In an attempt to understand cell kinetics of open neural tube defects
(ONTDs) in the embryonic stages, chronological changes of cell prolife
ration and cell death patterns in the surgically induced spinal ONTDs
of chick embryos were investigated using proliferating cell nuclear an
tigen (PCNA) staining and terminal deoxynucleotidyl transferase-mediat
ed deoxyuridine triphosphate (dUTP) nick end labeling (TUNEL) method.
ONTDs were induced at Hamburger and Hamilton stages 17-19. Compared wi
th the control group, the surgery group showed a lower PCNA labeling i
ndex for 5 days after surgery and demonstrated more TUNEL-positive cel
ls at 6 h, 3 and 5 days after surgery. Decreased cell proliferation an
d enhanced apoptosis were seen in the ventral as well as in the dorsal
spinal cord. These results partly explain the functional deficits of
ONTDs. (C) 1998 Elsevier Science Ireland Ltd.