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Unique localization of protein gene product 9.5 in type B synoviocytes in the joints of the horse.

Abstract: Fibroblast-like (Type B) synoviocytes are cells in the synovial membrane that are responsible for production of both synovial fluid and the extracellular matrix in the synovial intima. Immunostaining of the horse synovial membrane for protein gene product (PGP) 9.5, which is a neuron-specific ubiquitin C-terminal hydrolase, demonstrated selective localization of the immunoreactivity in a synoviocyte population different from acid phosphatase-positive Type A synoviocytes. The immunoreactive cells were lined up in the synovial intima and extended dendritic processes towards the joint cavity to form a dense plexus on the surface. Electron microscopic examination clearly identified the PGP 9.5-immunoreactive cells as Type B synoviocytes characterized by developed rough endoplasmic reticulum and free ribosomes. Immunoreactivity for PGP 9.5 was diffusely distributed throughout the cytoplasm, including the tips of fine processes. Western and Northern blot analyses could not distinguish the corresponding protein and mRNA obtained from the brain and synovial membrane. The existence of the neuron-specific PGP 9.5 in Type B synoviocytes suggests a common mechanism regulating the protein metabolism between neurons and synoviocytes, and also provides a new cytochemical marker for identification of the cells.
Publication Date: 1999-02-20 PubMed ID: 10026236DOI: 10.1177/002215549904700308Google Scholar: Lookup
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  • Journal Article

Summary

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The research paper presents a study of protein gene product (PGP) 9.5’s unique location within fibroblast-like (Type B) synoviocytes in horse joints. This protein, typically related to neuronal activity, points towards a common regulation mechanism for protein metabolism within the neurons and synoviocytes.

Understanding Type B synoviocytes

  • Fibroblast-like, or Type B, synoviocytes are cells that populate the synovial membrane in horse joints.
  • They are critical for the production of synovial fluid, a lubricant for joints, as well as the extracellular matrix within the synovial intima, the inner part of the synovial lining.

Exploration of Protein Gene Product 9.5

  • The research centered around protein gene product 9.5 (PGP 9.5), a unique protein generally associated with neurons and has a role as a ubiquitin C-terminal hydrolase, an enzyme that regulates protein degradation.
  • In their investigation, the researchers found that PGP 9.5 localizes and operates within a specific population subset of synoviocytes that differs from the acid phosphatase-positive Type A synoviocytes.

Identifying Unique Localization and Role

  • The researchers were able to determine the unique localization of PGP 9.5 through detailed immunostaining and electron microscopic examination, showing that these PGP 9.5-reactive cells are Type B synoviocytes.
  • These cells reveal developed rough endoplasmic reticulum and free ribosomes, suggesting an active role in protein synthesis and transportation.
  • The PGP 9.5 proteins spread throughout the cytoplasm, even extending into the fine processes of these cells.

Analysis of Protein and mRNA

  • The researchers procurred both protein and mRNA from the brain and the synovial membrane for Western and Northern blot analyses.
  • However, no clear distinction could be made between the protein and mRNA extracted from both sources using these techniques.

Implications and Conclusions of the Study

  • The presence of the neuron-specific PGP 9.5 in Type B synoviocytes poses a new perspective on the regulation of protein metabolism in these cells, suggesting a shared mechanism with neurons.
  • This conclusion also suggests a new cytochemical marker for identifying these particular synoviocyte cells, which could be beneficial in further studies or potential therapeutic applications.

Cite This Article

APA
Kitamura HP, Yanase H, Kitamura H, Iwanaga T. (1999). Unique localization of protein gene product 9.5 in type B synoviocytes in the joints of the horse. J Histochem Cytochem, 47(3), 343-352. https://doi.org/10.1177/002215549904700308

Publication

ISSN: 0022-1554
NlmUniqueID: 9815334
Country: United States
Language: English
Volume: 47
Issue: 3
Pages: 343-352

Researcher Affiliations

Kitamura, H P
  • Laboratories of Anatomy, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Yanase, H
    Kitamura, H
      Iwanaga, T

        MeSH Terms

        • Animals
        • Base Sequence
        • Blotting, Northern
        • Blotting, Western
        • Brain / metabolism
        • Cloning, Molecular
        • Horses / metabolism
        • Humans
        • Immunoenzyme Techniques
        • Male
        • Microscopy, Immunoelectron
        • Molecular Sequence Data
        • Neurons / metabolism
        • Rats
        • Sequence Alignment
        • Synovial Membrane / metabolism
        • Thiolester Hydrolases / genetics
        • Thiolester Hydrolases / metabolism
        • Ubiquitin Thiolesterase

        Citations

        This article has been cited 3 times.
        1. Zamith Cunha R, Zannoni A, Salamanca G, De Silva M, Rinnovati R, Gramenzi A, Forni M, Chiocchetti R. Expression of cannabinoid (CB1 and CB2) and cannabinoid-related receptors (TRPV1, GPR55, and PPARα) in the synovial membrane of the horse metacarpophalangeal joint. Front Vet Sci 2023;10:1045030.
          doi: 10.3389/fvets.2023.1045030pubmed: 36937015google scholar: lookup
        2. Emmi A, Stocco E, Boscolo-Berto R, Contran M, Belluzzi E, Favero M, Ramonda R, Porzionato A, Ruggieri P, De Caro R, Macchi V. Infrapatellar Fat Pad-Synovial Membrane Anatomo-Fuctional Unit: Microscopic Basis for Piezo1/2 Mechanosensors Involvement in Osteoarthritis Pain. Front Cell Dev Biol 2022;10:886604.
          doi: 10.3389/fcell.2022.886604pubmed: 35837327google scholar: lookup
        3. Fülber J, Maria DA, da Silva LC, Massoco CO, Agreste F, Baccarin RY. Comparative study of equine mesenchymal stem cells from healthy and injured synovial tissues: an in vitro assessment. Stem Cell Res Ther 2016 Mar 5;7:35.
          doi: 10.1186/s13287-016-0294-3pubmed: 26944403google scholar: lookup