@inproceedings {17749, title = {Dextran sulphate and ficcol fail as macromolecular crowders to enhance extracellular matrix deposition}, journal = {Journal of Tissue Engineering and Regenerative Medicine}, volume = {7}, year = {2013}, month = {2013-09-30 00:00:00}, pages = {6-52}, publisher = {John Wiley and Sons}, address = {Porto, Portugal}, abstract = {

The development of strategies based on the use of scaffolds for Tissue
Engineering and Regenerative Medicine(TERM) has been hindered by
the inability of researchers to present solutions to overcome problems
mainly related with the biocompatibility of materials andin vivoperfusion of the 3D structures. It is in this context that scaffold-free methodologies are being presented as increasingly attractive strategies for
TERM. Scaffold-free approaches in general rely on the production of
extracellular matrix(ECM) by the cells of interest. However, the creation of an ECM robust enough for use in TERM is many times a challenge. Therefore, there is an important need to develop protocols that
boost cell{\textquoteright}s ability to produce ECM. One way to achieve this is to expose
cells to an environment crowded with adequate macromolecules in
order to mimic the physiological cellular milieu. Dextran sulphate(DxS)
and Ficoll(Fc) have been suggested as compounds capable of increasing
ECM deposition. The involved mechanism is closely related to the \ increase in enzyme-mediated collagen deposition. In the present work,\ we hypothesized that the use of DxS or of a combination of Fc of different molecular weights (Fc70/Fc400) as crowders in culture medium
could increase the robustness of the ECM produced by humanfibroblasts(hFb) or human adipose-derived Stem Cells(hASCs). 5x104\ hFb\ or hASC were seeded on wells of 24 and 48 well plates, and cultured
for 24 h in a-MEM supplemented wih10\% FBS and 1\% antibiotics.
After thefirst 24 h, the medium was replaced by fresh medium supplemented with 1\% FBS and a)50lg/mL of Ascorbic Acid, b)50lg/mL of
Dextran Sulphate, or c)37.5 mg/mL of Fc70+25 mg/mL of Fc400.
Cells were cultured for further 2 and 5 days. dsDNA quantification
showed that in both conditions b) and c), and independently of the cell
type, cell proliferation was significantly reduced. ECM production was
evaluated by quantifying the deposited collagen using a semi-quantitative Sirius Red kit (Picrosirius, Chondrex, USA). Collagen quantification, normalized with dsDNA, demonstrated that for both cells types,
the presence of either DxS or Fc70/Fc400 resulted in the decrease of
ECM deposition. In conclusion, the use of DxS and Fc70/Fc under the
conditions herein described failed to increase the ECM production by
both hFb and hASCs.

}, keywords = {ecm, macromolecular crowding}, doi = {10.1002/term.1822}, url = {http://onlinelibrary.wiley.com/doi/10.1002/term.2013.7.issue-s1/issuetoc}, author = {Pirraco, R. P. and Carvalho, F. and Reis, R. L. and Marques, A. P.} }