4.7 Article

Radiotherapy Side Effects: Comprehensive Proteomic Study Unraveled Neural Stem Cell Degenerative Differentiation upon Ionizing Radiation

Journal

BIOMOLECULES
Volume 12, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/biom12121759

Keywords

radiation side effects; neural stem cell; redox proteomics

Funding

  1. National Key Research and Development Program of China
  2. Natural Science Foundation of Guangdong Province [2021YFA0719303]
  3. China Manned Space Flight Technology Project Chinese Space Station [2022A1515010952]
  4. [YYWT-0901-EXP-15]

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Cranial radiation therapy is effective for childhood brain cancers, but it can lead to cognitive impairment. This study found that radiation arrested the cell cycle and impacted differentiation of neural stem cells (NSCs). Proteomic analysis revealed that radiation suppressed protein transport and neuron projection development. Additionally, oxidative modifications were observed in proteins of differentiating NSCs. Some of the identified proteins were associated with neurodegenerative diseases. These findings have implications for understanding neurodegeneration and developing preventive strategies.
Cranial radiation therapy is one of the most effective treatments for childhood brain cancers. Despite the ameliorated survival rate of juvenile patients, radiation exposure-induced brain neurogenic region injury could markedly impair patients' cognitive functions and even their quality of life. Determining the mechanism underlying neural stem cells (NSCs) response to irradiation stress is a crucial therapeutic strategy for cognitive impairment. The present study demonstrated that X-ray irradiation arrested NSCs' cell cycle and impacted cell differentiation. To further characterize irradiation-induced molecular alterations in NSCs, two-dimensional high-resolution mass spectrometry-based quantitative proteomics analyses were conducted to explore the mechanism underlying ionizing radiation's influence on stem cell differentiation. We observed that ionizing radiation suppressed intracellular protein transport, neuron projection development, etc., particularly in differentiated cells. Redox proteomics was performed for the quantification of cysteine thiol modifications in order to profile the oxidation-reduction status of proteins in stem cells that underwent ionizing radiation treatment. Via conjoint screening of protein expression abundance and redox status datasets, several significantly expressed and oxidized proteins were identified in differentiating NSCs subjected to X-ray irradiation. Among these proteins, succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial (sdha) and the acyl carrier protein, mitochondrial (Ndufab1) were highly related to neurodegenerative diseases such as Parkinson's disease, Alzheimer's disease, and Huntington's disease, illustrating the dual-character of NSCs in cell differentiation: following exposure to ionizing radiation, the normal differentiation of NSCs was compromised, and the upregulated oxidized proteins implied a degenerative differentiation trajectory. These findings could be integrated into research on neurodegenerative diseases and future preventive strategies.

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