Selective Cell Recruitment and Spatially Controlled Cell Attachment on Instructive Chitosan Surfaces Functionalized with Antibodies
Author(s) -
Catarina A. Custódio,
A. M. Frias,
Aránzazu del Campo,
Rui L. Reis,
João F. Mano
Publication year - 2012
Publication title -
biointerphases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 45
eISSN - 1934-8630
pISSN - 1559-4106
DOI - 10.1007/s13758-012-0065-3
Subject(s) - tissue engineering , mesenchymal stem cell , chemistry , population , quartz crystal microbalance , cell , stem cell , regenerative medicine , covalent bond , antibody , chitosan , biophysics , nanotechnology , microbiology and biotechnology , materials science , biomedical engineering , biochemistry , immunology , biology , adsorption , demography , sociology , organic chemistry , medicine
Bioactive constructs to guide cellular mobilization
and function have been proposed as an approach for
a new generation of biomaterials in functional tissue
engineering. Adult mesenchymal stem cells have been
widely used as a source for cell based therapeutic strategies,
namely tissue engineering. This is a heterogeneous
cell population containing many subpopulations with distinct
regenerative capacity. Thus, one of the issues for the
effective clinical use of stem cells in tissue engineering is
the isolation of a highly purified, expandable specific
subpopulation of stem cells. Antibody functionalized biomaterials
could be promising candidates to isolate and
recruit specific cell types. Here we propose a new concept
of instructive biomaterials that are able to recruit and
purify specific cell types from a mixed cell population.
This biomimetic concept uses a target-specific chitosan
substrate to capture specific adipose derived stem cells.
Specific antibodies were covalently immobilized onto
chitosan membranes using bis[sulfosuccinimidyl] suberate
(BS3). Quartz crystal microbalance (QCM) was used to
monitor antibody immobilization/adsorption onto the
chitosan films. Specific antibodies covalently immobilized kept their bioactivity and captured specific cell types from
a mixed cell population. Microcontact printing allowed to
covalently immobilize antibodies in patterns and simultaneously
a spatial control in cell attachmentThe authors acknowledge the Portuguese Foundation for Science and Technology (FCT) for the fellowships SFRH/BD/61390/2009 (C.A.C) and SFRH/BPD/45206/2008 (A.M.F), and also to the International Max-Planck-Research School (C.A.C) for the financial support. We are grateful to Hospital da Prelada for the donations. This work was carried out under the scope of the EU 7th Framework Programme (FP7/2007-2013) under grant agreement no. NMP4-SL-2009-229292 (Find&Bind)
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