Pregnancy-induced maternal microchimerism shapes neurodevelopment and behavior in mice.
Steven SchepanskiMattia ChiniVeronika SternemannChristopher UrbschatKristin ThieleTing SunYu ZhaoMareike PoburskiAnna WoestemeierMarie-Theres ThiemeDimitra E ZazaraMalik AlawiNicole FischerJoerg HeerenNikita VladimirovAndrew WoehlerVictor G PuellesStefan BonnNicola GaglianiIleana L Hanganu-OpatzPetra Clara ArckPublished in: Nature communications (2022)
Life-long brain function and mental health are critically determined by developmental processes occurring before birth. During mammalian pregnancy, maternal cells are transferred to the fetus. They are referred to as maternal microchimeric cells (MMc). Among other organs, MMc seed into the fetal brain, where their function is unknown. Here, we show that, in the offspring's developing brain in mice, MMc express a unique signature of sensome markers, control microglia homeostasis and prevent excessive presynaptic elimination. Further, MMc facilitate the oscillatory entrainment of developing prefrontal-hippocampal circuits and support the maturation of behavioral abilities. Our findings highlight that MMc are not a mere placental leak out, but rather a functional mechanism that shapes optimal conditions for healthy brain function later in life.
Keyphrases
- pregnancy outcomes
- resting state
- white matter
- functional connectivity
- induced apoptosis
- mental health
- cerebral ischemia
- cell cycle arrest
- high fat diet induced
- high fat diet
- body mass index
- endoplasmic reticulum stress
- endothelial cells
- adipose tissue
- high glucose
- spinal cord injury
- brain injury
- subarachnoid hemorrhage
- weight gain
- mental illness
- transcranial magnetic stimulation
- skeletal muscle
- insulin resistance
- weight loss