Goury-Sistla Pavana, Nanjundiah Vidyanand, Pande Gopal
Centre for Cellular and Molecular Biology, Hyderabad, India.
Int J Dev Biol. 2012;56(4):263-72. doi: 10.1387/ijdb.113384ps.
Pre-starvation amoebae of Dictyostelium discoideum exhibit random movements. Starved cells aggregate by directed movements (chemotaxis) towards cyclic AMP and differentiate into live spores or dead stalk cells. Many differences between presumptive spore and stalk cells precede differentiation. We have examined whether cell motility-related factors are also among them. Cell speeds and localisation of motility-related signalling molecules were monitored by live cell imaging and immunostaining (a) in nutrient medium during growth, (b) immediately following transfer to starvation medium and (c) in nutrient medium that was re-introduced after a brief period of starvation. Cells moved randomly under all three conditions but mean speeds increased following transfer from nutrient medium to starvation medium; the transition occurred within 15 min. The distribution of speeds in starvation medium was bimodal: about 20% of the cells moved significantly faster than the remaining 80%. The motility-related molecules F-actin, PTEN and PI3 kinase were distributed differently in slow and fast cells. Among starved cells, the calcium content of slower cells was lower than that of the faster cells. All differences reverted within 15 min after restoration of the nutrient medium. The slow/fast distinction was missing in Polysphondylium pallidum, a cellular slime mould that lacks the presumptive stalk and spore cell classes, and in the trishanku (triA(-)) mutant of D. discoideum, in which the classes exist but are unstable. The transition from growth to starvation triggers a spontaneous and reversible switch in the distribution of D. discoideum cell speeds. Cells whose calcium content is relatively low (known to be presumptive spore cells) move slower than those whose calcium levels are higher (known to be presumptive stalk cells). Slow and fast cells show different distributions of motility-related proteins. The switch is indicative of a bistable mechanism underlying cell motility.
盘基网柄菌的饥饿前变形虫表现出随机运动。饥饿细胞通过向环磷酸腺苷的定向运动(趋化作用)聚集,并分化为活孢子或死柄细胞。在分化之前,推定的孢子细胞和柄细胞之间存在许多差异。我们研究了细胞运动相关因子是否也在这些差异之中。通过活细胞成像和免疫染色监测细胞速度以及运动相关信号分子的定位:(a) 在生长期间的营养培养基中;(b) 转移到饥饿培养基后立即进行;(c) 在短暂饥饿后重新引入的营养培养基中。在所有三种条件下细胞均随机移动,但从营养培养基转移到饥饿培养基后平均速度增加;这种转变在15分钟内发生。饥饿培养基中的速度分布是双峰的:约20%的细胞移动速度明显快于其余80%的细胞。运动相关分子F-肌动蛋白、PTEN和PI3激酶在慢速和快速细胞中的分布不同。在饥饿细胞中,较慢细胞的钙含量低于较快细胞。在恢复营养培养基后15分钟内,所有差异均恢复。在缺乏推定柄细胞和孢子细胞类别的细胞黏菌苍白聚孢霉以及盘基网柄菌的trishanku(triA(-))突变体中不存在慢/快区分,在该突变体中这些类别存在但不稳定。从生长到饥饿的转变触发了盘基网柄菌细胞速度分布的自发且可逆的转换。钙含量相对较低的细胞(已知为推定的孢子细胞)移动速度比钙水平较高的细胞(已知为推定的柄细胞)慢。慢速和快速细胞显示出运动相关蛋白的不同分布。这种转换表明细胞运动存在双稳态机制。