Fa. White et al., BIRTH DATES AND SURVIVAL AFTER AXOTOMY OF NEUROCHEMICALLY DEFINED SUBSETS OF TRIGEMINAL GANGLION-CELLS, Journal of comparative neurology, 352(2), 1995, pp. 308-320
Trigeminal (V) ganglion cells with different neurochemical phenotypes
or different birth dates are affected differently by neonatal axonal t
ransection. The aim of the present study was to determine if V ganglio
n cell birth date and neurochemical phenotype were correlated and if t
hese two variables could be related to responses to neonatal axonal tr
ansection. Immunocytochemistry, histochemistry, and [H-3]thymidine lab
elling were used to determine the birth dates of V ganglion cells reco
gnized by antibodies directed against neurofilament protein (NF), calc
itonin gene-related peptide (CGRP), and substance P (SP) and those tha
t bound the lectin Bandierea simplicifolia-I (BS-I). All V ganglion ce
lls were born between embryonic days (E-) 9.5 and 14.5. All ganglion c
ells were born between E-9.5 and E-14.5. In a normalized population (p
ercentages normalized to equal 100%), over 90% of NF-positive V gangli
on cells were born between E-10.5 and E-12.5. The majority of CGRP-pos
itive and SP-positive ganglion cells (> 90%) were generated from E-13.
5 to E-14.5 and E-12.5 through E-14.5, respectively. Almost 85% of BS-
I-positive ganglion cells were generated on E-12.5 through E-14.5. Pre
vious results and additional data from this study indicated that NF- a
nd BS-I-positive ganglion cells are proportionally more likely to be l
ost after neonatal axotomy and that SP-positive cells are more likely
to remain. The percentage of CGRP-positive cells in the V ganglion was
not significantly altered by neonatal infraorbital nerve transection.
Overall, these findings do not indicate a strong relationship between
cell birth date and the probability of survival after neonatal axonal
damage for all V ganglion cell phenotypes. (C) 1995 Wiley-Liss, Inc.