Aberrant choroid plexus formation in human cerebral organoids exposed to radiation.
Marco DuranteTamara BenderEsther SchickelMargot MayerJürgen DebusDavid GrosshansInsa SchroederPublished in: Research square (2023)
Brain tumor patients are commonly treated with radiotherapy, but the efficacy of the treatment is limited by its toxicity, particularly the risk of radionecrosis. We used human cerebral organoids to investigate the mechanisms and nature of postirradiation brain image changes commonly linked to necrosis. Irradiation of cerebral organoids lead to increased formation of ZO1 + /AQP1 + /CLN3 + -choroid plexus (CP) structures. Increased CP formation was triggered by radiation via the NOTCH/WNT signaling pathways and associated with delayed growth and neural stem cell differentiation, but not necrosis. The effect was more pronounced in immature than in mature organoids, reflecting the clinically-observed increased radiosensitivity of the pediatric brain. Protons were more effective than X-rays at the same dose, as also observed in clinical treatments. We conclude that radiation-induced brain image-changes can be attributed to aberrant CP formation, providing a new cellular mechanism and strategy for possible countermeasures.
Keyphrases
- radiation induced
- induced pluripotent stem cells
- cerebral ischemia
- subarachnoid hemorrhage
- endothelial cells
- radiation therapy
- resting state
- white matter
- newly diagnosed
- end stage renal disease
- deep learning
- signaling pathway
- functional connectivity
- brain injury
- ejection fraction
- stem cells
- early stage
- pluripotent stem cells
- ultrasound guided
- chronic kidney disease
- multiple sclerosis
- prognostic factors
- high resolution
- squamous cell carcinoma
- epithelial mesenchymal transition
- blood brain barrier
- patient reported outcomes
- machine learning
- rectal cancer
- induced apoptosis
- mass spectrometry
- combination therapy