Abstract: Cartilage canals have been shown to contain discontinuous blood vessels that enable circulating bacteria to bind to cartilage matrix, leading to vascular occlusion and associated pathological changes in pigs and chickens. It is also inconsistently reported that cartilage canals are surrounded by a cellular or acellular wall that may influence whether bacterial binding can occur. It is not known whether equine cartilage canals contain discontinuous endothelium or are surrounded by a wall. This study aimed to examine whether there were discontinuities in the endothelium of cartilage canal vessels, and whether canals had a cellular or acellular wall, in the epiphyseal growth cartilage of foals. Epiphyseal growth cartilage from the proximal third of the medial trochlear ridge of the distal femur from six healthy foals that were 1, 24, 35, 47, 118 and 122 days old and of different breeds and sexes was examined by light microscopy (LM), transmission electron microscopy (TEM) and immunohistochemistry. The majority of patent cartilage canals contained blood vessels that were lined by a thin layer of continuous endothelium. Fenestrations were found in two locations in one venule in a patent cartilage canal located deep in the growth cartilage and close to the ossification front in the 118-day-old foal. Chondrifying cartilage canals in all TEM-examined foals contained degenerated endothelial cells that were detached from the basement membrane, resulting in gap formation. Thirty-three percent of all canals were surrounded by a hypercellular rim that was interpreted as contribution of chondrocytes to growth cartilage. On LM, 69% of all cartilage canals were surrounded by a ring of matrix that stained intensely eosinophilic and consisted of collagen fibres on TEM that were confirmed to be collagen type I by immunohistochemistry. In summary, two types of discontinuity were observed in the endothelium of equine epiphyseal cartilage canal vessels: fenestrations were observed in a patent cartilage canal in the 118-day-old foal; and gaps were observed in chondrifying cartilage canals in all TEM-examined foals. Canals were not surrounded by any cellular wall, but a large proportion was surrounded by an acellular wall consisting of collagen type I. Bacterial binding can therefore probably occur in horses by mechanisms that are similar to those previously demonstrated in pigs and chickens.
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The study explores the structure of cartilage canals in young horses, specifically looking at the endothelium of these canals and how they might relate to bacterial infections leading to joint diseases. It was found that some of these canals are discontinuous, allowing bacteria to potentially bind to them, similar to observations in pigs and chickens.
Study Purpose and Methodology
The objective of the study was to investigate the endothelium of cartilage canals in the growth cartilage of foals. This exploration was guided by the assumption that these canals may have discontinuous endothelium and whether these canals are surrounded by a cellular or acellular wall.
The research analyzed the epiphyseal growth cartilage from six healthy foals of different breeds and sexes with varying ages, ranging from 1 to 122 days. The medium of study included light microscopy, transmission electron microscopy, and immunohistochemistry.
Findings
The majority of patent cartilage canals contained blood vessels that were lined by a thin layer of continuous endothelium.
On deeper examination, some discontinuity in the endothelium of these canals was found. This was noticed at two locations in a venule in one of the older foals (118 days old). This cartilage canal was located deep in the growth cartilage, close to the ossification front, an area where bone formation is taking place.
In addition, cartilage canals undergoing a process called chondrification were found to contain degenerated endothelial cells that have detached from the basement membrane, leaving gaps.
About 33% of canals had a hypercellular rim surrounding them, which was interpreted as a solution of chondrocytes to cartilage growth.
Visually, almost 70% of all cartilage canals were surrounded by a ring of matrix that stained intensely eosinophilic and contained collagen fibers. Further tests confirmed these to be collagen type I.
Implications
The study found two types of discontinuity in the endothelium of equine epiphyseal cartilage canal vessels.
It was also found that canals were not surrounded by any cellular wall, but a substantial number were surrounded by an acellular wall consisting primarily of collagen type I.
These findings suggest the potential for bacterial binding in these canals, akin to mechanisms previously demonstrated in pigs and chickens. This means that the breach in the endothelium may enable circulating bacteria to attach to cartilage matrix, which could lead to vascular occlusion and associated pathological changes.
Conclusion
The understanding of these structural details of cartilage canals could boost knowledge related to joint diseases in foals, particularly those associated with bacterial infections.
More research is necessary to definitively establish the correlation between these discontinuous canals and susceptibility to bacterial binding and subsequent joint diseases.
Cite This Article
APA
Hellings IR, Ekman S, Hultenby K, Dolvik NI, Olstad K.
(2015).
Discontinuities in the endothelium of epiphyseal cartilage canals and relevance to joint disease in foals.
J Anat, 228(1), 162-175.
https://doi.org/10.1111/joa.12391
Department of Companion Animal Clinical Sciences, Equine Section, Faculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences, Oslo, Norway.
Ekman, Stina
Department of Biomedical Sciences and Veterinary Public Health, Section of Pathology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Hultenby, Kjell
Department of Laboratory Medicine, Karolinska Institutet and University Hospital, Huddinge, Sweden.
Dolvik, Nils Ivar
Department of Companion Animal Clinical Sciences, Equine Section, Faculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences, Oslo, Norway.
Olstad, Kristin
Department of Companion Animal Clinical Sciences, Equine Section, Faculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences, Oslo, Norway.
MeSH Terms
Animals
Animals, Newborn
Cartilage, Articular / anatomy & histology
Cartilage, Articular / blood supply
Collagen Type I / analysis
Endothelium / anatomy & histology
Femur Head / anatomy & histology
Growth Plate / anatomy & histology
Growth Plate / blood supply
Horse Diseases / pathology
Horses / anatomy & histology
Immunohistochemistry
Joint Diseases / pathology
Microscopy, Electron
Regional Blood Flow
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