Mowat A M, Ferguson A
Gastroenterology. 1982 Aug;83(2):417-23.
We have used measurements of intestinal epithelial cell kinetics and counts of intraepithelial lymphocytes and mucosal mast cells to measure small intestinal mucosal changes during the proliferative and recovery phases of graft-vs.-host reaction in neonatal mice. Unirradiated (CBA x BALB/c)F1 mice were injected with parental spleen cells or with culture medium at 6-8 days of age, and followed up for 9 wk thereafter. The spleen index was used as a measure of the graft-vs.-host reaction, a stathmokinetic technique with microdissection was used to measure villus and crypt lengths and crypt cell production rate, and intraepithelial lymphocytes and mucosal mast cells were counted in histologic sections. Intraepithelial lymphocyte count rose within 24 h of induction of the graft-vs.-host reaction and increases in crypt length and in crypt cell production rate occurred within 3 days. These indices exactly parallel the spleen index during the proliferative phase of the graft-vs.-host reaction and the changes occurred in the absence of any villus damage. Mucosal mast cell numbers also increased, but the rise was delayed and sustained when compared with other mucosal changes. These results show that measurements of mucosal architecture and intraepithelial lymphocyte counts can be used to quantify mucosal cell-mediated immune reactions. In addition, this study provides further evidence to support our hypothesis that the mechanism of these changes is due to a delayed-type hypersensitivity reaction in the intestinal mucosa rather than to the action of cytotoxic T lymphocytes.
我们利用对小肠上皮细胞动力学的测量以及上皮内淋巴细胞和黏膜肥大细胞计数,来测定新生小鼠移植物抗宿主反应增殖期和恢复期小肠黏膜的变化。未受照射的(CBA×BALB/c)F1小鼠在6至8日龄时注射亲代脾细胞或培养基,此后随访9周。脾指数用作移植物抗宿主反应的指标,采用微切割的静止动力学技术测量绒毛和隐窝长度以及隐窝细胞产生率,并在组织学切片中计数上皮内淋巴细胞和黏膜肥大细胞。上皮内淋巴细胞计数在移植物抗宿主反应诱导后24小时内升高,隐窝长度和隐窝细胞产生率在3天内增加。在移植物抗宿主反应的增殖期,这些指标与脾指数完全平行,且这些变化发生时未出现任何绒毛损伤。黏膜肥大细胞数量也增加,但与其他黏膜变化相比,其增加延迟且持续。这些结果表明,黏膜结构测量和上皮内淋巴细胞计数可用于量化黏膜细胞介导的免疫反应。此外,本研究提供了进一步的证据来支持我们的假设,即这些变化的机制是由于小肠黏膜的迟发型超敏反应,而非细胞毒性T淋巴细胞的作用。