Dynamics of Intrinsic Glucose Uptake Kinetics in Human Mesenchymal Stem Cells During Chondrogenesis

被引:0
作者
Yi Zhong
Mostafa Motavalli
Kuo-Chen Wang
Arnold I. Caplan
Jean F. Welter
Harihara Baskaran
机构
[1] Case Western Reserve University,Department of Biomedical Engineering
[2] The Skeletal Research Center,Department of Biology
[3] Case Western Reserve University,Department of Chemical and Biomolecular Engineering
[4] Case Western Reserve University,undefined
[5] Case Center for Multimodal Evaluation of Engineered Cartilage,undefined
[6] Case Western Reserve University,undefined
来源
Annals of Biomedical Engineering | 2018年 / 46卷
关键词
Cartilage; Aggregate cultures; Mass transport; Glucose consumption; Diffusional limitation; Michaelis–Menten kinetics; Lactate production; Mathematical modeling;
D O I
暂无
中图分类号
学科分类号
摘要
Chondrogenesis of human mesenchymal stem cells (hMSCs) is an important biological process in many applications including cartilage tissue engineering. We investigated the glucose uptake characteristics of aggregates of hMSCs undergoing chondrogenesis over a 3-week period both experimentally and by using a mathematical model. Initial concentrations of glucose in the medium were varied from 1 to 4.5 g/L to mimic limiting conditions and glucose uptake profiles were obtained. A reaction–diffusion mathematical model was implemented and solved to estimate kinetic parameters. Experimental glucose uptake rates increased with culture time for aggregates treated with higher initial glucose concentrations (3 and 4.5 g/L), whereas they decreased or remained constant for those treated with lower initial glucose concentrations (1 and 2 g/L). Lactate production rate increased by as much as 40% for aggregates treated with higher initial glucose concentrations (2, 3 and 4.5 g/L), whereas it remained constant for those treated with 1 g/L initial glucose concentration. The estimated DNA-normalized maximum glucose uptake rate decreased by a factor of 9 from day 0–2 (12.5 mmol/s/g DNA) to day 6–8 (1.5 mmol/s/g DNA), after which it started to increase. On day 18–20, its value (17.5 mmol/s/g DNA) was about 11 times greater than its lowest value. Further, the extracellular matrix levels of aggregates at day 14 and day 21 correlated with their overall glucose uptake and lactate production. The results suggest that during chondrogenesis, for optimal results, cells require increasing amounts of glucose. Our results also suggest that diffusion limitations play an important role in glucose uptake even in the smaller size aggregate model of chondrogenesis. Further, the results indicate that glucose uptake or lactate production can be a tool for predicting the end quality of tissue during the process of chondrogenesis. The estimated kinetic parameters can be used to model glucose requirements in cartilage tissue engineering applications.
引用
收藏
页码:1896 / 1910
页数:14
相关论文
共 50 条
  • [41] Stiffness memory of indirectly 3D-printed elastomer nanohybrid regulates chondrogenesis and osteogenesis of human mesenchymal stem cells
    Wu, Linxiao
    Magaz, Adrian
    Wang, Tao
    Liu, Chaozong
    Darbyshire, Arnold
    Loizidou, Marilena
    Emberton, Mark
    Birchall, Martin
    Song, Wenhui
    BIOMATERIALS, 2018, 186 : 64 - 79
  • [42] Non-hypertrophic chondrogenesis of mesenchymal stem cells through mechano-hypoxia programing
    Li, David Xinzheyang
    Ma, Zhiyao
    Szojka, Alexander R. A.
    Lan, Xiaoyi
    Kunze, Melanie
    Mulet-Sierra, Aillette
    Westover, Lindsey
    Adesida, Adetola B.
    JOURNAL OF TISSUE ENGINEERING, 2023, 14
  • [43] Comparison of exosomes secreted by synovial fluid-derived mesenchymal stem cells and adipose tissue-derived mesenchymal stem cells in culture for microRNA-127-5p expression during chondrogenesis
    Sevimli, Tugba Semerci
    Sevimli, Murat
    Ekenel, Emilia Qomi
    Tasa, Burcugul Altug
    Soykan, Merve Nur
    Gucluer, Zilif Demir
    Inan, Ulukan
    Uysal, Onur
    Bagis, Sibel Gunes
    Cemrek, Fatih
    Sariboyaci, Ayla Eker
    GENE, 2023, 865
  • [44] Bioconjugated Carbon Dots for Delivery of siTnfα to Enhance Chondrogenesis of Mesenchymal Stem Cells by Suppression of Inflammation
    Liu, Jianwei
    Jiang, Tongmeng
    Li, Chun
    Wu, Yang
    He, Maolin
    Zhao, Jinmin
    Zheng, Li
    Zhang, Xingdong
    STEM CELLS TRANSLATIONAL MEDICINE, 2019, 8 (07) : 724 - 736
  • [45] Proteome analysis of human mesenchymal stem cells undergoing chondrogenesis when exposed to the products of various magnesium-based materials degradation
    Sanchez, Adela Helvia Martinez
    Omidi, Maryam
    Wurlitzer, Marcus
    Fuh, Marceline Manka
    Feyerabend, Frank
    Schlueter, Hartmut
    Willumeit-Roemer, Regine
    Luthringer, Berengere J. C.
    BIOACTIVE MATERIALS, 2019, 4 : 168 - 188
  • [46] Preliminary Characterization of the Epigenetic Modulation in the Human Mesenchymal Stem Cells during Chondrogenic Process
    Miceli, Marco
    Maruotti, Giuseppe Maria
    Sarno, Laura
    Carbone, Luigi
    Guida, Maurizio
    Pelagalli, Alessandra
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (17)
  • [47] Expression of exosomal microRNAs during chondrogenic differentiation of human bone mesenchymal stem cells
    Sun, Hao
    Hu, Shu
    Zhang, Ziji
    Lun, Jiayong
    Liao, Weiming
    Zhang, Zhiqi
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2019, 120 (01) : 171 - 181
  • [48] Chondrogenesis of Human Infrapatellar Fat Pad Stem Cells on Acellular Dermal Matrix
    Ye, Ken
    Traianedes, Kathy
    Choong, Peter F. M.
    Myers, Damian E.
    FRONTIERS IN SURGERY, 2016, 3
  • [49] Chondrogenesis of cocultures of mesenchymal stem cells and articular chondrocytes in poly(L-lysine)-loaded hydrogels
    Kim, Yu Seon
    Chien, Athena J.
    Guo, Jason L.
    Smith, Brandon T.
    Watson, Emma
    Pearce, Hannah A.
    Koons, Gerry L.
    Navara, Adam M.
    Lam, Johnny
    Scott, David W.
    Grande-Allen, K. Jane
    Mikos, Antonios G.
    JOURNAL OF CONTROLLED RELEASE, 2020, 328 : 710 - 721
  • [50] In vitro chondrogenesis of Wharton's jelly mesenchymal stem cells in hyaluronic acid-based hydrogels
    Aleksander-Konert, Ewelina
    Paduszynski, Piotr
    Zajdel, Alicja
    Dzierzewicz, Zofia
    Wilczok, Adam
    CELLULAR & MOLECULAR BIOLOGY LETTERS, 2016, 21