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Updated: May 4, 2026

Visualization of the Interstitial Cells of Cajal ICC Network in Mice
Published on: July 27, 2011
Appearance of interstitial cells of Cajal in the human midgut
Mirjana Abramovic1, Goran Radenkovic, Aleksandra Velickov
1Institute of Chemistry, Faculty of Medicine, University of Nis, 81 Dr Zorana Djindjica Blvd, 18000, Nis, Serbia.
Insights
Interstitial cells of Cajal (ICC) differentiate in the human midgut starting at week 9. These c-kit-positive cells appear in distinct patterns in the small intestine versus the proximal colon.
Area of Science:
- Developmental biology
- Gastroenterology
- Cell biology
Background:
- Interstitial cells of Cajal (ICC) are crucial for gastrointestinal motility.
- ICC express c-kit and rely on Kit receptor signaling for development and maintenance.
- c-kit-immunoreactive (c-kit-IR) cells appear early in the esophagus, stomach, and proximal duodenum.
Purpose of the Study:
- To determine the precise timing of c-kit-IR ICC appearance in the human midgut.
- To investigate the developmental patterns of ICC in the distal duodenum, jejunum, ileum, and proximal colon.
Main Methods:
- Examined human embryonic and fetal specimens (7-12 weeks gestational age).
- Used immunohistochemistry with anti-c-kit antibodies to identify ICC.
- Employed anti-PGP9.5 and anti-desmin antibodies to assess neuronal and smooth muscle differentiation.
Main Results:
- In the distal duodenum, jejunum, and ileum, c-kit-IR cells emerged at week 9 near the myenteric plexus.
- These early small intestine ICC were multipolar/spindle-shaped, forming a single row around ganglia.
- In the proximal colon, c-kit-IR cells appeared at weeks 9-10 in two parallel belts at submucosal and myenteric plexus levels.
Conclusions:
- ICC development in the human midgut follows two distinct patterns.
- The timing and spatial arrangement of ICC differentiation vary between the small intestine and proximal colon.
Abstract:
Several subtypes of the interstitial cells of Cajal (ICC) form networks that play a role in gastrointestinal motor control. ICC express c-kit and depend on signaling via Kit receptors for development and phenotype maintenance. At 7-8 weeks of development, c-kit-immunoreactive (c-kit-IR) cells are present in the human oesophagus, stomach and proximal duodenum wall. In the remaining small and large bowel, c-kit-IR cells appear later. The object of the present study is to determine the timing of the appearance of c-kit-IR ICC in the parts of the digestive tube originating from the midgut (distal duodenum, jejunum, ileum and proximal colon). Specimens were obtained from eight human embryos and 11 fetuses at 7-12 weeks of gestational age. The specimens were exposed to anti-c-kit antibodies to investigate ICC differentiation. The differentiation of enteric neurons and smooth muscle cells was immunohistochemically examined by using anti-PGP9,5 and anti-desmin antibodies, respectively. In the distal duodenum, jejunum and ileum, c-kit-IR cells emerged at week 9 at the level of the myenteric plexus in the form of a thin row of cells encircling the inception of the ganglia. These cells were multipolar or spindle-shaped with two long processes and corresponded to the ICC of the myenteric plexus. In the proximal colon, c-kit-IR cells emerged at week 9-10 in the form of two parallel belts of cells extending at the submucosal plexus and the myenteric plexus levels. We conclude that ICC develop following two different patterns in the human midgut.
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