An optical method to quantify the density of ligands for cell adhesion receptors in three-dimensional matrices

被引:14
作者
Tzeranis, Dimitrios S. [1 ]
Roy, Amit [1 ,3 ]
So, Peter T. C. [1 ,2 ]
Yannas, Ioannis V. [1 ,2 ]
机构
[1] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[3] Univ Massachusetts, Sch Med, Dept Ophthalmol, Worcester, MA 01655 USA
关键词
ligand density; biomaterials; extracellular matrix; collagen scaffolds; multiphoton microscopy; regenerative medicine/tissue engineering; FLUORESCENCE CORRELATION SPECTROSCOPY; STEM-CELLS; BINDING-SITE; IN-VITRO; OSTEOGENIC DIFFERENTIATION; INTEGRINS ALPHA(1)BETA(1); EXTRACELLULAR-MATRIX; COLLAGEN SUBTYPES; BOND FORMATION; A-DOMAIN;
D O I
10.1098/rsif.2010.0321.focus
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
07 ; 0710 ; 09 ;
摘要
The three-dimensional matrix that surrounds cells is an important insoluble regulator of cell phenotypes. Examples of such insoluble surfaces are the extracellular matrix (ECM), ECM analogues and synthetic polymeric biomaterials. Cell-matrix interactions are mediated by cell adhesion receptors that bind to chemical entities (adhesion ligands) on the surface of the matrix. There are currently no established methods to obtain quantitative estimates of the density of adhesion ligands recognized by specific cell adhesion receptors. This article presents a new optical-based methodology for measuring ligands of adhesion receptors on three-dimensional matrices. The study also provides preliminary quantitative results for the density of adhesion ligands of integrins alpha(1)beta(1) and alpha(2)beta(1) on the surface of collagen-based scaffolds, similar to biomaterials that are used clinically to induce regeneration in injured skin and peripheral nerves. Preliminary estimates of the surface density of the ligands of these two major collagen-binding receptors are 5775 +/- 2064 ligands mu m(-2) for ligands of alpha(1)beta(1) and 17 084 +/- 5353 ligands mu m(-2) for ligands of alpha(2)beta(1). The proposed methodology can be used to quantify the surface chemistry of insoluble surfaces that possess biological activity, such as native tissue ECM and biomaterials, and therefore can be used in cell biology, biomaterials science and regenerative medical studies for quantitative description of a matrix and its effects on cells.
引用
收藏
页码:S649 / S661
页数:13
相关论文
共 79 条
  • [1] New biarsenical Ligands and tetracysteine motifs for protein labeling in vitro and in vivo: Synthesis and biological applications
    Adams, SR
    Campbell, RE
    Gross, LA
    Martin, BR
    Walkup, GK
    Yao, Y
    Llopis, J
    Tsien, RY
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (21) : 6063 - 6076
  • [2] Stroma-derived three-dimensional matrices are necessary and sufficient to promote desmoplastic differentiation of normal fibroblasts
    Amatangelo, MD
    Bassi, DE
    Klein-Szanto, AJP
    Cukierman, E
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2005, 167 (02) : 475 - 488
  • [3] [Anonymous], 1974, Solving least squares problems
  • [4] [Anonymous], 2006, REMOTE SENSING DIGIT
  • [5] Osteogenic differentiation of dura mater stem cells cultured in vitro on three-dimensional porous scaffolds of poly(ε-caprolactone) fabricated via co-extrusion and gas foaming
    Aronin, C. E. Petrie
    Cooper, J. A., Jr.
    Sefcik, L. S.
    Tholpady, S. S.
    Ogle, R. C.
    Botchwey, E. A.
    [J]. ACTA BIOMATERIALIA, 2008, 4 (05) : 1187 - 1197
  • [6] Ligand density characterization of peptide-modified biomaterials
    Barber, TA
    Harbers, GM
    Park, S
    Gilbert, M
    Healy, KE
    [J]. BIOMATERIALS, 2005, 26 (34) : 6897 - 6905
  • [7] Imaging intracellular fluorescent proteins at nanometer resolution
    Betzig, Eric
    Patterson, George H.
    Sougrat, Rachid
    Lindwasser, O. Wolf
    Olenych, Scott
    Bonifacino, Juan S.
    Davidson, Michael W.
    Lippincott-Schwartz, Jennifer
    Hess, Harald F.
    [J]. SCIENCE, 2006, 313 (5793) : 1642 - 1645
  • [8] Single-photon counting multicolor multiphoton fluorescence microscope
    Buehler, C
    Kim, KH
    Greuter, U
    Schlumpf, N
    So, PTC
    [J]. JOURNAL OF FLUORESCENCE, 2005, 15 (01) : 41 - 51
  • [9] The integrin alpha 1 A-domain is a ligand binding site for collagens and laminin
    Calderwood, DA
    Tuckwell, DS
    Eble, J
    Kuhn, K
    Humphries, MJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (19) : 12311 - 12317
  • [10] Second-harmonic imaging microscopy for visualizing biomolecular arrays in cells, tissues and organisms
    Campagnola, PJ
    Loew, LM
    [J]. NATURE BIOTECHNOLOGY, 2003, 21 (11) : 1356 - 1360