Cellular migration to electrospun poly(lactic acid) fibermats

J Biomater Sci Polym Ed. 2012;23(15):1939-50. doi: 10.1163/092050611X599328. Epub 2012 May 8.

Abstract

Nonwoven fabrics prepared via an electrospinning method, so-called electrospun fibermats, are expected to be promising scaffold materials for bone tissue engineering. In the present work, poly(L-lactic acid) (PLLA) fibermats, consisting of fibers with diameters ranging from 1 to 10 μm, were prepared by electrospinning. Mouse osteoblast-like cells (MC3T3-E1) were seeded on the fibermats with various fiber diameters (10, 5 and 2 μm; they are denoted by samples A, B and C, respectively) and cultured in two different directions in order to compare the migration behaviours into the scaffold of the normal condition and the anti-gravity condition. The cells in/on the fibermats were observed by laser confocal microscopy to estimate the cellular migration ability into them. When the MC3T3-E1 cells were cultured in the normal direction, the thickness of their layer increased to approx. 90 μm in the sample A, consisting of 10-μm fibers after 13 days of culture, while that in the sample C, consisting of 2-μm fibers, did not increase. When the MC3T3-E1 cells were cultured in the anti-gravity condition, the thickness of the cell layer in the sample A increased to approx. 60 μm. These results mean that the MC3T3-E1 cells migrated into the inside of sample A in either the normal direction or the anti-gravity one. The cellular proliferation showed no significant difference among the fibermats with three different fiber diameters; MC3T3-E1 cells on the fibermat with 2 μm fiber diameter grew two-dimensionally, while they grew three-dimensionally in the fibermat with 10 μm fiber diameter.

Keywords: Electrospinning; MC3T3-E1 cell; cell migration; fibermat; poly(lactic acid); tissue-engineering scaffold.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Bone Substitutes / chemistry
  • Cell Movement / physiology*
  • Cell Proliferation / physiology
  • Lactic Acid* / chemistry
  • Mice
  • Microscopy, Confocal
  • Microscopy, Electron, Scanning
  • Osteoblasts / physiology
  • Polyesters
  • Polymers* / chemistry
  • Porosity
  • Time Factors
  • Tissue Engineering / instrumentation
  • Tissue Scaffolds* / chemistry

Substances

  • Bone Substitutes
  • Polyesters
  • Polymers
  • Lactic Acid
  • poly(lactide)