- Technical Note
- Open Access
A high throughput drug screening assay to identify compounds that promote oligodendrocyte differentiation using acutely dissociated and purified oligodendrocyte precursor cells
BMC Research Notesvolume 9, Article number: 419 (2016)
Multiple sclerosis is caused by an autoimmune response resulting in demyelination and neural degeneration. The adult central nervous system has the capacity to remyelinate axons in part through the generation of new oligodendrocytes (OLs). To identify clinical candidate compounds that may promote remyelination, we have developed a high throughput screening (HTS) assay to identify compounds that promote the differentiation of oligodendrocyte precursor cells (OPCs) into OLs.
Using acutely dissociated and purified rat OPCs coupled with immunofluorescent image quantification, we have developed an OL differentiation assay. We have validated this assay with a known promoter of differentiation, thyroid hormone, and subsequently used the assay to screen the NIH clinical collection library. We have identified twenty-seven hit compounds which were validated by dose response analysis and the generation of half maximal effective concentration (EC50) values allowed for the ranking of efficacy. The assay identified novel promoters of OL differentiation which we attribute to (1) the incorporation of an OL toxicity pre-screen to allow lowering the concentrations of toxic compounds and (2) the utilization of freshly purified, non-passaged OPCs. These features set our assay apart from other OL differentiation assays used for drug discovery efforts.
This acute primary OL-based differentiation assay should be of use to those interested in screening large compound libraries for the identification of drugs for the treatment of MS and other demyelinating diseases.
Multiple sclerosis (MS) is a devastating neurological disease, affecting over 2 million patients worldwide, caused by autoimmune-mediated destruction of the myelin sheaths that insulate and protect axons in the central nervous system. Most MS patients initially present with the relapsing-remitting form of MS (RRMS), in which cycles of immune-mediated axonal demyelination (relapse) are followed by periods of remyelination (remission). Over time, however, the majority of RRMS patients exhibit chronic, progressive decline in neurological function. This is believed to be the result of an accumulation of axonal damage, as well as an eventual loss of remyelination capacity . Although current MS therapies for RRMS provide significant relief from relapse, none have yet been demonstrated to prevent disease progression and none have been effective in treating progressive forms of MS. All of the disease-modifying therapies approved for treatment of RRMS do so by targeting the pathologic immune response . Currently, there are no therapies that function to directly protect or restore myelin, and identifying such therapies has been the focus of several groups in the field [3–7].
We have developed a high throughput drug screening assay to identify new therapeutic agents that accelerate the differentiation of immature OPCs into mature, myelin-producing OLs. The hope is that these newly differentiated OLs will accelerate the remyelination of axons following an immune attack. Here, we report the results of our screening campaign to identify drugs that stimulate oligodendrocyte differentiation. It is noteworthy that the assay that we employed differs in some details from those reported by others including (1) an OL toxicity prescreen which enabled lowering the concentrations of toxic compounds and (2) the utilization of freshly purified, non-passaged OPCs. We have screened the NIH collection of known drugs—a library of 727 drugs that have been approved for the treatment of various indications. Our screening efforts confirmed the activity of several drugs identified by other groups [3, 6, 7]. More importantly, we report the identification of a number of novel OL differentiation-promoting compounds not previously detected in other screening campaigns.
Development of an oligodendrocyte differentiation assay using acutely purified OPCs
In order to identify compounds with the potential to promote OL differentiation in vivo and thereby enhance remyelination, we first wanted to establish an in vitro assay system that would closely mimic conditions in vivo. To do this, we started by using OPCs acutely isolated from postnatal day 6–7 (P6–7) rat brains by O4 immunopanning . This allowed us to obtain an enriched population of primary OPCs that could be used directly in cell culture assays without the need for extensive passaging and expansion in vitro. OPCs were plated directly onto a biological substrate (PDL/laminin) in 96-well view plates at moderate density to allow for sufficient room to expand processes during differentiation. We plated cells in serum-free medium lacking OPC mitogens (no PDGF or FGF) to allow a basal level of OL differentiation to commence, and as a positive control added thyroid hormone (T3, 40 ng/ml) to accelerate differentiation (Fig. 1, flow scheme) . We found that T3 was able to consistently and significantly promote OL differentiation over the 0.1 % DMSO negative control, as measured by MBP expression after 4–5 days in culture in these conditions (Fig. 2a, b).
To quantify the extent of OL differentiation occurring in treatment conditions, we measured the overall amount of MBP expression/cell (see “Methods” section). Figure 2a depicts the mask created over MBP staining under which the MBP expression was quantified. The calculated MBP expression (OL differentiation) was then scaled to internal plate negative (0.1 % DMSO, set to 0) and positive (40 ng/ml T3, set to 100) control wells to generate percent OL differentiation score relative to the efficacy of positive control T3. This analysis of OL differentiation generated consistently significant results when T3 was compared to the DMSO negative control (Fig. 2b, inset). We used this analysis to determine the T3 dose response relationship and the EC50 value of 3.75 pg/ml (Fig. 2c).
OL toxicity assessment of the NIH Clinical Collection (NCC) library of known drugs
Having established a consistent assay for measuring OL differentiation in vitro, the next step was to utilize this assay to assess the ability of a wide array of compounds to promote OL differentiation. Prior to library screening, we first established the maximum non-toxic dose of each compound in the library. Our rationale was that there may be a number of compounds that could be toxic to OPCs cultured in serum-free media when applied at high doses, but which may be beneficially active at lower doses. Consequently, these beneficial activities would be missed if compounds were only tested at high, toxic doses. Therefore, we added each compound in the NIH clinical collection (NCC) library to OPCs at 10, 1, and 0.1 µM concentrations. Three days later, we assessed viability of the treated cells by measuring AlamarBlue fluorescence, a measure of cell viability (see “Methods” section). We found that 17.7 % of the compounds tested were significantly toxic to cultured OPCs at 10 µM, but non-toxic at lower doses. An additional 9.5 % of tested compounds were significantly toxic even at lower tested doses (Additional file 1: Table S1). Appropriately, we established three sets of screening concentrations for library compounds: non-toxic compounds were tested at 10 and 2 µM, slightly toxic compounds (only toxic at 10 µM) were tested at 2 and 0.4 µM, and very toxic compounds were tested at 0.4 and 0.08 µM.
NCC library screening for compounds that promote OL differentiation
Screening the NCC library of 727 known and FDA-approved drugs allowed us to test structurally distinct compounds with known safety profiles and biological activity in humans. Having established the peak non-toxic doses at which to test the NCC library compounds, we next screened this library using the acute OL differentiation assay. All compounds were tested at two concentrations, with positive (T3) and negative (0.1 % DMSO) control wells included on each assay plate. Additional file 2: Table S2 contains all of the acute OL differentiation assay NCC library screening data.
Hits were classified as compounds that increased OL differentiation from baseline to at least 50 % of T3-promoted levels. To evaluate efficiency and validity of our screening method, we used a scatter plot to visualize compounds relative to three standard deviations (SD) from the mean (Fig. 3a). While not a criterion in our assay for hit selection, it provided a common statistical assurance that we were well out of false-positive hit rate (0.15 %) range. This was also confirmed visually when plotted alongside our ≥50 % T3 threshold (Fig. 3b). Positive control T3 versus DMSO values from the entire screen for OL differentiation were highly statistically significant per assay plate (Fig. 3b, c) and averaged over entire screen (Fig. 3c, inset) as well as robust (overall Z prime = 0.2), indicating an acceptable screen window and reproducibility. We identified 36 actives (5 % primary hit rate) able to promote OL differentiation at one or both concentrations tested (Fig. 3d; Additional file 2: Table S2). Two of these compounds were T3 and the T3 precursor thyroxine (T4), known promoters of OL differentiation, and thus not followed up in future studies.
Independent confirmation and validation of identified hits
We next confirmed the differentiation-promoting activity of the 34 remaining identified compounds. We obtained all 34 hit compounds from various independent vendors to test in our OL differentiation assay. All compounds were tested at eight concentrations in at least two biological replicate experiments to generate dose-response curves for each candidate hit compound. Of the 34 initial hit compounds tested in this way, 26 (72 % hit confirmation rate) reproducibly promoted OL differentiation in a dose dependent manner (Table 1; Figs. 4, 5, 6, 7, 3d). Analysis of the EC50 values for each compound enabled the ranking of compound within each class. The average potency EC50, ranged from 30 nM to >20 µM (Table 1; Figs. 4, 5, 6, 7). Figures 4, 5, 6, 7 show each hit compound with the chemical structure, a representative MBP/DAPI screening image demonstrating numbers of OLs/field and OL morphology, and a representative OL differentiation EC50 curves. Table 1 shows the calculated average EC50 values for induction of differentiation obtained from independent biological replicates for the top hits from our initial OL differentiation screen. Based on the available literature on these previously characterized compounds, we grouped the hits by known mechanisms of action. Notably, our OL differentiation screen identified compounds from several distinct drug classes. Some of the hit compounds had been independently identified by other OL differentiation screening paradigms [3, 6, 7] (Table 2), whereas the refinement of using a toxicity prescreen and performing the assay on acutely purified OPCs allowed us to identify 16 additional novel compounds.
Although we observed that all actives could promote not only MBP expression, but also a morphological shift typical to OL differentiation (Figs. 4a–h, 5 i–p, 6q–x, 7y–c1), we nonetheless confirmed that active compounds could promote other markers of OL differentiation. In addition to MBP, we tested the ability of the 27 confirmed hit compounds to promote expression of 2′, 3′-cyclic-nucleotide 3′-phosphodiesterase (CNPase) and Galactocerebroside (GalC), two additional established markers of OL differentiation [10, 11]. All 27 confirmed hit compounds promoted CNP and GalC in our acute OL differentiation assay (Additional file 1: Figure S1A, B is shown).
Development of an acute OL differentiation compound screening assay
In an effort to identify possible therapeutic candidate compounds for multiple sclerosis and other demyelinating diseases, we have developed novel oligodendrocyte assays amenable to high throughput screening. We have established the first OL differentiation assay to utilize freshly purified, unpassaged OPCs. This distinguishes our assay from other OL differentiation assays used for drug discovery efforts, which used highly passaged OPCs or iPS-derived OPCs. Additionally, we used an OL toxicity pre-screening assay to customize our library screening efforts to account for compounds that may be toxic at high concentration, but efficacious at lower concentrations. This is an unusual precaution to take, as it is standard practice to screen an entire library at a single concentration (e.g., 10 µM) to minimize labor and time. Such a library is thus very different than a typical HTS library composed of novel, unknown and un-optimized compounds. This approach proved fruitful, as we identified several OL differentiation-promoting drugs in the NCC library that were not identified in another screen  that used this same library. Below is a discussion of some of the top hit compounds identified from our OL differentiation assay and their possible relevance to multiple sclerosis.
Other in vitro OL differentiation assays used for compound screening have only assessed differentiation using purified OPCs adapted to culture conditions by multiple passages , or differentiated from induced pluripotent stem cells . Mei et al. developed an HTS assay incorporating OL differentiation in the presence of inert micropillars allowing the quantification of pillar wrapping as a surrogate for myelination . We have noted the technical similarities and differences of our OL differentiation assay with these other studies in Table 2. The lead compounds that overlap with our findings are summarized in Table 3 and represent only about half of the leads we identified (in particular, the tricyclic anti-depressants and muscarinic drug classes), with the remaining compounds being identified and reported for the first time in our screen.
It should be noted that this in vitro OL differentiation screening assay only identifies compounds that promote OL differentiation and does not address whether the differentiated OLs also promote myelination. Additionally, this assay is performed in purified monoculture absent of other cell types that influence OL differentiation and myelination, e.g. neurons and astrocytes. Furthermore, this assay is performed under ideal OL differentiation conditions, unlike the inflammatory conditions present demyelination lesions. One should also be aware that the compounds identified in this screen have only been tested on rat OPCs. Mei et al. demonstrated cross-species compound activity in their OL differentiation assay, however, compounds identified from our OL differentiation screen have not been verified on mouse or human cells. Testing these compounds on OLs derived from human iPSCs would greatly increase the potential therapeutic value of these compounds. Nevertheless, OL differentiation-promoting compounds have the potential to increase the number of myelination competent OLs and therefore facilitate myelination. This hypothesis has been supported by the previously published work mentioned above that have identified pro-OL differentiating compounds that have facilitated myelination in vivo [3, 6, 7].
Confirmed hits group into multiple mechanistic classes
We found that the hits identified in the OL differentiation assay (Table 1) could be assigned into six broad categories, falling into common functional or structural categories. We have grouped these compounds into possible signaling pathways that feed into OL differentiation (Fig. 8).
Benztropine, donepezil, oxybutynin, vesamicol, and ipratropium all perturb the muscarinic acetylcholine signaling pathway. Indeed, the muscarinic receptor pathway has been previously implicated in OL differentiation and benztropine, oxybutynin and ipratropium were identified in other OL differentiation screens [3, 6, 7] (see Table 2, comparison). To supplement this class, we also tested clemastine, another muscarinic receptor antagonist characterized by Mei et al.  and found it too could promote OL differentiation in our assay similar to benztropine (Table 1; Figs. 4, 5, 6, 7; Additional file 1: Figure S1A). Both benztropine and clemastine have shown efficacy in stimulating remyelination in in vivo models [3, 6]. Previous work has demonstrated that M2 muscarinic receptor agonism has mitogenic activity increasing PDGFR∝ expression to keep OPCs in a proliferative state . Further, it was recently shown that treatment with solifenacin, an FDA-approved M3 muscarinic receptor antagonist, promoted oligodendrocyte differentiation of transplanted hOPCs in hypomyelinated shiverer/rag2 brain .
A second compound class uniquely identified by our OL differentiation assay was the selective estrogen receptor modulators (SERMs): raloxifene, toremifene, and tamoxifen. These compounds may be acting through the estrogen β receptor (EβR) and the PI3 K/Akt/mTOR signaling pathway, previously shown to stimulate OL differentiation and remyelination in vivo in demyelinating animal models of MS [14–18].
A third compound class includes perphenazine, prochlorperazine, fluphenazine, trifluorperazine, and QTP: five tricyclic antidepressant molecules with structural similarity believed to act primarily as serotonin/norepinephrine reuptake inhibitors (SNRIs) by blocking the serotonin transporter (SERT) and the norepinephrine transporter (NET). It must also be noted that these compounds also have significant off-target activity, including muscarinic antagonistic activity among others, which may account for OL differentiation-promoting activity. Perospirone, escitalopram, citalopram, metylperon, and bupropion are loosely grouped together as a class of non-tricyclic antidepressants that, with the exception of escitalopram and citalopram, do not share much structural similarity. These compounds have the properties of being selective serotonin reuptake inhibitors (SSRIs—escitalopram, citalopram, bupropion) or dopamine receptor antagonists (perospirone, metylperon). Since OPCs/pre-myelinating OLs express SERTs, NETs, serotonin receptors, and dopamine receptors , it is possible that the antidepressant class of compounds may function by modulating neurotransmitter levels and/or neurotransmitter receptor activity to facilitate OL differentiation .
Salmeterol, betaxolol, and esmolol all interact with the adrenergic receptor (AR) pathway . There is a paucity of data on AR function in OL differentiation. ARs are expressed in OL precursors  and the ∝1-AR has been demonstrated to play a role in OL specification and differentiation in vivo .
Finally, a broad class of ion channel modulators was identified: ifenprodil, benproperine, proxymetacaine, dofetilide, and dimethylphenylpiperazinium (DMPP). DMPP acts through the stimulation of the nicotinic acetylcholine receptor (nAChR) which may play a role in OL differentiation. Interestingly, it was recently demonstrated that donepezil-induced OL differentiation was mediated by the nACHR. Ifenprodil is an NMDA receptor (NMDAR) antagonist. It has been shown that NMDARs are present in precursor, immature and mature OLs [23, 24]. One additional active compound, bifonazole, is a known antifungal agent. A number of azole-containing anti-fungals have known effects on ion channels , but it is not known what role these may have in OL differentiation. By interacting with ion channels, these compounds may alter intracellular ion levels within OPCs/pre-myelinating OLs to facilitate OL differentiation .
Relevance to multiple sclerosis
There are many examples where repurposed drugs are making an impact in the field of MS. A few of note are BG-12 (Tecfidera®), a modification of a psoriasis drug; fingolimod (Gilenya®), originally developed for transplantation and alemtuzamab (Lemtrada™), originally an oncology drug. We found that a fair number of our hits aligned with current MS repositioning efforts in terms of patents, preclinical work, and clinical trials and are briefly cited here.
The SERMs represent a promising new class of compounds that promote OL differentiation not identified in other screens. Modulation of the estrogen receptor has been demonstrated to be effective in preventing demyelination in vivo and to stimulate differentiation and remyelination [27–30]. Specifically, raloxifene (Evista®) was shown to be effective in suppressing EAE . The pregnancy hormone estriol (Trimesta™) has shown efficacy in a clinical trial of MS reducing the lesion numbers and volumes .
A number of hits that we identified are covered in patents for oligodendrocyte directed differentiation. Notably trifluoperazine (Stelatzine®), benztropine (Cogentin®), and ipatropium (Atrovent®) are patented for the use of neurotransmitter receptor modulating agents for inducing OL differentiation, as well as methods for treating subjects with such agents in a demyelinating disease.
Other hits have been evaluated or will soon be tested in human MS trials. QTP (Seroquel XR®), an antipsychotic approved for schizophrenia is currently in clinical trials to determine tolerability to people with relapsing remitting multiple sclerosis (RRMS) and progressive MS (Clinicaltrials.gov identifier: NCT02087631). Selective serotonin re-uptake inhibitors (SSRIs) such as nitalapram (Celexa®) and escitalopram (Lexapro®) have also been in human MS trials. Nitalapram is one of three other SSRIs tested as an add-on with fingolimod, a current immunomodulatory treatment for MS (REGAIN Trial NCT01436643) in RRMS patients with depression. Escitalopram has been in a study to test improvement of depression in patients of MS or ALS (Trial NCT00965497). Donepezil (Aricept®), used as a treatment for dementia, has been used in a study to improve cognitive dysfunction in MS patients (NCT00315367) [33–35]. Oxybutynin (Ditropan XL®) is used currently in symptom management for MS to treat overactive bladder in MS (SONIC trial NCT00629642). Clemastine fumarate (Tavist®) originally approved as a first-generation antihistamine, is active in a current study to assess the drug as a remyelinating agent is RRMS patients (ReBUILD trial NCT02040298). Though not a hit in our screen, albuterol (compound #4, Additional file 3: Table S2), a short acting β2 adrenergic receptor agonist, was tested in a clinical trial (Trial NCT00039988) as an add-on therapy to capaxone (glatiramir acetate) for patients with RRMS and showed improved clinical outcomes. Perhaps the longer acting β2 adrenergic receptor agonist, salmeterol, which we identified in our screen, may also provide some clinical efficacy.
To our knowledge, the remainder of our confirmed hits has not been tested in any demyelinating diseases.
We have demonstrated here an OL differentiation assay with the robustness, scale and reproducibility amenable to HTS drug discovery. The assay was designed to preserve primary cell, in vivo-like characteristics in culture by using only acutely isolated cells (OL differentiation assay) and limited subculture to a single expansion (OL toxicity assay). Thus, we avoided undesirable changes in cellular phenotype (e.g. gene expression and/or unstable karyotypes) that multiple cell passages or derivation from large-scale stem cell cultures may introduce [3, 7, 36, 37]. Additionally, the OL toxicity pre-screen allowed us to reduce the top concentrations of toxic compounds and was essential to identifying compounds that were more efficacious at lower concentrations. Future studies should focus on testing these novel OL differentiation-promoting compounds both in vitro with human cells as well as in vivo models of MS. Furthermore, this assay is well-suited for screening larger compound libraries with novel chemical matter.
High glucose Dulbecco’s modified eagle medium (DMEM), neurobasal medium (NB), Earle’s balanced salt solution (EBSS), l-glutamine, fetal bovine serum (FBS), penicillin/streptomycin, sodium pyruvate, diamidino-2-phenylindole, dilactate (DAPI) were purchased from life technologies (Carlsbad, CA, USA). Normal goat serum, forskolin, triiodothyronine (T3, thyroid hormone), vitamin B12, hydrocortisone, d-biotin, apotransferrin, putrescine, progesterone, sodium selenite, poly-d-lysine (PDL), recombinant human (rh) insulin, bovine serum albumin, N-acetyl-l-cysteine, sodium phosphate (mono- and dibasic), sodium chloride, tris base, l-lysine, sodium azide, tunicamycin and DMSO were obtained from Sigma-Aldrich (St. Louis, MO, USA). Trace elements B, Dulbecco’s phosphate buffer saline (dPBS) and trypsin 0.05 %-EDTA were purchased from Mediatech, Inc. (Manassas, VA, USA). Human ceruloplasmin was purchased from EMD Millipore (Billerica, MA, USA). Recombinant rat (rr) CNTF, rrIFNγ, rrTNFα, rhNT-3 and rhPDGF-AA were purchased from PeproTech (Rock Hill, NJ, USA). Laminin was obtained from Trevigen (Gaithersburg, MD, USA). DNase, papain and ovomucoid inhibitor were purchased from Worthington Biochemical Corporation (Lakewood, NJ, USA). Paraformaldehyde solution was purchased from Electron Microscopy Science (Hatfield, PA). alamarBlue® (AB) was purchase from AbD Serotech (Killington, UK). Packard 96-well Viewplates were purchased from Perkin Elmer (Waltham, MA, USA). Falcon TC 96-well plates were purchase from corning (Corning, NY). Additional file 4: Table S3 lists the primary antibodies and their dilutions used in this study.
All compounds in the NIH Clinical Collection (NCC) library were supplied in DMSO at 10 mM in 96-well plates. Hit compounds were purchased as powders and stock solutions were dissolved in DMSO to 10 mM (see Additional file 2: Table S1, Additional file 3: Table S2 for complete listing of compounds).
Isolation and culture of neonatal rat OPCs
All animal work was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by the Institutional Use and Care and Use Committee at the Molecular Medicine Research Institute (Sunnyvale, CA). Animals used for OPC isolation in these studies were euthanized by decapitation. OPCs from brains of P6-P7 Sprague–Dawley rat pups (Charles River, Wilmington, MA, USA) were enriched by immunopanning as previously described (Dugas et al. 2006). Briefly, single cell suspensions were obtained from papain-digested neonatal brains and depleted of mature glial cells by successive panning with RAN-2- and GalC-coated plates, followed by enrichment for OPCs using O4-coated plates. OPCs were plated in differentiation media (DMEM, 100 U/ml Penicillin/100 µg/ml streptomycin, 2 mM l-glutamine, 1 mM Na pyruvate, 5 µg/ml insulin, 5 µg/ml N-acetyl-l-cysteine, 1× trace elements B,10 ng/ml d-Biotin, 100 µg/ml BSA, 100 µg/ml apo-transferrin, 16 µg/ml putrescine, 60 ng/ml progesterone, 40 ng/ml sodium selenite 5 ng/ml forskolin, 10 ng/ml CNTF, 1 ng/ml NT-3).
Oligodendrocyte toxicity assay
OPCs were expanded in vitro by seeding into PDL-coated tissue culture flasks at 1000–2000 cells/cm2 in differentiation media supplemented with 10 ng/ml PDGF-AA. Proliferating OPCs were fed every 2–3 days and supplemented with 2–3× concentration of PDGF as needed to prevent OPC differentiation. After 6–7 days of proliferation, OPCs were harvested by trypsinization, plated into PDL-coated 96-well Falcon plates and centrifuged at 200×g to facilitate cell attachment, survival, and even distribution of cells. Expanded OPCs were seeded in differentiation media at 10,000 cells/well and incubated for 2 h at 37 °C, 10 % CO2 prior to addition of compounds. The NCC library was diluted and added to cells at 10, 1, and 0.1 µM; each concentration was tested in quadruplicate. As a positive control for the induction of toxicity, 5 ng/ml tunicamycin was added to 8 wells in each plate. Three days later, a 1:10 dilution of alamarBlue® (AB) was added to each well and cells were incubated 4 h at 37 °C, 10 % CO2. AB fluorescence was measured using a PerkinElmer Victor II fluorescence microplate reader (PerkinElmer, Waltham, MA) with 560 nm excitation/590 nm emission filters. For library screening, the highest concentration of each compound was adjusted to a minimally toxic concentration based on this toxicity data. Compounds were additionally tested at a second concentration that was 1/5th of the top concentration. The final concentration of DMSO in each well was 0.1 %.
Acute oligodendrocyte differentiation assay
Acutely enriched OPCs were plated in differentiation media at 5000 cells/well into PDL/laminin coated 96-well view plates and centrifuged at 200×g to facilitate cell attachment, survival, and even distribution of OPCs. OPCs were pre-incubated for 1–2 h at 37 °C in 10 % CO2, followed by the addition of test compounds in quadruplicate. Controls were added in eight replicate wells, negative control = 0.1 % DMSO; positive control = 40 ng/ml T3. The day of OPC plating was considered DIV0. On DIV4, cells were fixed, immunostained for myelin basic protein (MBP) expression, imaged and quantified as described below.
Immunofluorescence staining and imaging
Following compound treatment, media was removed leaving 50 μl/well using an ELx405 microplate washer (BioTek, Winooski, VT, USA), the automated plate washer was also used for all subsequent washing steps during the staining. Cells were fixed for 14 min with 4 % paraformaldehyde at room temperature (RT). Following fixation, plates were washed with 1 ml PBS leaving 50 μl/well. Cells were then incubated in blocking buffer (10 % normal goat serum (NGS) diluted in antibody buffer: 150 mM NaCl, 50 mM Tris Base, 1 % BSA, 100 mM l-lysine, 0.04 % sodium azide, pH 7.4), with 0.4 % Triton X-100 for 1 h at RT, then stained overnight at 4 °C with rat anti-MBP antibodies (Additional file 4: Table S3) diluted in blocking buffer with 0.08 % Triton X-100. The cells were washed and incubated with secondary antibodies and 0.3 μM DAPI for 1 h at RT. After a final wash, 100 μl of PBS was added to each well and plates imaged. Images were captured with a Nikon Eclipse TE-2000-U microscope, Zyla cMOS megapixel camera (ANDOR Technology, Belfast, UK), fitted with an automated stage controlled by NIS Elements AR software 4.0 (Melville, NY, USA). An air 10× lens was used to capture 2–4 images per well with 16 bit resolution, 2560 × 2160 pixels. Images for each assay run were captured using identical camera settings. Images were exported as TIFF files for analysis and quantification.
TIFF files were analyzed using custom algorithms created with IN Cell Investigator Developer Toolbox (GE Health Sciences, Piscataway, NJ, USA). For each well of OL differentiation assay, four images were analyzed per well and the data from the duplicate wells was combined and averaged (total of eight images per test condition). For cytokine protection assay, two images were analyzed per well and the data from triplicate wells was combined and averaged (total of six images per test condition). The overall amount of MBP expression/cell was quantified in each image by calculating the density × area of MBP staining, and normalizing to the total number of DAPI-stained nuclei in the same field. The calculated extent of MBP expression (OL differentiation) was then scaled to internal plate negative (0.1 % DMSO) and positive controls (40 ng/ml T3) to generate percent OL differentiation scores relative to the efficacy of positive control. For the cytokine protection assay, the positive controls were either no insult or 1.1 μM QTP. This analysis consistently generated quantitatively similar results when scaled to internal plate negative and positive control wells.
Relative EC50 analysis
EC50 values were obtained by fitting the data to a sigmoidal dose–response curve-fitting function (Prism, GraphPad, San Diego, CA, USA). Serial dilutions of eight to ten different concentrations with three or four data points per concentration were used for curve fitting. Experiments were repeated at least two times.
For all experiments, assuming normal distribution, two-tailed t-tests were used to evaluate comparisons between two groups.
central nervous system
oligodendrocyte precursor cells
days in vitro
myelin basic protein
high throughput screening
NIH clinical collection
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DL, KLW, ER and JD conceived the assay; DW, KLW designed and performed the experiments; acquired, interpreted, provided intellectual content, statistical analysis of the data, drafted the manuscript, reviewed the manuscript critically and revised its final version; ER, JT, JD, and TC participated in the design of the study, helped revise the manuscript critically; TC and JT additionally gave the final approval of the version to be published. All authors read and approved the final manuscript.
We are grateful to Nicole Edwards for excellent administrative and data analysis support. We thank Russel Rydel for helpful discussions and comments on the manuscript. We gratefully thank Ben Barres for his continual support, guidance and generosity for providing antibodies. We are profoundly grateful to all the individual donors who have donated their time and funds to the Myelin Repair Foundation and the Translational Medicine Center.
The authors declare that they have no competing interests.
Availability of supporting data
Detailed protocols are available on request from D. Leonoudakis and K. Lariosa-Willingham at email@example.com and Karen.Lariosa-Willingham@tevapharm.com
Ethics approval and consent to participate
This study did not use any human subjects, human material or human data. All animal work was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was approved by the Institutional Use and Care and Use Committee at the Molecular Medicine Research Institute (Sunnyvale, CA).
About this article
- High throughput
- Drug screening
- Primary cell-based assay
- Image analysis
- Multiple sclerosis
- Myelin basic protein