Related Experiment Video
Updated: Jul 21, 2026

Isolating Lymphocytes from the Mouse Small Intestinal Immune System
Published on: February 28, 2018
Kit-like immunopositive cells in sheep mesenteric lymphatic vessels.
K D McCloskey1, M A Hollywood, K D Thornbury
1Smooth Muscle Group, Department of Physiology, Queen's University, 97 Lisburn Road, Belfast, BT9 7BL, UK.
This study investigated the structure of cells in sheep mesenteric lymphatic vessels using electron microscopy and immunohistochemistry. The researchers found a subpopulation of cells between the endothelium and smooth muscle layers that stained positively for Kit and vimentin. These cells had ultrastructural features similar to pacemaker cells in other tissues, including electron-dense cytoplasm, caveolae, and a well-developed endoplasmic reticulum. Smooth muscle cells in the lymphatic vessels were arranged in interlocking bundles rather than the circular and longitudinal layers seen in the gastrointestinal tract. Vimentin-positive cells were either branched or spindle-shaped, while myosin-staining cells had the typical smooth muscle cell appearance. The study provides the first morphological evidence that specialized cells exist in lymphatic vessels that may regulate contractile activity. These findings suggest that lymphatic vessels may contain pacemaker-like cells, but further research is needed to confirm their functional role.
Area of Science:
- Lymphatic system anatomy
- Cardiovascular physiology
- Cellular immunohistochemistry
Background:
Prior research has shown that lymphatic vessels exhibit spontaneous contractile activity, but the cellular mechanisms behind this phenomenon remain unclear. Established knowledge includes the role of Kit and vimentin in identifying pacemaker-like cells in the gastrointestinal tract. However, no prior work had resolved whether similar cells exist in lymphatic vessels. This gap motivated the investigation into the morphology of cells within sheep mesenteric lymphatic vessels. The absence of clear structural parallels to gastrointestinal interstitial cells of Cajal in lymphatic tissue raised uncertainty about the presence of analogous pacemaker cells. No prior studies had combined electron microscopy and immunohistochemistry to examine lymphatic wall composition in this species. The lack of ultrastructural data on lymphatic pacemaker candidates limited understanding of their functional potential. This uncertainty highlights the need for detailed morphological analysis to identify potential pacemaker cells in lymphatic vessels. The study addresses this by exploring the spatial arrangement and ultrastructural features of cells in sheep mesenteric lymphatic vessels.
Purpose Of The Study:
The aim of this study was to investigate the morphology of cells within sheep mesenteric lymphatic vessels using electron microscopy and immunohistochemical techniques. The specific problem addressed was the absence of clear evidence for pacemaker-like cells in lymphatic tissue. The motivation stemmed from the need to understand how spontaneous contractile activity is regulated in lymphatic vessels. Prior studies had identified Kit and vimentin as markers for pacemaker cells in the gastrointestinal tract, but their presence in lymphatic tissue was unknown. The study sought to determine whether similar cells exist in lymphatic vessels and whether they share ultrastructural features with known pacemaker cells. The researchers aimed to examine the spatial distribution and ultrastructural characteristics of Kit and vimentin-positive cells in sheep mesenteric lymphatic vessels. This investigation was driven by the hypothesis that such cells might regulate contractile activity in lymphatic vessels. The study's contribution lies in providing the first morphological evidence of pacemaker-like cells in lymphatic tissue.
Main Methods:
The study employed electron microscopy and immunohistochemical techniques to examine sheep mesenteric lymphatic vessels. Tissue samples were prepared for ultrastructural analysis using electron microscopy to assess cellular morphology. Immunohistochemistry was performed using antibodies to Kit and vimentin to identify specific cell populations. The spatial arrangement of smooth muscle cells was compared to that of gastrointestinal tract smooth muscle cells. Electron-dense cells between the endothelium and smooth muscle were analyzed for ultrastructural features. The study compared the morphology of Kit and vimentin-positive cells to that of smooth muscle cells. Cells were stained for vimentin and myosin to distinguish between different cell types. The presence of caveolae, Golgi complexes, and endoplasmic reticulum was assessed in Kit and vimentin-positive cells.
Main Results:
The study found that smooth muscle cells in sheep mesenteric lymphatic vessels were arranged in interlocking bundles rather than circular or longitudinal layers. Kit and vimentin-positive cells were identified between the endothelium and smooth muscle layers. These cells exhibited electron-dense cytoplasm and contained caveolae, Golgi complexes, and mitochondria. The cells also displayed 10-nm filaments and a well-developed endoplasmic reticulum. Smooth muscle cells contained caveolae, dense bodies, and abundant filaments. Vimentin-positive cells were either branched or spindle-shaped, resembling smooth muscle cells. Myosin-staining cells had the typical spindle appearance of smooth muscle cells. The presence of a basal lamina in both Kit and vimentin-positive cells and smooth muscle cells was confirmed.
Conclusions:
The study provides the first morphological evidence that Kit and vimentin-positive cells exist in sheep mesenteric lymphatic vessels. These cells share ultrastructural features with pacemaker cells in other tissues, including electron density and caveolae. The researchers propose that these cells may regulate spontaneous contractile activity in lymphatic vessels. The findings suggest that lymphatic vessels may contain a subpopulation of pacemaker-like cells. The presence of 10-nm filaments and a well-developed endoplasmic reticulum supports this hypothesis. The study does not confirm the functional role of these cells but highlights their potential significance. The spatial arrangement of Kit and vimentin-positive cells between the endothelium and smooth muscle is notable. The results suggest that further research is needed to determine the physiological role of these cells.
Frequently Asked Questions
These cells share ultrastructural features with pacemaker cells in other tissues, suggesting a potential regulatory role in lymphatic contractile activity.
Immunohistochemical techniques using antibodies to Kit and vimentin were employed to label these cells in sheep mesenteric lymphatic vessels.
The interlocking bundle arrangement differs from the circular and longitudinal layers seen in the gastrointestinal tract, indicating unique structural adaptations.
Kit and vimentin-positive cells contain caveolae, Golgi complexes, and 10-nm filaments, whereas smooth muscle cells have dense bodies and abundant filaments.
Vimentin is a marker used to identify specialized cells, such as interstitial cells of Cajal in the gastrointestinal tract, and was used here to label potential pacemaker cells.
The researchers propose that these cells may regulate spontaneous contractile activity in lymphatic vessels, based on their ultrastructural similarities to pacemaker cells.

