Mjh. Petersvandersanden et al., REGIONAL DIFFERENCES BETWEEN VARIOUS AXIAL SEGMENTS OF THE AVIAN NEURAL CREST REGARDING THE FORMATION OF ENTERIC GANGLIA, Differentiation, 53(1), 1993, pp. 17-24
The vagal neural crest adjacent to somites 1-7 gives rise to the enter
ic ganglia along the entire digestive tract. It is generally assumed t
hat formation of enteric ganglia in preumbilical gut is independent of
the axial segment from which the neural crest originates. In postumbi
lical gut, however, there is evidence that the axial segment of origin
of the neural crest might be relevant to neural differentiation. In t
his part of the gut, we previously identified a subpopulation of HNK-1
-immunoreactive cells within the enteric mesenchyme. This immunoreacti
vity disappeared upon formation of the enteric nervous system. We stud
ied the interaction between various axial segments of quail neural cre
st and the microenvironment in aneural chicken hindgut using chorioall
antoic membrane cocultures. We found that neural crest cells from vari
ous axial segments could migrate into the gut and home to the correct
sites. However, whereas vagal neural crest cells differentiated into e
nteric neurons, neural crest cells from truncal segments mainly differ
entiated into melanocytes. The HNK-1-immunoreactivity within the enter
ic mesenchyme only disappeared when neural crest cell colonization was
followed by differentiation into enteric neurons and subsequent forma
tion of enteric ganglia. To determine whether differentiation of neura
l crest cells in chorioallantoic membrane cocultures was influenced by
the prolonged presence of the neural tube and notochord, we developed
a new coculture system, using neural crest cells cultured in vitro. W
e found that the differentiation of vagal and trunk neural crest cells
within the enteric mesenchyme was not influenced by the prolonged pre
sence of the neural tube and notochord after 24 h, suggesting that the
re are intrinsic differences between these neural crest cell populatio
ns. Upon prolonged in vitro culturing, the properties of vagal neural
crest cells changed, and concomitantly, they lost the ability to diffe
rentiate into enteric neurons and instead differentiated into melanocy
tes. We conclude that the disappearance of the HNK-1-immunoreactivity
within the enteric mesenchyme is correlated with formation of enteric
ganglia. In our experimental system, cells from the vagal neural crest
are more capable of neural differentiation in the hindgut than cells
from other axial levels of the neural crest.