Stereotypical alterations in cortical patterning are associated with maternal illness-induced placental dysfunction
Pamela A Carpentier1, Ursula Haditsch, Amy E Braun
1Stanford University, Institute for Stem Cell Biology and Regenerative Medicine, Stanford, California 94305-5454.
Summary
Maternal illness during a specific gestational window can disrupt fetal brain development, altering neuronal positioning and leading to behavioral changes relevant to autism spectrum disorders.
Area of Science:
- Neuroscience
- Developmental Biology
- Immunology
Background:
- Cytokine-mediated placental damage can impair fetal nutrient and oxygen supply.
- Placental vulnerability to maternal inflammation changes throughout gestation.
Purpose of the Study:
- To investigate the impact of maternal illness during a specific gestational window on fetal neurodevelopment.
- To determine if placental vulnerability timing influences neuroanatomical development and behavior.
Main Methods:
- Mice models were used to study maternal illness effects during critical gestation periods.
- Analysis of neuronal subtype abundance and laminar positioning in the fetal brain cortex.
- Assessment of adult social behavior and cognitive function.
Main Results:
- Maternal illness during a specific gestational window altered neuronal subtype abundance and laminar positioning.
- Disturbances in the Tbr1, Satb2, and Ctip2/Fezf2 patterning axis were observed.
- Laminar imbalance in neuron types led to altered social behavior and cognition in adults.
Conclusions:
- The timing of placental vulnerability to maternal illness critically impacts fetal neurodevelopment.
- Developmental alterations in neuroanatomical systems and behaviors are linked to autism spectrum disorders.
- Illness-induced placental compromise during specific gestation periods has long-term neurodevelopmental consequences.
More Related Videos
Related Concept Videos
Teratogenicity
4.2K
The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
4.2K
Genomic Imprinting and Inheritance
30.4K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
30.4K
Alzheimer Disease ll: Pathophysiology
44
Alzheimer disease involves structural changes in the brain that begin long before symptoms appear. The most distinctive features are extracellular neuritic plaques and intracellular neurofibrillary tangles.Neuritic plaques form in the cerebral cortex and around blood vessels. These plaques contain a dense core of beta-amyloid (Aβ)—a toxic protein fragment that clumps outside neurons. The core is surrounded by damaged neuronal extensions, as well as reactive astrocytes and...
44
Pathophysiology of Diabetes
3.9K
Diabetes mellitus is a chronic metabolic disorder characterized by hyperglycemia. The four categories of diabetes are type 1 diabetes, type 2 diabetes, other specific types of diabetes, and gestational diabetes.
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
3.9K
Biological Causes of Schizophrenia
1.2K
Schizophrenia, a severe psychiatric disorder, arises from a complex interplay of biological factors, including genetic predisposition, structural brain abnormalities, neurotransmitter dysregulation, and developmental irregularities. These factors collectively contribute to the onset and progression of the disorder, which typically manifests in late adolescence or early adulthood.
Genetic Factors in Schizophrenia
The genetic basis of schizophrenia is strongly supported by family and twin...
Genetic Factors in Schizophrenia
The genetic basis of schizophrenia is strongly supported by family and twin...
1.2K


