Simon Timothy M, Van Sickle David C, Kunishima Dennis H, Jackson Douglas W
Orthopaedic Research Institute at the Southern California Center for Sports Medicine, 2760 Atlantic Avenue, Long Beach 90806, USA.
J Orthop Res. 2003 May;21(3):470-80. doi: 10.1016/S0736-0266(02)00206-1.
An autograft of periosteal tissue containing cambium cells has potential to become chondrogenic or osteogenic depending on the regeneration repair strategies. The potential number of harvestable cambium cells diminishes with age. Other factors may be associated with a reduction in the number or variable yields of cambium cells including harvest technique, harvest site location, and the time interval from harvest to implantation. Attempts to increase the number of cambium cells have included improvements in harvesting and handling technique, and expansion of the cells in tissue culture. An "in situ" stimulation and proliferation technique would offer the potential for increasing the number of cambium cells in a cost-effective manner for transplantation without the need for expansion in tissue culture. The hypothesis tested was that surgical release of the periosteum and its deep inner underlying cambium layer by sharply incising through the superficial periosteal fibrous layer down to and scoring the cortical bone surface would increase the number of cambium cells that could be harvested at a later time period. Two techniques for periosteal release were used to stimulate a proliferation of the underlying cambium layer and increase the cambium cells for harvest in skeletally mature goats: (1) sharply scoring all four-sides of the tissue test site perimeter, and (2) sharply scoring only two sides of the tissue test site. The two-sided and four-sided release scoring of the periosteum induced stimulatory responses in the number of cambium cells. In addition, a marked increase in mRNA expression for BMP-2 (p<0.001) was observed within 24 h and remained elevated over baseline values for up to 96 h after this stimulation to the cambium layer.
含有形成层细胞的骨膜组织自体移植根据再生修复策略有成为软骨生成或骨生成的潜力。可收获的形成层细胞数量会随着年龄增长而减少。其他因素可能与形成层细胞数量减少或产量变化有关,包括收获技术、收获部位位置以及从收获到植入的时间间隔。增加形成层细胞数量的尝试包括改进收获和处理技术,以及在组织培养中扩增细胞。一种“原位”刺激和增殖技术有可能以经济有效的方式增加用于移植的形成层细胞数量,而无需在组织培养中扩增。所测试的假设是,通过锐性切开浅表骨膜纤维层直至皮质骨表面并进行划痕,对骨膜及其深层下方的形成层进行手术松解,会增加在稍后时间段可收获的形成层细胞数量。在骨骼成熟的山羊中,使用两种骨膜松解技术来刺激下方形成层的增殖并增加用于收获的形成层细胞:(1) 在组织测试部位周边的所有四边进行锐性划痕,以及 (2) 仅在组织测试部位的两边进行锐性划痕。骨膜的双边和四边松解划痕诱导了形成层细胞数量的刺激反应。此外,在对形成层进行这种刺激后 24 小时内观察到 BMP - 2 的 mRNA 表达显著增加(p<0.001),并且在长达 96 小时内一直高于基线值。