Table 1.

Effects of AChE on neurite growth in vitro

Construct injected1-aTotal neurite length per cell (μm)Growth rate (μm/hr)Number of branchesNumber of cells (embryos)
at 6–7 hrat 9–10 hr
ACHE-E6+64.6  ± 6.5124.0  ± 11.7*37.9  ± 5.2*1.8  ± 0.132 (7)
55.2  ± 5.988.2  ± 10.312.9  ± 2.71.6  ± 0.133 (7)
ACHE-I4/E5+62.0  ± 10.677.5  ± 8.211.6  ± 2.11.7  ± 0.127 (8)
52.9  ± 5.092.7  ± 6.214.7  ± 1.91.6  ± 0.131 (8)
ACHE-E6-IN+91.2  ± 9.8*156.9  ± 13.6*33.6  ± 3.7*2.0  ± 0.125 (3)
47.4  ± 5.162.5  ± 9.611.2  ± 2.11.5  ± 0.128 (3)
ACHE-E4+48.0  ± 7.094.2  ± 9.111.9  ± 3.71.7  ± 0.216 (4)
51.6  ± 7.4126.2  ± 20.413.0  ± 4.21.8  ± 0.220 (4)
  • F1-a  cDNA vectors were injected intoXenopus embryos at the two-cell stage using rhodamine–dextran as a marker. Cultures were made from injected embryos 1 d later. “+” indicates rhodamine–dextran-positive neurons; “−” indicates rhodamine–dextran-negative neurons in the same cultures.

  • * Significant difference was found between + and − groups (two-tailed t test; p < 0.005).