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基底膜成分在体内刺激肠道缺损的上皮形成。

Basement membrane components stimulate epithelialization of intestinal defects in vivo.

作者信息

Thompson J S

机构信息

Surgical Service, Omaha VAMC, NE.

出版信息

Cell Tissue Kinet. 1990 Sep;23(5):443-51. doi: 10.1111/j.1365-2184.1990.tb01136.x.

DOI:10.1111/j.1365-2184.1990.tb01136.x
PMID:2245441
Abstract

Subepithelial tissues have an important role in the structure and function of the intestinal epithelium. Basement membrane components (BMC) stimulate epithelial cell migration and differentiation in vitro. The aim of this study was to determine the effect of BMC and/or interstitial tissue collagen (type I) on the in vivo intestinal regenerative response to intestinal patching. Twenty rabbits had two 2 x 5 cm ileal defects patched with the serosal surface of adjacent caecum. Group 1 (n = 5) were controls; group 2 (n = 5), group 3 (n = 5) and group 4 (n = 5) had collagen, collagen plus BMC, and BMC respectively applied to the distal patched defect. Animals were killed at 7 d and evaluated grossly for epithelialization and contraction of the defects. Epithelial coverage was greatest in the distal patch of group 4 animals (62 +/- 9%) and was significantly greater than the group 4 proximal patch and control values (43 +/- 7 and 40 +/- 14%, P less than 0.05). Contraction was similar in all groups (38 +/- 5 to 45 +/- 5%). Crypt cell production rate, villus height, and disaccharidase activities were similar in all groups. BMC stimulated epithelialization via a local mechanism since only the distal patch was affected. Type I collagen did not stimulate epithelialization and inhibited the effect of BMC. Since crypt cell production rate was similar in all groups, the enhanced epithelialization seen with BMC is primarily due to increased cell migration.

摘要

上皮下组织在肠上皮的结构和功能中发挥着重要作用。基底膜成分(BMC)在体外可刺激上皮细胞迁移和分化。本研究的目的是确定BMC和/或间质组织胶原蛋白(I型)对肠道修补术后体内肠道再生反应的影响。20只兔子的两个2×5 cm回肠缺损用相邻盲肠的浆膜面进行修补。第1组(n = 5)为对照组;第2组(n = 5)、第3组(n = 5)和第4组(n = 5)分别将胶原蛋白、胶原蛋白加BMC和BMC应用于远端修补缺损处。在第7天处死动物,对缺损处的上皮化和收缩情况进行大体评估。第4组动物远端修补处的上皮覆盖度最大(62±9%),且显著高于第4组近端修补处和对照组的值(43±7%和40±14%,P<0.05)。所有组的收缩情况相似(38±5%至45±5%)。所有组的隐窝细胞产生率、绒毛高度和双糖酶活性相似。BMC通过局部机制刺激上皮化,因为仅远端修补处受到影响。I型胶原蛋白不刺激上皮化,且抑制BMC的作用。由于所有组的隐窝细胞产生率相似,BMC所见的上皮化增强主要是由于细胞迁移增加。

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