Discriminant Principal Component Analysis of ToF-SIMS Spectra for Deciphering Compositional Differences of MSC-Secreted Extracellular Matrices

被引:7
作者
Zimmermann, Ralf [1 ]
Nitschke, Mirko [1 ]
Magno, Valentina [1 ]
Freudenberg, Uwe [1 ]
Sockel, Katja [2 ]
Stoelzel, Friedrich [2 ,3 ]
Wobus, Manja [2 ]
Platzbecker, Uwe [4 ]
Werner, Carsten [1 ,5 ,6 ]
机构
[1] Leibniz Inst Polymer Res Dresden, Max Bergmann Ctr Biomat, D-01069 Dresden, Germany
[2] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Med Clin & Policlin 1, D-01307 Dresden, Germany
[3] Univ Hosp Schleswig Holstein, Dept Internal Med 2, Div Stem Cell Transplantat & Cellular Immunothera, Arnold Heller Str 3, D-24105 Kiel, Germany
[4] Univ Hosp Leipzig, Hematol & Cellular Therapy, D-04103 Leipzig, Germany
[5] Tech Univ Dresden, Ctr Regenerat Therapies Dresden, D-01307 Dresden, Germany
[6] Tech Univ Dresden, Cluster Excellence Phys Life, D-01307 Dresden, Germany
关键词
discriminant principal component analysis; extracellular matrices; multivariate data analysis; myelodysplastic syndrome; proteome; time-of-flight secondary ion mass spectrometry; ADSORBED PROTEIN FILMS; MESENCHYMAL STROMAL CELLS; ION MASS-SPECTROMETRY; BONE-MARROW FIBROSIS; LYSYL-OXIDASE; IN-VITRO; ASCORBIC-ACID; NICHE; DEPOSITION; MICROENVIRONMENT;
D O I
10.1002/smtd.202201157
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Identifying characteristic extracellular matrix (ECM) variants is a key challenge in mechanistic biology, bioengineering, and medical diagnostics. The reported study demonstrates the potential of time-of-flight secondary ion mass spectrometry (ToF-SIMS) to detect subtle differences between human mesenchymal stromal cell (MSC)-secreted ECM types as induced by exogenous stimulation or emerging pathology. ToF-SIMS spectra of decellularized ECM samples are evaluated by discriminant principal component analysis (DPCA), an advanced multivariate analysis technique, to decipher characteristic compositional features. To establish the approach, signatures of major ECM proteins are determined from samples of pre-defined mixtures. Based on that, sets of ECM variants produced by MSCs in vitro are analyzed. Differences in the content of collagen, fibronectin, and laminin in the ECM resulting from the combined supplementation of MSC cultures with polymers that induce macromolecular crowding and with ascorbic acid are detected from the DPCA of ToF-SIMS spectra. The results are verified by immunostaining. Finally, the comparative ToF-SIMS analysis of ECM produced by MSCs of healthy donors and patients suffering from myelodysplastic syndrome display the potential of the novel methodology to reveal disease-associated alterations of the ECM composition.
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页数:14
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