生物
诱导多能干细胞
表观遗传学
细胞生物学
补体系统
神经干细胞
人口
分泌物
信号转导
免疫系统
神经科学
计算生物学
干细胞
胚胎干细胞
免疫学
遗传学
基因
人口学
社会学
生物化学
作者
Francesca Rapino,Ted Natoli,Francesco Limone,Erin O’Connor,Jack Blank,Matthew Tegtmeyer,William Chen,Erika M. Norabuena,Juhi G. Narula,Dane Z. Hazelbaker,Gabriella Angelini,Lindy E. Barrett,Alison O’Neil,Ursula K. Beattie,Jessica M. Thanos,Heather de Rivera,Steven D. Sheridan,Roy H. Perlis,Steven A. McCarroll,Beth Stevens
标识
DOI:10.1016/j.stemcr.2022.11.018
摘要
In the brain, the complement system plays a crucial role in the immune response and in synaptic elimination during normal development and disease. Here, we sought to identify pathways that modulate the production of complement component 4 (C4), recently associated with an increased risk of schizophrenia. To design a disease-relevant assay, we first developed a rapid and robust 3D protocol capable of producing large numbers of astrocytes from pluripotent cells. Transcriptional profiling of these astrocytes confirmed the homogeneity of this population of dorsal fetal-like astrocytes. Using a novel ELISA-based small-molecule screen, we identified epigenetic regulators, as well as inhibitors of intracellular signaling pathways, able to modulate C4 secretion from astrocytes. We then built a connectivity map to predict and validate additional key regulatory pathways, including one involving c-Jun-kinase. This work provides a foundation for developing therapies for CNS diseases involving the complement cascade.
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