Sobolewski A, Weeks G
Department of Microbiology, University of British Columbia, Vancouver, Canada.
Dev Biol. 1988 Jun;127(2):296-303. doi: 10.1016/0012-1606(88)90316-8.
In Dictyostelium discoideum stalk cell formation is induced by cyclic AMP and differentiation-inducing factor (DIF) when cells are plated in in vitro monolayers (Kay et al., 1979, Differentiation 13: 7-14). The in vivo developmental stages at which cells became independent of these factors were determined. Independence was defined as the stage at which dispersed cells no longer required the factors for stalk cell formation in low density monolayers. Cyclic AMP independent cells were first detected at around 12 hr of development, a time that corresponds to the transition between the tipped aggregate and the first finger stages. In contrast cells did not become independent of DIF until late culmination. The prestalk cell-specific isozyme acid phosphatase II and a stalk cell-specific 41,000 Mr antigen (ST 41) were expressed during differentiation in low density monolayers in the presence of both cyclic AMP and DIF, but neither component was expressed in the presence of cyclic AMP alone. This result implies that DIF is essential for both prestalk and stalk cell formation. The two components were expressed within 2 hr of each other during differentiation in vitro, whereas during development in vivo acid phosphatase II was first detected at the first finger stage and ST 41 was first detected during late culmination, 8-12 hr later. These contrasting results suggest that the conversion of prestalk cells to stalk cells is unrestrained in monolayers, following directly after prestalk cell induction, but restrained in vivo until the culmination stage. This interpretation is consistent with the finding that cells become independent of DIF early during in vitro differentiation (A. Sobolewski, N. Neave, and G. Weeks, 1983, Differentiation 25, 93-100), but do not become independent of DIF until the culmination stage when differentiating in vivo.
在盘基网柄菌中,当细胞接种于体外单层培养时,环磷酸腺苷(cAMP)和分化诱导因子(DIF)可诱导柄细胞形成(Kay等人,1979年91979年,《分化》13: 7 - 14)。确定了细胞在体内发育过程中不再依赖这些因子的阶段。独立性被定义为分散细胞在低密度单层培养中不再需要这些因子来形成柄细胞的阶段。最早在发育约12小时时检测到不依赖cAMP的细胞,这个时间对应于顶端聚集体和第一指状阶段之间的转变。相比之下,细胞直到发育后期才不再依赖DIF。在前柄细胞特异性同工酶酸性磷酸酶II和一种柄细胞特异性的41,000道尔顿抗原(ST 41)在低密度单层培养中,在同时存在cAMP和DIF的情况下分化过程中表达,但单独存在cAMP时这两种成分均不表达。这一结果表明DIF对于前柄细胞和柄细胞的形成都是必不可少的。在体外分化过程中,这两种成分在彼此2小时内相继表达,而在体内发育过程中,酸性磷酸酶II最早在第一指状阶段检测到,ST 41最早在发育后期检测到,时间上要晚8 - 12小时。这些对比结果表明,在前柄细胞诱导后,前柄细胞向柄细胞的转化在单层培养中不受限制,但在体内直到发育后期才受到限制。这一解释与以下发现一致:体外分化早期细胞就不再依赖DIF(A. Sobolewski、N. Neave和G. Weeks,1983年,《分化》25, 93 - 100),但在体内分化时直到发育后期才不再依赖DIF。