CELLULAR FEEDBACK NETWORKS AND THEIR RESILIENCE AGAINST MUTATIONS

被引:0
作者
Bailey, Lora D. [1 ]
Komarova, Natalia L. [2 ]
机构
[1] Grand Valley State Univ, Allendale, MI 49401 USA
[2] Univ Calif Irvine, Dept Math, Irvine, CA 92697 USA
关键词
Cancer; Feedback; Stem Cells; Cellular Control Networks; Cellular Feedback; Resilience; Mutation; Stem Cell Lineages; CELLS; MODELS; FATE;
D O I
10.1142/S0218339021400039
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many tissues undergo a steady turnover, where cell divisions are on average balanced with cell deaths. Cell fate decisions such as stem cell (SC) differentiations, proliferations, or differentiated cell (DC) deaths, may be controlled by cell populations through cell-to-cell signaling. Here, we examine a class of mathematical models of turnover in SC lineages to understand engineering design principles of control (feedback) loops, that may operate in such systems. By using ordinary differential equations that describe the co-dynamics of SCs and DCs, we study the effect of different types of mutations that interfere with feedback present within cellular networks. For instance, we find that mutants that do not participate in feedback are less dangerous in the sense that they will not rise from low numbers, whereas mutants that do not respond to feedback signals could rise and replace the wild-type population. Additionally, we asked if different feedback networks can have different degrees of resilience against such mutations. We found that all minimal networks, that is networks consisting of exactly one feedback loop that is sufficient for homeostatic stability of the wild-type population, are equally vulnerable. Mutants with a weakened/eliminated feedback parameter might expand from lower numbers and either enter unlimited growth or reach an equilibrium with an increased number of SCs and DCs. Therefore, from an evolutionary viewpoint, it appears advantageous to combine feedback loops, creating redundant feedback networks. Interestingly, from an engineering prospective, not all such redundant systems are equally resilient. For some of them, any mutation that weakens/eliminates one of the loops will lead to a population growth of SCs. For others, the population of SCs can actually shrink as a result of "cutting" one of the loops, thus slowing down further unwanted transformations.
引用
收藏
页码:325 / 374
页数:50
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共 42 条
  • [1] Regulatory T Cells in Skin Facilitate Epithelial Stem Cell Differentiation
    Ali, Niwa
    Zirak, Bahar
    Rodriguez, Robert Sanchez
    Pauli, Mariela L.
    Hong-An Truong
    Lai, Kevin
    Ahn, Richard
    Corbin, Kaitlin
    Lowe, Margaret M.
    Scharschmidt, Tiffany C.
    Taravati, Keyon
    Tan, Madeleine R.
    Ricardo-Gonzalez, Roberto R.
    Nosbaum, Audrey
    Bertolini, Marta
    Liao, Wilson
    Nestle, Frank O.
    Paus, Ralf
    Cotsarelis, George
    Abbas, Abul K.
    Rosenblum, Michael D.
    [J]. CELL, 2017, 169 (06) : 1119 - +
  • [2] STABILITY ANALYSIS OF MODELS OF CELL PRODUCTION SYSTEMS
    ARINO, O
    KIMMEL, M
    [J]. MATHEMATICAL MODELLING, 1986, 7 (9-12): : 1269 - 1300
  • [3] T Helper Cell Cytokines Modulate Intestinal Stem Cell Renewal and Differentiation
    Biton, Moshe
    Haber, Adam L.
    Rogel, Noga
    Burgin, Grace
    Beyaz, Semir
    Schnell, Alexandra
    Ashenberg, Orr
    Su, Chien-Wen
    Smillie, Christopher
    Shekhar, Karthik
    Chen, Zuojia
    Wu, Chuan
    Ordovas-Montanes, Jose
    Alvarez, David
    Herbst, Rebecca H.
    Zhang, Mei
    Tirosh, Itay
    Dionne, Danielle
    Nguyen, Lan T.
    Xifaras, Michael E.
    Shalek, Alex K.
    von Andrian, Ulrich H.
    Graham, Daniel B.
    Rozenblatt-Rosen, Orit
    Shi, Hai Ning
    Kuchroo, Vijay
    Yilmaz, Omer H.
    Regev, Aviv
    Xavier, Ramnik J.
    [J]. CELL, 2018, 175 (05) : 1307 - +
  • [4] ACTION OF CHALONES
    BULLOUGH, WS
    [J]. AGENTS AND ACTIONS, 1971, 2 (01): : 1 - &
  • [5] Molecular Pathways: Targeting Cancer Stem Cells Awakened by Chemotherapy to Abrogate Tumor Repopulation
    Chan, Keith Syson
    [J]. CLINICAL CANCER RESEARCH, 2016, 22 (04) : 802 - 806
  • [6] Toward a universal treatment for cancer: cell inflation assisted chemotherapy
    Corcos, Daniel
    [J]. CANCER MEDICINE, 2013, 2 (04): : 421 - 426
  • [7] Compartmental Architecture and Dynamics of Hematopoiesis
    Dingli, David
    Traulsen, Arne
    Pacheco, Jorge M.
    [J]. PLOS ONE, 2007, 2 (04):
  • [8] Neutrophil elastase enzymatically antagonizes the in vitro action of G-CSF: implications for the regulation of granulopoiesis
    El Ouriaghli, F
    Fujiwara, H
    Melenhorst, JJ
    Sconocchia, G
    Hensel, N
    Barrett, AJ
    [J]. BLOOD, 2003, 101 (05) : 1752 - 1758
  • [9] The Importance of Spatial Distribution of Stemness and Proliferation State in Determining Tumor Radioresponse
    Enderling, H.
    Park, D.
    Hlatky, L.
    Hahnfeldt, P.
    [J]. MATHEMATICAL MODELLING OF NATURAL PHENOMENA, 2009, 4 (03) : 117 - 133
  • [10] Myc, cell competition, and compensatory proliferation
    Gallant, P
    [J]. CANCER RESEARCH, 2005, 65 (15) : 6485 - 6487