Astrocytes — named for their star-like shape — are a type of brain cell as abundant as neurons in the central nervous system, but little is known about their role in brain health and disease.
Many neurological diseases are caused by or result in the loss of cells in the central nervous system. Some diseases are a result of the loss of specific cells, such as the loss of motor neurons in amyotrophic lateral sclerosis (ALS), the loss of dopaminergic neurons in Parkinson’s disease, and the loss of GABAergic neurons in Huntington’s disease.
For other neurodegenerative conditions, like Alzheimer’s disease, a key hallmark is the general loss of cells in brain regions responsible for memory formation.
Although many brain diseases are marked by the loss of specific cells, a common link among these diseases is the loss of astrocytes. Interestingly, in some animal studies involving cases such as ALS, introducing disease-causing mutations selectively in astrocytes alone produces ALS symptoms and disease progression.
Transplantation therapy
Emerging evidence indicates that astrocytes take part in major functions of the brain, including homeostasis and neural network modulation that are essential to everyday cognition. A functioning brain requires healthy astrocytes, and finding strategies to heal or replace damaged astrocytes could help in the treatment of neurological diseases.
Cell replacement therapy involves transplanting functional cells in patients. In recent years there have been exciting developments in this area with respect to astrocyte transplantation in animal disease models, with one approach even moving to early clinical trial in ALS patients. While there have been some promising outcomes, treatment success varies from one study to the other.
Our recent study, published in The Journal of Neuroscience, examines how transplanted astrocyte integrate into the recipient central nervous system. We studied the types of transplanted astrocytes, timing of treatment and routes of transplantation.
Preparing astrocytes
First, we prepared astrocyte cultures in petri dishes by extracting immature astrocytes from the cerebral cortex of newborn mice and expanding the cell population. To track the development of transplanted astrocytes following their delivery to recipient mice, we used astrocytes from genetically modified mice in which astrocytes glow red, and they are transplanted into the brain of mice where astrocytes glow green.
We found that the transplanted astrocytes could survive for up to one year after transplantation, developing normally and integrating into the recipient brain just like the native astrocytes, with just minor differences.
Astrocytes depend on their capability to sense signals and exchange materials within the brain environment through molecules such as receptors and ion channels located on their cell surface. Transplanted astrocytes displayed comparable numbers of such receptors and channels and possessed similar sizes and complexity when compared to native astrocytes.
Transplanted astrocytes do appear to take some time to catch up to and perfectly match astrocytes in the recipient mice in terms of the production of these receptors and ion channels.
