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利用在羊膜上培养的口腔角质形成细胞构建的组织工程化生物人工黏膜制作肌黏膜瓣。

Fabrication of myomucosal flap using tissue-engineered bioartificial mucosa constructed with oral keratinocytes cultured on amniotic membrane.

作者信息

Ahn Kang-Min, Lee Jong-Ho, Hwang Soon-Jung, Choung Pill-Hoon, Kim Myung-Jin, Park Hee-Jung, Park Jung-Keug, Jahng Jeongwon, Yang Eun-Kyung

机构信息

Department of Oral and Maxillofacial Surgery, School of Medicine, Ulsan University, Asan Medical Center, Ulsan, Korea.

出版信息

Artif Organs. 2006 Jun;30(6):411-23. doi: 10.1111/j.1525-1594.2006.00236.x.

Abstract

The purpose of this study was to fabricate bioartificial mucosa using cultured oral keratinocytes (OKCs) on an amniotic membrane (AM), and to evaluate the possibility of developing a prelaminated myomucosal flap using the fabricated bioartificial mucosa and local muscle flap. Buccal mucosa was harvested from male New Zealand rabbits (n = 40, 2.5-3.0 kg) and primary cultivation was performed. The cultured OKCs were seeded on the AM and a submerged culture was performed. Prelamination of the bioartificial mucosa was performed on the latissimus dorsi (LD) muscle of rabbits. Survival rate, layer of OKCs, and Cinamon's score (CS) based on macroscopic and microscopic examinations were evaluated 7, 10, 14, and 21 days after prelamination (n = 10 per day). The OKCs cultured on AM showed multiple layers (3.85 +/- 1.32) and cells were tightly adhered with desmosomes. Basal layer cells adhered to the AM with hemidesmosomes. In addition, the AM played an excellent role as a substrate for the OKCs and simplified handling during prelamination. A myomucosal flap with OKCs cultured on AM was fabricated within 2 weeks (CS: 11.05 +/- 2.63). The basement component of laminin was observed 2 weeks after prelamination and showed enough strength to adhere to the underlying fascia. A myomucosal flap was successfully developed using prelamination of bioartificial mucosa on the LD muscle between 10 and 14 days.

摘要

本研究的目的是在羊膜(AM)上使用培养的口腔角质形成细胞(OKCs)制备生物人工黏膜,并评估使用制备的生物人工黏膜和局部肌瓣制作预层压肌黏膜瓣的可能性。从雄性新西兰兔(n = 40,体重2.5 - 3.0 kg)采集颊黏膜并进行原代培养。将培养的OKCs接种到AM上并进行浸没培养。在兔的背阔肌(LD)上进行生物人工黏膜的预层压。在预层压后7、10、14和21天评估存活率、OKCs层数以及基于宏观和微观检查的肉桂评分(CS)(每天n = 10)。在AM上培养的OKCs显示出多层(3.85 +/- 1.32),细胞通过桥粒紧密粘附。基底层细胞通过半桥粒粘附到AM上。此外,AM作为OKCs的基质发挥了出色的作用,并简化了预层压过程中的操作。在2周内制作出了在AM上培养有OKCs的肌黏膜瓣(CS:11.05 +/- 2.63)。预层压2周后观察到层粘连蛋白的基底成分,并且显示出足够的强度粘附于下方的筋膜。在10至14天之间,通过在LD肌肉上预层压生物人工黏膜成功制作出了肌黏膜瓣。

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