Cell Surface Engineering to Control Cellular Interactions

被引:92
作者
Custodio, Catarina A. [1 ]
Mano, Joao F. [1 ]
机构
[1] Univ Aveiro, Dept Chem, CICECO Aveiro Inst Mat, P-3810193 Aveiro, Portugal
基金
欧洲研究理事会;
关键词
cell membranes; cell surface engineering; nanoparticles; nanopatches; ligands; STEM-CELLS; CHEMICAL-MODIFICATION; BIOTIN LIGASE; LIVING CELLS; ADHESION; CHEMISTRY; PROTEINS; DNA; FUNCTIONALIZATION; OLIGONUCLEOTIDES;
D O I
10.1002/cnma.201600047
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Cell surface composition determines all interactions of the cell with its environment, thus cell functions such as adhesion, migration and cell-cell interactions can potentially be controlled by engineering and manipulating the cell membrane. Cell membranes present a rich repertoire of molecules, therefore a versatile ground for modification. However the complex and dynamic nature of the cell surface is also a major challenge for cell surface engineering that should also involve strategies compatible with cell viability. Cell surface engineering by selective chemical reactions or by the introduction of exogenous targeting ligands can be a powerful tool for engineering novel interactions and controlling cell function. In addition to chemical conjugation and modification of functional groups, ligands of interest to modify the surface of cells include recombinant proteins, liposomes or nanoparticles. Here, we review recent efforts to perform changes to cell surface composition. We focus on the engineering of the cell surface with biological, chemical or physical methods to modulate cell functions and control cell-cell and cell-microenvironment interactions. Potential applications of cell surface engineering are also discussed.
引用
收藏
页码:376 / 384
页数:9
相关论文
共 62 条
[1]
DNA modification of live cell surface [J].
Borisenko, Grigory G. ;
Zaitseva, Marina A. ;
Chuvilin, Andrey N. ;
Pozmogova, Galina E. .
NUCLEIC ACIDS RESEARCH, 2009, 37 (04)
[2]
Membrane-Anchored DNA Assembly for Energy and Electron Transfer [J].
Borjesson, Karl ;
Tumpane, John ;
Ljungdahl, Thomas ;
Wilhelmsson, L. Marcus ;
Norden, Bengt ;
Brown, Tom ;
Martensson, Jerker ;
Albinsson, Bo .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (08) :2831-2839
[3]
Magnetic Force-Based Tissue Engineering and Regenerative Medicine [J].
Castro, Emilio ;
Mano, Joao F. .
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2013, 9 (07) :1129-1136
[4]
Chandra R., 2006, Angewandte Chemie, V118, P910
[5]
Site-specific labeling of cell surface proteins with biophysical probes using biotin ligase [J].
Chen, I ;
Howarth, M ;
Lin, WY ;
Ting, AY .
NATURE METHODS, 2005, 2 (02) :99-104
[6]
Improving cell-based therapies by nanomodification [J].
Chen, Wei ;
Fu, Liwu ;
Chen, Xiaoyuan .
JOURNAL OF CONTROLLED RELEASE, 2015, 219 :560-575
[7]
Nanoparticulate Cellular Patches for Cell-Mediated Tumoritropic Delivery [J].
Cheng, Hao ;
Kastrup, Christian J. ;
Ramanathan, Renuka ;
Siegwart, Daniel J. ;
Ma, Minglin ;
Bogatyrev, Said R. ;
Xu, Qiaobing ;
Whitehead, Kathryn A. ;
Langer, Robert ;
Anderson, Daniel G. .
ACS NANO, 2010, 4 (02) :625-631
[8]
Engineering a biospecific communication pathway between cells and electrodes [J].
Collier, JH ;
Mrksich, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (07) :2021-2025
[9]
Engineering Biomolecular Microenvironments for Cell Instructive Biomaterials [J].
Custodio, Catarina A. ;
Reis, Rui L. ;
Mano, Joao F. .
ADVANCED HEALTHCARE MATERIALS, 2014, 3 (06) :797-810
[10]
Synthetic Chemoselective Rewiring of Cell Surfaces: Generation of Three-Dimensional Tissue Structures [J].
Dutta, Debjit ;
Pulsipher, Abigail ;
Luo, Wei ;
Yousaf, Muhammad N. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (22) :8704-8713