Modeling dynamics of mutants in heterogeneous stem cell niche

被引:15
作者
Shahriyari, L. [1 ]
Mahdipour-Shirayeh, A. [2 ]
机构
[1] Ohio State Univ, Math Biosci Inst, Columbus, OH 43210 USA
[2] Univ Waterloo, Dept Appl Math, Biomed Res Grp, Waterloo, ON N2L 3G1, Canada
基金
美国国家科学基金会;
关键词
fixation probability; cancer; cell migration; central and border stem cells; stem cell niche; bi-compartmental stochastic model; IMMORTAL STRAND HYPOTHESIS; CANCER; DIFFERENTIATION; TUMORS; CRYPT; SELECTION; PROGENY; P53;
D O I
10.1088/1478-3975/aa5a61
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studying the stem cell (SC) niche architecture is a crucial step for investigating the process of oncogenesis and obtaining an effective stem cell therapy for various cancers. Recently, it has been observed that there are two groups of SCs in the SC niche collaborating with each other to maintain tissue homeostasis: border stem cells (BSCs), which are responsible in controlling the number of non-stem cells as well as stem cells, and central stem cells (CeSCs), which regulate the SC niche. Here, we develop a bi-compartmental stochastic model for the SC niche to study the spread of mutants within the niche. The analytic calculations and numeric simulations, which are in perfect agreement, reveal that in order to delay the spread of mutants in the SC niche, a small but non-zero number of SC proliferations must occur in the CeSC compartment. Moreover, the migration of BSCs to CeSCs delays the spread of mutants. Furthermore, the fixation probability of mutants in the SC niche is independent of types of SC division as long as all SCs do not divide fully asymmetrically. Additionally, the progeny of CeSCs have a much higher chance than the progeny of BSCs to take over the entire niche.
引用
收藏
页数:15
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