Background
Embryonic stem (ES) cells possess the capacity for unlimited self renewal and can be induced
in vitro to become neural precursors with the potential for therapeutic treatment of nervous system disorders [
1‐
5]. Neural stem cells (NSCs) are mobile [
6], are attracted to regions of brain injury and can migrate great distances to reach a site of neural damage [
7‐
10]. In addition, through unknown mechanisms, they exhibit tropism to brain tumors, including glioma cells that have left the main tumor mass and have infiltrated adjacent brain parenchyma [
6,
8,
11,
12].
In vitro migration assays confirm the ability of isolated NSCs, including those derived from mouse embryonic stem cells [
13], to migrate toward factors produced by glioma cells [
8,
14].
Recent studies suggest that stem cell factor (SCF) and stromal cell-derived factor 1α (SDF1α) act as chemoattractants, capable of inducing neural stem cell migration into regions of brain injury/inflammation. For example, Sun et al. [
15] report that in normal mouse brains, endogenous NSCs are attracted to regions where recombinant SCF has been introduced, SCF elicits selective migration of neural stem/progenitor cells
in vitro, and after a freezing brain injury SCF is up-regulated in neurons at the site of injury. Also, Imitola et al. [
16] found in a mouse stroke model that SDF1α synthesis by astrocytes and endothelial cells is increased at the site of injury and that exogenous human NSCs migrate to sites of injury from as far as the contralateral hemisphere to intermingle with SDF1α-expressing cells. These studies suggest that cytokines, such as SCF and SDF1α may be involved in attracting stem cells to regions of injury and inflammation [
17].
Since brain tumors can also attract stem cells, perhaps their mechanism of attraction is similar to that of injury and inflammation. Support for this comes from reports of the expression of SCF by certain glioma cell lines [
18,
19] and expression of
c-kit, the tyrosine kinase receptor for SCF ligand, by neural stem/progenitor cells [
15,
20]. Clearly, it is important to characterize the reactions of stem cells to gliomas, including whether they display the capacity for selective attraction to tumor cells. In the present study, we performed
in vitro migration assays to compare the behavior of undifferentiated and neuralized mouse ES cells toward the human glioma lines U87 and N1321, rat glioma line C6 and SCF. In addition, we tested for expression of SCF by the tumor lines and of
c-kit by the ES cells.
Discussion
Our results show that neural progenitors derived from mouse ES cells migrate toward factor(s) secreted by glioma cell lines U87, N1321 and C6. We show that these glioma lines can synthesize SCF and that recombinant SCF elicits migration by neuralized ES cells in an apparent dose-dependent manner. This selective migration is consistent with the expression of c-kit, the receptor for SCF, by the ES cell-derived neural progenitors.
Prior to this study, little was known about the migratory properties of undifferentiated ES cells [
21‐
23]. In contrast to neuralized ES cells, we found that
in vitro undifferentiated ES cells are highly migratory in all conditions. The highly migratory nature of undifferentiated ES cells may contribute to their unique roles in early embryonic development, such as migration events leading to gastrulation.
The migration of neuralized ES cells towards conditioned medium in vitro may not be selective for SCF because the glioma cell lines likely produce other attractant factors. However, the production of SCF by glioma cells and expression of c-kit by neural precursors suggests that SCF could mediate selective migration towards gliomas in vivo.
Our initial migration studies led to the question: what factors are secreted by the gliomas that act on neuralized ES cells to elicit selective migration? Malignant gliomas secrete a wide variety of factors, associated with their proliferative and invasive programs, including cytokines, interleukins and growth factors, such as TGF-β1 [
24‐
26], and matrix metalloproteinases [
27]. The cytokine SCF elicits selective migration of brain-derived neural stem/progenitor cells
in vitro [
28] and is up-regulated in response to brain injury [
15]. We confirmed expression of SCF by the human glioma cell line, U87 [
19]. In addition, we found that the human glioma cell line, N1321, and the rat glioma cell line, C6, both express SCF, and the version of SCF expressed by these cell lines contains exon 6. Exon 6 is present in the splice variant of SCF from which soluble SCF is produced [
18]. It is also known that many types of stem cells express the receptor for SCF,
c-kit [
20,
29,
30]. We confirmed expression of
c-kit by undifferentiated mouse ES cells [
31] and found that neuralized ES cells also express
c-kit. The latter result is consistent with expression of
c-kit by neural stem cells as well as with the attractant and survival effects of SCF on neural stem cells [
20,
28]. It is possible that expression of
c-kit in Day 8 embryoid bodies (Fig.
3B) is due to the presence of neural progenitors [
1,
3]. While our data suggest that SCF may be involved in eliciting selective migration by neuralized ES cells, glioma cell lines likely produce other attractants. In the future, it will be important to test the contribution of SCF (if any) to selective migration documented here by adding antibodies to SCF to the top well, to potentially block the actions of SCF diffusing from the bottom well.
Neural stem cells demonstrate remarkable tropism to factors produced by gliomas
in vivo [
8,
12,
16,
32]. Importantly, they can be genetically modified to express therapeutic transgenes. These transgenes can encode oncolytic agents, apoptosis-inducing factors, interleukins, factors that inhibit angiogenesis and factors that sensitize tumor cells to traditional treatments for gliomas, such as chemotherapy and radiation [
11,
32,
33]. Recent results show that transplanted neural precursors can improve survival and reduce tumor volume in rodent models with introduced glioblastomas [
8,
11,
34]. In fact, transplanted and endogenous neural precursors as well as bone marrow-derived mesenchymal cells [
35,
36], may enhance survival after induction of glioblastomas in rodent models [
37]. The 4-/4+ induction protocol used here produces a heterogeneous mixture of neural cells within the EBs. It will be important to test whether neural progenitors, or more mature neural cells present in Day 8 EBs, contribute to the cell population that is selectively attracted to SCF and to medium conditioned by the glioma cell lines.
Methods
ES Cell cultures and neural induction
The B5 mouse ES cell line [
3,
40] was used for all experiments. The ES cells were grown in embryonic stem cell growth medium (ESGM) (as described previously [
3]) for 2 days on gelatin-coated flasks until 70% confluent. The cells were then dissociated at 37°C for 5 minutes (0.25% Trypsin with 1 mM EDTA), passed into 4 gelatin-coated flasks and incubated for an additional 2 days (37°C, 5% C0
2). Then dissociated ES cells were transferred to uncoated petri plates and induced (i.e., neuralized) to become neural precursors as free floating embryoid bodies (EBs), using a retinoic acid induction protocol developed by Gottlieb and colleagues [
1,
3]. Prior to migration assays, EBs were grown for 4 days (Day 4) in embryonic stem cell induction medium (ESIM = ESGM without β-mercaptoethanol and Leukemia Inhibitory Factor) or for an additional 4 days (Day 8) in ESIM plus all-trans retinoic acid (500 nM).
As we reported previously [
3], post-induction EBs obtained using B5 ES cells contain a majority of cells that express the neural precursor marker Nestin, but these EBs have substantial numbers of cells that label for neuronal markers, such as β-III Tubulin and Neurofilament-M. Therefore, cells used for the migration assays represent a heterogeneous population, consisting primarily of neural progenitors and/or neural-like cells. After induction, EBs were treated with 0.25% Trypsin with 1 mM EDTA, dissociated mechanically to a single cell suspension and 25,000 cells were added to each well of the top chamber.
Tumor cell lines
Human glioma cell lines N1321 and U87 and rat glioma cell line C6 were grown in DMEM and 10% fetal bovine serum supplemented with 100 U/ml Penicillin, 100 μg/ml Streptomycin [
41] for 2 days in Tissue Culture BD Falcon Flasks (Fisher; Cat. # 13-680-65). The U87 and C6 cell lines were dissociated at 37°C for 2.5 minutes using 0.25% Trypsin with 1 mM EDTA. The N1321 cell line was also dissociated for 2 minutes but using 0.05% Trypsin with 1 mM EDTA. Cells were then passaged and incubated for an additional 2 days (37°C, 5% C0
2). All cells (ES and glioma cells) were tested for viability using Trypan blue stain and live cells were counted using a hemocytometer.
Migration assays and statistical analyses
Cell migration tests were performed using the Neuro Probe Standard 48 Well Chemotaxis Chamber (Cat. # AP48). The lower well was filled with either Unconditioned Medium, medium conditioned by one of the glioma cell lines (i.e., Conditioned Medium) or glioma cells at a density of 50,000 cells per 30 μl. Conditioned Medium was obtained by collecting medium from glioma cell cultures after 2 days of incubation. In migration assays involving SCF, recombinant SCF was added in the bottom well at selected concentrations. A porous polycarbonate membrane (8 μm pores) was coated with entactin-collagen IV-laminin (Upstate Biotechnologies, Cat. # 08–110) and placed on top of the bottom chamber.
Wells of the top chamber were filled with a suspension of stem/progenitor cells in DMEM at a density of 25,000 cells per 50 μl with cells at three different stages of differentiation as follows: undifferentiated embryonic stem cells (Day 0) or stem cells at Day 4 or Day 8 of the induction protocol. Table
1 lists the components found in the top and bottom wells for experiments described here. Negative controls for cellular migration through the membrane included: 1- DMEM alone in the top well and glioma cells in the bottom well, and 2- DMEM alone in the top well and Unconditioned Medium (DMEM and FBS) in the bottom well (Table
1). The entire chamber was placed in an incubator (37°C, 5% C02) for 4 hours. The chamber was separated and cells on the polycarbonate membrane were fixed in methanol for 10 minutes and washed in PBS (4X for 2 minutes each). The fixed membrane was stained for 3 hours with Hoechst 33358 nuclear stain at 50 μg/ml to identify cells that had migrated through the membrane pores. After staining, the membrane was washed with PBS (5X for 2 minutes each). The membrane was then placed on a slide for subsequent epifluorescence microscopy.
Table 1
Contents of Top and Bottom Wells for Migration Experiments
Top Well | | | | | | |
| DMEM | X | X | X | X | X |
| Stem Cells | X | X | X | | |
Bottom Well | | | | | | |
| DMEM | X | X | X | X | X |
| FBS | X | X | X | X | X |
| Glioma Cells | X | | | X | |
| Factors Secreted by Tumor Cells | X | X | | X | |
| rSCF | | | X | | |
Images were captured digitally using a Leica stereoscope, Model MZFLIII, equipped with a CCD camera. Images were saved as TIFF files using MagnaFire (Ver. 2.1c) and analyzed using NIH Image (Ver. 1.62). The total numbers of cells that migrated through the pores of the membrane were counted. All experimental conditions were replicated a minimum of three times, and all experiments were performed at least three times.
Statistical comparisons of cell counts were made using One-Way ANOVA and post hoc Dunnet Test and/or Newman-Keuls Multiple Comparisons Test. Significance is given at p < 0.05 level, unless otherwise noted.
RT-PCR
Total RNA isolation was performed using GenElute according to manufacturer's instructions (Sigma-Aldrich, Cat# RTN 10). The 50 μl isolate was treated with 5 μl DNase1 and 5 μl Reaction Buffer for 10 minutes at 37°C. Then, 5 μl stop buffer was added and the mixture held at 70°C for 10 minutes. The cDNA was created with Marligen Biosciences Inc. First-Strand cDNA Synthesis System (Cat#11801-100) as directed by the manufacturer. PCR was run using Eppendorf's HotMasterMix (2.5X) (Cat# 954140181), 200 uM primers and 7 μl of cDNA template. Controls lacking Reverse Transcriptase were included. In Figure
3B, no RT controls were pooled prior to PCR. The SCF primers used were 5'-AAGGGATCTGCAGGAATCGTGTGA-3' (forward) and 5'-TGCCCTTGTAAGACTTGG CTGTCT-3' (reverse). The parameters were 32 cycles at 94°C for 1 min, 55°C for 1 min, and 72°C for 1 min, with final elongation at 72°C for 10 minutes. The mouse
c-kit primers used were 5'-CCATGTGGCTAAAGATGAAC-3' (upstream) and 5'-CTGCTGGTGCTCGGGTTTG-3' (downstream) [
15]. The GAPDH primers used were 5'- TGATGGGTGTGAACCACGAGAA -3' (upstream) and 5'- AGTGATGGCATGGACTGTGGTCAT-3' (downstream). The parameters for
c-kit and GAPDH amplification were as follows: 30 cycles at 94°C for 30 sec, 54°C for 45 sec, 69°C for 45 sec, with final elongation at 69°C for 10 minutes.
Competing interests
The author(s) declare that they have no competing interests.
Authors' contributions
PS & MS carried out the cell cultures and migration assays. CP & MS participated in the RT-PCR. BM & MK conceived of the study and participated in its design and coordination. MS & MK drafted the manuscript. All authors read and approved the final manuscript.