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Updated: Aug 7, 2026

Visualization of the Interstitial Cells of Cajal (ICC) Network in Mice
Published on: July 27, 2011
Insights into the interstitium of ventricular myocardium: interstitial Cajal-like cells (ICLC)
L M Popescu1, Mihaela Gherghiceanu, M E Hinescu
1Victor Babes National Institute of Pathology, Bucharest, Romania. LMP@jcmm.org
Insights
Interstitial Cajal-like cells (ICLC) in the ventricular myocardium were identified using multiple techniques. These cells, distinct from cardiomyocytes, may play roles in cardiac signaling, repair, and disease.
Area of Science:
- Cardiovascular Biology
- Cell Biology
- Histology
Background:
- Interstitial Cajal-like cells (ICLC) have been previously identified in human atrial myocardium.
- Their presence and characteristics in ventricular myocardium require further investigation.
Purpose of the Study:
- To verify the existence and characterize ICLC in rat and human ventricular myocardium.
- To elucidate the potential roles of ICLC in cardiac function and pathology.
Main Methods:
- Multiple complementary approaches including primary cell cultures, vital and traditional stainings, light and transmission electron microscopy (TEM).
- Stereology, immunohistochemistry (IHC), and immunofluorescence (IF) with molecular probes were employed.
- Specific markers such as CD34, EGFR, vimentin, CD117, and connexin 43 were assessed.
Main Results:
- ICLC were confirmed in the ventricular interstitium, constituting approximately 32% of interstitial cells.
- ICLC possess characteristic long, thin cytoplasmic processes with dilations containing mitochondria and endoplasmic reticulum.
- ICLC establish contacts with nerve fibers, myocytes, capillaries, and express connexin 43, CD34, EGFR, and vimentin.
Conclusions:
- ICLC are a distinct cell population in the ventricular myocardium with unique morphological and molecular features.
- Potential roles in intercellular signaling, chemomechanical sensing, cardiac repair, arrhythmogenesis, and sudden death are suggested.
- Further research is warranted to fully understand ICLC function in the heart.
Abstract:
We have previously described interstitial Cajal-like cells (ICLC) in human atrial myocardium. Several complementary approaches were used to verify the existence of ICLC in the interstitium of rat or human ventricular myocardium: primary cell cultures, vital stainings (e.g.: methylene blue), traditional stainings (including silver impregnation), phase contrast and non-conventional light microscopy (Epon-embedded semithin sections), transmission electron microscopy (TEM) (serial ultrathin sections), stereology, immunohistochemistry (IHC) and immunofluorescence (IF) with molecular probes. Cardiomyocytes occupy about 75% of rat ventricular myocardium volume. ICLC represent approximately 32% of the number of interstitial cells and the ratio cardiomyocytes/ICLC is about 70/1. In the interstitium, ICLC establish close contacts with nerve fibers, myocytes, blood capillaries and with immunoreactive cells (stromal synapses). ICLC show characteristic cytoplasmic processes, frequently two or three, which are very long (tens up to hundreds of microm), very thin (0.1-0.5 microm thick), with uneven caliber, having dilations, resulting in a moniliform aspect. Gap junctions between such processes can be found. Usually, the dilations are occupied by mitochondria (as revealed by Janus green B and MitoTracker Green FM) and elements of endoplasmic reticulum. Characteristically, some prolongations are flat, with a veil-like appearance, forming a labyrinthic system. ICLC display caveolae (about 1 caveola/ 1 microm cell membrane length, or 2-4% of the relative cytoplasmic volume). Mitochondria and endoplasmic reticulum (rough and smooth) occupy 5-10% and 1-2% of cytoplasmic volume, respectively. IHC revealed positive staining for CD34, EGFR and vimentin and, only in a few cases for CD117. IHC was negative for: desmin, CD57, tau, chymase, tryptase and CD13. IF showed that ventricular ICLC expressed connexin 43. We may speculate that possible ICLC roles might be: intercellular signaling (neurons, myocytes, capillaries etc.) and/or chemomechanical sensors. For pathology, it seems attractive to think that ICLC might participate in the process of cardiac repair/remodeling, arrhythmogenesis and, eventually, sudden death.
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