Lab-Grown Human Cerebellar Cells Enable Study Of Autism.
In a new study, researchers at Boston Children's Hospital used stem cell technology to create cerebellar cells known as Purkinje cells from patients with tuberous sclerosis complex (TSC), a genetic syndrome that often includes ASD-like features.
In the lab, the cells showed several characteristics that may help explain how ASD develops at the molecular level.
TSC, a rare condition in which benign tumors grow in multiple organs of the body, is associated with ASD in about half of all cases.
Previous brain autopsies have shown that patients with TSC, as well as patients with ASD, have reduced numbers of Purkinje cells, the main type of neuron that communicates out of the cerebellum.
In a 2012 mouse study, Sahin and colleagues knocked out a TSC gene (Tsc1) in Purkinje cells and found social deficits and repetitive behaviors in the mice, together with abnormalities in the cells.
In the new paper, the researchers took their observations to humans, studying Purkinje cells derived from three patients with TSC (two also had ASD symptoms, and all three also had epilepsy).
"Developmentally, stem-cell derived neurons are close to a fetal state, recapitulating early differentiation of cells," said Maria Sundberg, the paper's first author.
To make the cells, the researchers first created induced pluripotent stem cells from patients' blood cells or skin cells, then differentiated these into neural progenitor cells and finally Purkinje cells.
The team then compared them with Purkinje cells derived from unaffected people (parents or gender-matched controls) and with cells whose TSC mutation was corrected using CRISPR-Cas9 gene editing.
They saw changes. The cells are bigger and fire less than control cells, exactly what is seen in the mouse model.
Purkinje cells with the TSC genetic defect were harder to differentiate from neural progenitor cells, suggesting that TSC may impair the early development of cerebellar tissue.
The patient-derived Purkinje cells showed structural abnormalities in dendrites (the projections neurons use to take in signals) and signs of impaired development of synapses (junctions with other neurons).
The TSC Purkinje cells also showed over-activation of a cell growth pathway called mTOR. The team treated the cells with rapamycin, an mTOR inhibitor that is already used clinically in TSC to reduce the size of TSC-related tumors and prevent TSC-related seizures.
Added to patient-derived cells in culture, rapamycin enabled the development of more Purkinje precursor cells, improved the functioning of their synapses and increased their tendency to fire.
Lastly, the researchers also compared what genes were being "turned on" in Purkinje cells from TSC patients versus controls. Unexpectedly, the patient-derived cells showed reduced production of FMRP, a protein that is associated with Fragile X syndrome, a common genetic cause of ASD and intellectual disability. FMRP is known to help regulate synapse function, so it may contribute to the abnormalities seen in Purkinje cell functioning in TSC.
These conditions may have a common downstream pathway.
The analysis also showed reduced production of two proteins important for neuron-to-neuron communication at synapses: synaptophysin and a glutamate receptor protein.
The study was the first to create human Purkinje cells using TSC patients' own stem cells. In future studies, the researchers hope to generate larger numbers of patient-derived cells to investigate differences between patients with TSC alone and those who also have ASD.
They also plan to use the Purkinje cell platform to study other ASD-related genetic disorders, including Fragile X and SHANK3 mutation, and to test potential drugs. Sundberg also plans to create other types of neurons for modeling ASD.
Looking at cell-type-specific changes is very important. In TSC, in different cell types, the mutation causes different effects.
Citation: Maria Sundberg et al., "Purkinje cells derived from TSC patients display hypoexcitability and synaptic deficits associated with reduced FMRP levels and reversed by rapamycin," Molecular Psychiatry, 2018; DOI: 10.1038/s41380-018-0018-4
Contact: Mustafa Sahin, email@example.com
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|Title Annotation:||Basic Research|
|Publication:||Stem Cell Research News|
|Date:||Feb 26, 2018|
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