Neural tissue engineering using embryonic and induced pluripotent stem cells
© BioMed Central Ltd 2011
Published: 15 April 2011
With the recent start of the first clinical trial evaluating a human embryonic stem cell-derived therapy for the treatment of acute spinal cord injury, it is important to review the current literature examining the use of embryonic stem cells for neural tissue engineering applications with a focus on diseases and disorders that affect the central nervous system. Embryonic stem cells exhibit pluripotency and thus can differentiate into any cell type found in the body, including those found in the nervous system. A range of studies have investigated how to direct the differentiation of embryonic cells into specific neural phenotypes using a variety of cues to achieve the goal of replacing diseased or damaged neural tissue. Additionally, the recent development of induced pluripotent stem cells provides an intriguing alternative to the use of human embryonic stem cell lines for these applications. This review will discuss relevant studies that have used embryonic stem cells to replicate the tissue found in the central nervous system as well as evaluate the potential of induced pluripotent stem cells for the aforementioned applications.
The human nervous system can be divided into two major components: the central nervous system (CNS) and the peripheral nervous system . The CNS consists of the brain and the spinal cord with the blood-brain barrier restricting the types of biomolecules that can reach these organs . The majority of neural tissue found in the CNS consists of two cell types: neuronal cells and glial cells. Neurons serve as the main information transmitting unit of the nervous system, which can be classified as either sensory, allowing them to detect stimuli from the environment, or motor, responsible for the generation of movement through signaling with muscle tissue . Glial cells encompass a number of different types of support cells, including astrocytes and oligodendrocytes found in the CNS [4, 5]. This review will discuss the use of embryonic stem (ES) cell therapy as a method of treating injuries and diseases that inflict damage to the CNS. These studies are particularly relevant now as the first human ES-cell-derived therapy is currently being evaluated in clinical trials as a potential method for treating spinal cord injury (SCI) .
Many of the studies detailed in this review use mouse ES cells as a model system for studying cell behavior with the goal of translating this knowledge to human ES cells. While this approach does have merit, it is important to note some of the differences between mouse and human ES cell lines. One of the major differences is that mouse ES cells can be maintained in the presence of leukemia inhibitory factor (LIF) on gelatin substrates in a relatively cost effective manner while human ES cells are cultured either on a feeder layer of cells or on a Matrigel surface in the presence of defined media . Mouse and human ES cells differ in protein expression patterns, including the signaling pathways that regulate differentiation and the markers that indicate pluripotency . For example, undifferentiated mouse ES cells express stage-specific embryonic antigen (SSEA)-1 while undifferentiated human ES cells express the SSEA-3 and SSEA-4 markers . Thus, the information gained in mouse ES cell studies does not always directly translate to human ES cell lines due to these intrinsic differences.
Both human ES and iPS cells exhibit high variability between different cell lines as illustrated by a recent study published in Cell that mapped the genome-wide DNA methylation patterns and gene expression for 20 ES and 12 iPS cell lines . They used the information obtained from the ES cell lines as a reference to evaluate the expression patterns of the iPS cell lines to see if they fell within an acceptable range of 'stemness'. Another study used transcriptional profiling analysis to show that the iPS cell lines have residual gene expression from the donor cells after reprogramming, with certain donor cells being reprogrammed more efficiently . Both of these studies illustrate the need for defined standards to use for evaluating newly derived ES and iPS cell lines to determine their suitability for clinical applications.
Embryonic stem-cell-based therapies for neural tissue replacement
The use of embryonic stem and induced pluripotent stem cell derived therapies for neural tissue engineering applications
Traumatic brain injury
Mouse embryonic stem cells
Mouse embryonic stem cells
Human embryonic stem cells
Mouse induced pluripotent cells
Human embryonic stem cells
Mouse embryonic stem cells
Spinal cord injury
Mouse embryonic stem cells
Human embryonic stem cells
Mouse induced pluripotent cells
While specific protocols for directing stem cell differentiation into neural lineages will not be reviewed in depth here, several reviews on the subject describe these processes in more detail [21, 22]. When developing ES-cell-based treatments for neural diseases and disorders, it is important to consider what specific cell populations could potentially restore lost function. For certain neuro-degenerative disorders that affect specific neuronal populations, the goal is to transplant a highly differentiated mature population of neurons to replace the lost cells. For promoting recovery after traumatic CNS injury, a variety of ES-cell-based therapies have been explored as neural progenitors could potentially secrete regeneration-promoting factors while the transplantation of ES-cell-derived neurons and oligodendrocytes to restore the lost mature cellular populations has also been studied. The method of transplanting the cells in the desired location in the CNS should also be carefully evaluated to ensure cell viability and prevent unwanted differentiation. Other relevant issues relating to ES-cell-based therapies include the potential of the transplanted cells to induce an immune response. These issues will be discussed along with the relevant studies for each of the following diseases and disorders.
Traumatic brain injury
It is estimated that 3.2 million people in the United States currently suffer from reduced function after hospitalization as a result of traumatic brain injury (TBI) . The impact and resulting lesion from TBI often results in cognitive, sensory, motor, and emotional impairments. Several studies have investigated the use of ES-cell-derived therapies, specifically the transplantation of neural progenitors and undifferentiated ES cells, as a way of treating TBI with the hope of alleviating the afore-mentioned symptoms as these cells could secrete factors that would induce regeneration. In one of the first studies to investigate such a strategy, neural progenitors produced by treating mouse ES cells with retinoic acid were transplanted into the lesion site one week after administration of a cortical impact injury . They found that these cells were able to prevent the formation of necrotic cavities that would normally occur after injury and were able to improve the sensorimotor function. Another group showed transplanted mouse ES cells migrated to the injury sites consisting of lesions induced by fluid injection in the mouse brain, suggesting that the damaged brain tissue secreted factors to induce ES cell migration . In a similar study, the ability of undifferentiated mouse ES cells to promote recovery after TBI was evaluated . The animals that received the ES cells performed better on the Rotorod test, measuring the animal's ability to stay on a moving rod, and had better Neuroscores, reflecting an improvement in their neuromotor function. However, they observed tumor formation in two of the ten animals receiving the cells, illustrating a limitation of using undifferentiated ES cells as a therapy. In a follow-up study, they reported that the inflammatory response associated with TBI impaired ES cell survival and integration after implantation into injured rat brain . These studies illustrate the potential of ES cell therapies for the treatment of TBI, but much work remains before such therapies will be suitable for evaluation in clinical trials.
The loss of dopaminergic neurons located in the substantia nigra is one of the major hallmarks of Parkinson's disease (PD) . These neurons secrete dopamine, which regulates cortical and thalamic activity. Loss of these dopamine neurons in the substantia nigra results in motor dysfunction, including tremor, rigidity, and brady-kinesia, as well as non-motor symptoms, including anxiety and depression. The current treatment for PD consists of the drug levodopa, often referred to as L-dopa, which is a dopamine precursor that can cross the blood-brain barrier, where it is then metabolized into dopamine . However, long-term use of levodopa leads to more motor function dysregulation . Additionally, the transplantation of fetal tissue as a method of replacing the lost dopamine neurons has also been investigated, but the most recent clinical trials did not show any benefit to receiving this treatment [31–33]. The goal of ES-cell-based therapies for PD is to generate a highly defined, dopaminergic neuron population suitable for transplantation into the substantia nigra.
Many groups have investigated the use of ES -cell-derived dopaminergic neurons for their potential to treat PD as an alternative to the current standard of care. One group implanted undifferentiated mouse ES cells directly into the mid-brain, where the cells differentiated into functional dopaminergic neurons and promoted functional recovery in a rat model of PD induced by injections of 6-hydroxydopamine . Another study developed an extensive five step protocol for generating dopaminergic neurons from mouse ES cells and showed that trans-plantation of these cells improved function in the same PD rat model . Similar studies were also performed using human ES-cell-derived dopaminergic neurons and showed that transplantation of these cells into a rat model of PD produced similar improvements in function [36–39]. Other groups have shown that co-cultures of ES cells with astrocytes and stromal cells induces differentiation into dopaminergic neurons [37, 40, 41]. Finally, a recent study developed an efficient protocol for large scale production of dopaminergic neurons from human ES cells that reduces the potential for tumor formation, bringing this therapy closer to standards required for clinical testing .
Huntington's disease (HD) is a rare, inherited neuro-degenerative disorder characterized by a loss of medium spiny projection neurons in the striatum . Symptoms include loss of muscular coordination along with progressive cognitive decline. Many clinical studies have investigated the transplantation of fetal-derived tissue into the brain as a potential treatment for HD [43–46] and ES cells provide an alternative to the use of such tissues by providing an alternative way to replace the lost neuronal population.
One study induced human ES cells to differentiate into neural progenitors and then transplanted these cells into a rat model of HD induced using quinolinic acid . The animals receiving the treatment performed better on an apomorphine-induced rotation test compared to sham treated animals and no tumor formation was observed. While they did observe neuronal differentiation of the transplanted progenitors, they did not investigate the mechanism behind the observed recovery to determine if it was due to the secretion of factors that preserved the existing cells or if the transplanted cells were contributing to the functional recovery. A second study utilized a three step protocol to induce human ES cells to differentiate specifically into striatal spiny neurons for transplantation . While the initial results were promising, after 13 weeks, the grafts overgrew the implantation site, leading to deleterious side effects. However, these grafts did not contain undifferentiated ES cells, but the regions of overgrowth did contain nestin-positive neural progenitor cells. A different study showed that treatment of neural progenitors derived from human ES cells with the protein Noggin enhanced neuronal differentiation post-implantation in a rat model of HD . These studies demonstrate the viability of using ES-cell-derived therapies as a way to replace the lost neuronal populations due to HD. However, the issue of graft overgrowth as well as determining how these transplanted cells contribute to function recovery will have to be addressed and characterized before these therapies can be translated to the clinic.
Similar to HD, Alzheimer's disease (AD) is another neurodegenerative disease that tends to affect people over the age of 65 years. The clinical symptoms of AD include progressive cognition deterioration due to the loss of cholinergic neurons . In terms of histology, AD is associated with the appearance of amyeliod plaques and neurofibrillary tangles in the brain. Many groups have investigated the use of ES-cell-derived therapies as a means of treating AD in pre-clinical models by differentiating ES cells into cholinergic neurons as this cell population is one the most affected by AD.
One group derived neurospheres from mouse ES cells and transplanted the resulting cells into a mouse model of AD . These cells differentiated into choline acteyl-transferase-positive neurons and reduced memory deterioration compared to control mice that received undifferentiated ES cells. The control mice receiving the undifferentiated ES cell transplants also showed tumor formation and significant memory deterioration. Another study took a similar approach to differentiating mouse ES cells and also examined the effect of adding the growth factor sonic hedgehog (Shh) during the neurosphere formation step. They observed that the differentiation of neural progenitors into cholinergic neurons was enhanced by priming the neurospheres with Shh and the treated animals that received these cells showed a significant improvement in memory as indicated by performance in a water maze test . These studies provide preliminary evidence for an ES-cell-based therapy for AD, but such results would need to be repeated with human ES cells in pre-clinical testing to determine the viability of such a strategy.
Spinal cord injury
The complex arrangement of neurons, oligodendrocytes, and astrocytes allow the spinal cord to coordinate movement and sensation between the brain and the limbs and disruption of this structure due to mechanical injury can result in paralysis . The extent of paralysis depends on the degree of trauma and the location of the injury in the spinal cord. The initial mechanical injury triggers a secondary cascade of events and damage from both of these processes must be addressed when designing a suitable therapeutic repair strategy. ES-cell-based therapies for the treatment of SCI have focused on generating both neurons and oligodendrocytes to promote recovery after injury.
The McDonald group  transplanted retinoic-acid-treated ES cells into a rat model of SCI and these cells were able to survive and differentiate into neurons, oligodendrocytes, and astrocytes while promoting recovery as indicated by regained hind limb function. Other groups using similar approaches observed improvements in motor and sensory function after transplantation of pre-differentiated mouse ES cells [55–57]. Another group showed that transplantation of bone marrow stromal cells along with retinoic-acid -treated mouse ES cells prevented tumor formation in a rat model of SCI . Other studies have used genetically modified ES cell lines to improve cell survival and differentiation after transplantation, but the use of virus-mediated transfection methods limit the feasibility of such approaches [59–62].
More recent work has focused on the production of specific cellular populations from ES cells for treatment of SCI. Many groups have chosen to differentiate ES cells into motor neurons as a therapeutic strategy. One approach involved inducing mouse ES cells to differentiate into motor neurons using a combination of retinoic acid and Shh and transplanted these cells into a virus-mediated rat model of SCI, with approximately 25% of these cells surviving one month after transplantation  Another group transplanted ES-cell-derived motor neurons along with olfactory ensheathing cells into a rat model of SCI and observed partial functional recovery . The Keirstead group has shown that motor neurons derived from human ES cells can also promote functional recovery after SCI in a rat model . This strategy also holds potential for the treatment of amyotrophic lateral sclerosis, a neurodegenerative disease characterized by the loss of motor neurons .
The other major therapeutic strategy has involved differentiating ES cells into oligodendrocytes for treating SCI [67–74]. One of the most promising approaches to treatment of SCI involves differentiating human ES cells into oligodendrocyte precursors using an extensive 42-day differentiation protocol  and then transplanting these cells into the site of SCI [70, 72–74]. This therapy showed promising results in pre-clinical trials as these oligodendrocyte precursors differentiated into mature oligodendrocytes, promoting functional recovery in two distinct models of SCI [72, 74]. This therapy has become the first human ES-cell-derived therapy to be evaluated in clinical trials , with the first patient having already been enrolled . The Keirstead group  has also begun researching the effects of transplanting motor neuron progenitors into the injured rat spinal cord with some promising results.
Several groups have used tissue engineering approaches that combine biomaterial scaffolds with ES cells for the treatment of SCI. The Sakiyama-Elbert group [76–81] has used a fibrin-based scaffold to deliver growth factors that promote ES cells to differentiate into neurons and oligo-dendrocytes and this approach has been shown to enhance functional recovery in a rat model of SCI. The Baharvand group  has investigated the transplantation of neural progenitors derived from human ES cells inside of collagen scaffolds for the treatment of SCI and this approach also resulted in an increase in locomotor function post-transplantation. Another group developed electrospun poly (ε)-caprolactone scaffolds, which support mouse ES cell culture and promoted differentiation into nestin-positive neural progenitors in an in vitro setting . Many other biomaterials have been investigated for the treatment of SCI, but not in combination with stem cells [84, 85].
Reprogramming somatic cells and the potential for engineering neural tissue
As mentioned in the Introduction, the recent development of iPS cells provides an exciting alternative to the use of ES cells. These cells are generated from somatic cells, such as fibroblasts, by upregulating the expression of specific genes (Oct3/4, Sox2, c-Myc, and Klf4) that restore pluripotency [9, 10]. Unlike traditional ES cell lines, the use of iPS cells allows for generation of pluripotent cell lines without the use of embryos as well as for the production of patient-specific iPS cell lines, which should reduce the risk of rejection after transplantation.
An alternative approach to differentiating pluripotent stem cells is to directly convert one mature cell type into the desired cell type by manipulating cell signaling pathways. The Wernig group  recently demonstrated that mouse embryonic fibroblasts can be directly converted to neurons if the appropriate factors were expressed, offering a potential method of engineering neural tissue without the use of pluripotent stem cells. Much work remains to be done to determine the feasibility of such an approach for clinical applications.
Overall, a large body of work exists showing the potential of using pluripotent stem cells to produce replacement tissue for the CNS as discussed in this review. The current evaluation of oligodendrocytes derived from human ES cells shows the promise of this technology for the treatment of SCI and other neurological disorders and diseases while the generation of iPS cell lines now allows for generation of patient-specific neural tissue derived from pluripotent stem cells. Additionally, the recent work from the Wernig group showing the direct conversion of somatic cells into neurons provides an intriguing alternative to differentiating pluripotent stem cells as a means of replacing lost neural tissue.
central nervous system
induced pluripotent stem
spinal cord injury
traumatic brain injury.
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