Перегляд вихідного коду сторінки Ideal Course Of Action For CX-5461

?5E). By the 48?hpf two-arm pluteus stage, the ECPN cells were restricted to the aboral ectoderm (Fig.?3C) and the blastocoel (Fig.?5F�CK). In the ectoderm, the cells were mostly round (Fig.?5F�CI) or bipolar (Fig.?5J,K). By the 72?hpf four-arm pluteus stage, the number of ECPN cells in the ectoderm was reduced considerably, and they converged at the [http://www.selleckchem.com/products/forskolin.html Forskolin nmr] tips of the larval arms and the posterior end of the body in the blastocoel (Fig.?5L�CN). This pattern of distribution of ECPN cells persisted in 96?hpf four-arm plutei (Fig.?5O, arrows). Immediately before metamorphosis at the 1?mpf eight-arm pluteus stage, the ECPN cells were packed at the tips of the larval arms and the posterior end of the larval body (Fig.?5P). The larvae oriented their arms in the direction of swimming. Pigment cells and ECPN cells were present in the tips of these larval arms (Figs?5L�CP and 6A), which suggested that the ECPN cells contribute to light sensitivity of larvae. To examine whether the distribution pattern or number of ECPN cells had any relationship to light condition, the pattern of Hp-ECPN expression was examined by WMIHC (Fig.?6C�CE). The number of ECPN cells per larva was found to be decreased significantly in conditions of continuous dark to 9.3?�� 1.02 cells from 15.7?��?1.2 cells in conditions of continuous light in the 50?hpf two-arm plutei (P?[https://en.wikipedia.org/wiki/Dipivefrine Dipivefrine] whether the above close relationship between the number of ECPN cells and light condition was initiated by Hp-ECPN expression or vice versa, expression of Hp-ECPN was inhibited by functional knockdown of Hp-ecpn mRNA with Hp-ecpn-MASO. The development of embryos injected with 750?��mol/L Hp-ecpn-MASO was delayed slightly, although their overall [http://www.selleckchem.com/products/cx-5461.html CX-5461 datasheet] morphology appeared to be unaffected. The swimming activity of 48?hpf two-arm plutei that had been injected with Hp-ecpn-MASO was not different from that of the larvae injected with the standard control-MASO at the start of the bioassay (Fig.?7A, red columns). However, from 12?h after the onset of the bioassay, which corresponded to the 60?hpf two-arm pluteus stage, the number of Hp-ecpn-MASO-injected larvae that sank to the bottom of the bioassay cuvettes was increased significantly as compared with the control larvae (P?