Mathematical modeling of growth and death dynamics of mouse embryonic stem cells irradiated with γ-rays

被引:1
作者
Terranova, N. [1 ]
Rebuzzini, P. [2 ]
Mazzini, G. [3 ]
Borella, E. [1 ]
Redi, C. A. [2 ,4 ]
Zuccotti, M. [5 ]
Garagna, S. [2 ,6 ]
Magni, P. [1 ,6 ]
机构
[1] Univ Pavia, Dipartimento Ingn Ind & Informaz, I-27100 Pavia, Italy
[2] Univ Pavia, Dipartimento Biol & Biotecnol Lazzaro Spallanzani, Lab Biol Sviluppo, I-27100 Pavia, Italy
[3] CNR, Ist Genet Mol, Sez Istochim & Citometria, I-27100 Pavia, Italy
[4] Fdn IRCCS Policlin San Matteo, Pavia, Italy
[5] Univ Parma, Dipartimento Sci Biomed Biotecnol & Traslaz SBiBi, Unita Anat Istol & Embriol, I-43100 Parma, Italy
[6] Univ Pavia, CIT, I-27100 Pavia, Italy
关键词
Cell growth; Cell death; Ionizing irradiation; DNA-DAMAGE; TUMOR-GROWTH; IONIZING-RADIATION; ANTICANCER AGENTS; STRESS DEFENSE; APOPTOSIS; KINETICS; REPAIR; DIFFERENTIATION; COMMITMENT;
D O I
10.1016/j.jtbi.2014.08.042
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Following ionizing radiation, mouse embryonic stem cells (mESCs) undergo both apoptosis and block at G2/M phase of the cell cycle. The dynamics of cell growth and the transition through the apoptotic phases cannot be directly inferred from experimental data, limiting the understanding of the biological response to the treatment. Here, we propose a semi-mechanistic mathematical model, defined by five compartments, able to describe the time curves of untreated and gamma-rays irradiated mESCs and to extract the information therein embedded. To this end, mESCs were irradiated with 2 or 5 Gy gamma-rays, collected over a period of 48 h and, at each time point, analyzed for apoptosis by using the Annexin V assay. When compared to unirradiated mESCs, the model estimates an additional 0.2 probability to undergo apoptosis for the 5 Gy-treated cells, and only a 0.07 (not statistically significantly different from zero) when a 2 Gy-irradiation dose is administered. Moreover, the model allows us to estimate the duration of the overall apoptotic process and also the time length of its early, intermediate, and late apoptotic phase. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:374 / 380
页数:7
相关论文
共 37 条
  • [1] ES cells do not activate p53-dependent stress responses and undergo p53-independent apoptosis in response to DNA damage
    Aladjem, MI
    Spike, BT
    Rodewald, LW
    Hope, TJ
    Klemm, M
    Jaenisch, R
    Wahl, GM
    [J]. CURRENT BIOLOGY, 1998, 8 (03) : 145 - 155
  • [2] [Anonymous], 2013, NEWNES
  • [3] Mammalian G1- and S-phase checkpoints in response to DNA damage
    Bartek, J
    Lukas, J
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (06) : 738 - 747
  • [4] Commitment to cell death measured by loss of clonogenicity is separable from the appearance of apoptotic markers
    Brunet, CL
    Gunby, RH
    Benson, RSP
    Hickman, JA
    Watson, AJM
    Brady, G
    [J]. CELL DEATH AND DIFFERENTIATION, 1998, 5 (01) : 107 - 115
  • [5] The impacts of geometry and binding on CaMKII diffusion and retention in dendritic spines
    Byrne, Michael J.
    Waxham, M. Neal
    Kubota, Yoshihisa
    [J]. JOURNAL OF COMPUTATIONAL NEUROSCIENCE, 2011, 31 (01) : 1 - 12
  • [6] A model-based approach to the in vitro evaluation of anticancer activity
    Del Bene, Francesca
    Germani, Massimiliano
    De Nicolao, Giuseppe
    Magni, Paolo
    Re, Claudia Ernestina
    Ballinari, Dario
    Rocchetti, Maurizio
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2009, 63 (05) : 827 - 836
  • [7] ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS
    EVANS, MJ
    KAUFMAN, MH
    [J]. NATURE, 1981, 292 (5819) : 154 - 156
  • [8] Acute and Fractionated Irradiation Differentially Modulate Glioma Stem Cell Division Kinetics
    Gao, Xuefeng
    McDonald, J. Tyson
    Hlatky, Lynn
    Enderling, Heiko
    [J]. CANCER RESEARCH, 2013, 73 (05) : 1481 - 1490
  • [9] Goldstein JC, 2000, ANN NY ACAD SCI, V926, P132
  • [10] Mathematical Modeling of Tumor Growth, Drug-Resistance, Toxicity, and Optimal Therapy Design
    Hadjiandreou, Marios M.
    Mitsis, Georgios D.
    [J]. IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2014, 61 (02) : 415 - 425