Hasegawa N
Shika Kiso Igakkai Zasshi. 1989 Aug;31(4):392-403. doi: 10.2330/joralbiosci1965.31.392.
An attempt to develop a new pulp-dentin slice culture system was carried out using thin slices of rat incisors in order to obtain a better culture method which will be useful for studies of the physiological function of odontoblasts including the mechanism of dentiogenesis. The thin slices of incisors were prepared from mandibles of 4-5-day-old rats, using original equipment that was developed in the present study. They were incubated under stationary and rocking culture conditions with two oxygen tensions (50 and 95%). The hyperbaric condition (30% O2, 2 atm) was also tested. Histological observations, [3H]-proline uptake examination and [3H]-proline autoradiography were carried out in order to estimate the matrix formative ability of odontoblasts. The results showed that the pulp-dentin slice culture system successfully preserved the viability and the matrix formative function of odontoblasts. The rocking culture was more favorable than the stationary culture to maintain the cell viability. The higher oxygen tension improved the matrix formative function of odontoblasts. Satisfactory results were obtained from the rocking culture (95% O2) and the hyperbaric stationary culture (30% O2, 2 atm). These results suggest that a large amount of oxygen may be required for maintaining the functions of odontoblasts in this new pulp-dentin slice culture system.
为了获得一种更适合研究成牙本质细胞生理功能(包括牙本质形成机制)的培养方法,我们尝试利用大鼠切牙薄片开发一种新的牙髓 - 牙本质切片培养系统。切牙薄片取自4 - 5日龄大鼠的下颌骨,使用本研究中开发的原始设备制备。将其在两种氧张力(50%和95%)的静态和摇晃培养条件下进行培养。还测试了高压条件(30% O₂,2个大气压)。为了评估成牙本质细胞的基质形成能力,进行了组织学观察、[³H] - 脯氨酸摄取检测和[³H] - 脯氨酸放射自显影。结果表明,牙髓 - 牙本质切片培养系统成功地保留了成牙本质细胞的活力和基质形成功能。摇晃培养比静态培养更有利于维持细胞活力。较高的氧张力改善了成牙本质细胞的基质形成功能。摇晃培养(95% O₂)和高压静态培养(30% O₂,2个大气压)均获得了满意的结果。这些结果表明,在这种新的牙髓 - 牙本质切片培养系统中,维持成牙本质细胞的功能可能需要大量的氧气。