Hamaji Masatsugu, Kojima Fumitsugu, Koyasu Sho, Tsuruyama Tatsuaki, Komatsu Teruya, Ikuno Tsuyoshi, Date Hiroshi, Nakamura Tatsuo
Department of Bioartificial Organs, Institute for Frontier Medical Sciences, Kyoto University, Sakyo-ku, Kyoto, Japan Department of Thoracic Surgery, Kyoto University, Sakyo-ku, Kyoto, Japan
Department of Bioartificial Organs, Institute for Frontier Medical Sciences, Kyoto University, Sakyo-ku, Kyoto, Japan Department of Thoracic Surgery, Kyoto University, Sakyo-ku, Kyoto, Japan.
Interact Cardiovasc Thorac Surg. 2014 Sep;19(3):357-62. doi: 10.1093/icvts/ivu177. Epub 2014 Jun 3.
We herein report on development of a composite (synthetic and biological) tracheal scaffold with vascularized autologous connective tissue in the omentum, followed by in situ tissue engineering of the composite scaffold with the pedicled omentum. In this preliminary report, we focus on development and evaluation of the vascularized autologous connective tissue in the omentum.
In animal experiment 1, a polypropylene framework as a synthetic component was placed in the omental sac for 3 weeks and another was placed in the pouch of Douglas as a control in five beagle dogs. In animal experiment 2, a polypropylene framework placed in the omental sac for 3 weeks was compared with a polypropylene framework coated with porcine atelocollagen, which was also placed in the omental sac in another five dogs, to investigate whether the coating of porcine atelocollagen contributes to development of more vascularized connective tissue. Macroscopic, radiological and histological evaluations were performed for developed autologous connective tissue on the frameworks, with a focus on its thickness and capillary vessels.
In animal experiment 1, the polypropylene framework in the omentum developed a composite tracheal scaffold with homogeneous and significantly thicker (2.6 ± 0.5 vs 1.2 ± 0.4 mm, P <0.0001) connective tissue in which more capillary vessels per 10-power field of view (3.5 ± 2.2 vs 0 ± 0, P = 0.015) were identified, compared with the control in the pouch of Douglas. In animal experiment 2, the omentum developed significantly thicker connective tissue on the polypropylene framework coated with porcine atelocollagen (3.6 ± 0.7 vs 2.2 ± 0.4 mm, P <0.0001) in which not significantly more capillary vessels were identified (3.5 ± 2.2 vs 5.0 ± 2.7, P = 0.12), compared with the framework that was not coated.
Placement of the polypropylene framework in the omental sac resulted in development of homogeneous and vascularized autologous connective tissue on the polypropylene framework for a composite tracheal scaffold. The framework coated with porcine atelocollagen did not show an additional benefit in inducing vascularization. This preliminary report will be followed by the long-term evaluations of in situ tissue engineering of the composite tracheal scaffold.
我们在此报告一种复合(合成与生物)气管支架的研发情况,该支架带有大网膜内血管化的自体结缔组织,随后利用带蒂大网膜对复合支架进行原位组织工程构建。在本初步报告中,我们重点关注大网膜内血管化自体结缔组织的研发与评估。
在动物实验1中,将一个聚丙烯框架作为合成组件置于五只比格犬的网膜囊中3周,另一个置于道格拉斯窝作为对照。在动物实验2中,将置于网膜囊3周的聚丙烯框架与另一个涂有猪去端胶原蛋白的聚丙烯框架进行比较,后者也置于另外五只犬的网膜囊中,以研究猪去端胶原蛋白涂层是否有助于形成血管化程度更高的结缔组织。对框架上形成的自体结缔组织进行宏观、放射学和组织学评估,重点关注其厚度和毛细血管。
在动物实验1中,网膜囊内的聚丙烯框架形成了一个复合气管支架,其结缔组织均匀且明显更厚(2.6±0.5 vs 1.2±0.4毫米,P<0.0001),每10倍视野中的毛细血管数量更多(3.5±2.2 vs 0±0,P = 0.015),与道格拉斯窝中的对照相比。在动物实验2中,与未涂层的框架相比,涂有猪去端胶原蛋白的聚丙烯框架上的网膜形成了明显更厚的结缔组织(3.6±0.7 vs 2.2±0.4毫米,P<0.0001),但其中识别出的毛细血管数量没有显著增加(3.5±2.2 vs 5.0±2.7,P = 0.12)。
将聚丙烯框架置于网膜囊中可在聚丙烯框架上形成用于复合气管支架的均匀且血管化的自体结缔组织。涂有猪去端胶原蛋白的框架在诱导血管化方面未显示出额外益处。本初步报告之后将对复合气管支架的原位组织工程进行长期评估。