Evans C M, Phillips A D, Walker-Smith J A, MacDonald T T
Academic Department of Paediatric Gastroenterology, St Bartholomew's Hospital, London.
Gut. 1992 Feb;33(2):230-5. doi: 10.1136/gut.33.2.230.
An organ culture model has been used to study the effects of T cell activation in the human colon. Lamina propria T cells in explant cultures of human fetal colon (11 to 23 weeks gestation) were activated in situ using pokeweed mitogen or an anti-CD3 monoclonal antibody, and compared with unstimulated controls. After three days of culture, there was a two to four-fold increase in crypt epithelial cell proliferation in T cell stimulated explants of more than 15 weeks gestation, associated with a fall in crypt goblet cell numbers of up to 20-fold. By three days, the surface epithelium of stimulated explants appeared thin with loss of goblet cells, and by day 7, severe and extensive mucosal damage was observed by light and electron microscopy. These changes did not occur in control cultures and explants deficient in T cells (less than 16 weeks gestation), and were inhibited by cyclosporin A. These experiments indicate that the increase in epithelial cell proliferation and accompanying goblet cell depletion observed in colorectal crypts in chronic inflammatory bowel disease may be mediated by activated T cells.
一种器官培养模型已被用于研究T细胞活化对人类结肠的影响。使用商陆有丝分裂原或抗CD3单克隆抗体在原位激活人胎儿结肠(妊娠11至23周)外植体培养物中的固有层T细胞,并与未刺激的对照进行比较。培养三天后,妊娠超过15周的T细胞刺激外植体中隐窝上皮细胞增殖增加了两到四倍,同时隐窝杯状细胞数量下降高达20倍。到第三天,刺激外植体的表面上皮变薄,杯状细胞减少,到第7天,通过光学显微镜和电子显微镜观察到严重且广泛的粘膜损伤。这些变化在对照培养物和缺乏T细胞的外植体(妊娠小于16周)中未发生,并且被环孢素A抑制。这些实验表明,在慢性炎症性肠病的结直肠隐窝中观察到的上皮细胞增殖增加和伴随的杯状细胞耗竭可能由活化的T细胞介导。