In silico modeling the potential clinical effect of growth factor treatment on the metabolism of human nucleus pulposus cells

被引:1
|
作者
Mcdonnell, Emily E. [1 ,2 ]
Ni Neill, Tara [1 ,2 ]
Wilson, Niamh [1 ,2 ]
Darwish, Stacey L. [3 ,4 ,5 ,6 ]
Butler, Joseph S. [1 ,3 ,4 ]
Buckley, Conor T. [1 ,2 ,7 ,8 ]
机构
[1] Univ Dublin, Trinity Biomed Sci Inst, Trinity Coll Dublin, Trinity Ctr Biomed Engn, Dublin, Ireland
[2] Univ Dublin, Trinity Coll Dublin, Sch Engn, Discipline Mech Mfg & Biomed Engn, Dublin, Ireland
[3] Mater Misericordiae Univ Hosp, Natl Spinal Injuries Unit, Dublin, Ireland
[4] Univ Coll Dublin, Sch Med, Dublin, Ireland
[5] Natl Orthopaed Hosp, Dept Trauma & Orthopaed, Dublin, Ireland
[6] St Vincents Univ Hosp, Dept Orthopaed, Dublin, Ireland
[7] Univ Dublin, Royal Coll Surg Ireland, Trinity Coll Dublin, Adv Mat & Bioengn Res AMBER Ctr, Dublin, Ireland
[8] Royal Coll Surgeons Ireland, Dept Anat & Regenerat Med, Tissue Engn Res Grp, Dublin, Ireland
来源
JOR SPINE | 2024年 / 7卷 / 03期
基金
欧洲研究理事会;
关键词
GDF5; growth factors; in silico; intervertebral disc; metabolism; regeneration; INTERVERTEBRAL DISC; DIFFERENTIATION FACTOR-5; ENERGY-METABOLISM; OXYGEN; INJECTION; GLUCOSE; VIVO; VIABILITY; REPAIR; RATES;
D O I
10.1002/jsp2.1352
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
BackgroundWhile growth factors have the potential to halt degeneration and decrease inflammation in animal models, the literature investigating the effect of dosage on human cells is lacking. Moreover, despite the completion of clinical trials using growth differentiation factor-5 (GDF-5), no results have been publicly released.AimsThe overall objective was to quantitatively assess the effect of three clinically relevant concentrations of GDF-5 (0.25, 1, and 2 mg) as a therapeutic for disc regeneration.Materials and methodsFirstly, this work experimentally determined the effects of GDF-5 concentration on the metabolic and matrix synthesis rates of human nucleus pulposus (NP) cells. Secondly, in silico modeling was employed to predict the subsequent regenerative effect of different GDF-5 treatments (+/- cells).ResultsThis study suggests a trend of increased matrix synthesis with 0.25 and 1 mg of GDF-5. However, 2 mg of GDF-5 significantly upregulates oxygen consumption. Despite this, in silico models highlight the potential of growth factors in promoting matrix synthesis compared to cell-only treatments, without significantly perturbing the nutrient microenvironment.DiscussionThis work elucidates the potential of GDF-5 on human NP cells. Although the results did not reveal statistical differences across all doses, the variability and response among donors is an interesting finding. It highlights the complexity of human response to biological treatments and reinforces the need for further human research and personalized approaches. Furthermore, this study raises a crucial question about whether these potential biologics are more regenerative in nature or better suited as prophylactic therapies for younger patient groups.ConclusionBiological agents exhibit unique characteristics and features, demanding tailored development strategies and individualized assessments rather than a one-size-fits-all approach. Therefore, the journey to realizing the full potential of biological therapies is long and costly. Nonetheless, it holds the promise of revolutionizing spinal healthcare and improving the quality of life for patients suffering from discogenic back pain. This study's focus on growth differentiation factor-5 (GDF-5) highlights the potential of growth factors to enhance extracellular matrix synthesis in human nucleus pulposus (NP) cells, while minimally affecting their metabolism or disrupting the nutrient microenvironment. Our results indicate a trend of increased matrix synthesis at specific GDF-5 concentrations, though individual donor variability must be taken into account. This variability emphasizes the complexity of human responses to biological treatments and underscores the necessity for further research and personalized approaches. image
引用
收藏
页数:18
相关论文
共 50 条
  • [1] ROLE OF HYPOXIA AND GROWTH AND DIFFERENTIATION FACTOR-5 ON DIFFERENTIATION OF HUMAN MESENCHYMAL STEM CELLS TOWARDS INTERVERTEBRAL NUCLEUS PULPOSUS-LIKE CELLS
    Stoyanov, J. V.
    Gantenbein-Ritter, B.
    Bertolo, A.
    Aebli, N.
    Baur, M.
    Alini, M.
    Grad, S.
    EUROPEAN CELLS & MATERIALS, 2011, 21 : 533 - 547
  • [2] The Combined Effects of Transforming Growth Factor-β and basic Fibroblast Growth Factor on the Human Degenerated Nucleus Pulposus Cells in Monolayer Culture
    He, Erxing
    Cui, Ji Hao
    Li, Chuang
    Tang, Cheng
    Kim, In-Sung
    Kim, Young-Woo
    Chang, Ho-Guen
    Cha, Jae-Ryong
    Byung, Oh-Jong
    Kim, Yong-Chan
    TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2013, 10 (03) : 146 - 154
  • [3] Screening for Growth-Factor Combinations Enabling Synergistic Differentiation of Human MSC to Nucleus Pulposus Cell-Like Cells
    Morita, Kosuke
    Schol, Jordy
    Volleman, Tibo N. E.
    Sakai, Daisuke
    Sato, Masato
    Watanabe, Masahiko
    APPLIED SCIENCES-BASEL, 2021, 11 (08):
  • [4] The combined effects of transforming growth factor-β and basic fibroblast growth factor on the human degenerated nucleus pulposus cells in monolayer culture
    Erxing He
    Ji Hao Cui
    Chuang Li
    Cheng Tang
    In-Sung Kim
    Young-Woo Kim
    Ho-Guen Chang
    Jae-Ryong Cha
    Oh-Jong Byung
    Yong-Chan Kim
    Tissue Engineering and Regenerative Medicine, 2013, 10 : 146 - 154
  • [5] Transforming growth factor β mediates communication of co-cultured human nucleus pulposus cells and mesenchymal stem cells
    Lehmann, Tomasz P.
    Glowacki, Jakub
    Harasymczuk, Jerzy
    Jagodzinski, Pawel P.
    JOURNAL OF ORTHOPAEDIC RESEARCH, 2018, 36 (11) : 3023 - 3032
  • [6] Enhancing human nucleus pulposus cells for biological treatment approaches of degenerative intervertebral disc diseases: a systematic review
    Mern, Demissew Shenegelegn
    Beierfuss, Anja
    Thome, Claudius
    Hegewald, Aldemar Andres
    JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2014, 8 (12) : 925 - 936
  • [7] The effect of prolonged rhBMP-2 treatment on telomerase activity, replicative capacity and senescence of human nucleus pulposus cells
    Kim, Ki-Won
    Jeong, Seo-Won
    Park, Hyung-Youl
    Heu, Jun-Young
    Jung, Ho-Young
    Lee, Jun-Seok
    BIOTECHNIC & HISTOCHEMISTRY, 2020, 95 (07) : 490 - 498
  • [8] Vascular endothelial growth factor-A is a survival factor for nucleus pulposus cells in the intervertebral disc
    Fujita, Nobuyuki
    Imai, Jun-ichi
    Suzuki, Toru
    Yamada, Masayuki
    Ninomiya, Ken
    Miyamoto, Kana
    Iwasaki, Ryotaro
    Morioka, Hideo
    Matsumoto, Morio
    Chiba, Kazuhiro
    Watanabe, Shinya
    Suda, Toshio
    Toyama, Yoshiaki
    Miyamoto, Takeshi
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 372 (02) : 367 - 372
  • [9] Effect of Whole Tissue Culture and Basic Fibroblast Growth Factor on Maintenance of Tie2 Molecule Expression in Human Nucleus Pulposus Cells
    Sako, Kosuke
    Sakai, Daisuke
    Nakamura, Yoshihiko
    Schol, Jordy
    Matsushita, Erika
    Warita, Takayuki
    Horikita, Natsumi
    Sato, Masato
    Watanabe, Masahiko
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (09)
  • [10] Potential of Human Nucleus Pulposus-Like Cells Derived From Umbilical Cord to Treat Degenerative Disc Disease
    Perez-Cruet, Mick
    Beeravolu, Naimisha
    McKee, Christina
    Brougham, Jared
    Khan, Irfan
    Bakshi, Shreeya
    Chaudhry, G. Rasul
    NEUROSURGERY, 2019, 84 (01) : 272 - 283