Comparison of models of neural stem cell heterogeneity for radiation research

31 Oct 2025, 14:00
20m
3d floor, 310 (MLIT)

3d floor, 310

MLIT

Oral Radiation Research in Life Science Radiation research in Life Science

Speaker

Artem Glebov (LRB)

Description

Radiation-induced impairments in memory and learning are associated to the death of neural stem cells (NSCs) in the dentate gyrus of the hippocampus [1, 2]. Three types of NSCs have been identified distinguished by their self-renewal rates: active cells, long-term self-renewing cells, and resting cells [3]. Additionally, has been established the coexistence of three NSC types — alpha, beta, and omega, which differ in morphological characteristics, proliferative activity, and response to external stimuli [4, 5]. Differences in the sensitivity of various NSC types to radiation may determine the extent of radiation-induced impairments in the hippocampus.

Previously, we proposed a model describing the dynamics of NSCs with varying self-renewal rates [6]. In this study, we focused on modeling the morphological heterogeneity of NSCs. We developed a model describing the dynamics of alpha and beta NSCs in response to irradiation. The modeling results were compared with models of homogeneous and heterogeneous NSC populations after irradiation with iron particles. Models according to populations of long-term self-renewing and resting cells demonstrated the highest accuracy. Further development of models that account for the effects of radiation on different NSC types may facilitate a more precise assessment of the risks of memory and learning impairments after irradiation.

  1. Rivera, Phillip D., et al. "Acute and fractionated exposure to high-LET 56Fe HZE-particle radiation both result in similar long-term deficits in adult hippocampal neurogenesis." Radiation research 180.6 (2013): 658-667.

  2. DeCarolis, Nathan A., et al. "56Fe particle exposure results in a long-lasting increase in a cellular index of genomic instability and transiently suppresses adult hippocampal neurogenesis in vivo." Life sciences in space research 2 (2014): 70-79.

  3. Wu, Yicheng, et al. "Chronic in vivo imaging defines age-dependent alterations of neurogenesis in the mouse hippocampus." Nature Aging 3.4 (2023): 380-390.

  4. Gebara, Elias, et al. "Heterogeneity of radial glia-like cells in the adult hippocampus." Stem cells 34.4 (2016): 997-1010.

  5. Martín‐Suárez, Soraya, et al. "Phenotypical and functional heterogeneity of neural stem cells in the aged hippocampus." Aging cell 18.4 (2019): e12958.

  6. Glebov, A. A., E. A. Kolesnikova, and A. N. Bugay. "Modeling the survival rate of a heterogeneous population of neural stem cells in response to irradiation with 56Fe particles." Particles Physics of Particles and Nuclei Letters 22.5 (2025): 1203-1206.

Authors

Artem Glebov (LRB) Elena Kolesnikova (JINR) Александр Бугай (Joint Institute for Nuclear Research)

Presentation materials