Merguerian P, Chavez D R, Hakim S
Department of Surgery, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
J Urol. 1994 Aug;152(2 Pt 2):671-4. doi: 10.1016/s0022-5347(17)32677-0.
Urinary tract reconstruction using bowel can result in acid-base and electrolyte abnormalities. We tested the feasibility of grafting bladder mucosa and urothelial cells grown on a biodegradable polyglactin 910 scaffold onto de-epithelialized segments of bowel in the rabbit. A segment of de-epithelialized colon was either grafted with cultured urothelium on a collagen mesh scaffold (12 rabbits) or with free bladder mucosa (11 rabbits). In 10 rabbits that served as a control group another segment of bowel was isolated and de-epithelialized. No urothelial or bowel epithelial growth was present 4 weeks later in 10 of the isolated de-epithelialized colonic segments grafted with the cultured urothelium. In 2 segments a minute focus of epithelium staining positively for anticytokeratin antibodies AE1 and AE3 was seen but this could not be histologically differentiated as either urothelium or native colonic epithelium. All 7 surviving animals that underwent a bladder mucosal graft had viable urothelium at sacrifice 30 days postoperatively. In 2 of the 7 rabbits microscopic nests of colonic epithelium were also found underneath the urothelial layer. Of the 7 internal controls 6 had no evidence of bowel epithelial regrowth 4 weeks after de-epithelialization. This study demonstrated that a confluent layer of urothelial cells could be grown in culture using a scaffold of biodegradable mesh and rat tail collagen. We also showed that bladder mucosal grafts can be grown on de-epithelialized bowel segments. We were unable to graft successfully cultured urothelial cells onto a de-epithelialized bowel segment. Further improvement in understanding the role of the submucosal matrix in cell growth may lead to future success in covering large segments of de-epithelialized bowel with autologous urothelium.
使用肠道进行尿路重建可能会导致酸碱和电解质异常。我们测试了将在可生物降解的聚乙醇酸910支架上生长的膀胱黏膜和尿路上皮细胞移植到兔去上皮化肠段的可行性。将一段去上皮化的结肠要么移植在胶原网支架上培养的尿路上皮(12只兔),要么移植游离的膀胱黏膜(11只兔)。在10只作为对照组的兔中,分离出另一段肠并去上皮化。4周后,在10个移植了培养尿路上皮的分离去上皮化结肠段中没有出现尿路上皮或肠上皮生长。在2个肠段中,可见一小片上皮对抗细胞角蛋白抗体AE1和AE3呈阳性染色,但在组织学上无法区分是尿路上皮还是天然结肠上皮。所有7只接受膀胱黏膜移植的存活动物在术后30天处死时都有存活的尿路上皮。在7只兔中的2只,在尿路上皮层下方也发现了结肠上皮的微小巢状结构。在7个内部对照中,6个在去上皮化4周后没有肠上皮再生的迹象。本研究表明,使用可生物降解网和大鼠尾胶原支架在培养中可以生长出汇合的尿路上皮层。我们还表明膀胱黏膜移植物可以在去上皮化的肠段上生长。我们未能成功地将培养的尿路上皮细胞移植到去上皮化的肠段上。对黏膜下层基质在细胞生长中作用的进一步了解可能会导致未来成功地用自体尿路上皮覆盖大片去上皮化的肠段。