Byers S W, Musto N A, Dym M
J Androl. 1985 Sep-Oct;6(5):271-8. doi: 10.1002/j.1939-4640.1985.tb00845.x.
The isolation and culture of ciliated and nonciliated cells from rat ductuli efferentes is described. Fragments of epithelium obtained after two collagenase digestions attached to plastic and to extracellular matrix and could be maintained in culture for at least 2 weeks. Ciliary beating in cells grown on epididymal extracellular matrix-coated plastic could be observed for up to 7 days in culture. Although cells maintained on this substrate retained organelles characteristic of cells in vivo, they assumed a flattened, squamous appearance. In contrast, cells growing on the surface of permeable supports impregnated with extracellular matrix were polarized and exhibited a cuboidal/columnar appearance. Androgen binding protein conjugated to colloidal gold was taken up by these cells via coated pits and was found sequentially in uncoated endosomes, multivesicular bodies and lysosomes.
本文描述了从大鼠输出小管分离和培养纤毛细胞和非纤毛细胞的方法。经两次胶原酶消化后获得的上皮碎片可附着于塑料和细胞外基质上,并能在培养中维持至少2周。在附睾细胞外基质包被的塑料上生长的细胞,其纤毛摆动在培养中可持续观察到7天。虽然在这种基质上培养的细胞保留了体内细胞特有的细胞器,但它们呈现出扁平的鳞状外观。相比之下,在浸有细胞外基质的可渗透支持物表面生长的细胞呈极化状态,并呈现出立方形/柱状外观。与胶体金偶联的雄激素结合蛋白通过有被小窝被这些细胞摄取,并依次出现在无被内体、多囊泡体和溶酶体中。