Yj. Sun et al., PERIKARYAL MYELINATION OF CULTURED CHICK-EMBRYO STATOACOUSTIC GANGLION-CELLS - AN ELECTRON-MICROSCOPIC STUDY, Acta oto-laryngologica, 118(3), 1998, pp. 344-351
Perikaryal myelin formation on cultured chick embryo statoacoustic gan
glion (SAG) cells was studied using electron microscopy. SAGs were dis
sected from 13-day embryos and cultured for 1 to 6 weeks. Myelinated p
erikarya, which were completely encircled by two or more layers of loo
se and/or compact myelin lamellae like those in vivo in the chick, wer
e first observed in 3-week-cultured SAGs; myelinated axons appeared in
2-week-cultured SAGs. The perikaryal myelination progressively increa
sed loose and compact lamellae and the axonal myelination increased co
mpact lamellae. In 4- to 6-week-cultured SAGs, 11 to 12% of SAG cells
had the myelinated perikaryon of which perikaryal myelin lamellae term
inated at the axon hillock in the same manner as those in vivo in the
chick. The number of layers of myelin lamellae around the myelinated p
erikaryon in 5- to 6-week-cultured SAGs and around the myelinated axon
in 4- to 6-week-cultured SAGs ranged between 2 and 15, and between 12
and 26, respectively. Since these numbers were consistent with those
in vivo in chicks 3 days after hatching, it is suggested that the cult
ure provides perikaryal myelin sheaths, which are equivalent to those
in vivo in structure, in more than 10% of SAG cells, while the myelina
tion process in vitro is carried our much more slowly than that in viv
o.