Determination of tenogenic differentiation in human mesenchymal stem cells by terahertz waves for measurement of the optical property of cellular suspensions

被引:2
作者
Morita, Yasuyuki [1 ]
Azuchi, Kosuke [1 ]
Ju, Yang [1 ]
Suzuki, Satoshi [1 ]
Xu, Baiyao [1 ]
Yamamoto, Shuhei [1 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Mech Sci & Engn, Nagoya, Aichi 4648601, Japan
关键词
cell differentiation; terahertz; mesenchymal stem cell; tenocyte; nondestructive evaluation; cellular suspension; TO-TENOCYTE DIFFERENTIATION; TIME-DOMAIN SPECTROSCOPY; FOCAL ADHESION KINASE; COLLAGEN TYPE-I; MECHANICAL STRETCH; TENASCIN-C; TENDON; TECHNOLOGY; BONE; EXPRESSION;
D O I
10.1088/0957-0233/25/6/065703
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Technology for identifying stem cell-to-tenocyte differentiation that is non-contact and non-destructive in vitro is essential in tissue engineering. It has been found that expression of various RNA and proteins produced by differentiated cells is elevated when human bone marrow mesenchymal stem cells (hBMSCs) differentiate into tenocytes. Also, such biomolecules have absorption bands in the terahertz range. Thus, we attempted to evaluate whether terahertz waves could be used to distinguish hBMSC-to-tenocyte differentiation. Terahertz time-domain spectroscopy (THz-TDS) using femtosecond laser pulses was used for terahertz measurements. HBMSCs differentiated into tenocytes with mechanical stimulation: 10% cyclical uniaxial stretching at 1 Hz for 24 or 48 h. Cellular suspensions before and after differentiation were measured with terahertz waves. Complex refractive index, consisting of a refractive index (real) and an extinction coefficient (imaginary) obtained from the transmitted terahertz signals, was evaluated before and after differentiation at 1.0 THz. As a result, the THz-TDS system enabled discrimination of hBMSC-to-tenocyte differentiation due to the marked contrast in optical parameter before and after differentiation. This is the first report of the potential of a THz-TDS system for the detection of tenogenic differentiation using a non-contact and non-destructive in vitro technique.
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页数:8
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