Literature DB >> 2475153

Expression of the vitronectin receptor during embryonic development; an immunohistological study of the ontogeny of the osteoclast in the rabbit.

A Simpson1, M A Horton.   

Abstract

The development of the osteoclast during embryogenesis was studied in the rabbit by immunohistological techniques. Two monoclonal antibodies, 13C2 and 23C6, which react with the alpha-chain of the vitronectin receptor were used to define mono and multi-nucleate osteoclasts; being unreactive with other haemopoietic cells these antibodies could discriminate between osteoclasts and cells of the mononuclear phagocyte system. Staged rabbit embryos, from 14 to 28 days of age, were analysed and compared with findings from newborn and adult rabbits. No 13C2/23C6 immunoreactivity was seen in any of the tissues studied prior to day 17. 13C2/23C6-positive, mononuclear cells--presumptive osteoclast precursors--were first observed in the outer perichondrium of long-bones adjacent to the zone of hypertrophic cartilage in day 17 embryos. From day 17 onwards mono and multi-nucleate cells accumulated progressively in the perichondrium/periosteum, and by day 22 within the developing bone marrow cavity attached to bone spicules. No cells expressing the vitronectin receptor were seen at sites of embryonic or foetal haemopoiesis in yolk sac or foetal liver, that is, prior to the formation of the marrow cavity. Macrophages, defined by cross-reactivity with an antibody to human HLA-DR, first appeared in developing marrow spaces 11 days after the first osteoclast precursor appeared, suggesting that osteoclasts and definitive macrophages might develop from separate cell lineages, or that they diverge at an early stage of differentiation of haemopoietic stem cells.

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Year:  1989        PMID: 2475153      PMCID: PMC2040572     

Source DB:  PubMed          Journal:  Br J Exp Pathol        ISSN: 0007-1021


  18 in total

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Authors:  T J Chambers
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Authors:  M E Hemler
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3.  The role of mesenchyme in embryonic long bones as early deposition site for osteoclast progenitor cells.

Authors:  C W Thesingh; E H Burger
Journal:  Dev Biol       Date:  1983-02       Impact factor: 3.582

Review 4.  The origin of osteoclasts: evidence, clinical implications and investigative challenges of an extra-skeletal source.

Authors:  S C Marks
Journal:  J Oral Pathol       Date:  1983-08

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Authors:  N M Le Douarin
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6.  Fine structure of fetal rat calvarium; provisional identification of preosteoclasts.

Authors:  B R Rifkin; J S Brand; J E Cushing; S J Coleman; F Sanavi
Journal:  Calcif Tissue Int       Date:  1980       Impact factor: 4.333

7.  Monoclonal antibodies to osteoclastomas (giant cell bone tumors): definition of osteoclast-specific cellular antigens.

Authors:  M A Horton; D Lewis; K McNulty; J A Pringle; T J Chambers
Journal:  Cancer Res       Date:  1985-11       Impact factor: 12.701

8.  Cell surface characterization of the human osteoclast: phenotypic relationship to other bone marrow-derived cell types.

Authors:  M A Horton; E F Rimmer; D Lewis; J A Pringle; K Fuller; T J Chambers
Journal:  J Pathol       Date:  1984-12       Impact factor: 7.996

9.  A 125/115-kDa cell surface receptor specific for vitronectin interacts with the arginine-glycine-aspartic acid adhesion sequence derived from fibronectin.

Authors:  R Pytela; M D Pierschbacher; E Ruoslahti
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205

10.  In vitro formation of osteoclasts from long-term cultures of bone marrow mononuclear phagocytes.

Authors:  E H Burger; J W Van der Meer; J S van de Gevel; J C Gribnau; G W Thesingh; R van Furth
Journal:  J Exp Med       Date:  1982-12-01       Impact factor: 14.307

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  4 in total

Review 1.  Vitronectin receptor: tissue specific expression or adaptation to culture?

Authors:  M Horton
Journal:  Int J Exp Pathol       Date:  1990-10       Impact factor: 1.925

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4.  The osteoclast functional antigen, implicated in the regulation of bone resorption, is biochemically related to the vitronectin receptor.

Authors:  J Davies; J Warwick; N Totty; R Philp; M Helfrich; M Horton
Journal:  J Cell Biol       Date:  1989-10       Impact factor: 10.539

  4 in total

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