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Actin cytoskeleton dynamics in stem cells from autistic individuals. | LitMetric

AI Article Synopsis

  • Researchers found evidence suggesting that cytoskeletal dynamics, crucial for the development of neurons, could be disrupted in autism spectrum disorders (ASD) due to gene mutations or expression changes.
  • The study specifically investigated actin cytoskeleton dynamics in stem cells from children with ASD and compared them to controls by examining actin filament behavior after certain activations.
  • Results indicated that over half of the ASD patients exhibited abnormal actin filament reconstruction, hinting that these cellular dynamics could contribute to the neuronal issues seen in some ASD patients.

Article Abstract

Several lines of indirect evidence, such as mutations or dysregulated expression of genes related to cytoskeleton, have suggested that cytoskeletal dynamics, a process essential for axons and dendrites development, is compromised in autism spectrum disorders (ASD). However, no study has yet examined whether cytoskeleton dynamics is functionally altered in cells from ASD patients. Here we investigated the regulation of actin cytoskeleton dynamics in stem cells from human exfoliated deciduous teeth (SHEDs) of 13 ASD patients and 8 control individuals by inducing actin filament depolymerization and then measuing their reconstruction upon activation of the RhoGTPases Rac, Cdc42 or RhoA. We observed that stem cells from seven ASD individuals (53%) presented altered dymanics of filament reconstruction, including a patient recently studied by our group whose iPSC-derived neuronal cells show shorten and less arborized neurites. We also report potentially pathogenic genetic variants that might be related to the alterations in actin repolymerization dynamics observed in some patient-derived cells. Our results suggest that, at least for a subgroup of ASD patients, the dynamics of actin polymerization is impaired, which might be ultimately leading to neuronal abnormalities.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057935PMC
http://dx.doi.org/10.1038/s41598-018-29309-6DOI Listing

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