The use of nanovibration to discover specific and potent bioactive metabolites that stimulate osteogenic differentiation in mesenchymal stem cells

被引:28
作者
Hodgkinson, Tom [1 ,2 ]
Tsimbouri, P. Monica [1 ]
Llopis-Hernandez, Virginia [1 ]
Campsie, Paul [3 ]
Scurr, David [4 ]
Childs, Peter G. [5 ]
Phillips, David [6 ]
Donnelly, Sam [1 ]
Wells, Julia A. [7 ]
O'Brien, Fergal J. [2 ]
Salmeron-Sanchez, Manuel [5 ]
Burgess, Karl [8 ]
Alexander, Morgan [4 ]
Vassal, Massimo [5 ]
Oreffo, Richard O. C. [7 ]
Reid, Stuart [3 ]
France, David J. [6 ]
Dalby, Matthew J. [1 ]
机构
[1] Univ Glasgow, Coll Med Vet & Life Sci, Ctr Cellular Microenvironm, Inst Mol Cell & Syst Biol, Glasgow G12 8QQ, Lanark, Scotland
[2] Royal Coll Surgeons Ireland, Dept Anat & Regenerat Med, Tissue Engn Res Grp, Dublin D2, Ireland
[3] Univ Strathclyde, SUPA Dept Biomed Engn, Glasgow G1 1QE, Lanark, Scotland
[4] Univ Nottingham, Sch Pharm, Nottingham NG7 2RD, England
[5] Univ Glasgow, Ctr Cellular Microenvironm, Sch Engn, Div Biomed Engn, Glasgow G12 8LT, Lanark, Scotland
[6] Univ Glasgow, Coll Sci & Engn, Sch Chem, Glasgow G12 8QQ, Lanark, Scotland
[7] Univ Southampton, Bone & Joint Res Grp, Ctr Human Dev Stem Cells & Regenerat, Inst Dev Sci, Glasgow SO16 6YD, Lanark, Scotland
[8] Univ Glasgow, Coll Med Vet & Life Sci, Glasgow Polyom, Switchback Rd, Glasgow G61 1BD, Lanark, Scotland
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会; 欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
MASS-SPECTROMETRY DATA; MOLECULAR-MECHANISMS; CHOLESTEROL SULFATE; METABOLOMICS; MEMBRANE; ADHESION; INDENTATION; MODULATION; OSTEOBLAST; MATRIX;
D O I
10.1126/sciadv.abb7921
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bioactive metabolites have wide-ranging biological activities and are a potential source of future research and therapeutic tools. Here, we use nanovibrational stimulation to induce osteogenic differentiation of mesenchymal stem cells, in the absence of off-target, nonosteogenic differentiation. We show that this differentiation method, which does not rely on the addition of exogenous growth factors to culture media, provides an artifact-free approach to identifying bioactive metabolites that specifically and potently induce osteogenesis. We first identify a highly specific metabolite, cholesterol sulfate, an endogenous steroid. Next, a screen of other small molecules with a similar steroid scaffold identified fludrocortisone acetate with both specific and highly potent osteogenic-inducing activity. Further, we implicate cytoskeletal contractility as a measure of osteogenic potency and cell stiffness as a measure of specificity. These findings demonstrate that physical principles can be used to identify bioactive metabolites and then enable optimization of metabolite potency can be optimized by examining structure-function relationships.
引用
收藏
页数:16
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