A quantitative immunohistochemical study of the endoneurium in the rat dorsal and ventral spinal roots
Language English Country Germany Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Axons chemistry MeSH
- Chondroitin Sulfate Proteoglycans analysis MeSH
- Diagnostic Imaging methods MeSH
- Extracellular Matrix Proteins analysis MeSH
- Fibronectins analysis MeSH
- Fluorescent Antibody Technique MeSH
- Immunohistochemistry MeSH
- Rats MeSH
- Spinal Nerve Roots chemistry MeSH
- Peripheral Nerves chemistry MeSH
- Rats, Wistar MeSH
- Tenascin analysis MeSH
- Thrombospondins analysis MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Chondroitin Sulfate Proteoglycans MeSH
- Extracellular Matrix Proteins MeSH
- Fibronectins MeSH
- Tenascin MeSH
- Thrombospondins MeSH
The dorsal and ventral spinal roots contain different types of axons. The endoneurial extracellular matrix (ECM) among them is produced by Schwann cells and fibroblasts under the control of the axons. Chondroitin sulfate proteoglycan, fibronectin, tenascin-C, and thrombospondin are common components of the endoneurial ECM involved in the normal function as well as regeneration of the peripheral nerve. The present paper demonstrates a comparison of immunofluorescence staining for chondroitin sulfate proteoglycan, fibronectin, tenascin-C, and thrombospondin in the endoneurium of the rat dorsal and ventral spinal roots. Sections through the dorsal and ventral roots were cut simultaneously and adhered to the same microscopic slide. They were incubated simultaneously and the intensity of immunofluorescence staining was assessed by computer-assisted image analysis using interactive segmentation of digitized pictures to select the areas of measurement. The measurement of the immunofluorescence brightness revealed that the endoneurium of the dorsal roots was immunostained for the studied molecules at a higher intensity than in the ventral roots. The results suggest quantitative differences of the endoneurial content of the spinal dorsal and ventral roots probably corresponding to the presence of various types of axons. On the other hand, the different concentration of ECM molecules in the endoneurium of dorsal and ventral roots might be related to the formation of extrinsic conditions differently supporting regeneration of afferent and motor axons after their injury.
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