Wild-type but not mutant SOD1 transgenic astrocytes promote the efficient generation of motor neuron progenitors from mouse embryonic stem cells
© Christou et al.; licensee BioMed Central Ltd. 2013
Received: 11 June 2013
Accepted: 9 October 2013
Published: 17 October 2013
The efficient derivation of mature (Hb9+) motor neurons from embryonic stem cells is a sought-after goal in the understanding, and potential treatment, of motor neuron diseases. Conditions that promote the robust generation of motor neuron progenitors from embryonic stem cells and that promote the survival of differentiated motor neurons ex vivo are likely, therefore, to be critical in future biological/therapeutic/screening approaches. Previous studies have shown that astrocytes have a protective effect on differentiated motor neurons (in vivo and ex vivo), but it remains unclear whether astrocytes also play a beneficial role in the support of motor neuron progenitors. Here we explore the effect of murine astrocyte-conditioned medium on monolayer cultures of mouse embryonic stem cell-derived motor neuron progenitors.
Our data show that wild-type astrocyte-conditioned medium significantly increases the number of Olig2+/Hb9- progenitors, which subsequently differentiate into Hb9+/Islet1+ post-mitotic motor neurons. Intriguingly, while astrocyte-conditioned medium derived from mice transgenic for wild-type human SOD1 mimics the effect of wild-type astrocytes, conditioned medium derived from astrocytes carrying an amyotrophic lateral sclerosis-related SOD1-G93A mutation shows no such beneficial effect. The effect of astrocyte-conditioned medium, moreover, is specific to motor neurons: we find that interneurons generated from mouse embryonic stem cells are unaffected by conditioned media from any type of astrocyte.
Our study indicates that conditioned medium derived from wild type astrocytes enhances the efficient generation of motor neurons from mouse embryonic stem cells by enhancing motor neuron progenitors. In contrast, conditioned medium from SOD1-G93A astrocytes does not show a similar enhancing effect.
KeywordsES cells G93A astrocytes Motor neuron Progenitor Differentiation ALS
Motor neurons (MNs) are selectively depleted, or diminished, in motor neuron diseases such as amyotrophic lateral sclerosis (ALS). Various factors contribute to the pathogenesis of ALS including mutations in the SOD1 gene, mutations in the ALS2 (Alsin) [1, 2], FUS (RNA-binding protein FUS) , TARDBP (TAR DNA-binding protein 43) [4, 5], ATXN2 (Ataxin-2)  and ANG (Angiogenin)  genes, and the recently-discovered intronic hexanucleotide expansions in C9ORF72 [8, 9]. In mutant SOD1 disease models, non-neuronal cells, such as astrocytes have been implicated in the pathogenesis of MN degeneration [10–12]. The mechanism by which astrocytes facilitate MN loss has not yet been fully identified, but a number of potential mechanisms have been reported. The production of NGF (nerve growth factor) (or related species such as NGF-precursor forms (pro-NGF)) in reactive SOD1-G93A (change of alanine to glycine at position 93 of the SOD1 protein) astrocytes can induce death of rat MNs expressing p75-receptor, through a mechanism that involves nitric oxide and peroxynitrite formation . The increased secretion of pro-NGF and subsequent induction of toxic p75 receptor signalling within neighbouring motor neurons is believed to be a key element of the toxicity of mutant SOD1-expressing astrocytes to motor neurons . Studies in mouse have similarly shown that astrocytes expressing mutant forms of SOD1-G37R (change of arginine to glycine at position 37), SOD1-G85R (change of arginine to glycine at position 85), and SOD1-G93A (change of alanine to glycine at position 93), release soluble factors that can selectively kill embryonic stem (ES) cell-derived or primary MNs in vitro, and have demonstrated that neurotoxicity by SOD1-G93A astrocytes is mediated through the recruitment of the Bax-dependent death machinery. By contrast, conditioned medium from wild-type SOD1-expressing astrocytes displays a supportive/survival effect on MNs similar to that observed with non-transgenic astrocytes . Co-culture of ES cell-derived MNs with SOD1-G93A astrocytes markedly decreases MN survival relative to primary wild-type SOD1 astrocytes . In vivo, the transplantation of glial-restricted precursor cells into the vicinity of cervical spinal cord respiratory MNs in a SOD1-G93A rat model of motor neuron disease limits progression of the disease, resulting in enhanced motor and respiratory physiological functions and enhanced survival . The neuroprotective effects have been partly attributed to increased expression of the astrocytic glutamate transporter, GLT1. Taken together, the evidence from these studies suggests that astrocytes are critically involved in MN depletion in ALS, most likely acting through multiple mechanisms.
As yet, no study has examined whether astrocytes exert an effect on MN-progenitor cells. Two factors suggest this is an important question. First, the efficient derivation of mature (Hb9+) MNs from embryonic stem cells is a sought-after goal in the understanding, and potential treatment, of motor neuron diseases: factors that enhance early steps in MN differentiation will therefore contribute to the derivation of MNs ex vivo. Second, the realisation that new neurons can be generated within the adult brain suggests the possibility that ALS-driven MN depletion may result from the loss of adult-born neurons. Recent experiments in songbirds show that adult neurogenesis can result in the addition of new neurons to cortical premotor circuits that govern peripheral muscle control , while dopamine produced by projections of the brain promotes adult MN regeneration in lesioned spinal cord in zebrafish , supporting this idea. Thus, we aimed to extend current knowledge by examining the potential effect of astrocytes on MN progenitors. Here we show that wild-type astrocyte-conditioned medium promotes the efficient generation of MN progenitors from mouse ES cells. By contrast, SOD1-G93A astrocytes are less supportive for the generation of these MN progenitors.
Spatio-temporal expression profiles of transcription factors in MN development in mouse neural tube
As a basis for monitoring MN differentiation from mouse ES cells in vitro, we first examined the expression profiles of the transcription factors Olig2, Hb9/MNR2 and Islet1 in the embryonic mouse neural tube at E10.5; all have been previously demonstrated to be involved in MN fate determination [20–22].
Wild-type but not mutant SOD1-G93A astrocyte-conditioned medium promotes the generation of MN progenitors from mouse ES cells and subsequent MN differentiation
To determine whether the increased proportion of differentiated MNs might be due, in part, to enhanced numbers of progenitors, we analysed expression of the b-HLH (basic helix-loop helix) transcription factor, Olig2 [20, 25]. Many Olig2+ cells were detected within the cultures (Figure 2a,e). High magnification views after combinatorial labelling with Olig2, Hb9:eGFP and β3-tubulin, or Olig2, Hb9:eGFP and Islet1 revealed that the vast majority of Olig2+ cells did not co-express either β3-tubulin (Figure 2c,d, red arrows) or Islet 1 (Figure 2h,i, red arrows). Quantitative analyses revealed that only a very minor proportion of Olig2+ cells co-expressed β3-tubulin (0.2%) or Islet1 (0.17%) (green arrow, Figure 2e-i). A significantly higher percentage of Olig2+ MN-progenitor cells was detected in cultures grown in wt non-Tg astrocyte CM, compared to those in control medium (Figure 2k). Quantitative analyses showed that the percentage of Olig2+ MN-progenitors in wt non-Tg astrocyte CM was increased by 1.5-fold compared to the control (p <0.001). These data suggest that a primary effect of wt non-Tg astrocyte CM is to increase the number of MN progenitor cells. Importantly, moreover, culture with wt non-Tg astrocyte CM appeared to result in a more robust conversion of Olig2+ progenitors to MNs or survival of MNs. In the case of controls, approximately 8.8% of Olig2+ progenitors differentiated to MNs, whereas with wt non-Tg astrocyte CM, approximately 16.8% of Olig2+ progenitors differentiated to MNs. Thus, wt non-Tg astrocyte CM may promote the generation of differentiated MNs in two ways: first, by increasing the numbers of progenitors, and second, by supporting their robust differentiation/survival.
In contrast to the effects of wt non-Tg astrocyte CM, medium conditioned by astrocytes derived from transgenic mice expressing mutant SOD1-G93A (Tg SOD1-G93A) did not show a supportive effect on Olig2+ MN progenitors. Quantitative analyses showed that in Tg SOD1-G93A CM, the number of Olig2+ MN-progenitors was similar to those in the control (p >0.05, not significant), but decreased significantly (p<0.001: a 1.6-fold decrease) compared to the littermate wt non-Tg CM (Figure 2k). Tg SOD1-G93A astrocyte CM similarly appeared far less able to support eGFP+ MNs, compared to wt non-Tg astrocyte CM. Quantitative analyses revealed a two-fold difference in the percentage of eGFP+ MNs in Tg SOD1-G93A CM compared to the littermate wt non-Tg CM (p <0.001) (Figure 2j). Notably, however, the efficiency of differentiation to MNs from Olig2+ progenitors in Tg SOD1-G93A CM appears comparable to that in wt non-Tg astrocyte CM (differentiation/survival coefficient of 13% which is closer to the wt non-Tg astrocyte CM than to the control: see Methods). To determine whether Tg SOD1-G93A CM decreases the numbers of MN progenitors and MNs by increasing apoptosis, indicative of the presence of a toxic factor , we analysed chromatin condensation and nuclear fragmentation after DAPI-labelling . Quantitative analyses revealed no statistically significant association of the number of apoptotic cells with any of the three media (Additional file 1: Figure S1). Taken together, these results indicate that, while CM from wt non-Tg astrocytes is strongly supportive of both Olig2+ MN progenitor cells and eGFP+ MNs, CM from Tg SOD1-G93A astrocytes appears to lack, in particular, a trophic support factor to motor neuron progenitors.
In order to confirm that the significant differences found in the proportion of Olig2+ MN-progenitor cells and eGFP+ MNs between the wt non-Tg astrocyte CM and the SOD1-G93A or the control medium were indeed due to the presence of the G93A mutation and not to the presence of the transgene, a similar study was performed, this time using conditioned medium from transgenic astrocytes over-expressing human wild-type SOD1 (Tg WTSOD1), or, for comparison, CM from their wt non-Tg littermates. As expected, the percentage of eGFP+ MNs detected after culture with either wt non-Tg or WTSOD1 CM was similar (p >0.05, not significant; Figure 2l), while both media evoked a higher proportion of differentiated MNs than control medium (Figure 2l; p <0.001; a two-fold increase of eGFP+ MNs compared to the control; coefficient of differentiation is 11% for control; 16% for wt non-Tg; 18% for Tg WTSOD1). Similarly, there was a significant difference in the percentage of Olig2+ MN-progenitor cells in cultures grown in wt non-Tg astrocyte CM compared to control medium (p <0.01; Figure 2m). However, there was almost no difference in the proportion of Olig2+ cells supported through wt non-Tg murine astrocyte CM, compared to CM from Tg WTSOD1 littermates (Figure 2m; p <0.05). The similar proportion of Olig2+ progenitors and eGFP+ MNs generated in the presence of wt non-Tg and Tg WTSOD1 astrocyte CM (Figure 2l,m) suggests that the presence and over-expression of the human transgene in mouse astrocytes is not the reason for any observed differences in the numbers of eGFP+ MNs. Therefore, the difference in the proportion of eGFP+ MNs in the wt non-Tg and Tg SOD1-G93A astrocyte CM is likely to be due to the effect of the SOD1-G93A mutation.
Neither wild type astrocyte CM nor mutant SOD1G93A astrocyte CM affects the generation of Lhx1/5+ interneurons from mouse ES cells
Published studies over the last few years have demonstrated negative effects of mutant SOD1 astrocytes on MN survival [12–14, 17] but no study has so far examined any potential effects on MN progenitor cells. The question of how astrocyte CM may impact on MN progenitors is important, both from the perspective of ex vivo differentiation strategies and, from the perspective of adult neurogenesis, since buffering of the niche from localised astrocytes may affect survival and differentiation efficiency of the progenitors. Here we demonstrate an impact of astrocyte CM on both MN progenitors and MNs, and demonstrate that mutant SOD1 astrocytes fail, particularly, to provide survival/trophic support to MN progenitors.
Our study reveals markedly higher numbers of Olig2+ MN progenitor cells and eGFP+ MNs in wt non-Tg astrocyte CM and consistently lower numbers in littermate Tg SOD1-G93A CM. In contrast, Tg WTSOD1 and littermate wt non-Tg CM have similar effects on eGFP+ MNs and Olig2+ MN-progenitors, indicating that our findings are likely due to the presence of mutant SOD1-G93A, rather than over-expressed SOD1 per se.
The significantly higher number of Olig2+ MN progenitor cells in the wt non-Tg astrocyte CM supports the idea that normal astrocytes favour MN development potentially by secreting supportive and/or trophic factors that promote MN progenitors. The positive role of astrocytes in promoting MN growth and maturation in in vitro cultures is already established . Wild-type and mutant SOD1 astrocytes produce substantial amounts of functionally-variable factors that can positively or negatively affect MN survival. Such factors include trophic factors (GDNF -glial-derived neurotrophic factor, NGF) [30, 31], pro-inflammatory/inflammatory proteins (iNOS -inducible nitric oxide synthase, cystatin-C, interferon-α, prostaglandin-D2) [32, 33], proteases (complement 3α,β) and protease inhibitors, carrier proteins (apolipoprotein E, IBP-2 -insulin-like growth factor binding protein-2), extracellular matrix binding proteins (cyclophilin-A) and anti-oxidant proteins (peroxiredoxins) . Our study extends current knowledge by showing that astrocytes also positively affect MN progenitor cells, potentially governing Olig2+ cell-proliferation or Olig2+ cell-survival.
Unlike wt non-Tg astrocyte CM, Tg SOD1-G93A astrocyte CM does not favour MN progenitor cell growth: similar numbers of Olig2+ cells are found in Tg SOD1-G93A CM and in control non-conditioned medium. The relatively high numbers of differentiated MNs found with SOD1-G93A CM, compared to control non-conditioned medium, however, suggests that the mutant astrocyte CM does support MN differentiation/survival. It is therefore likely that a number of the aforementioned factors that are produced by astrocytes and that affect MN survival are secreted in the conditioned medium and are also able to affect MN progenitor cell survival, growth or differentiation.
Our findings support a previous study that shows a halving in the number of primary and ES cell-derived MNs when cultured in Tg SOD1-G93A astrocyte CM compared to wt non-Tg astrocyte CM . Our results differ from this study, however, in that they provide no evidence for MN death through increased apoptosis of MN progenitors or MNs: nuclear fragmentation was not increased by SOD1-G93A CM, nor do we observe a significant decrease in Olig2+ MN progenitor cells or MNs in Tg SOD1-G93A astrocyte CM compared to the baseline level in the presence of control non-conditioned medium. Why might our findings differ from this study, that demonstrated neurotoxicity by SOD1-G93A astrocytes mediated through the recruitment of the Bax-dependent death machinery? Notably, in our study, we analysed the effects of SOD1-G93A CM at an earlier time-point. Potentially, then, the neurotoxic effects of SOD1-G93A CM are realised later than the effects we examine here. While we cannot exclude the possibility that cell-death (through non-apoptotic pathways) contributes to the reduced numbers of MN progenitor cells, our data indicate that the mutant SOD1-G93A in astrocytes affects a secretory mechanism/product which renders the CM less supportive/trophic to MN-progenitors, potentially affecting either Olig2+ cell-proliferation or Olig2+ cell-survival. Thus, the beneficial effect observed with wt non-Tg CM is likely due to the presence of a supportive factor(s) that is absent or reduced from the Tg SOD1-G93A CM.
We also determined whether the effects of Tg SOD1-G93A and wt non-Tg astrocyte CM were specific to MNs and their progenitor cells by examining the effect on Lhx1/5+/Hb9- interneurons. Both the Tg SOD1-G93A and wt non-Tg CM were as trophic/supportive to interneurons as the control medium indicating that mutant SOD1-G93A in astrocytes did not affect interneurons and that the effects of wt non-Tg and Tg SOD1-G93A astrocyte CM were selective for MNs and MN progenitor cells. This is in agreement with Nagai et al. who reported no effects on primary spinal GABAergic or dorsal root ganglion neurons and ES cell-derived interneurons grown in SOD1-G93A compared to non-Tg astrocyte CM .
Astrocytes are actively implicated in the neurodegeneration in ALS. The exact mechanisms by which mutant SOD1 in astrocytes can exert negative effects on MNs and MN-progenitors still remain obscure, although existing evidence indicates that astrocytes exert their effects on MNs through several different mechanisms. Our study extends current knowledge by showing a negative effect of the SOD1-G93A mutation on Olig2+ MN-progenitor cells, possibly revealing new mechanisms of MN loss at the early stages of MN development.
Primary antibodies used were: anti-Olig2 rabbit polyclonal (Chemicon), anti-Lim1/2 (4F2) mouse monoclonal (Developmental Studies Hybridoma Bank), anti-Islet1 (4D5) mouse monoclonal (Developmental Studies Hybridoma Bank), anti-Hb9/MNR2 (5C10) mouse monoclonal (Developmental Studies Hybridoma Bank), β3-tubulin (class 3 beta-tubulin) mouse monoclonal or rabbit polyclonal (Covance), anti-Ki67 rabbit polyclonal (Novocastra). Secondary antibodies used were anti-rabbit IgG-Alexa 594 and anti-mouse IgG-Alexa 594 (Molecular Probes), anti-mouse IgG-Cy5 (Jackson laboratories).
Animal ethics statement
All experiments were conducted according to the Animal (Scientific Procedures) Act 1986, under Project License 40/3089 reviewed and approved by the University of Sheffield Ethical Review Sub-Committee, and the UK Animal Procedures Committee (London, UK). The UK Home Office code of practice for the housing and care of animals used in scientific procedures was followed. We adhere to the ARRIVE guidelines for reporting animal research .
Mouse embryos at E10.5 were washed with PBS and fixed in 4% PFA for 2 hours at 4°C, then rinsed with PBS and incubated in 0.2M phosphate buffer with 30% sucrose at 4°C overnight. Whole mount embryos were sectioned in slices of 15 μm thickness using a cryostat at -25°C. Slices were collected on glass slides, allowed to dry for 30 min-1 hour, then washed with PBS, permeabilised with PBS/1% goat serum/0.1% Triton X-100 and incubated with primary antibodies at 4°C overnight. Incubation with secondary antibodies was performed at room temperature for 1 hour. The specimens were mounted in Vectashield Mounting medium with DAPI and sealed with cover glass. Microscopy was performed using ZEISS Axio Imager.Z1 microscope and AxioVision 4.6.3 software.
Cell cultures were fixed with 4% paraformaldehyde, permeabilised with PBS/ 2% goat serum/ 0.2% Triton X-100 and incubated with primary antibodies at 4°C overnight. Incubation with secondary antibodies was performed at room temperature for 1 hour and the specimens were mounted in Vectashield Mounting medium with DAPI. A ZEISS Axio Imager.Z1 microscope was used and images were captured using AxioVision 4.6.3 software. Islet1+, β3-tubulin+ and Olig2+ cells were counted in 44 random fields and co-expression of the markers was estimated as a percentage of Olig2+ cells. For apoptosis assessment of Olig2+ and Hb9:eGFP+ cells, apoptotic nuclei exhibiting chromatin condensation and nuclear fragmentation after DAPI-labelling were counted in a total of 30 random fields per condition. For the conditioned media experiments, Olig2+, Hb9:GFP+ and Lhx1/5+ cells (the mammalian orthologue of chick Lim1/2, recognised by the anti-Lim1/2 antibody) were counted in 30 random fields per technical replica of each of the conditions (control, wt non-Tg or Tg) and per experiment and calculated as the percentage of total cells (DAPI nuclei) per field. The percentages calculated from similar conditions within each experiment were pooled together. The mean percentages of positive cells for each marker and per condition were statistically analysed.
The data used for the statistical analyses were collected from n independent biological replicates as noted in the figure legends. In each biological replica, there were 3 technical replicas per condition (control medium, transgenic or wild-type non-transgenic mouse). Ten random fields per technical replica were used for cell counting. Thus at least 30 random fields were used per condition and per experiment; therefore at least 90 random fields were counted in total. Each field contains between 250–300 cells. Therefore for each experiment, a sample size of at least 7500 cells was used per condition. Statistical analysis was performed using GraphPad Prism 5.0 software. Data were examined and fitted a normal distribution and therefore were analysed using one-way ANOVA followed by Tukey’s multiple comparison post-test, with Confidence Interval 95% and alpha=0.05. Differences were considered significant for P values less than 0.05. For apoptosis assessment, association of the number of apoptotic cells with the media was examined using the Chi-square test with 95% Confidence Interval.
Calculation of differentiation/survival coefficient
For each condition (control, wt non-Tg or Tg conditioned medium) the number of Olig2+ and eGFP+ cells was used in the following formula:
Differentiation/survival coefficient= Y/X *100; where X is the mean percentage of Olig2+ cells of the treatment group; Y is the mean percentage of eGFP+ cells of the treatment group.
The formula translates as follows: In a total of 100 cells, X cells are Olig2+ and Y cells differentiate to eGFP+ cells. Therefore, in 100 Olig2+ cells the proportion of cells to differentiate/survive towards eGFP+ cells is Y/X *100.
Preparation of SHH-N protein
SHH-N protein containing culture supernatant was prepared as described previously . Briefly, 3 days post transfection of a ShhN-pIRES2-eGFP construct into HEK/293T cells, the culture supernatant was collected and concentrated up to 10× or 25× by repetitive centrifugation in columns of a 10 kDa threshold (Amicon Bioseparations) according to the manufacturer’s instructions.
Preparation of murine primary astrocyte cultures
Primary astrocyte cultures were prepared from the cortices of SOD1-G93A (B6SJLTg(SOD1*G93A)1Gur/J purchased from Jackson Laboratories), WT SOD1 and non-Tg littermate neonate 1–2 day old (p1-p2) mice. The total number of mice used were, eight Tg SOD1-G93A and ten wt non-Tg mice from four litters, six Tg WTSOD1 and six wt non-Tg from 3 litters. The cortices were stripped of meninges, washed and triturated in Hank’s balanced salt solution (HBSS) with Ca2+/Mg2+ containing 0.04% trypsin (Sigma), 0.1 mg/ml collagenase (Calbiochem) and 0.05 mg/ml DNaseI (Sigma). Following trituration, the enzymatic process was terminated by addition of an equal volume of complete medium [Dulbecco’s modified Eagle’s medium (DMEM, Cambrex), 10% heat inactivated fetal calf serum (FCS, BioSera), 100 units/ml penicillin and 100 μg/ml streptomycin (Gibco)] and the cells plated in complete medium [10% FCS, 2 mM L-glutamine, 100 U/ml Penicillin and 100 μg/ml Streptomycin] in a T25 (P1). The cell preparations were allowed to attach. After 48 hours, the medium with any cell debris was removed, cells were washed once with PBS and fresh complete medium was added. Astrocytes and microglia were allowed to grow to confluency for 2 weeks.
Purification of astrocytes from microglia
The overlying microglia cells were removed by shaking overnight on a rotatory shaker (Weiss Gallenkamp) at 37°C between 180-220 rpm. Pure astrocyte cultures were next established by mild trypsinisation (0.25% trypsin and 1mM EDTA in HBSS (-Ca/Mg), added in a ratio of 1:2 with serum-free DMEM/F12), followed by trypsinisation with 2.5% trypsin in PBS and trituration up to single cells. Trypsin was inactivated with complete medium and the suspension was centrifuged. The astrocytes were plated in complete medium in T25 flasks (P2) and allowed to grow to confluency for 10 days before harvesting for conditioned medium.
Preparation of astrocyte conditioned medium
Conditioned medium was prepared by incubation with the astrocytes. The maintenance medium was removed from the cultures and astrocytes were rinsed with PBS. N2B27 medium (see below) was added and the medium was conditioned for 48 hours. Conditioned medium was collected, centrifuged to remove any cells present and stored at 4°C to be used immediately.
Differentiation of mouse ES cells in monolayer culture
MNs expressing eGFP were derived from the transgenic Hb9:eGFP mouse ES cell-line HBG3  (generous gift from Professor Thomas Jessell, Columbia University). Mouse ES cells were removed from the flask by trypsinisation, resuspended in mESC-medium [DMEM (4.5 g/L glucose and 0.11 g/L sodium pyruvate), L-glutamine (2 mM), penicillin/streptomycin (100 μg/ml) (all from Gibco), 15% FCS (Globepharm) and 0.1 mM β-mercaptoethanol (Sigma)] and plated on tissue culture plastic substrate pre-coated with 0.1% w/v gelatin overnight. Mouse ES cells-medium was next replaced by N2B27 (1:1) medium. N2 consisted of DMEM:F12, BSA fraction-V (50 μg/ml, Gibco), insulin (25 μg/ml), transferrin (100 μg/ml), progesterone (20 nM), putrescine (100 μM), sodium selenite (20 nM) (all from Sigma), L-glutamine (2 mM), penicillin/streptomycin (100 μg/ml). B27 consisted of neurobasal medium (Gibco), B27 (1:50), L-glutamine (2 mM), penicillin/streptomycin (100 μg/ml). The differentiating cells were cultured in N2B27 for 7 days, RA (0.1 μM) and SHH-N (1×) added on days 3 and 4. On day 7, the cells were trypsinised and replated on PDL (10 μg/ml)/laminin (5 μg/ml) coated 8-well chamber slides at 5×104 cells/cm2 in control N2B27 or astrocyte conditioned N2B27 supplemented with bFGF (10 ng/ml) for 2 days. After 2 days, bFGF was withdrawn and fresh control or conditioned N2B27 were added. The differentiation cultures were grown for another 3 days, prior to immunocytochemical analysis.
Amyotrophic lateral sclerosis
- ES cells:
Embryonic stem cells
Nerve growth factor
We thank Professor Thomas Jessell (Columbia University) for the HBG3 mESC line. This study was supported by the Department of Neuroscience (PJ Shaw) and the MRC Centre for Developmental and Biomedical Genetics (M Placzek) of the University of Sheffield. PJS is supported as an NIHR Senior Investigator.
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