Wechselberger Gottfried, Russell Robert C, Neumeister Michael W, Schoeller Thomas, Piza-Katzer Hildegunde, Rainer Christian
Department of Plastic and Reconstructive Surgery, University Hospital Innsbruck, Leopold-Franzens University, Anichstrasse 35, A-6020 Innsbruck, Austria.
Plast Reconstr Surg. 2002 Jul;110(1):123-9. doi: 10.1097/00006534-200207000-00022.
Recent advances in cell biology and tissue engineering have used various delivery vehicles for transplanting varying cell cultures with limited success. These techniques are frequently complicated by tissue necrosis, infection, and resorption. The purpose of this study was to investigate whether urothelium cells, tracheal epithelial cells, and preadipocytes cultured in vitro could be successfully transplanted onto a prefabricated capsule surface by using fibrin glue as a delivery vehicle, with the ultimate goal for use in reconstruction. In the first step of the animal study, tissue specimens (bladder urothelium, tracheal epithelial cells, epididymal fat pad) were harvested for in vitro cell culturing, and a silicone block was implanted subcutaneously or within the anterior rectus sheath to induce capsule formation. After 6 to 10 days, when primary cultures were confluent, the animals were re-anesthetized, the newly formed capsule pouches were incised, and the suspensions of cultured urothelia cells (n = 40), tracheal epithelial cells (n = 32), and preadipocytes (n = 40) were implanted onto the capsule surface in two groups, one using standard culture medium as a delivery vehicle and the second using fibrin glue. Histologic sections were taken, and different histomorphologic studies were performed according to tissue type. Consistently in all animals, a highly vascularized capsule was induced by the silicon material. In all animals in which the authors used fibrin glue as a delivery vehicle, they could demonstrate a successful reimplantation of cultured urothelium cells, tracheal epithelial cells, or preadipocytes. Their animal studies showed that capsule induction in combination with fibrin glue as a delivery vehicle is a successful model for transplantation of different in vivo cultured tissue types.
细胞生物学和组织工程学的最新进展使用了各种递送载体来移植不同的细胞培养物,但成功率有限。这些技术常常因组织坏死、感染和吸收而变得复杂。本研究的目的是调查体外培养的尿路上皮细胞、气管上皮细胞和前脂肪细胞是否可以通过使用纤维蛋白胶作为递送载体成功移植到预制的胶囊表面,最终目标是用于重建。在动物研究的第一步,采集组织标本(膀胱尿路上皮、气管上皮细胞、附睾脂肪垫)进行体外细胞培养,并将硅橡胶块皮下植入或植入腹直肌鞘内以诱导胶囊形成。6至10天后,当原代培养物汇合时,再次对动物进行麻醉,切开新形成的胶囊袋,并将培养的尿路上皮细胞(n = 40)、气管上皮细胞(n = 32)和前脂肪细胞(n = 40)的悬浮液分成两组植入胶囊表面,一组使用标准培养基作为递送载体,另一组使用纤维蛋白胶。取组织学切片,并根据组织类型进行不同的组织形态学研究。在所有动物中,硅材料均诱导出高度血管化的胶囊。在所有使用纤维蛋白胶作为递送载体的动物中,作者都能证明培养的尿路上皮细胞、气管上皮细胞或前脂肪细胞成功重新植入。他们的动物研究表明,胶囊诱导结合纤维蛋白胶作为递送载体是一种成功的不同体内培养组织类型移植模型。