Until recently, the embryological origin of the interstitial cells of Cajal
(ICC) within the intestine was unclear. An origin from the neural crest or
from the mesenchyme was considered possible because ICC possess some chara
cteristics in common with neural crest-derived cells, and some characterist
ics in common with cells derived from the mesenchyme, Experiments in both m
ammalian and avian species, in which segments of embryonic gut were removed
prior to the arrival of neural crest cells and grown in organ culture, hav
e now shown that ICC do not arise from the neural crest. It appears that IC
C and smooth muscle cells arise from common mesenchymal precursor cells. Fr
om mid-embryonic stages, ICC precursors express Kit, which is a receptor ty
rosine kinase, Both ICC and many smooth muscle cell precursors initially ex
press Kit, and then the cells destined to become smooth muscle cells down-r
egulate Kit and up-regulate the synthesis of myofilament proteins, whereas
cells destined to differentiate into ICC maintain their expression of Kit.
Adult mice with mutations that block the activity of Kit have disrupted arr
ays of ICC, whereas normal ICC are present until shortly after birth in suc
h mice. It, therefore, appears that the Kit signalling pathway in not neces
sary for the embryonic development of ICC, but rather the post-natal prolif
eration of ICC. (C) 1999 Wiley-Liss, Inc.