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Organoids missing the TSC2 gene form rogue astrocytes; and more

Here is a roundup of autism-related news and research spotted around the web for the week of 28 September.

By Jill Adams
29 September 2026 | 2 min read

Two roads diverge: Human brain organoids missing the gene TSC2 have overreactive astrocytes that are similar to those found in tubers from people with tuberous sclerosis complex, according to a new study. The findings substantiate the idea that glial pathology results from altered protein expression and activity—specifically, high mTORC1 signaling—rather than from seizures themselves. “These results implicate glial dysfunction as a driver of TSC pathogenesis and highlight reactive astrocytes as potential therapeutic targets for TSC-related neuropathology,” the investigators write.

Autism research spotted this week:

  • “Postnatal maturation of putamen microstructure accompanies topographic white matter connectivity and altered circuits in autism” bioRxiv
  • “A retinoic acid autoregulatory loop governing prefrontal-motor arealization” Nature
  • “Developmental cerebellar pathology in mouse models of SCN2A premature termination codon variants” bioRxiv
  • “Maternal-fetal immune conflict contributes to male-specific impairments in a mouse model of neurodevelopmental disorders” Science Advances
    See also: “Post-infection immune conflict alters fetal development in some male mice”
  • “Parvalbumin interneurons and dentate gyrus homeostatic dysregulation shape epileptogenesis in Angelman syndrome model mice” bioRxiv
Research image of perineuronal nets.
Seizure susceptibility: Atypical accumulation of perineuronal nets (red stain) in the dentate gyrus occurs with seizure kindling in a mouse model of Angelman syndrome (left panel) but not in mice that have UBE3A present in GABA-containing neurons (right panel).
  • “The uneven landscape of cognitive domains in 22q11.2 deletion syndrome: A large consortium study” Psychological Medicine
  • “A cell type-specific switch in GluN2D NMDA receptors drives cortical circuit hyperexcitability and sensory-driven cortical synchronization deficits in a fragile X syndrome model” Biological Psychiatry
  • “A rare recurring gain-of-function variant in BMPR2 causes neurodevelopmental phenotypes in humans and flies” American Journal of Human Genetics
  • “Congenital TORCH infections and neurodevelopmental outcomes” JAMA Pediatrics
  • “Kennedy announces new effort to speed up autism diagnoses” STAT
  • “Molecular biologist and neuroscientist Catherine Dulac wins the 2026 Pearl Meister Greengard Prize” Rockefeller University

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