Farkas R, Sutáková G
Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava.
In Vitro Cell Dev Biol Anim. 1998 Nov-Dec;34(10):813-23. doi: 10.1007/s11626-998-0036-7.
Alterations in the ultrastructure of in vitro cultured larval salivary glands of Drosophila melanogaster in response to the steroid hormone ecdysone were studied in relation to complex changes in puffing patterns. We found that the changes in the fine structure of cultured glands reflected progression of the puffing pattern, and they paralleled those seen in vivo. We observed that glue secretion by exocytosis, the main function of salivary glands, took place between puff stage 5 (PS5) and PS7. Glue could not be expectorated under culture conditions but was slowly released from the lumen through a duct into the medium. After the cultured glands reached PS13/PS14, further progress of puffing and fine structural alterations required that the ecdysteroid titer be transiently extremely low or absent. Under in vitro conditions we did not observe the putative new secretory program(s) described for glands in vivo after PS12. However, ultrastructural changes which unambiguously indicated that an autohistolytic process had begun in vitro started to appear after PS17. Many salivary gland cells developed numerous features of progressive self-degradation between PS18 and PS21. Actual degradation of salivary glands in vivo seemed to be rapid, but in vitro degradation was never completed, probably due to a lack of exogenous factors from the hemolymph. Manipulations of ecdysone titer in vitro in the culture medium, known during the larval puffing cycle to cause premature induction of developmentally specific puffing patterns, did not affect the normal development of ultrastructural features of the cytoplasm and nucleus.
研究了黑腹果蝇体外培养幼虫唾液腺的超微结构变化对类固醇激素蜕皮激素的响应,并将其与胀泡模式的复杂变化联系起来。我们发现,培养腺体的精细结构变化反映了胀泡模式的进展,并且与体内观察到的变化相似。我们观察到,唾液腺的主要功能——通过胞吐作用分泌黏液,发生在胀泡阶段5(PS5)和PS7之间。在培养条件下,黏液无法咳出,而是通过导管从管腔缓慢释放到培养基中。培养的腺体达到PS13/PS14后,胀泡的进一步进展和精细结构的改变需要蜕皮甾类激素滴度暂时极低或不存在。在体外条件下,我们没有观察到体内腺体在PS12之后所描述的假定新分泌程序。然而,在PS17之后开始出现明确表明体外自溶过程已经开始的超微结构变化。许多唾液腺细胞在PS18和PS21之间出现了许多渐进性自我降解的特征。唾液腺在体内的实际降解似乎很快,但体外降解从未完成,这可能是由于缺乏来自血淋巴的外源性因素。在幼虫胀泡周期中,已知在培养基中体外操纵蜕皮激素滴度会导致发育特异性胀泡模式的过早诱导,但这并不影响细胞质和细胞核超微结构特征的正常发育。