Nonomura A, Kono N, Yoshida K, Nakanuma Y, Ohta G
Department of Pathology, School of Medicine, Kanazawa University, Japan.
Liver. 1988 Feb;8(1):32-41. doi: 10.1111/j.1600-0676.1988.tb00964.x.
Electron microscopic features of intrahepatic bile ducts of experimental mouse graft-versus-host disease (GVHD) across minor histocompatibility barriers were studied for 14 months after transplantation. In GVHD mice, the bile duct epithelial layer was consistently infiltrated by lymphoid cells and often accompanied by polymorphonuclear leukocytes, monocytes and rarely by plasma cells. The epithelial cells in close contact with and in the vicinity of these infiltrated cells showed a variety of degenerative changes, including darkness of the cytoplasm and the nucleus with shrunken, irregular contours, increase in the amount of endoplasmic reticulum and number of mitochondria, and formation of intracytoplasmic vesicles and diverticula, cytoplasmic blebs, and apoptopic bodies. Lymphocytes were in close contact with epithelial cells through a number of point-contacts and located in the lateral intercellular spaces and/or between the basement membranes and the epithelial cells. The localization of infiltrating lymphocytes beneath the epithelial cells with conspicuous detachment from the basement membranes strongly suggested a link with subsequent epithelial cell injury and death. The lymphoid cells had irregular cytoplasmic projections which occasionally extended into spaces created by retractions of the epithelial cell membranes, reflecting an activation of the lymphocytes. These findings support the notion that the bile duct lesions in GVHD across minor histocompatibility barriers are mediated by specifically sensitized lymphocytes against epithelial cell membrane antigens. From our previous finding that a large majority of the infiltrating lymphocytes had a phenotype of helper/inducer T cells, a putative role of these lymphocytes in the induction of the bile duct lesions is discussed.
对移植后14个月的实验性小鼠经次要组织相容性屏障发生移植物抗宿主病(GVHD)时肝内胆管的电子显微镜特征进行了研究。在GVHD小鼠中,胆管上皮层持续被淋巴细胞浸润,且常伴有多形核白细胞、单核细胞,很少有浆细胞。与这些浸润细胞紧密接触及在其附近的上皮细胞呈现出多种退行性变化,包括细胞质和细胞核变暗,轮廓收缩、不规则,内质网数量和线粒体数量增加,细胞质内小泡和憩室形成,细胞质泡和凋亡小体形成。淋巴细胞通过许多点接触与上皮细胞紧密接触,并位于细胞间侧间隙和/或基底膜与上皮细胞之间。浸润淋巴细胞位于上皮细胞下方且与基底膜明显脱离,这强烈提示其与随后的上皮细胞损伤和死亡有关。淋巴细胞具有不规则的细胞质突起,偶尔延伸到上皮细胞膜回缩形成的间隙中,这反映了淋巴细胞的激活。这些发现支持这样一种观点,即经次要组织相容性屏障发生的GVHD中的胆管病变是由针对上皮细胞膜抗原的特异性致敏淋巴细胞介导的。根据我们之前的发现,即绝大多数浸润淋巴细胞具有辅助/诱导性T细胞表型,讨论了这些淋巴细胞在胆管病变诱导中的假定作用。