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The effect of particles, including nanoparticles, on macrophages in vitro and in vivo

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Macrophages remove foreign material from the body and are recruited to sites were there are particles present. Multinucleate giant cells from by the fusion of macrophages. In the presence of particles, macrophages produce various chemical mediators, known as cytokines, as well as enzymes. Some of the cytokines are pro-inflammatory (for example, IL1Beta, IL6 and TNFalpha) while others promote giant cell formation (GM-CSF, M-CSF, TGF). The presence of these cellular products can be shown by examining tissue sections with immunohistochemistry and by western blotting. The message (mRNA) for the synthesis of these molecules can be demonstrated by in situ hybridization and the polymerase chain reaction. Macrophages process ingested material and present it as antigen to lymphocytes. Antigen-presenting macrophages play an important part in the initiation of metal sensitization. Surface receptors and their counterligands are expressed on macrophages and lymphocytes during antigen presentation. The particles present in tissues around joint prostheses have been isolated and characterized. Over 95% of these are less than 1 micron (ECD) in size. Transmission electron microscopy has revealed nanoparticles of metal in the range 15-20 nm. Such particles are too small to be phagocytosed. Hydroxyapatite, diamond-like carbon (nano-diamond) and metal particles are being studied and results compared with those of particles in the micrometer range. There is a different response to different nanoparticles.
Rocznik
Strony
29--31
Opis fizyczny
Bibliogr. 27 poz., rys., wykr.
Twórcy
autor
  • Eastman Dental Institute, UCL, London, England
autor
  • Eastman Dental Institute, UCL, London, England
autor
  • Eastman Dental Institute, UCL, London, England
autor
  • Technical University of Lodz, Poland
autor
  • Eastman Dental Institute, UCL, London, England
Bibliografia
  • [1] Yamac T, The extraction and characterisation of wear particles from tissues around failed orthopaedic implants of different designs PhD Thesis, University of London; 1999.
  • [2] Kobayashi A, Bonfield W, Kadoya Y, Yamac T, Freeman MAR, Scott G and Revell PA, The size and shape of particulate polyethylene wear debris in total joint replacements. Proc Instn Mech Engrs [H] 211, 11-15; 1997.
  • [3] Maloney WJ, Smith RL, Schmalzreid TP, Chiba J, Huene D and Rubash H, Isolation and characterisation of wear particles generated in patients who have had failure of hip arthroplasty without cement. J Bone Jt Surg 77A, 1301-1310; 1995.
  • [4] Revell PA. Tissue reactions to joint prostheses and the products of wear and corrosion. Curr Top Pathol 71, 73-101; 1982
  • [5] Revell PA, Al-Saffar N and Kobayashi A. Biological reaction to debris in relation to joint prostheses. Proc Instn Mech Engrs 211 H, 187-197; 1997.
  • [6] Al-Saffar N and Revell PA, Pathology of the Bone-Implant Interfaces. J Long-term Effects of Medical Implants 9, 319-347; 1999
  • [7] Revell PA and Jellie SE. Interleukin 15 production by macrophages in the implant interface membrane of aseptically loosened joint replacements. J Mater.Sci; Mater in Med 9, 727-730;1998.
  • [8] Clarke SA and Revell PA. Expression of Beta2 integrins at the bone/biomaterial interface. Proc Soc Biomat, San Diego, California;1998.
  • [9] Clarke SA. Integrin expression at the bone biomaterial interface. PhD Thesis. University of London, 1999
  • [10] Al-Saffar N and Revell PA, Pathology of the Bone-Implant Interfaces. J Long-term Effects of Medical Implants 9, 319-347; 1999.
  • [11] Al-Saffar N and Revell PA. Interleukin-1 production by activated microphages surrounding loosened orthopaedic implants: a potential role in osteolysis. Br J Rheumatol 33, 309-316: 1994.
  • [12] Al-Saffar N and Revell PA. Differential expression of transforming growth factor-alpha and macrophage colony-stimulating factor/colony stimulating factor-1R (c-fms) by multinucleated gian cells involved in pathological bone resorption at the site of orthopaedic implants. J Orthop Res 18, 800-807; 2000.
  • [13] Chiba J, Rhubash HE, Kim KJ and Iwaki Y. The characterization of cytokines in the interface tissue obtained from tailed cementless total hip arthroplasty with and without femoral osteolysis. Clin Orthop 300, 304-312; 1994.
  • [14] Al-Saffar N, Revell PA, Khwaja HA and Bonfield W. Assessment of the role of cytokines in bone resorption in patients with total hip replacement. J Mater Sci; Mater in Med 5; 762-767; 1995.
  • [15] Al-Saffar N, Revell PA, Khwaja HA and Kadoya Y. Assessment of the role of GM-CSF in the cellular transformation and the development of erosive lesions around orthopaedic implants. Am J Clin 105, 628-639; 1996.
  • [16] Xu JW, Kontinnen YT, Li TF, Waris TF, Lassus J, Matucci-Cerinic M, Sorsa T and Snatavirta TS. Production of platelet-derived growth factor in aseptic loosening of total hip replacement. Rheumatol Int 17, 215-221; 1998.
  • [17] Hercus B, Saeed S and Revell PA. Expression profile of T cell associated molecules in the interfacial tissue of aseptically loosened prosthetic joints. J Mater Sci: Mater Med 13,1153-1156;2002.
  • [18] Lalor PA, Revell PA. Gray AB, Wright S, Railton GT and Freeman MAR. Sensitivity to titanium. A cause for implant failure? J Bone Jt Surg 73B, 25-28; 1991.
  • [19] Weyand CM, Geisler A, Brack ME, Bolander ME and Goronzy JJ. Oligoclonal T-cell proliferation and interferon-gamma production in periprosthetic inflammation. Lab Invest 78, 677- 685; 1998.
  • [20] Hercus B and Revell PA. Phenotypic characteristics of T lymphocytes in the interfacial tissue of aseptically loosened prosthetic joints. J Mater Sci: Mater Med 12,1063-1067; 2001.
  • [21] Bainbridge JA, Revell PA and Al-Saffar N. Costimulatory molecule expression following exposure to orthopaedic implants wear J Biomed Mater Res 54, 328-334; 2001.
  • [22] Al-Saffar N, Revell PA and Kobayashi A. Modulation of the phenotypic and functional properties of phagocytic macrophages by wear particles from orthopaedic implants. J Mater Sci: Mater Med 8, 641-648; 1997.
  • [23] Altaf H, Saeed S, Bhatt R and Revell PA The assessment of antigen presenting cells In the bone-implant interface. Biomaterialen 4, 86; 2003.
  • [24] Altaf H and Revell PA. The characterisation of antigen presenting cells in the bone implant interface & in response to biomaterials. Proc 7th World Biomaterials Congress, Sydney, Australia, 686; 2004.
  • [25] Bhatt R, Saeed S, Altaf H and Revell PA. In vitro assessment of interactions between T-cells and antigen-presenting cells (Apcs) when challenged with biomaterials: the CD40-CD40L interaction. Proc 7th World Biomaterials Congress, Sydney, Australia, 488; 2004.
  • [26] Saeed S and Revell PA. Production and distribution of interleukin 15 and its receptors (IL-15R? and IL-R2Beta) in the implant interface tissues obtained during revision of failed total joint replacement. Int J Exp Path 82, 201-209; 2001.
  • [27] Saeed S, Al-Saffar N and Revell PA. Expression of interleukin-15 (IL-15) and its receptors by U937 cells stimulated by metal wear particles retrieved from periprosthetic tissue. Proc 6th World Biomaterials Congress, Hawaii, 401; 2000.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-AGH5-0008-0076
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