech) and Cy3-anti-mouse (Jackson Immunoresearch) for enhanced GFP detection. The Cy3 fluorescence was converted to the green channel in the RGB color mode in Photoshop.
Stereotaxic rAAV delivery into brains of newborn mice
Stereotaxic rAAV injection into neonate C57BL6/N mice at P0 was performed as described previously . The following coordinates relative to lambda were used for injection: Lateral ventricle (LV), rostral 1 mm, lateral 1 mm and ventral 1.5 mm; HPC, rostral 2 mm, lateral 0.7 mm and ventral 1.5 mm. Briefly, newborn pubs were separated from their mother and cryoanesthetized for 5 min. Purified rAAV1/2 were infused into LV and HPC (1 μl virus per injection site) of neonates according to the defined coordinates at 200 nl/sec through a 33-gauge beveled needle via microprocessor-controlled WPI (World Precision Instruments) infusion-pump driving a 100 μl syringe. After injection, the hand-held needle was kept in place for additional 3 s to avoid backflow of the injected virus. Following injection the pups were collected on a 37°C warm plate for recovery. After regaining normal body color and full mobility, the injected pups were rolled in home cage bedding and returned to their mother as a group. Injected animals were kept until experiments were performed.
Middle cerebral artery occlusion (MCAO)
Eight-week-old male C57BL/6 N mice that had been infected with rAAV vectors on P0 were anesthetized by intraperitoneally injecting 15 μl of 2.5% avertin per g body weight. Middle cerebral artery occlusion (MCAO) was performed as described previously [47, 48]. A skin incision was made between the ear and the orbit on the left side and the temporal muscle was removed by electrical coagulation. Then, the MCA was exposed and occluded by microbipolar coagulation. Rectal temperature was maintained at 37°C during surgery by a heating pad and monitored continuously. After 48 hours of MCAO, mice were deeply anesthetized with avertin and perfused transcardially with Ringer’s solution. Brains were removed and immediately frozen on dry ice. Serial coronal cryosections (20 μm in thickness) were cut every 400 μm and stained with a silver technique . Stained sections were scanned at 300 d.p.i., and the infarct area was measured using ImageJ (NIH). To correct for edema formation, the difference between areas of the left and right hemispheres was subtracted from the measured silver-negative area . For calculating the infarct volume, the infarct areas were added and multiplied by the distance between the sections (400 μm). Based on previous MCAO experiments in our laboratory we calculated that, in experiments with four groups, 12 mice per group were required to detect a 40% change of infarct size with a power of >0.8 and a p < 0.05 by one-way ANOVA. Experimenters were blinded for the treatment group.
TUNEL staining and quantification
For quantification of apoptosis after MCAO, terminal deoxynucleotidyl transferase- mediated dUTP-biotin nick end labeling (TUNEL) was performed on cryosections using the in-situ-cell death detection kit (Roche). Sections were air-dried for 10 min at RT and postfixed in 4% PFA for 30 min. Then, sections were washed twice in PBS for 5 min and subsequently permeabilized in 0.1% sodium citrate, 0.1% TrtionX-100 in PBS. Sections were washed twice in PBS for 5 min and incubated with TUNEL reaction mix (50 μl per section, TUNEL-enzyme: labeling solution, 1:7) in a humid chamber for 2 h in the dark. After washing in PBS and DAPI-staining for 5 min at RT sections were washed in PBS and mounted with Mowiol/DABCO (Merck/Sigma-Aldrich). For combined TUNEL and fluorescence immunostaining, immunohistochemistry was performed as described above. To quantify the percentage of apoptotic cells fluorescence images were acquired at 10x magnification in three optical fields of the penumbra and analyzed using ImageJ (NIH). The number of DAPI and TUNEL positive cells was counted manually. Experimenters were blinded for the treatment group.
Culture supernatants or lysates of infected PCN were collected and BMP2-immunoassay was performed in a 96-well plate according the manufacturer’s instructions (R&D systems). The optical density of each well was measured at 450 nm using the VersaMax microplate reader (Molecular Devices). Protein concentrations were determined according to appropriate BMP2 standard curves.
Data were analyzed using GraphPad Prism 5 (Graphpad) and results are presented as mean ± standard error of the mean (SEM) of the indicated number of independent replicates unless otherwise indicated. Two-tailed Student’s t test was used for comparisons between two independent groups. For comparing more than two groups one way analysis of variance (ANOVA) was performed followed by Turkey’s multiple comparison post hoc test.
Analysis of variance
Bovine growth hormone polyadenylation
Bone morphogenic proteins
Chicken beta-actin enhanced cytomegalovirus promoter
Central nervous system
Days in vitro
Day post infection
Enzyme linked immunosorbent assay
Green fluorescent protein
Inverted terminal repeats
Middle cerebral artery occlusion
Middle cerebral artery
Multiplicities of infection
Phosphate buffered saline
Primary cortical neurons
Recombinant adeno-associated virus
Recombinant adeno-associated viruses
Recombinant-bone morphogenic protein
Sodium dodecyl sulfate polyacrylamide gel electrophoresis
Standard error of the mean
Transforming growth factor beta
Terminal deoxynucleotidyl transferase dUTP nick end labeling
Viral expressed-bone morphogenic protein
Woodchuck posttranscriptional regulatory element
We thank Dr. P.H. Seeburg and the Max Planck Society for generous support. We thank Dr. Uwe Zillmann for veterinarian and Annette Herold and Sabine Grünewald for technical assistance, Ulrike Mersdorf for performing EM and Christine L. Mummery for providing the BRE: GFP mice. This work was supported by funds to MS from the European Union’s 7, Framework program, FP7/2007-2013, grant agreements 201024 and 202213 (European Stroke Network) and by the German research foundation grant to RS (SFB636/A4).
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