Sánchez L, Andrade J L, Cisneros R, Zúñiga G
Departamento de Zoología, Escuela Nacional de Ciencias Biológicas-IPN, Prol. de Carpio y Plan de Ayala s/n, C.P. 11340, México D.F., México.
In Vitro Cell Dev Biol Anim. 2004 Jan-Feb;40(1-2):8-13. doi: 10.1290/1543-706X(2004)40<8:MOMECF>2.0.CO;2.
This article describes the culture of epithelial cells from anterior and posterior midgut regions of adult Dendroctonus valens. Culture conditions were established, and cell adherence was improved by means of a new technique that allowed the cells to grow between two glass coverslips. Cytoplasmic projections occur as anterior midgut cells grow to confluence; these projections were not observed in cells of the posterior midgut. The optimal culture medium for the maintenance of these epithelial cells was Roswell Park Memorial Institute 1640 medium at 25 degrees C. Cells in Grace's medium died in 24 h. Cultures did not require CO(2) atmosphere, but culture development was favored by the microaerophilic environment and the dark conditions in which the cells were grown, between the coverslips.
本文描述了成年红脂大小蠹前、中肠后部上皮细胞的培养。建立了培养条件,并通过一项新技术改善了细胞贴壁情况,该技术使细胞能在两个盖玻片之间生长。前肠中部细胞生长至汇合时会出现细胞质突起;后肠细胞中未观察到这些突起。维持这些上皮细胞的最佳培养基是罗斯韦尔帕克纪念研究所1640培养基,培养温度为25摄氏度。处于格雷斯培养基中的细胞在24小时内死亡。培养不需要二氧化碳环境,但微需氧环境以及细胞在盖玻片之间生长的黑暗条件有利于培养的发展。