Biomaterial Strategies of Macrophage Behaviour in Bone Regeneration

被引:0
作者
Chocholata, Petra Kocanek [1 ]
Dvorakova, Jana [1 ]
Babuska, Vaclav [1 ]
Cedikova, Miroslava [2 ,3 ]
机构
[1] Charles Univ Prague, Fac Med Pilsen, Dept Med Chem & Biochem, Alej Svobody 76, Plzen 32300, Czech Republic
[2] Charles Univ Prague, Fac Med Pilsen, Dept Physiol, Alej Svobody 76, Plzen 32300, Czech Republic
[3] Charles Univ Prague, Fac Med Pilsen, Biomed Ctr, Lab Tumor Biol & Immunotherapy, Alej Svobody 76, Plzen 32300, Czech Republic
关键词
Biomaterials; Macrophages; Monocytes; Immune reaction; Inflammation; Bone tissue engineering; CENTRAL-NERVOUS-SYSTEM; FOREIGN-BODY REACTION; IN-VITRO; ALVEOLAR MACROPHAGES; HYALURONIC-ACID; TISSUE-REPAIR; GIANT-CELLS; SCAFFOLDS; POLARIZATION; HYDROGELS;
D O I
10.1007/s40883-025-00443-8
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Macrophages are essential mediators in the immune response to biomaterials, significantly influencing the success and longevity of bone tissue implants and engineered scaffolds. Their ability to transition between pro-inflammatory (M1) and anti-inflammatory (M2) phenotypes offers unique opportunities for modulating tissue healing processes. This review examines current biomaterial strategies that harness macrophage plasticity to enhance bone regeneration, with a focus on surface modifications, mechanical properties, and scaffold biodegradability. We discuss the interactions between macrophages and various biomaterials used in bone tissue engineering, highlighting methods to promote M2 polarization and mitigate chronic inflammation. The findings underscore the importance of designing biomaterials that not only support structural integrity but also actively participate in immune modulation, aiming to improve scaffold integration, tissue regeneration, and overall therapeutic outcomes in bone repair.
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页数:15
相关论文
共 165 条
[111]   Biomaterials & scaffolds for tissue engineering [J].
O'Brien, Fergal J. .
MATERIALS TODAY, 2011, 14 (03) :88-95
[112]   Neutrophil morphology and migration are affected by substrate elasticity [J].
Oakes, Patrick W. ;
Patel, Dipan C. ;
Morin, Nicole A. ;
Zitterbart, Daniel P. ;
Fabry, Ben ;
Reichner, Jonathan S. ;
Tang, Jay X. .
BLOOD, 2009, 114 (07) :1387-1395
[113]   Reduced substrate stiffness promotes M2-like macrophage activation and enhances peroxisome proliferator-activated receptor γ expression [J].
Okamoto, Takayuki ;
Takagi, Yoshimi ;
Kawamoto, Eiji ;
Park, Eun Jeong ;
Usuda, Haruki ;
Wada, Koichiro ;
Shimaoka, Motomu .
EXPERIMENTAL CELL RESEARCH, 2018, 367 (02) :264-273
[114]   Adsorbed Fibrinogen stimulates TLR-4 on monocytes and induces BMP-2 expression [J].
Oliveira, Marta I. ;
Pinto, Marta L. ;
Goncalves, Raquel M. ;
Martins, M. Cristina L. ;
Santos, Susana G. ;
Barbosa, Mario A. .
ACTA BIOMATERIALIA, 2017, 49 :296-305
[115]   Macrophage Polarization: Different Gene Signatures in M1(LPS+) vs. Classically and M2(LPS-) vs. Alternatively Activated Macrophages [J].
Orecchioni, Marco ;
Ghosheh, Yanal ;
Pramod, Akula Bala ;
Ley, Klaus .
FRONTIERS IN IMMUNOLOGY, 2019, 10
[116]  
Pan Y, 2023, ACS Appl Polym Mater.
[117]   IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MONOCYTE SUBPOPULATION IN HUMAN PERIPHERAL-BLOOD [J].
PASSLICK, B ;
FLIEGER, D ;
ZIEGLERHEITBROCK, HWL .
BLOOD, 1989, 74 (07) :2527-2534
[118]   Osteal macrophages: A new twist on coupling during bone dynamics [J].
Pettit, Allison R. ;
Chang, Ming K. ;
Hume, David A. ;
Raggatt, Liza-Jane .
BONE, 2008, 43 (06) :976-982
[119]   Bone Aging, Cellular Senescence, and Osteoporosis [J].
Pignolo, Robert J. ;
Law, Susan F. ;
Chandra, Abhishek .
JBMR PLUS, 2021, 5 (04)
[120]   Modulating immune microenvironment during bone repair using biomaterials: Focusing on the role of macrophages [J].
Ping, Jianfeng ;
Zhou, Chao ;
Dong, Yongqiang ;
Wu, Xudong ;
Huang, Xiaogang ;
Sun, Bin ;
Zeng, Bin ;
Xu, Fangming ;
Liang, Wenqing .
MOLECULAR IMMUNOLOGY, 2021, 138 :110-120