Dental Pulp Stem Cells (DPSCs) differentiation study by Confocal Raman Microscopy

被引:0
作者
Salehi, H. [1 ]
Collart-Dutilleul, P-Y [1 ]
Gergely, C. [2 ,3 ]
Cuisinier, F. J. G. [1 ]
机构
[1] Univ Montpellier I, UFR Odontol, EA 4203, Lab Biol Sante Nanosci, F-34193 Montpellier, France
[2] Univ Montpellier 2, Lab Charles Coulomb, UMR 5221, F-34095 Montpellier, France
[3] CNRS, Lab Charles Coulomb, UMR 5221, Montpellier, France
来源
IMAGING, MANIPULATION, AND ANALYSIS OF BIOMOLECULES, CELLS, AND TISSUES XII | 2014年 / 8947卷
关键词
Dental Pulp Stem cells DPSC; Raman microscopy; differentiation; living cell; SPECTROSCOPY;
D O I
10.1117/12.2041346
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Regenerative medicine brings a huge application for Mesenchymal stem cells such as Dental Pulp Stem Cells (DPSCs). Confocal Raman microscopy, a non-invasive, label free, real time and high spatial resolution imaging technique is used to study osteogenic differentiation of DPSCs. Integrated Raman intensities in the 2800-3000 cm(-1) region (C-H stretching) and 960 cm(-1) peak (phosphate PO43-) were collected. In Dental Pulp Stem Cells 21st day differentiated in buffer solution, phosphate peaks nu(1) PO43- (first vibrational mode) at 960cm(-1) and nu(2) PO43- at 430cm(-1) and nu(4) PO43- at 585cm(-1) are obviously present. Confocal Raman microscopy enables the detection of cell differentiation and it can be used to investigate clinical stem cell research.
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页数:10
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