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Zentralblatt fur Veterinarmedizin. Reihe A1994; 41(1); 31-36; doi: 10.1111/j.1439-0442.1994.tb00062.x

Preparation and characterization of monoclonal antibodies against equine chondrocytes, osteoblasts and osteocytes.

Abstract: Three monoclonal antibodies capable of individually recognizing chondrocytes, osteoblasts and osteocytes were prepared. EB-1 reacted with a 55-kDa antigen on the chondrocyte membrane, EB-2 with a 110-kDa antigen on the membrane of osteoblasts and/or partial osteocytes, and EB-3 with a 130-kDa antigen on the membrane of osteocytes. These monoclonal antibodies may be useful probes for studying the differentiation and maturation of osteogenic cells.
Publication Date: 1994-02-01 PubMed ID: 8085396DOI: 10.1111/j.1439-0442.1994.tb00062.xGoogle Scholar: Lookup
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  • Journal Article

Summary

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This research focuses on the creation and examination of three different monoclonal antibodies that have the capability to individually identify chondrocytes, osteoblasts, and osteocytes. These antibodies could be significant for studying the maturation and development processes of cells that contribute to bone formation.

Preparation of Monoclonal Antibodies

Researchers prepared three separate monoclonal antibodies each with the distinctive capacity to react with and identify a specific type of cell. These cells – chondrocytes, osteoblasts and osteocytes – are key components contributing to the structure and function of bones.

  • EB-1: This antibody reacted with a particular 55-kDa antigen found on the chondrocyte membrane. Chondrocytes are cells responsible for the synthesis and maintenance of cartilaginous matrix in the body.
  • EB-2: This antibody interacted with a 110-kDa antigen located on the membrane of osteoblasts and/or partial osteocytes. Osteoblasts are cells active in the formation of bone, while osteocytes are mature bone cells.
  • EB-3: The third antibody detected a 130-kDa antigen present on the membrane of osteocytes.

Significance of Findings

The successful preparation and characterization of these monoclonal antibodies provides a potential pathway for further understanding the differentiation and maturation of osteogenic cells.

  • The fact that each antibody is able to individually recognize and react with a specific cell type could help to shed light on how these cells function and interact during the process of bone formation.
  • Identification of antigens specific to the cell type could provide crucial targets for future research or therapeutic approaches in diseases related to bone tissue such as osteoporosis or arthritis.
  • The antibodies may also be used as probes in a laboratory setting to observe and study osteogenic cells behaviour during their life cycle.

Cite This Article

APA
Katayama Y, Oikawa M, Kaneko M, Yoshihara T, Yoshikawa H, Yoshikawa T. (1994). Preparation and characterization of monoclonal antibodies against equine chondrocytes, osteoblasts and osteocytes. Zentralbl Veterinarmed A, 41(1), 31-36. https://doi.org/10.1111/j.1439-0442.1994.tb00062.x

Publication

ISSN: 0514-7158
NlmUniqueID: 0331323
Country: Germany
Language: English
Volume: 41
Issue: 1
Pages: 31-36

Researcher Affiliations

Katayama, Y
  • Pathology Division, Equine Research Institute, Japan Racing Association, Tokyo.
Oikawa, M
    Kaneko, M
      Yoshihara, T
        Yoshikawa, H
          Yoshikawa, T

            MeSH Terms

            • Animals
            • Antibodies, Monoclonal / biosynthesis
            • Antibodies, Monoclonal / immunology
            • Cartilage / cytology
            • Cartilage / immunology
            • Horses / immunology
            • Hybridomas
            • Mice
            • Osteoblasts / immunology
            • Osteocytes / immunology

            Citations

            This article has been cited 1 times.
            1. Maeda Y, Hanada M, Oikawa MA. Epidemiology of racing injuries in Thoroughbred racehorses with special reference to bone fractures: Japanese experience from the 1980s to 2000s.. J Equine Sci 2016;27(3):81-97.
              doi: 10.1294/jes.27.81pubmed: 27703403google scholar: lookup