Literature DB >> 2546991

Polarized distribution of Na+,K+-ATPase in giant cells elicited in vivo and in vitro.

A Vignery1, T Niven-Fairchild, D H Ingbar, M Caplan.   

Abstract

Giant cell formation was analyzed to determine whether it results in the high level of Na+,K+-ATPase expression that characterizes multinucleated cells such as osteoclasts. Giant cells and fusing alveolar macrophages were subjected to morphological, immunological, and biochemical studies. Both subunits of the Na+,K+-ATPase were found to be present on the plasma membrane of giant cells. Their localization was restricted to the non-adherent domain of the cell surface. Dynamic studies of giant cell differentiation demonstrated that on culture and/or multinucleation, an increase in sodium pump alpha-subunit synthesis occurred and led to a high level of expression of Na pumps. Conversely, the adherent plasma membrane of giant cells was enriched in a lysosomal membrane antigen. This study demonstrates that culture and/or multinucleation induces a significant increase in the expression of sodium pumps. The polarized distribution of these pumps and of a lysosomal component suggests that fusing macrophages undergo biochemical and morphological alterations which prepare them for a new and specialized function in chronic inflammatory reactions. Giant cells may offer a suitable model system to study the differentiation of other related multinucleated cells, such as osteoclasts.

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Year:  1989        PMID: 2546991     DOI: 10.1177/37.8.2546991

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  11 in total

1.  Generation of multinucleated giant cells in vitro by culture of human monocytes with Mycobacterium bovis BCG in combination with cytokine-containing supernatants.

Authors:  A Gasser; J Möst
Journal:  Infect Immun       Date:  1999-01       Impact factor: 3.441

Review 2.  Osteoclasts and giant cells: macrophage-macrophage fusion mechanism.

Authors:  A Vignery
Journal:  Int J Exp Pathol       Date:  2000-10       Impact factor: 1.925

3.  Identification of an inducible surface molecule specific to fusing macrophages.

Authors:  C Saginario; H Y Qian; A Vignery
Journal:  Proc Natl Acad Sci U S A       Date:  1995-12-19       Impact factor: 11.205

4.  Macrophage multinucleation is accompanied by the expression of new soluble and membrane antigens in mice.

Authors:  A Vignery
Journal:  Am J Pathol       Date:  1989-09       Impact factor: 4.307

5.  The intracellular domain of CD44 promotes the fusion of macrophages.

Authors:  Weiguo Cui; Juan Zhang Ke; Qing Zhang; Hua-Zhu Ke; Cécile Chalouni; Agnès Vignery
Journal:  Blood       Date:  2005-09-29       Impact factor: 22.113

6.  Beta1 and beta2 integrins mediate adhesion during macrophage fusion and multinucleated foreign body giant cell formation.

Authors:  Amy K McNally; James M Anderson
Journal:  Am J Pathol       Date:  2002-02       Impact factor: 4.307

7.  Foreign body-type multinucleated giant cell formation is potently induced by alpha-tocopherol and prevented by the diacylglycerol kinase inhibitor R59022.

Authors:  Amy K McNally; James M Anderson
Journal:  Am J Pathol       Date:  2003-09       Impact factor: 4.307

8.  Monocyte, macrophage and foreign body giant cell interactions with molecularly engineered surfaces.

Authors:  J M Anderson; K Defife; A McNally; T Collier; C Jenney
Journal:  J Mater Sci Mater Med       Date:  1999 Oct-Nov       Impact factor: 3.896

9.  MFR, a putative receptor mediating the fusion of macrophages.

Authors:  C Saginario; H Sterling; C Beckers; R Kobayashi; M Solimena; E Ullu; A Vignery
Journal:  Mol Cell Biol       Date:  1998-11       Impact factor: 4.272

10.  CD44 occupancy prevents macrophage multinucleation.

Authors:  H Sterling; C Saginario; A Vignery
Journal:  J Cell Biol       Date:  1998-11-02       Impact factor: 10.539

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