Quantifying the relation between adhesion ligand-receptor bond formation and cell phenotype

被引:75
作者
Kong, Hyun Joon
Boontheekul, Tanyarut
Mooney, David J. [1 ]
机构
[1] Harvard Univ, Div Engn & Appl Sci, Cambridge, MA 02138 USA
[2] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[3] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
关键词
fluorescence resonance energy transfer; myoblast; osteoblast; proliferation; RGD peptides; EXTRACELLULAR-MATRIX; INTEGRIN BINDING; GENE-EXPRESSION; IN-VITRO; DIFFERENTIATION; MORPHOGENESIS; FIBRONECTIN; DENSITY; PROTEIN; TRANSDUCTION;
D O I
10.1073/pnas.0605960103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
One of the fundamental interactions in cell biology is the binding of cell receptors to adhesion ligands, and many aspects of cell behavior are believed to be regulated by the number of these bonds that form. Unfortunately, a lack of methods to quantify bond formation, especially for cells in 3D cultures or tissues, has precluded direct probing of this assumption. We now demonstrate that a FRET technique can be used to quantify the number of bonds formed between cellular receptors and synthetic adhesion oligopeptides coupled to an artificial extracellular matrix. Similar quantitative relations were found between bond number and the proliferation and differentiation of MC3T3-E1 preosteoblasts and C2C12 myoblasts, although the relation was distinct for each cell type. This approach to understanding 3D cell-extracellular matrix interactions will allow one to both predict cell behavior and to use bond number as a fundamental design criteria for synthetic extracellular matrices.
引用
收藏
页码:18534 / 18539
页数:6
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