In the small intestine of both embryonic birds and mammals, neuron precurso
rs aggregrate first at the site of the myenteric plexus, and the submucous
plexus develops later. However, in the large intestine of birds, the submuc
osal region is colonised by neural-crest-derived cells before the myenteric
region (Burns and Le Douarin, Development 125:4335-4347, 1998). Using anti
sera that recognize undifferentiated neural-crest-derived cells (p75(NTR))
and differentiated neurons (PGP9.5), we examined the colonisation of the mu
rine large intestine by neural-crest-derived cells and the development of t
he myenteric and submucosal plexuses. At E12.5, when the neural crest cells
were migrating through and colonising the hindgut, the hindgut mesenchyme
was largely undifferentiated, and a circular muscle layer could not be disc
erned. Neural-crest-derived cells migrated through, and settled in, the out
er half of the mesenchyme. By E14.5, neural-crest-derived cells had colonis
ed the entire hindgut; at this stage the circular muscle layer had started
to differentiate. From E14.5 to E16.5, p75(NTR-) and PGP9.5-positive cells
were observed on the serosal side of the circular muscle, in the myenteric
region, but not in the submucosal region. Scattered, single neurons were fi
rst observed in the submucosal region around E18.5, and groups of neurons f
orming ganglia were not observed until after birth. The development of the
enteric plexuses in the murine large intestine therefore differs from that
in the avian large intestine.