WANG Yan-jun, WANG Gui-wen, YAO Hui-lu. Study on Liver Cancer Cells (HepG2) Under Simulated Microgravity Based on Raman Spectroscopy[J]. Chinese Journal of Luminescence, 2013,34(10): 1408-1411
WANG Yan-jun, WANG Gui-wen, YAO Hui-lu. Study on Liver Cancer Cells (HepG2) Under Simulated Microgravity Based on Raman Spectroscopy[J]. Chinese Journal of Luminescence, 2013,34(10): 1408-1411 DOI: 10.3788/fgxb20133410.1408.
Study on Liver Cancer Cells (HepG2) Under Simulated Microgravity Based on Raman Spectroscopy
HepG2 was cultured onto biodegradable polyglycolic acid(PGA) polymer scaffolds
which was cultured in a rotating cell culture system (RCCS) to form a three-dimensional (3D) and human liver cancer cells cultured in common plate. We detected the spectra of HepG2 cells under two culture conditions and compared the spectra changes of the different cells under two culture conditions. The results show that Raman spectroscopy can differentiate among HepG2 cells under two culture conditions. 527 cm
-1
and 1 357 cm
-1
peaks of HepG2 cells under simulated microgravity are higher than that of HepG2 cells in common plate. 1 438 cm
-1
and 1 659 cm
-1
peaks of HepG2 cells under simulated microgravity are lower than that of HepG2 cells in common plate. It is known that 527 cm
-1
represents Fe(Ⅱ)
N
N
-MeIm
1 357 cm
-1
represents Guanine
porphyrins (haemoglobin)
lipids
1 438 cm
-1
represents CH
2
deformation (lipids)
cholesterol
and 1 659 cm
-1
represents Amide I: proteins. These biomaterials which induce these peak changes are possibly related to 3D culture.
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references
Nakamura K, Kuga H, Morisaki T, et al. Simulated microgravity culture system for a 3-D carcinoma tissue model [J]. Biotechniques, 2002, 33(5):1068-1070.[2] Wang X, Wei G, Yu W, et al. Scalable producing embryoid bodies by rotary cell culture system and constructing engineered cardiac tissue with ESDerived cardiomyocytes in vitro [J]. Biotechnol. Prog., 2006, 22(3):811-818.[3] Martin A, Zhou A, Gordon R E, et al. Thyroid organoid formation in simulated microgravity: Influence of keratinocyte growth factor [J]. Thyroid, 2000, 10(6):481-487.[4] Draux F, Jeannesson P, Beljebbar A, et al. Raman spectral imaging of single living cancer cells: A preliminary study [J]. Analyst, 2009, 134(3):542-548.[5] Kang L L, Huang Y X, Luo M. Confocal Raman microscopy on single living young and old erythrocytes [J]. Spectrosc. Spect. Anal.(光谱学与光谱分析), 2008, 28(10):2343-2347 (in Chinese).[6] Schrader B, Schulz H, Andreev G N, et al. On-destructive NIR-FT-Raman spectroscopy of plant and animal tissues, of food and works of art [J]. Talanta, 2000, 53(1):35-45.[7] Xie C A, Li Y Q. Confocal micro-Raman spectroscopy of single biological cells using optical trapping and shifted excitation difference techniques [J]. Appl. Phys., 2003, 93(5):2982-2986.[8] Xie C A, Li Y Q, Tang W J. Study of dynamical process of heat denaturation in optically trapped single microorganisms by near-infrared Raman spectroscopy [J]. Appl. Phys., 2003, 94(9):6138-6142.[9] Potten C S, Loeffler M. Stem cells: Attributes, cycles, spirals, pitfalls and uncertainties. Lessons for and from the crypt [J]. Development, 1990, 110(4):1001-1020.[10] Fischbach C, Kong H J, Hsiong S X, et al. Cancer cell angiogenic capability is regulated by 3D culture and integrin engagement [J]. Proc. Natl. Acad. Sci. USA, 2009, 106(2):399-404.[11] Kinasiewiczi A, Kawiak J, Werynski A. 3D matrigel culture improves differentiated functions of HepG2 cells in vitro [J]. Biocybern. Biomed. Eng., 2006, 26(4):47-55.[12] Fisher K E, Pop A, Koh W, et al. Tumor cell invasion of collagen matrices requires coordinate lipid agonist-induced G-protein and membrane-type matrix metalloproteinase-1-dependent [J]. Mol. Cancer, 2006, 5:69-72.