Fabrication of nanofibrous microcarriers mimicking extracellular matrix for functional microtissue formation and cartilage regeneration

Biomaterials. 2018 Jul:171:118-132. doi: 10.1016/j.biomaterials.2018.04.033. Epub 2018 Apr 16.

Abstract

Cartilage has rather limited capacities for self-repair and regeneration. To repair complexly shaped cartilage tissue defects, we propose the application of microtissues fabricated from bone marrow-derived mesenchymal stem cells (BMSCs) cultured in natural bionic nanofibrous microcarriers (NF-MCs). The NF-MCs were structurally and functionally designed to mimic natural extracellular matrix (ECM) by crosslinking dialdehyde bacterial cellulose (DBC) with DL-allo-hydroxylysine (DHYL) and complexing chitosan (CS) with DHYL through electrostatic interactions. The orthogonal design allows for fine tuning of fiber diameter, pore size, porosity, mechanical properties, and biodegradation rate of the NF-MC. BMSCs cultured in NF-MCs showed improved proliferation compared with those cultured in chitosan microcarriers (CS-MCs). After three-week culture under microgravity conditions, functional cartilage microtissues were generated. When implanted into a knee articular cartilage defect in mice, the microtissue showed superior in vivo cartilage repair as characterized by cell tracking, histology, micro CT image, and gait analysis. Versatile in natural biopolymer design and biomimetic in nanofibrous component embedded in macroporous microcarriers, these injectable NC-MCs demonstrate to be effective carriers for cell proliferation and differentiation. Furthermore, the functional microtissues also show their prospect in repair of cartilage tissue, and suggest their potential for other tissues in general.

Keywords: Cartilage regeneration; Chitosan; Dialdehyde bacterial cellulose; Microtissue; Nanofibrous microcarriers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomimetic Materials / chemistry*
  • Cartilage, Articular / physiology*
  • Cell Proliferation
  • Cell Survival
  • Cells, Cultured
  • Cellulose / chemistry
  • Cellulose / pharmacology
  • Cellulose / ultrastructure
  • Disease Models, Animal
  • Extracellular Matrix / chemistry*
  • Femur / pathology
  • Gait
  • Green Fluorescent Proteins / metabolism
  • Hydroxylysine / chemistry
  • Imaging, Three-Dimensional
  • Mesenchymal Stem Cells / cytology
  • Microtechnology / methods*
  • Nanofibers / chemistry*
  • Rats, Sprague-Dawley
  • Regeneration*
  • Tissue Engineering / methods*
  • X-Ray Microtomography

Substances

  • Green Fluorescent Proteins
  • Hydroxylysine
  • Cellulose