Ll. Bruce et al., THE DEVELOPMENT OF VESTIBULOCOCHLEAR EFFERENTS AND COCHLEAR AFFERENTSIN MICE, International journal of developmental neuroscience, 15(4-5), 1997, pp. 671-692
We have reinvestigated the embryonic development of the vestibulocochl
ear system in mice using anterograde and retrograde tracing techniques
. Our studies reveal that rhombomeres 4 and 5 include five motor neuro
n populations. One of these, the abducens nucleus, will not be dealt w
ith here. Rhombomere 4 gives rise to three of the remaining population
s: the facial branchial motor neurons; the vestibular efferents; and t
he cochlear efferents. The migration of the facial branchial motor neu
rons away from the otic efferents is completed by 13.5 days post coitu
m (dpc). Subsequently the otic efferents separate into the vestibular
and cochlear efferents, and complete their migration by 14.5 dpc. In a
ddition to their common origin, all three populations have perikarya t
hat migrate via translocation through secondary processes, form a cont
inuous column upon completion of their migrations, and form axonal tra
cts that run in the internal facial genu. Some otic efferent axons tra
vel with the facial branchial motor nerve from the internal facial gen
u and exit the brain with that nerve. These data suggest that facial b
ranchial motor neurons and otic efferents are derived from a common pr
ecursor population and use similar cues for pathway recognition within
the brain. In contrast, rhombomere 5 gives rise to the fourth populat
ion to be considered here, the superior salivatory nucleus, a visceral
motor neuron group. Other differences between this group and those de
rived from rhombomere 4 include perikaryal migration as a result of tr
anslocation first through primary processes and only then through seco
ndary processes, a final location lateral to the branchial motor/otic
efferent column, and axonal tracts that are completely segregated from
those of the facial branchial and otic efferents throughout their cou
rse inside the brain. Analysis of the peripheral distribution of the c
ochlear efferents and afferents show that efferents reach the spiral g
anglion at 12.5 dpc when postmitotic ganglion cells are migrating away
from the cochlear anlage. The efferents begin to form the intragangli
onic spiral bundle by 14.5 dpc and the inner spiral bundle by 16.5 dpc
in the basal turn. They have extensive collaterals among supporting s
ells of the greater epithelial ridge from 16.5 dpc onwards. Afferents
and efferents in the basal turn of the cochlea extend through all thre
e rows of outer hair cells by 18.5 dpc. Selective labeling of afferent
fibers at 20.5 dpc (postnatal day 1) shows that although some afferen
ts are still in early developmental stages, some type II spiral gangli
on cells already extend for long distances along the outer hair cells,
and some type I spiral ganglion cells end on a single inner hair cell
. These data support previous evidence that in mice the early outgrowt
h of afferent and efferent fibers is essentially achieved by birth. (C
) 1997 ISDN.