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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
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