Finkbeiner W E, Nadel J A, Basbaum C B
In Vitro Cell Dev Biol. 1986 Oct;22(10):561-7. doi: 10.1007/BF02623514.
Bovine tracheal submucosal gland cells have been isolated by enzymatic digestion and serially propagated in tissue culture for more than 12 mo. (40 passages). The cells exhibit an epithelioid appearance at confluence and contain alcian blue (pH 2.5)/periodic acid-Schiff-positive material within cytoplasmic granules. By electron microscopy numerous osmiophilic secretory granules are seen. Maximal growth is observed when the cells are grown on human placental collagen-coated culture vessels in medium supplemented with 20% fetal bovine serum. Scintillation spectrometry revealed that radiolabeled precursor (35SO4) was incorporated into high molecular weight molecules and released from cells. Isoproterenol (10(-6) to 10(-3) M) stimulated the release of 35SO4. The maximal response to isoproterenol was completely inhibited by the beta-adrenergic antagonist propranolol. It is concluded that the cultured cells retain features of tracheal gland cells and may serve as a useful model of synthesis and secretion of macromolecules by tracheal gland cells.
牛气管黏膜下腺细胞已通过酶消化法分离,并在组织培养中连续传代培养超过12个月(40代)。细胞在汇合时呈现上皮样外观,细胞质颗粒内含有阿尔辛蓝(pH 2.5)/过碘酸希夫阳性物质。通过电子显微镜可见大量嗜锇性分泌颗粒。当细胞在补充有20%胎牛血清的培养基中,在人胎盘胶原包被的培养容器上生长时,观察到最大生长。闪烁光谱法显示,放射性标记的前体(35SO4)被整合到高分子量分子中并从细胞中释放出来。异丙肾上腺素(10^(-6)至10^(-3) M)刺激了35SO4的释放。β-肾上腺素能拮抗剂普萘洛尔完全抑制了对异丙肾上腺素的最大反应。结论是,培养的细胞保留了气管腺细胞的特征,可作为气管腺细胞合成和分泌大分子的有用模型。