Mechanisms of Foreign Body Giant Cell Formation in Response to Implantable Biomaterials

被引:17
作者
Eslami-Kaliji, Farshid [1 ]
Nia, Niloufar Hedayat [2 ]
Lakey, Jonathan R. T. [3 ]
Smink, Alexandra M. [4 ]
Mohammadi, Mohammadreza [5 ]
机构
[1] ACECR, Royan Inst Biotechnol, Cell Sci Res Ctr, Dept Anim Biotechnol, Esfahan 8159358686, Iran
[2] Univ Calif Irvine, Dept Publ Hlth, Irvine, CA 92617 USA
[3] Univ Calif Irvine, Dept Surg & Biomed Engn, Orange, CA 92868 USA
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, NL-9701 Groningen, Netherlands
[5] Chapman Univ, Dale E & Sarah Ann Fowler Sch Engn, Orange, CA 92866 USA
关键词
macrophages fusion; biomaterials; foreign body giant cells (FBGCs); immune response; mechanotransduction; actin cytoskeleton; SOFT-TISSUE AUGMENTATION; MACROPHAGE FUSION; MONOCYTES MACROPHAGES; VITAMIN-E; ADHESION; ACTIN; RECEPTOR; KINASE; INVADOPODIA; PODOSOMES;
D O I
10.3390/polym15051313
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Long term function of implantable biomaterials are determined by their integration with the host's body. Immune reactions against these implants could impair the function and integration of the implants. Some biomaterial-based implants lead to macrophage fusion and the formation of multinucleated giant cells, also known as foreign body giant cells (FBGCs). FBGCs may compromise the biomaterial performance and may lead to implant rejection and adverse events in some cases. Despite their critical role in response to implants, there is a limited understanding of cellular and molecular mechanisms involved in forming FBGCs. Here, we focused on better understanding the steps and mechanisms triggering macrophage fusion and FBGCs formation, specifically in response to biomaterials. These steps included macrophage adhesion to the biomaterial surface, fusion competency, mechanosensing and mechanotransduction-mediated migration, and the final fusion. We also described some of the key biomarkers and biomolecules involved in these steps. Understanding these steps on a molecular level would lead to enhance biomaterials design and improve their function in the context of cell transplantation, tissue engineering, and drug delivery.
引用
收藏
页数:16
相关论文
共 113 条
[41]   Biomimetic surfaces for control of cell adhesion to facilitate bone formation [J].
García, AJ ;
Keselowsky, BG .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2002, 12 (02) :151-162
[42]   Lamellipodial actin mechanically links myosin activity with adhesion-site formation [J].
Giannone, Gregory ;
Dubin-Thaler, Benjamin J. ;
Rossier, Olivier ;
Cai, Yunfei ;
Chaga, Oleg ;
Jiang, Guoying ;
Beaver, William ;
Dobereiner, Hans-Gunther ;
Freund, Yoav ;
Borisy, Gary ;
Sheetz, Michael P. .
CELL, 2007, 128 (03) :561-575
[43]   CD47, a ligand for the macrophage fusion receptor, participates in macrophage multinucleation [J].
Han, X ;
Sterling, H ;
Chen, YM ;
Saginario, C ;
Brown, EJ ;
Frazier, WA ;
Lindberg, FP ;
Vignery, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37984-37992
[44]   VASP is a processive actin polymerase that requires monomeric actin for barbed end association [J].
Hansen, Scott D. ;
Mullins, R. Dyche .
JOURNAL OF CELL BIOLOGY, 2010, 191 (03) :571-584
[45]   Cell Adhesion Molecules and Their Roles and Regulation in the Immune and Tumor Microenvironment [J].
Harjunpaa, Heidi ;
Asens, Marc Llort ;
Guenther, Carla ;
Fagerholm, Susanna C. .
FRONTIERS IN IMMUNOLOGY, 2019, 10
[46]   Focal adhesion kinase functions as a receptor-proximal signaling component required for directed cell migration [J].
Hauck, CR ;
Klingbeil, CK ;
Schlaepfer, DD .
IMMUNOLOGIC RESEARCH, 2000, 21 (2-3) :293-303
[47]   Macrophage fusion induced by IL-4 alternative activation is a multistage process involving multiple target molecules [J].
Helming, Laura ;
Gordon, Siamon .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2007, 37 (01) :33-42
[48]   Molecular mediators of macrophage fusion [J].
Helming, Laura ;
Gordon, Siamon .
TRENDS IN CELL BIOLOGY, 2009, 19 (10) :514-522
[49]   Essential Role of DAP12 Signaling in Macrophage Programming into a Fusion-Competent State [J].
Helming, Laura ;
Tomasello, Elena ;
Kyriakides, Themis R. ;
Martinez, Fernando O. ;
Takai, Toshiyuki ;
Gordon, Siamon ;
Vivier, Eric .
SCIENCE SIGNALING, 2008, 1 (43)
[50]   Molecular Mechanisms Underlying the Force-Dependent Regulation of Actin-to-ECM Linkage at the Focal Adhesions [J].
Hirata, Hiroaki ;
Sokabe, Masahiro ;
Lim, Chwee Teck .
MECHANOTRANSDUCTION, 2014, 126 :135-154