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Updated: Aug 8, 2026

Visualization of the Interstitial Cells of Cajal (ICC) Network in Mice
Published on: July 27, 2011
Embryological origin of interstitial cells of Cajal
1Department of Anatomy and Cell Biology, University of Melbourne, Parkville, 3052, VIC, Australia. h.young@anatomy.unimelb.edu.au
Insights
Interstitial cells of Cajal (ICC) originate from mesenchymal precursors, not the neural crest. The Kit signaling pathway is crucial for post-natal ICC proliferation, not embryonic development.
Area of Science:
- Gastroenterology
- Developmental Biology
- Cell Biology
Background:
- The embryological origin of interstitial cells of Cajal (ICC) in the intestine was previously uncertain.
- ICC share characteristics with both neural crest-derived cells and mesenchymal cells, leading to debate about their origin.
Purpose of the Study:
- To elucidate the embryological origin of intestinal interstitial cells of Cajal (ICC).
- To investigate the role of the Kit signaling pathway in ICC development and proliferation.
Main Methods:
- Experiments involving organ culture of embryonic gut segments from mammalian and avian species, with and without neural crest cell presence.
- Analysis of Kit expression in ICC and smooth muscle cell precursors during embryonic development.
- Study of ICC development in adult mice with mutations affecting Kit activity.
Main Results:
- Experiments demonstrated that ICC do not arise from the neural crest.
- ICC and smooth muscle cells appear to originate from common mesenchymal precursor cells.
- While ICC precursors express Kit, the Kit signaling pathway is essential for post-natal ICC proliferation, not embryonic development.
Conclusions:
- Interstitial cells of Cajal (ICC) originate from mesenchymal precursors in the embryonic intestine.
- The Kit signaling pathway plays a critical role in the post-natal proliferation and maintenance of ICC, rather than their initial embryonic development.
Abstract:
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 characteristics in common with neural crest-derived cells, and some characteristics in common with cells derived from the mesenchyme. Experiments in both mammalian and avian species, in which segments of embryonic gut were removed prior to the arrival of neural crest cells and grown in organ culture, have now shown that ICC do not arise from the neural crest. It appears that ICC and smooth muscle cells arise from common mesenchymal precursor cells. From mid-embryonic stages, ICC precursors express Kit, which is a receptor tyrosine kinase. Both ICC and many smooth muscle cell precursors initially express Kit, and then the cells destined to become smooth muscle cells down-regulate 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 arrays of ICC, whereas normal ICC are present until shortly after birth in such mice. It, therefore, appears that the Kit signalling pathway in not necessary for the embryonic development of ICC, but rather the post-natal proliferation of ICC.
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