AI Article Synopsis

  • Researchers modified cellulose to promote better attachment of MG-63 cells by adding positively charged trimethylammonium groups, achieving over 90% cell attachment at low modification levels.
  • Cell attachment leveled off at a specific degree of substitution, indicating a link between surface charge and cell adherence, while stiffness was varied using glyoxal crosslinking.
  • The development of these tailored biomaterials represents a significant advancement towards creating scaffold materials that support cell growth and shape without needing additional proteins or ligands.

Article Abstract

Combining surface chemical modification of cellulose to introduce positively charged trimethylammonium groups by reaction with glycidyltrimethylammonium chloride (GTMAC) allowed for direct attachment of mammalian MG-63 cells, without addition of protein modifiers, or ligands. Very small increases in the surface charge resulted in significant increases in cell attachment: at a degree of substitution (DS) of only 1.4%, MG-63 cell attachment was > 90% compared to tissue culture plastic, whereas minimal attachment occurred on unmodified cellulose. Cell attachment plateaued above DS of ca. 1.85% reflecting a similar trend in surface charge, as determined from ζ-potential measurements and capacitance coupling (electric force microscopy). Cellulose film stiffness was modulated by cross linking with glyoxal (0.3-2.6% degree of crosslinking) to produce a range of materials with surface shear moduli from 76 to 448 kPa (measured using atomic force microscopy). Cell morphology on these materials could be regulated by tuning the stiffness of the scaffolds. Thus, we report tailored functionalised biomaterials based on cationic cellulose that can be tuned through surface reaction and glyoxal crosslinkin+g, to influence the attachment and morphology of cells. These scaffolds are the first steps towards materials designed to support cells and to regulate cell morphology on implanted biomaterials using only scaffold and cells, i.e. without added adhesion promoters.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954015PMC
http://dx.doi.org/10.1007/s10570-017-1612-3DOI Listing

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