Brockmeyer C, Emura M, Ochiai A, Riebe M, Mohr U, Hilfrich J
Institut für Experimentelle Pathologie, Medizinische Hochschule Hannover, FRG.
Exp Pathol. 1990;39(1):11-7. doi: 10.1016/s0232-1513(11)80214-8.
Human fetal bronchial epithelial (HFBE) cells at 6-8 passages were cultivated on a collagen gel for 10 days. A basal differentiative medium (BDM), consisting of RPMI 1640 supplemented with hormones and growth factors, was employed. Histochemistry, scanning electron microscopy and transmission electron microscopy revealed that HFBE cells developed secretory granules when cultivated on collagen gel in BDM. They were electron-dense and stained positive for PAS but negative for alcian blue. On additional treatment with 8 micrograms/ml vitamin A (VA), the number of secretory granules was increased. Moreover, the HFBE cells lost their surface microvilli, and dilation of rough endoplasmic reticulum was more marked than in culture without VA.
将6 - 8代的人胎儿支气管上皮(HFBE)细胞在胶原凝胶上培养10天。使用由补充了激素和生长因子的RPMI 1640组成的基础分化培养基(BDM)。组织化学、扫描电子显微镜和透射电子显微镜显示,HFBE细胞在BDM中的胶原凝胶上培养时会形成分泌颗粒。这些颗粒电子密度高,PAS染色呈阳性,但阿尔辛蓝染色呈阴性。用8微克/毫升维生素A(VA)进一步处理后,分泌颗粒的数量增加。此外,HFBE细胞失去了表面微绒毛,粗面内质网的扩张比未添加VA的培养更为明显。