Spatiotemporal evolution of early innate immune responses triggered by neural stem cell grafting
© Reekmans et al.; licensee BioMed Central Ltd. 2012
Received: 17 September 2012
Accepted: 12 December 2012
Published: 14 December 2012
Transplantation of neural stem cells (NSCs) is increasingly suggested to become part of future therapeutic approaches to improve functional outcome of various central nervous system disorders. However, recently it has become clear that only a small fraction of grafted NSCs display long-term survival in the (injured) adult mouse brain. Given the clinical invasiveness of NSC grafting into brain tissue, profound characterisation and understanding of early post-transplantation events is imperative to claim safety and efficacy of cell-based interventions.
Here, we applied in vivo bioluminescence imaging (BLI) and post-mortem quantitative histological analysis to determine the localisation and survival of grafted NSCs at early time points post-transplantation.
An initial dramatic cell loss (up to 80% of grafted cells) due to apoptosis could be observed within the first 24 hours post-implantation, coinciding with a highly hypoxic NSC graft environment. Subsequently, strong spatiotemporal microglial and astroglial cell responses were initiated, which stabilised by day 5 post-implantation and remained present during the whole observation period. Moreover, the increase in astrocyte density was associated with a high degree of astroglial scarring within and surrounding the graft site. During the two-week follow up in this study, the NSC graft site underwent extensive remodelling with NSC graft survival further declining to around 1% of the initial number of grafted cells.
The present study quantitatively describes the early post-transplantation events following NSC grafting in the adult mouse brain and warrants that such intervention is directly associated with a high degree of cell loss, subsequently followed by strong glial cell responses.
Neural stem cells (NSCs) are defined as a population of self-renewing multipotent progenitor cells present in the developing and adult central nervous system (CNS) . Despite their specific spatiotemporal occurrence in vivo, ex vivo culture expansion of NSCs derived from various sources (for example, embryonic or postnatal brain and embryonic stem cells) was shown to be relatively straightforward. Moreover, given the observation that ex vivo cultured neurosphere-derived NSCs and monolayer-cultured NSC populations can be triggered to differentiate into neurons, astrocytes and oligodendrocytes, it is hoped that NSCs, or more committed (progenitor) cells derived thereof, will become part of novel treatment options for a variety of CNS disorders. To date, several studies have reported the clinical benefit of NSCs following intraperitoneal, intravenous, intraventricular, intrathecal and intra-tissue grafting in various models of neuroinflammation, neurodegeneration or injury [1–4]. However, despite many suggestive literature reports, it still remains elusive whether the actual clinical benefit of grafted NSCs is due to cell integration, trophic support, immunomodulation or other yet to be defined mechanisms [5–7]. In this context, preceding work by others  and us  determined the actual survival of grafted NSCs after at least two weeks to be less then 2% upon direct grafting into healthy or inflamed brain tissue. In addition, our preceding histological analyses indicated the presence of both microglia and astrocytes within and surrounding the NSC graft site at two weeks post-implantation . Following these observations, our next research aim was to determine whether the observed glial cell responses: (i) were directly executed against the grafted NSC (or their reporter proteins), or (ii) resulted as a consequence of immediate cell graft mortality. In order to investigate both hypotheses, the present study determined the following parameters at multiple early time points (that is, day 0, 1, 3, 5, 7 and 14) post-implantation: (i) the actual survival of grafted NSC, (ii) the occurrence of cellular hypoxia, and (iii) the occurrence and/or maintenance of cell graft-induced glial cell responses.
Materials and methods
Cell implantation experiments
NSC genetically engineered with the Luciferase and eGFP reporter proteins (NSC-Luc/eGFP, FVB-background) were cultured and characterised as previously described . For cell implantation experiments, adult female Friend leukemia virus B (FVB)/NCrl mice (n = 33) were obtained from Charles River Laboratories (Wilmington, MA, USA - strain code 207). Cell implantation of NSC-Luc/eGFP (2.5 × 105 cells in 2 μl PBS) was reproducibly targeted to the right hemisphere at the following coordinates relative to bregma: 2 mm posterior, 2 mm lateral, and 2.25 mm ventral. All surgical interventions were performed under sterile conditions, as previously described [9–11]. For all experiments, mice were kept in a normal day-night cycle (12/12) with free access to food and water. All experimental procedures were approved by the Ethics Committee for Animal Experiments of the University of Antwerp (UA) (approval no. 2011/13).
In vivo bioluminescence imaging
In vivo bioluminescence imaging (BLI) was performed at different time points post-implantation (day 1, 3, 5, 7, 10 and 14) using a real-time photon-imager system (Biospace, Centennial, CO, USA), according to previously optimised procedures [10–12]. Using the M3 Vision software (Biospace, Centennial, CO, USA), light emission was measured from a fixed region of interest on the mouse head, and values of signal intensity are presented as the average number of photons/s/sr/cm2 over a 3-minute time period. An additional region of interest was drawn on the mouse shoulder and considered as background signal.
Histological analysis - immunofluorescence staining
Before sacrifice (1.5 hours), mice used in this study were injected intraperitoneally with Hypoxyprobe-1 (HPI Inc, Burlington, MA, USA), according to the manufacturer's instructions. Preparation of brain tissue for histological examination was performed according to previously optimised procedures . Serial 10-μm thick cryosections were obtained from the entire implant region using a Microm HM5000 cryostat (Prosan, Merelbeke, Belgium), consecutively marked and missing slides were noted. For further immunofluorescence analysis of tissue sections, antibody staining was performed as previously described [9, 10, 12], using the following antibodies: (i) a rabbit anti-mouse ionized calcium binding adaptor molecule 1 (Iba1) antibody (1/200) (Wako chemicals, Osaka, Japan; 019-19714) and (ii) a rabbit anti-pimonidazole (Hypoxyprobe-1) antibody (1/200) (HPI Inc., Burlington, MA, USA; Pab2627), all in combination with a secondary donkey anti-rabbit AlexaFluor 555 antibody (1/500) (Life Technologies, Carlsbad, CA, USA; A31572), (iv) a rabbit anti-mouse S100B antibody (1/200) (Abcam, Cambridge, UK; 52642) in combination with a secondary donkey anti-rabbit AlexaFluor 555 antibody (1/1000) (Life Technologies, Carlsbad, CA, USA; A31572), (v) a mouse anti-mouse GFAP antibody (1/400) (Millipore, Billerica, MA, USA; MAB360) in combination with a secondary goat anti-mouse AlexaFluor 555 (1/1000) (Life Technologies, Carlsbad, CA, USA; A21127), and (vi) a chicken anti-mouse MBP antibody (1/200) (Millipore, Billerica, MA, USA; AB9348) in combination with a secondary donkey anti-chicken DyLight 549 (Jackson Immunoresearch, Suffolk, UK; 703-506-155). The presence of terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL)+ apoptotic cells was investigated using the In Situ Cell Death Detection Kit TMR Red (Roche, Penzberg, Germany; 12156792910), according to manufacturer's instructions. Nuclear staining was performed using a TOPRO3 deep red stain (1/200) (Life Technologies, Carlsbad, CA, USA).
Histological analysis - quantitative analysis
Quantitative analysis of cell graft survival, glial cell responses and cellular hypoxia were performed using NIH ImageJ analysis software (ImageJ) and TissueQuest immunofluorescence analysis software (TissueGnostics GmbH, Vienna, Austria), allowing determination of the following parameters: (i) total graft site volume in mm3, (ii) density of eGFPpos NSC-luc/eGFP within the graft site provided in number of cells/mm3 (six data counts per cell graft analysed), (iii) cell graft survival provided in absolute numbers and as % calculated to the initial number of grafted cells, (iv) density of Iba1pos microglia within the graft site provided in number of cells/mm3 (three data counts per cell graft analysed), (v) density of Iba1pos microglia within the implant border (that is, region extending 100 μm from the implant site) provided in number of cells/mm3 (three data counts per cell graft analysed), (vi) density of S100Bpos astrocytes within the graft site in number of cells/mm3 (three data counts per cell graft analysed), (vii) density of S100Bpos astrocytes within the implant border provided in number of cells/mm3 (three data counts per cell graft analysed), (viii) the degree of glial fibrillary acidic protein (GFAP)pos astrogliosis within the graft site provided as % astrogliosis (that is, image-covering of GFAP staining) (one data count per cell graft analysed), (ix) the degree of GFAPpos astrogliosis within the implant border provided as % astrogliosis (one data count per cell graft analysed), (x) the percentage of Hypoxyprobe-1pos eGFPpos NSC versus total eGFPpos NSC within the implant zone (one data count per cell graft analysed).
All statistical analyses were performed using the statistical package R, version 2.13.1, with linear mixed models fitted using the lme function in the nlme package. Differences in graft site volume between day 0 and day 14 post-grafting were tested using the Mann-Withney U-test. The evolution over time of NSC graft survival was modelled using piecewise linear regression, taking the knot at day 1 post-implantation. Using this model, separate regression slopes up to day 1 and beyond day 1 (that is, from on day 3) were estimated and tested for significance. The evolution over time of the obtained in vivo bioluminescence signal intensities, microglia densities, astrocyte densities and the degree of astrogliosis was modelled using piecewise linear mixed model analysis. A random intercept for individual was added to the model to account for the dependence between observations from the same individual. Values for bioluminescence signal intensity, microglia densities and astrocyte densities were log-transformed to obtain a more normally distributed outcome variable. The position of the knot was determined based upon visual inspection of the data. Separate regression slopes before and after the knot were estimated and tested for significance. For all analyses, a P-value < 0.05 was considered statistically significant.
Longitudinal in vivo bioluminescence imaging of neural stem cell grafts
Quantitative analysis of neural stem cell graft survival
Excessive apoptotic cell loss coincides with cellular hypoxia within NSC grafts
Quantitative analysis of glial cell responses following neural stem cell grafting
Astroglial and microglial densities following intracerebral implantation of NSC-Luc/eGFP.
1,293 ± 768
10,017 ± 10,678
104,712 ± 75555
146,551 ± 188,791
94,803 ± 126,268
24,017 ± 250,036
5,382 ± 5,483
7,376 ± 5,653
18,059 ± 12,436
25,515 ± 5,986
28,900 ± 9,807
32,647 ± 15,108
1,537 ± 1,071
5,367 ± 5,951
24,551 ± 17,042
34,467 ± 33,349
25,062 ± 22,264
41,693 ± 44,628
22,010 ± 6,202
17,757 ± 3,149
22,798 ± 4,216
25,308 ± 4,943
27,262 ± 5,647
34,603 ± 11,392
Disruption of CNS architecture following neural stem cell transplantation
Inevitably, cell grafting in the CNS will induce damage to the CNS architecture due to needle insertion and the subsequent injection of a cell suspension. As shown by the representative images in Figure 2 (sixth row), it is clear that both the CNS architecture, as visualised by staining for myelin basic protein (MBP), and the NSC-Luc/eGFP graft site, as visualised by the presence of eGFP-expressing cells, undergo significant changes at early stages post-grafting. While initially grafted NSC-Luc/eGFP are clustered together and myelin conformation of the capsula externa is temporally spread out, this gradually remodels as the limited number of surviving NSC-Luc/eGFP spread along the capsula externa/corpus callosum, and the disturbance in myelin conformation partially restores itself. The latter is accompanied with a reduction of graft site volume (that is, the area in which eGFP-expressing cells can be found) from 0.35 ± (SD) 0.09 mm3 at day 0 post-grafting to 0.07 ± 0.07 mm3 at day 14 post-grafting (P = 0.015).
Over the past years, neural stem cell transplantation has been recognized as a promising novel therapeutic tool to treat CNS disorders for which today, no effective therapies are available. However, successful functional integration of grafted NSCs (or in vitro/in vivo NSC-derived cell types) is one of the major challenges in current neuroscience research, and if successful, will have an enormous impact on the future development of cell replacement therapies for CNS disorders. In order to contribute to this understanding, we have investigated the spatiotemporal evolution of NSC graft behaviour and endogenous glial cell responses at early time points post-implantation.
With regard to direct grafting of NSCs in CNS tissue, our results demonstrate that this procedure immediately results in: (i) significant disruption of the CNS architecture (Figure 2, sixth row) and (ii) substantial cell graft mortality (Figure 3a). First, the observed disruption of CNS architecture (although partially restored over time) will remain inevitable as long as cells (or cell-seeded scaffolds) are directly implanted into CNS tissue. Although alternative administration routes (that is, intraventricular, intrathecal or intravenous) have been suggested to facilitate cell delivery into injured CNS tissue, the cell number arriving at the target site is generally nihil to a few representative cells detected by histological analysis [13–15]. Second, apoptotic cell death within the first 24 hours post-grafting (Figure 4) can most likely be explained by the lack of oxygen (Figure 2, second row) and/or nutrients delivered to the NSC graft, which, in fact, is introduced without any structural and/or functional support. More recently, novel biomimetic strategies are emerging aiming to create a permissive micro environmental niche, thereby enhancing survival, differentiation and integration of grafted NSCs [16–18]. The latter will be inevitable, as a substantial amount of grafted cells need to survive following transplantation in order to functionally participate in neuronal circuitries. Of note, while we used both in vivo BLI (Figure 1c) and post-mortem histological analysis (Figure 3a) to determine cell graft survival, it should be noted that the observed in vivo BLI signals at day 1 and day 3 post-grafting are resulting from respectively 20% and 5% of the original number of grafted cells. Although we and others have associated this early in vivo BLI signal with complete cell graft survival, our results now clearly indicate that precaution has to be taken in the interpretation of early in vivo BLI data [10, 11]. Nevertheless, in vivo BLI remains an interesting tool for longitudinal assessment of cell graft survival, as progressive cell loss of implanted NSC could clearly be demonstrated from on day 3 post-implantation (Figure 1c).
With regard to the observed glial cell responses, these are not surprising as the majority (up to 95%) of grafted NSCs already die within the first 24 to 48 hours post-grafting (Figure 3a). However, in our preceding studies regarding autologous and allogeneic stem cell grafting in the CNS of immune competent mice, we suggested that the occurrence of glial cell responses was most likely due to the recognition of the cellular implant itself, whereby autologous reporter-gene modified cellular grafts were immune-tolerated and allogeneic cellular grafts were immune-rejected. However, our early studies did not include full quantitative analysis of in vivo BLI and histology data. Based on our new data showing that NSC grafts already display a high degree of mortality before the initiation of glial cell responses (Figure 3b-f), the observed glial cell responses are more likely to be associated with phagocytocis of cellular debris rather than active recognition of grafted autologous NSC. Nevertheless, based on our preceding data regarding full rejection of allogeneic (but not autologous) cellular grafts, active distinguishment of autologous and allogeneic cellular grafts by microglia (or astrocytes) will thus most likely be occurring during or after the initial clearance of cellular debris. Following initial activation of glial cell responses, survival of grafted autologous NSC further declines to around 1% by week 2 post-implantation. Moreover, although endogenous microglia and astrocytes are able to produce either pro-inflammatory/neurotoxic or anti-inflammatory/neuroprotective factors depending on the type of activation [19, 20], it is highly likely that the evoked immune responses following NSC implantation create an inhibitory pro-inflammatory environment, thereby further limiting the long-term survival of transplanted NSC . Of note, additional immunophenotypical stainings were performed to determine the in vivo differentiation potential of the few surviving NSC-Luc/eGFP (data not shown). Results indicated that grafted NSC-Luc/eGFP did not change phenotypic properties between day 0 and day 14 post-grafting, that is, They remained SOX2pos (as NSC marker), S100Bneg (as astrocyte marker), NeuNneg (as neuronal marker) and CC1neg (as oligodendrocytes marker). Likewise, proper in vivo differentiation and functional integration of the few surviving NSC is most likely inhibited by an endogenous glial-cell-induced pro-inflammatory immune environment [22–24].
The present study quantitatively describes the early post-transplantation events following NSC grafting in the adult mouse brain and warrants that such intervention is associated with an immediate high degree of cell loss. The latter is subsequently followed by strong glial cell responses, presumably creating a non-permissive environment, which limit proper migration, differentiation and integration of grafted NSC into the host tissue. Unfortunately, these observations are generally not considered when evaluating the potential of pre-clinical cell therapy studies, as most reports lack detailed cell graft survival and/or glial reactivity analysis at early and late time-points post-grafting. Moreover, it is important to note that early NSC graft mortality and subsequent glial cell responses themselves might be responsible for many of the observed beneficial effects following cell transplantation in CNS disorders . We therefore underscore the current need for a profound characterisation of all cellular and/or molecular interactions following cell grafting in the CNS, as the full potential of NSC transplantation therapy can only be determined following better understanding (and manipulation) of NSC graft survival and inhibitory immune responses.
anti-APC (Adenomatous polyposis coli protein) antibody
central nervous system
enhanced green fluorescent protein
glial fibrillary acidic protein
ionized calcium binding adaptor molecule 1
myelin basic protein
neural stem cell
S100 calcium binding protein B
sex-determining region Y-box 2
terminal deoxynucleotidyl transferase dUTP nick end labeling.
This work was supported by research grants G.0136.11 and G.0130.11 (granted to ZB, AvDL and PP) of the Fund for Scientific Research-Flanders (FWO-Vlaanderen, Belgium), in part by a Methusalem research grant from the Flemish government (granted to ZB and HG) and in part by funding received from the European Union's Seventh Framework Programme (FP7/2007-2013) under grant agreement number 278850 (INMiND) (granted to AvDL). Nathalie De Vocht holds a PhD-studentship from the FWO-Vlaanderen. Debbie Le Blon holds a PhD-studentship from the Flemish Institute for Science and Technology (IWT-Vlaanderen). Peter Ponsaerts is a post-doctoral fellow of the FWO-Vlaanderen.
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