Analyzing brain stem cells of patients with autism spectrum disorder (ASD), Rutgers scientists have found evidence of irregularities in very early brain development that may contribute to the neuropsychiatric disorder.
The findings support a concept scientists have long suspected: ASD arises early in fetal development during the period when brain stem cells divide to form the elements of a functioning brain.
Writing in the journal Stem Cell Reports, Rutgers scientists examined brain stem cells – known as neural precursor cells (NPCs) of patients with ASD. They found the NPCs – responsible for producing the three main kinds of brain cells: neurons, oligodendrocytes and astrocytes – either overproduced or underproduced the number of permanent brain cells.
“The NPCs we studied from all samples showed abnormal proliferation, either ‘too little’ or ‘too much,’ which suggests that poor control of proliferation of brain cells is an important basis for ASD causation,” said Emanuel DiCicco-Bloom, a professor of neuroscience and cell biology, and pediatrics at Rutgers Robert Wood Johnson Medical School and author of the paper. “This study demonstrates at the cellular level that altered proliferation is indeed one likely mechanism of the disorder, supporting implications obtained from previous research.”
The study focused on the stem cell activity of five individuals with ASD, including those with idiopathic autism where there is no known genetic cause, and others with genetically defined 16p11.2 deletion. Those with macrocephaly, a medical term for an abnormally large head, had NPCs that produced too many brain cells. The remaining two patients, who did not have macrocephaly, had NPCs that produced too few brain cells.
ASD is a neurodevelopmental disorder characterized by difficulties with social interactions and communication and the presence of repetitive and restricted behaviors. Most ASD cases are idiopathic. About 15 percent to 20 percent of ASD cases are caused by specific genetic mutations.
NPCs are formed prenatally during a period that stretches from the end of the first trimester through the second, about weeks eight to 24 of the 40-week gestation period of a human fetus.
“We’ve actually measured proliferation of human neural precursors and greatly advanced our understanding,” DiCicco-Bloom said. “In the future, once we have reproduced these studies and extended them, we also may be able to use this knowledge as a biomarker, which could signal when to introduce therapy, or to identify signaling pathways to target with drugs.”
Other Rutgers researchers involved in the study include James Millonig, senior associate dean of the Rutgers School of Graduate Studies and member of the Center for Advanced Biotechnology and Medicine; Robert Connacher, Madeline Williams, Smrithi Prem, Xiaofeng Zhou, Courtney McDermott, and Zhiping Pang of the Department of Neuroscience and Cell Biology of Rutgers Robert Wood Johnson Medical School; Percy Yeung and Che-Wei Lu of the Child Health Institute of New Jersey; Paul Matteson and Monal Mehta of CABM; Anna Markov of the Department of Molecular Biology and Biochemistry; Cynthia Peng of the Department of Cell Biology and Neuroscience; and Judy Flax and Linda Brzustowicz of the Department of Genetics.
Stem Cell Reports
Method of Research
Subject of Research
Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses
Article Publication Date