Hybrid Cell Membrane-Functionalized Matrixes for Modulating Inflammatory Microenvironment and Improving Bone Defect Repair

被引:15
作者
Qiao, Fangyu [1 ]
Lv, Yonggang [2 ]
机构
[1] Chongqing Univ, Bioengn Coll, Mechanobiol & Regenerat Med Lab, Chongqing 400044, Peoples R China
[2] Wuhan Text Univ, State Key Lab New Text Mat & Adv Proc Technol, Wuhan 430200, Peoples R China
基金
中国国家自然科学基金;
关键词
bone repair; cell membrane-functionalized matrixes; electrospinning; hybrid membrane; inflammation; MANNOSE-RECEPTOR; BIOMIMETIC PLATFORM; CANCER-CELLS; MACROPHAGES; PLASMA; GROWTH; NANOPARTICLES; METASTASIS; MECHANISM; IMMUNITY;
D O I
10.1002/adhm.202203047
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cell membranes from different sources retain the integrity of the original membrane structure and special membrane protein functions. However, the diversity function of membrane surface proteins is underutilized in bone defect repair. The current study creatively prepared a hybrid membrane (HM) (diameter, 92.25 +/- 16.47 nm) and coated it on a poly-epsilon-caprolactone (PCL) (diameter, 313.79 +/- 4.69 nm) electrospinning membrane for cell membrane-functionalized matrixes (MFMs) (diameter, 368.76 +/- 5.90 nm) preparation. The effects of the HM and MFMs on inflammatory regulation and bone formation are further explored in vitro and in vivo. The results showed that MFMs can regulate macrophage into anti-inflammatory phenotype and promote alkaline phosphatase secretion and mineralization deposition of mesenchymal stem cells (MSCs) in vitro. The foreign body response is alleviated and bone regeneration is facilitated in rat calvarial critical-size defect in vivo. The study provides an innovative approach to applicate the cell membrane functions from different sources for immunomodulatory and osteogenic differentiation and provides a promising choice for designing bone repair materials.
引用
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页数:13
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共 58 条
[1]   Endocytic control of signaling at the plasma membrane [J].
Barbieri, Elisa ;
Di Fiore, Pier Paolo ;
Sigismund, Sara .
CURRENT OPINION IN CELL BIOLOGY, 2016, 39 :21-27
[2]  
BEVAN MJ, 1976, J IMMUNOL, V117, P2233
[3]   Modulation of macrophage phenotype and protein secretion via heparin-IL-4 functionalized supramolecular elastomers [J].
Bonito, V. ;
Smits, A. I. P. M. ;
Goor, O. J. M. ;
Ippel, B. D. ;
Driessen-Mol, A. ;
Munker, T. J. A. G. ;
Bosman, A. W. ;
Mes, T. ;
Dankers, P. Y. W. ;
Bouten, C. V. C. .
ACTA BIOMATERIALIA, 2018, 71 :247-260
[4]   Receptor clustering as a cellular mechanism to control sensitivity [J].
Bray, D ;
Levin, MD ;
Morton-Firth, CJ .
NATURE, 1998, 393 (6680) :85-88
[5]   3D Scaffolds with Different Stiffness but the Same Microstructure for Bone Tissue Engineering [J].
Chen, Guobao ;
Dong, Chanjuan ;
Yang, Li ;
Lv, Yonggang .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (29) :15790-15802
[6]   Hybrid cell membrane-coated nanoparticles: A multifunctional biomimetic platform for cancer diagnosis and therapy [J].
Chen, Hong-Ying ;
Deng, Jiang ;
Wang, Yu ;
Wu, Cheng-Qiong ;
Li, Xian ;
Dai, Hong-Wei .
ACTA BIOMATERIALIA, 2020, 112 :1-13
[7]   Mesenchymal Stem Cell-Immune Cell Interaction and Related Modulations for Bone Tissue Engineering [J].
Chen, Renxin ;
Hao, Zhuowen ;
Wang, Yi ;
Zhu, Hongzhen ;
Hu, Yingkun ;
Chen, Tianhong ;
Zhang, Peng ;
Li, Jingfeng .
STEM CELLS INTERNATIONAL, 2022, 2022
[8]   Coating nanofiber scaffolds with beta cell membrane to promote cell proliferation and function [J].
Chen, Wansong ;
Zhang, Qiangzhe ;
Luk, Brian T. ;
Fang, Ronnie H. ;
Liu, Younian ;
Gao, Weiwei ;
Zhang, Liangfang .
NANOSCALE, 2016, 8 (19) :10364-10370
[9]   Superabsorbent 3D Scaffold Based on Electrospun Nanofibers for Cartilage Tissue Engineering [J].
Chen, Weiming ;
Chen, Shuai ;
Morsi, Yosry ;
El-Hamshary, Hany ;
El-Newehy, Mohamed ;
Fan, Cunyi ;
Mo, Xiumei .
ACS APPLIED MATERIALS & INTERFACES, 2016, 8 (37) :24415-24425
[10]   Fracture healing under healthy and inflammatory conditions [J].
Claes, Lutz ;
Recknagel, Stefan ;
Ignatius, Anita .
NATURE REVIEWS RHEUMATOLOGY, 2012, 8 (03) :133-143