Literature DB >> 7047375

Inflammatory giant cells.

T J Chambers, W G Spector.   

Abstract

Giant cells are commonly seen in granulomas produced by a wide variety of known and unknown agents. It is widely accepted that giant cell formation results from fusion of mononuclear phagocytes. Both experimental and circumstantial evidence suggests that fusion takes place following the attachment of more than one macrophage to the same endocytic material. This view is in keeping with the consistent observation of giant cell formation in granulomas, where macrophages are actively ingesting material in close apposition to other macrophages. The experimental evidence for this view derives from the finding that if more than one macrophage is attached simultaneously to the same endocytic material in vitro, fusion results. Study of the phagocytic capacity of giant cells formed in vivo suggests that the same mechanism of fusion operates in granulomatous inflammation. Giant cell formation in granulomas thus appears to be the incidental result of macrophages ingesting material in close apposition to other macrophages. The material responsible for fusion may either be the visible particulate cause of granuloma formation or the denatured macromolecules formed by the inflammatory process.

Entities:  

Mesh:

Year:  1982        PMID: 7047375     DOI: 10.1016/S0171-2985(82)80084-3

Source DB:  PubMed          Journal:  Immunobiology        ISSN: 0171-2985            Impact factor:   3.144


  19 in total

1.  The scavenger receptor CD36 plays a role in cytokine-induced macrophage fusion.

Authors:  Laura Helming; Julia Winter; Siamon Gordon
Journal:  J Cell Sci       Date:  2009-01-20       Impact factor: 5.285

Review 2.  Biocompatibility of implants: lymphocyte/macrophage interactions.

Authors:  James M Anderson; Amy K McNally
Journal:  Semin Immunopathol       Date:  2011-01-27       Impact factor: 9.623

3.  Continuous cultures of macrophages derived from the 8-day epiblast of the pig.

Authors:  N C Talbot; M Worku; M J Paape; P Grier; C E Rexroad; V G Pursel
Journal:  In Vitro Cell Dev Biol Anim       Date:  1996-10       Impact factor: 2.416

4.  Senescence and quiescence induced compromised function in cultured macrophages.

Authors:  Dolly J Holt; David W Grainger
Journal:  Biomaterials       Date:  2012-07-17       Impact factor: 12.479

Review 5.  Macrophage form, function, and phenotype in mycobacterial infection: lessons from tuberculosis and other diseases.

Authors:  Colleen M McClean; David M Tobin
Journal:  Pathog Dis       Date:  2016-07-10       Impact factor: 3.166

6.  B-1 cells are pivotal for in vivo inflammatory giant cell formation.

Authors:  Cristina Stewart Bittencourt Bogsan; Ronni Rômulo Novaes e Brito; Maiko da Cruz Palos; Renato Arruda Mortara; Sandro Rogério Almeida; José Daniel Lopes; Mario Mariano
Journal:  Int J Exp Pathol       Date:  2005-08       Impact factor: 1.925

Review 7.  The aetiology of Crohn's disease.

Authors:  G N Tytgat; C J Mulder
Journal:  Int J Colorectal Dis       Date:  1986-07       Impact factor: 2.571

8.  Spontaneous cell transformation: karyoplasts derived from multinucleated cells produce new cell growth in senescent human epithelial cell cultures.

Authors:  Kirsten H Walen
Journal:  In Vitro Cell Dev Biol Anim       Date:  2004 May-Jun       Impact factor: 2.416

9.  Interleukin-4-induced macrophage fusion is prevented by inhibitors of mannose receptor activity.

Authors:  A K McNally; K M DeFife; J M Anderson
Journal:  Am J Pathol       Date:  1996-09       Impact factor: 4.307

10.  Foreign body-type multinucleated giant cell formation requires protein kinase C beta, delta, and zeta.

Authors:  Amy K McNally; Sarah R Macewan; James M Anderson
Journal:  Exp Mol Pathol       Date:  2007-11-09       Impact factor: 3.362

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