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Folia Neuropathologica
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Original article
Heterogeneity of local tissue microenvironment influences differentiation of oligodendroglial progenitors

Joanna Sypecka
,
Anna Sarnowska

Folia Neuropathol 2013; 51 (2): 103-110
Online publish date: 2013/06/26
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- Heterogeneity.pdf  [0.36 MB]
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Introduction

Oligodendrocyte progenitors (OPCs) are NG2-positive cells abundantly populating the young and adult central nervous system (CNS). They are capable of mye­linogenesis, but they are also among the first cells to react to CNS dysfunction [32]. They are known to be affected in many inherited [15,44,54] and acquired disorders, both acute like spinal cord injury and brain trauma [1,6,49] and chronic like intoxication or im­munological diseases [39]. The resulting depletion of functio­nal oligodendrocytes accompanied by ongoing hypo/ demyelination leads to an urgent need for cell replacement therapies based on either recruitment of endogenous progenitors or cell transplantation.

Endogenous OPCs are generated during perinatal gliogenesis and remain scattered across white and grey matter in large quantities [26,36,52]. In adult CNS, they could also be derived from neural stem cells inhabiting the subventricular zone (SVZ) [10,28] and the hilus of the dentate gyrus (DG), a part of the hippocampal non-neurogenic area [23]. Thus, there is a natural and abundant reservoir of cells existing within CNS, which could be mobilized for neurorepair purposes. In the case of inherited diseases leading to oligodendrocyte malfunction and myelin disturbances, the cell transplantation would presumably be the best solution. However, the fate of both recruited endogenous precursors and the transplanted cells is considerably affected by the local tissue microenvironment, composed of a cocktail of active compounds like trophic factors, cytokines, morphogenes and extracellular matrix components [18,22,40]. Over the past decade, the neurogenic po­tential of glia-committed precursors has been intensively investigated. In our previous reports, the ability of the neonatal OPCs to express the spectrum of pro-neuronal markers in the microenvironment created by hippocampal slices was shown. A fraction of the labelled OPCs seeded onto the slices, which migrated and integrated to the tissue, adopted the neuronal phenotype [45]. The results have also revealed that the neurogenic effect could be exerted by paracrine signalling. This points to the presence of soluble active compounds governing cell commitment.

Our observations together with reports coming from other laboratories lead to a question concerning differences in the composition of nervous tissue derived from distinct CNS regions [2,34,46,50]. To address this issue, organotypic slices from the hippocampus (as

a well-recognised neurogenic area) and from the spi­nal cord (where gliogenic signals are assumed to predominate) were subjected to a molecular analysis of those selected factors which regulate crucial cell pro­cesses. Additionally, the ability of these two microenvironments to promote the astrocytic differentiation was studied to verify the postulated multipotency of the oli­godendroglial progenitors.

Material and methods

Oligodendrocyte progenitors isolation and culturing



Oligodendrocyte progenitors were isolated from

a mixed primary glial culture, established from brain hemispheres of neonatal Wistar Cmd:(WI)WU rats.

The procedure was approved by the Local Ethics Committee on Animal Care and Use. The detailed procedure is described elsewhere [22,45]. Briefly, the method is based on sequentially dislodging separate glial fractions (first microglia and subsequently oligodendrocyte precursors, while astrocytes remain strongly adhered to plastic) [24] from a 2-week-old primary culture. The shaken-off progenitors were spun down and the resulting pellet was mechanically dispersed with a 22-m needle in serum-free standard DMEM medium, supplemented with a solution of antibiotics. The cell suspension was purified from contaminating non-oligodendroglial cells by filtration through 80 m and subsequently through 41-m Millipore membranes. The additional step of the OPC purification was based on the poor adhesion of the progenitors to the uncoated plastic, while the other glial fractions stick to the plastic surface within 2-3 hours. After collecting of the supernatant containing floating OPCs, the cells were seeded onto poly-L-lysine-coat­ed cover slips placed in 6-well plates (NUNC) at 2x105/cm2 density and cultured for the subsequent 10 DIV in se­rum-free culture medium.



Organotypic hippocampal culture (OHC)



A hippocampal organotypic culture was esta­blished from the brains of 7-day-old Wistar rats according to the previously described method [38,42]. All the procedures of animal handling practices were accepted by the Lo­cal Ethics Committee on Animal Care and Use. Briefly,

the anesthetized animals were decapitated and their brains were carefully isolated and inserted into ice-cold HBSS (Gibco) buffer. The 400-m thin hippocampal slices, cut by a McIlwain tissue chopper, were placed onto Millicell-CM (Millipore) membranes and inserted in 6-well plates (NUNC). The slices were then cultured in a defined medium composed of DMEM 50%, HEPES, HBSS 25%, horse serum 25% (Gibco), 2 mmol/l L-glutamine, 5 mg/ml glucose, 1% amphotericin B and 0.4% penicillin-streptomycin. The serum concentration in the culture medium was gradually lowered and from the 7th DIV on­wards, the slices were cultured in serum-free conditions. On the 8th DIV the organotypic slices were used for co-culture experiments.



Organotypic spinal cord culture (OSC)



The organotypic longitudinal spinal cord slice culture was established according to the procedure des­cribed elsewhere [19]. The spinal cords were extracted from the same animals used for isolating the hippo­campi. After dissection, 10 mm longitudinal sagittal sli­ces of the spinal cord were cut using a tissue chopper (McIlwain) at a thickness of 350 m and transferred onto a permeable Millicell-CM (4 slices per membrane) and cultured according to the protocol used for OHC.



Co-culturing of OPCs with organotypic slices (OHC/OSC)



The purified OPC fraction was left to adhere to poly-L-lysine-coated cover slips for approximately 1 h and was used for setting up the co-culture experiments with either the spinal cord or the hippocampal organotypic slices. The Millicell-CM membranes containing the slices were transferred to the plates with OPCs and co-cultured in indirect contact (Fig. 1) for the next 5 days in serum-free DMEM supplemented with an AAS antibiotic solution (Gibco). The culture medium was changed every second day. On the 5 DIV, the organotypic slices were gently removed from the membranes with an ultra-thin brush, put into RNAlater Solution (Applied Biosystems) and stored at 4°C until the nucleic acid had been extracted.



Reverse transcription and quantitative real-time RT-PCR analysis



In order to extract total RNA, the Trizol reagent (Invitrogen) was applied and the purified samples were subjected to reverse transcription reaction by application of High Capacity RNA-to-cDNA Kit (Applied Biosystems), following the manufacturer’s instructions. To measure the selected trophic factors (including neurotrophins) and cytokines, the commercial RT2 Profiler™ PCR Ar­ray for rat neurotrophins (SABioscience) was applied according to the supplier’s protocol. The samples containing 50, 75 and 100 ng of cDNA were amplified using SYBR Green PCR Master Mix (Applied Biosystems) and ABI Prism 7500 Sequence Detection System. Each sample was tested in triplicate during three analyses and the parameters selected for the performed PCR reactions were as follows: 2 min at 50°C, 10 min at 95°C, 40 cycles of 15 s at 95°C and 1 min at 60°C. To determine the PCR product specificity, a dissociation curve was plotted and 1.5 % agarose gel electrophoresis was performed to check the amplicon size. The obtained data were normalized against that of the -actin gene and threshold cycle values (Ct) were quantified as fold changes by the 2–Ct method [20].



Immunocytochemical analysis



The cell commitment and differentiation were as­sessed by staining the PFA-fixed cells with a panel of specific antibodies. To ensure the specificity of binding, the cells were immersed in 10% normal goat serum in PBS in at 25°C for an hour and then the primary antibodies were applied overnight. The stages of oligoden­drocyte maturation were verified by applying the following: rabbit polyclonal anti-PDGFR (Santa Cruz) and anti-NG2 (Chemicon) – for the precursor state; mono­clonal anti-mouse against O4 (Sigma), CNP-ase (Sigma) and GalC (Chemicon) – for immature oligodendrocytes; monoclonal anti-mouse anti-MBP (Sigma) for myelinating cells. To identify the generated astrocytes, rabbit polyclonal antibody against GFAP (Dako) was used. Appropriate secondary antibodies, conjugated to either Alexa-488 or Alexa-546 (Molecular Probes), were ap­plied for 1 hour at RT. Before immersing in Fluoromont, the cell nuclei were stained with 5 m Hoechst 33258 (Sigma). The labelled cells were examined using an Axio­vert 25 fluorescence microscope (Zeiss). Four randomly selected fields on each slide were taken by a Videotro­nic CCD-4230 camera and a cell count was done.



Statistical analysis



The data obtained due to molecular and immunocytochemical examinations were subjected to a statis­tical analysis with one-way analysis of variance

(ANOVA) followed by the Bonferroni’s Multiple Comparison Test. All the values were expressed as mean ± SEM, *p < 0.05.

Results

To assess the ability of the oligodendroglial precursor to acquire the astrocytic phenotype in various microenvironment conditions, a purified cell population from neonatal rat brains was co-cultured with organotypic slices derived from distinct CNS regions. Before establishing the OPC co-cultures, both the spinal cord and hippocampal slices were deprived of serum supplement to prevent the cell from being stimulated by additional, undefined compounds. Subsequently, an indirect co-culture system (Fig. 1) was set up to study the influence of the soluble factors released from the organotypic slices into the culture medium on OPCs differentiating into astrocytes. Simultaneously, the OPCs were allowed to spontaneously differentiate in the same, serum-free medium as the control in order to evaluate the potential stimulating effect exerted by the CNS slices. The data obtained as a result of immunocytochemical analysis showed that 99.2 ± 0.92% of OPCs had matured from NG2 antigen expressing cells (Figs. 2A-C) into O4 and GalC-positive oligodendrocytes during the 5-day – in vitro period. Another interesting finding concerned the promotion of astroglial differentiation by slightly elevating the serum content in the culture media. By adding 1% serum, the number of GFAP-positive cells in the differentiating population increased by 2.48 ± 0.8%.

The examination of how the cells differentiated in the co-cultures with organotypic slices led to some more interesting observations. While the GFAP+ cells constituted a very minor population in control experi­ments, their amount increased as much as 18.5 ± 2.31% of the total cell number in the medium continuously conditioned by either hippocampal or the spinal cord slices (Figs. 2D-F). A quantitative analysis of both co-culture types revealed approximately comparative (15-19%) content of astrocytes with no statistically signi­ficant differences.

The observed potent capability of the paracrine signals provided by organotypic slices to trigger astroglial differentiation prompted us to check the expression of the selected cytokines and trophic factors at the mRNA level by means of semi-quantitative molecular methods. The microarray screening for neurotrophins and related factors which are known to be engag­ed in main cellular functions revealed a significantly elevated expression of all of the examined factors in organotypic slices in relation to housekeeping genes (B-actin, ribosomal protein L13A, lactate dehydrogenase A). In turn, a comparison between hippocampal and spinal cord slices showed that out of the 15 ana­lysed factors the expression of nine in the hippo­campal slices was noticeably elevated, two were downregulated and only the other four were similarly expressed (Fig. 3). The factors, of which the mRNA expression is elevated, include neurotrophins such as brain-derived trophic factor (BDNF), nerve growth factor (NGF), ciliary neurotrophic factor (CNTF), glial-derived neuro­trophic factor (GDNF) and other factors too, such as neurotrophin-5 (NTF5), fibroblast growth factor 9 (FGF 9), Signal Transducer and Activator of Transcription protein (STAT4) and glial maturation factor (GMF, isoforms  and ). The factors, which are strongly expressed in the spinal cord, are VGF nerve growth factor inducible protein and neurotrophin 3 (NTF3). Those without noticeably changed expression include leukemia inhibitory factor (LIF) as well as STAT1, STAT2 and STAT3.

Discussion

Over the past decade, oligodendrocyte disorders accompanied by myelin deficit, malformation or its loss have become targets for cell-based therapies. Oligodendrocyte progenitors may be most conveniently used for the complex neurorepair strategies. First of all, they are already glia-commitment progenitors themselves, which considerably reduces the danger of neoplasia and assures their differentiating into myelinating cells [4,12,16,24,43,51]. Moreover, there is a growing list of evidence that OPCs exhibit some important properties of neural stem cells in a conducive microenvironment. They have been shown to be sensitive to being stimulated by the external clues and prove to be multipotential. However, even in the highly stimulus milieu, part of the OPC population is still proliferative.

The enumerated properties could be beneficial to the process of restoring a damaged tissue. While promoting neurogenesis is usually highly desirable, the ability of differentiating into astrocytes might however prove be a serious obstacle. Many CNS injuries are associated with the glial scar formation, which significantly hinders precursors from migrating and delivering anti-inflammatory and trophic factors [9,37,41,50].

The objective of our studies was to assess the ability of OPCs to acquire the astroglial phenotype in

a microenvironment created by the nervous tissue derived from distinct CNS regions. While in controls, all of the progenitors matured into oligodendrocytes expressing myelin components, the medium continuously conditioned by either the spinal cord or hippocampal slices triggered astroglial differentiation of a part of the cultured OPCs. What has been known for a long time is that astrocytes can be derived from common glial precursors in vitro while being cultured in high concentrations of serum [14,30,31,47]. This observation contributed to one of the pioneer terms for describing oligodendrocyte progenitors: O-A2. In our serum free co-culture system with the organotypic slices (i.e. with the preserved tissue organization) the paracrine signals proved to be potent to force the as­troglial commitment of OPCs. There are also reports describing a similar in vivo effect, found in different CNS regions [33,56]. The observation coming from our study concerning the promotion of astroglial differentiation in co-cultures with hippocampal and spinal cord sli­ces are in agreement with the reports about the glial scar formation in injuries occurring to the brain and spinal cord.

The heterogeneity of the nervous tissue microenvironment, suggested by the results obtained in our and other laboratories, prompted us to analyse a spectrum of active compounds that are known to regulate the main biological functions like proliferation, survival, commitment and differentiation. A comparison of data gathered from molecular studies showed that certain crucial factors involved in important biological processes occurring in cells are differently expressed. The ex­pression of nine examined factors (out of fifteen) turned out to be increased in the hippocampal slices when compared to the spinal cord slices, two others were down-regulated, while only four were similarly ex­pressed. These findings prove conclusively that the local tissue microenvironment within the nervous system is heterogenic.

What is worth noting is that among factors being highly expressed in the hippocampus are those exerting the neurotrophic effects: neurotrophins NGF and BDNF [5] as well as CNTF [3,27] and GDNF [7,57]. They supposedly play a role in recruiting new neurons, protecting them and regenerating nerves [13,57]. GMFs were shown to be involved in regulating glia activity and in enhancing the pro-inflammatory responses in a range of selected diseases [53]. Signal Transducer and Activator of Transcription together with FGF-2 are en­gaged in regulating genes responsible for cell proliferation, migration, differentiation, and survival, as well as for neurogenesis and axon growth [8,35]. Up-regulation of those selected genes is presumably associated with the neurogenic regions characteristic of hippocampus.

The specificity of different CNS regions, indicated by the results obtained in the presented study, might significantly modify cell commitment and differentiation. Since therapies based on mobilizing endogenous progenitors or on transplanting stem cells are intensely pursued [11,17,21,29,48], the cell fate in various local microenvironments should be investigated for the purpose of predicting the outcome of the applied treatment.

In conclusion, the presented work shows the substantial differences in the expression of the factors governing the crucial processes involved in oligodendroglial precursors biology between organotypic slices derived from distinct CNS regions. The stated local tissue heterogeneity should be taken into consideration when planning cell-based therapies.

Acknowledgements

We thank Mrs Hanna Winiarska and Mr Lukasz Strojek for excellent technical assistance. This work is supported by the Polish Ministry of Science and Higher Education grant 0345/B/P01/2010/38 and 05728/B/NZ4/ 2011/01.

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