4.8 Article

The effect of nanofibrous galactosylated chitosan scaffolds on the formation of rat primary hepatocyte aggregates and the maintenance of liver function

Journal

BIOMATERIALS
Volume 30, Issue 14, Pages 2753-2763

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2009.01.053

Keywords

Chitosan; Scaffolds; Nanotopography; Hepatocyte; Cell culture

Funding

  1. Jiangsu Science and Technology Department [BK2006509]
  2. National Natural Science Foundation of China [60121101]
  3. International Cooperation Program of Jiangsu Pi-ovine [BZ2007062]
  4. Ministry of Science and Technology of China [2008DFA51180]

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Liver tissue engineering requires a perfect extracellular matrix (ECM) for primary hepatocytes culture to maintain high level of liver-specific functions and desirable mechanical stability. The aim of this study was to develop a novel natural nanofibrous scaffold with surface-galactose ligands to enhance the bioactivity and mechanical stability of primary hepatocytes in culture. The nanofibrous scaffold was fabricated by electrospinning a natural material, galactosylated chitosan (GC), into nanofibers with an average diameter of similar to 160 nm. The CC nanofibrous scaffolds displayed slow degradation and suitable mechanical properties as an ECM for hepatocytes according to the evaluation of disintegration and Young's modulus testing. The results of morphology characterization, double-staining fluorescence assay and function detection showed that hepatocytes cultured on CC nanofibrous scaffold formed stably immobilized 3D flat aggregates and exhibited superior cell bioactivity with higher levels of liver-specific function maintenance in terms of albumin secretion, urea synthesis and cytochrome P-450 enzyme than 3D spheroid aggregates formed on CC films. These spheroid aggregates could be detached easily during culture period from the flat CC films. We suggest such GC-based nanofibrous scaffolds could be useful for various applications Such as bioartificial liver-assist devices and tissue engineering for liver regeneration as primary hepatocytes culture substrates. (C) 2009 Elsevier Ltd. All rights reserved.

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