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Increased matrix synthesis by fibroblasts with decreased proliferation on synthetic chitosan-gelatin porous structures
Biotechnology and bioengineering, 2012-05, Vol.109 (5), p.1314-1325
Iyer, Pooja
Walker, Kenneth J.
Madihally, Sundararajan V.
2012
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Iyer, Pooja
Walker, Kenneth J.
Madihally, Sundararajan V.
Titel
Increased matrix synthesis by fibroblasts with decreased proliferation on synthetic chitosan-gelatin porous structures
Ist Teil von
Biotechnology and bioengineering, 2012-05, Vol.109 (5), p.1314-1325
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2012
Quelle
MEDLINE
Beschreibungen/Notizen
Influence of mechanical characteristics and matrix architecture of substrates used in cell culture is an important issue to tissue engineering. Chitosan‐based materials have been processed into porous structures, injectable gels and membranes, and are investigated to regenerate various tissues. However, the effect of these structures on cell growth and matrix production in accordance with each of the differing scaffolds has not been examined. We investigated the influence of porous structures, hydrogels, and membranes on the growth of normal human fibroblasts and their matrix production in a serum‐free system. We used chitosan alone and in combination with gelatin. Injectable hydrogels were prepared using 2‐glycerol phosphate. From the same solution, porous scaffolds and membranes were formed using controlled rate freezing and lyophilization, and air‐drying, respectively. Fibroblast growth was evaluated on the 4th and 10th days using flow cytometry and CFDA‐SE pre‐staining. Cell morphology was assessed using actin and nucleus staining. Total protein content, collagen, tropoelastin, and MMP2/MMP‐9 activity in the media supernatant were assessed by BCA, Sircol™, Fastin Elastin, and fluorogeneic peptide assays. Collagen accumulated in the matrix was assessed by Sircol™ assay after pepsin/acetic acid digestion and by Masson's Trichrome staining. These results showed increased viability of fibroblasts on chitosan–gelatin porous scaffold with decreased proliferation relative to tissue culture plastic (TCP) surface despite the cells showing spindle shape. The total protein, collagen, and tropoelastin contents were higher in the spent media from chitosan–gelatin porous scaffolds compared to other conditions. MMP2/MMP9 activity was comparable to TCP. An increase in collagen content was also observed in the matrix, suggesting increased matrix deposition. In summary, matrix production is influenced by the form of chitosan structures, which significantly affects the regenerative process. Biotechnol. Bioeng. 2012; 109:1314–1325. © 2011 Wiley Periodicals, Inc. The authors demonstrate the effect of presenting chitosan and chitosan‐gelatin in 3D porous structures, membranes and hydrogels on fibroblast growth and production of matrix elements. Despite reduced proliferation on 3D chitosan‐gelatin porous structures relative to tissue culture plastic, fibroblasts show increased production of collagen, tropoelastin and other proteins. Other structures show reduced matrix production. Increased gelatinase (MMP‐2/MMP‐9) expressions are also observed in all gelatin containing structures independent of their form. Matrix assembly essential for the regenerative process is affected by structural form.
Sprache
Englisch
Identifikatoren
ISSN: 0006-3592
eISSN: 1097-0290
DOI: 10.1002/bit.24396
Titel-ID: cdi_proquest_miscellaneous_928906333
Format
–
Schlagworte
Bioassays
,
Cell culture
,
Cell growth
,
Cell Proliferation
,
Chitosan
,
Extracellular Matrix - metabolism
,
Fibroblasts - metabolism
,
Fibroblasts - physiology
,
Flow Cytometry
,
Gelatin
,
Humans
,
Hydrogels
,
matrix synthesis
,
membranes
,
Morphology
,
scaffolds
,
Staining and Labeling
,
Tissue engineering
,
Tissue Engineering - methods
,
Tissue Scaffolds - chemistry
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