Origin of Interstitial Cells of Cajal in the Mouse Intestine

• Published in: Developmental biology Vol. 180; no. 1; pp. 97 - 107
• Main Authors: Young, H.M., Ciampoli, D., Southwell, B.R., Newgreen, D.F.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 25-11-1996
• Subjects: Aging; Animals; Calbindin 2; Embryonic and Fetal Development; Female; Fetal Tissue Transplantation; Gestational Age; Immunohistochemistry; Intestines - cytology; Intestines - embryology; Intestines - growth & development; Kidney; Mice; Mice, Inbred BALB C; Models, Biological; Muscle Development; Muscle, Smooth - cytology; Muscle, Smooth - embryology; Muscle, Smooth - growth & development; Nerve Tissue Proteins - analysis; Neural Crest - physiology; Neuroglia - cytology; Neuroglia - physiology; Neurons - cytology; Neurons - physiology; Phosphopyruvate Hydratase - analysis; Pregnancy; Proto-Oncogene Proteins c-kit - analysis; Receptors, Neurokinin-1 - analysis; S100 Calcium Binding Protein G - analysis; Substance P - analysis; Transplantation, Heterotopic
• ISSN: 0012-1606; 1095-564X
• DOI: 10.1006/dbio.1996.0287

The interstitial cells of Cajal (ICC) are found in a number of different locations in the gastrointestinal tract, where they form close associations with both muscle cells and nerve terminals. In this study we examined the embryological origin of ICC in the mouse intestine to determine whether they arise from the neural crest or from the intestinal wall. Segments of intestine were removed from embryonic mice either before or after the arrival of neural crest cells (the precursors of enteric neurons and glial cells) and transplanted under the renal capsule of host (adult) mice and allowed to develop for 18–41 days. In the mouse intestine, antibodies to c-kitprotein selectively label ICC at a variety of locations, and antibodies to the NK1 receptor (the receptor for substance P) labels ICC at the level of the deep muscular plexus in the small intestine and a subpopulation of enteric neurons in the large intestine. The presence of neurons in the explants was examined using antisera to neuron-specific enolase, substance P, and calretinin. In segments of small and large intestine explanted after the arrival of neural crest cells, immunoreactive neurons and c-kit- and NK1-immunoreactive ICC were present with a distribution similar to that seen in control tissue at a similar developmental age. In segments of large intestine explanted before the arrival of neural crest cells, neurons were not present; however, c-kit-immunoreactive ICC were present in these aneuronal explants, indicating that ICC do not arise from the neural crest. The source of ICC in mammals is therefore likely to be the mesenchyme of the gut.