Roti L W, Stevens A R
J Cell Sci. 1975 May;17(3):503-15. doi: 10.1242/jcs.17.3.503.
Differentiation of Acanthamoeba castellanii into dormant cysts occurs spontaneously in stationary phase cultures, or can be induced experimentally by starvation. Although no further increase in cell density occurred after induction in either case, incorporation of [H]thymidine into DNA continued at a reduced rate through the period when differentiated products (cyst wall components) were formed. No net accumulation of DNA occurred during differentiation, indicating that the DNA synthesis occurring at this time was balanced by breakdown. When either 5-fluorodeoxyuridine (FUdR) or hydroxyurea was added to exponentially growing cultures, growth was terminated and the subsequent spontaneous encystment was delayed in comparison with untreated stationary phase cultures. A similar delay was observed for experimentally induced encystment of FUdR-pretreated cells. In all cases, delay of encystment was correlated with inhibition of 32PO4 incorporation into DNA, and unexpectedly also into RNA. Addition of FUdR at zero-time of experimental induction of cells not previously exposed to FUdR, on the other hand, had no effect on encystment or on 32PO4 incorporation. The delay of encystment produced by FUdR and hydroxyurea, therefore, appeared to reflect a requirement for normal synthesis of DNA and/or RNA not only during encystment, but also during the period of exponential growth just before encystment induction.
卡氏棘阿米巴向休眠包囊的分化在静止期培养物中会自发发生,或者也可以通过饥饿实验诱导。尽管在这两种情况下诱导后细胞密度都没有进一步增加,但在形成分化产物(包囊壁成分)的整个时期,[H]胸苷掺入DNA的过程仍以较低速率持续进行。分化过程中DNA没有净积累,这表明此时发生的DNA合成与分解处于平衡状态。当向指数生长的培养物中添加5-氟脱氧尿苷(FUdR)或羟基脲时,生长终止,与未处理的静止期培养物相比,随后的自发包囊化延迟。对于经FUdR预处理的细胞实验诱导的包囊化也观察到类似的延迟。在所有情况下,包囊化延迟都与32PO4掺入DNA的抑制相关,而且出乎意料的是也与掺入RNA的抑制相关。另一方面,在实验诱导之前未接触过FUdR的细胞的零时间添加FUdR,对包囊化或32PO4掺入没有影响。因此,FUdR和羟基脲产生的包囊化延迟似乎不仅反映了在包囊化期间,而且在包囊化诱导前的指数生长期间对DNA和/或RNA正常合成的需求。