Brockbank K G, Voerman J S
Department of Cell Biology and Genetics, Erasmus University, Rotterdam, the Netherlands.
Thymus. 1987;10(3-4):169-77.
We describe a clonal culture technique for assay of thymic reticular-fibroblast progenitors. The adherent stromal cells in the colonies were pleomorphic fibroblast-like cells with oval nuclei containing several nucleoli. These cells were also nonphagocytic and negative for 4 of 5 epithelial markers employed. A minor population (less than 5%) were positive for the fifth epithelial marker ER-TR4. The majority of cells in all colonies were positive for the connective tissue marker ER-TR7. Treatment of mice with bacterial lipopolysaccharide, a mobiliser of splenic and bone marrow and reticular-fibroblast progenitors into circulation, failed to alter thymic clonogenic stromal cell numbers. These observations suggest that the colonies formed by thymic stromal progenitors consist of reticular-fibroblasts and that these progenitors are isolated from the fibroblast progenitor populations of other hemopoietic organs.
我们描述了一种用于检测胸腺网状成纤维细胞祖细胞的克隆培养技术。集落中的贴壁基质细胞是多形性的成纤维细胞样细胞,具有含有多个核仁的椭圆形细胞核。这些细胞也不具有吞噬作用,并且在所使用的5种上皮标志物中有4种呈阴性。少数群体(不到5%)对第五种上皮标志物ER-TR4呈阳性。所有集落中的大多数细胞对结缔组织标志物ER-TR7呈阳性。用细菌脂多糖(一种将脾脏、骨髓和网状成纤维细胞祖细胞动员到循环中的物质)处理小鼠,未能改变胸腺克隆性基质细胞的数量。这些观察结果表明,胸腺基质祖细胞形成的集落由网状成纤维细胞组成,并且这些祖细胞是从其他造血器官的成纤维细胞祖细胞群体中分离出来的。