Covalent immobilization of MSC-affinity peptide on poly(L-lactide-co-ε-caprolactone) copolymer to enhance stem cell adhesion and retention for tissue engineering applications

Muhammad Shafiq, Soo Hyun Kim

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Electrospun nanofibers mimicking the extracellular microenvironment have tremendous potential for tissue regeneration applications. However, a lack of bioactive functionalities limits the effective utilization of nanofibers fabricated from synthetic biodegradable polymers. The objective of this study was to conjugate mesenchymal stem cell affinity peptide (EPLQLKM, E7) with star-shaped poly(L-lactide-co-ε-caprolactone) (PLCL) copolymer and to evaluate the potential of this modified polymer to enhance stem cell adhesion and proliferation in vitro. MSCadhesive peptide was covalently conjugated with the hydroxyl functionalities of the star-shaped PLCL copolymer and nanofibers were prepared by mixing appropriate proportions of linear PLCL and E7-conjugated star-shaped PLCL copolymers using electrospinning. Nuclear magnetic resonance and amino acid composition analysis revealed that E7 was successfully conjugated to PLCL copolymers. Nanofibers were smooth and homogenous as examined using scanning electron micrography. Nanofibrous meshes containing PLCL-E7 showed significantly higher cell viability and proliferation compared with the control group. In addition, cells spread well on meshes containing PLCL-E7 compared with the control group. The strategy adopted here may be very useful for designing stem cell adhesive polymeric biomaterials to enhance stem cell-based tissue repair. In addition, E7-immobilized PLCL copolymers can be fabricated into different shapes and structures as needed for various tissue engineering applications. [Figure not available: see fulltext.]

Original languageEnglish
Pages (from-to)986-994
Number of pages9
JournalMacromolecular Research
Volume24
Issue number11
DOIs
Publication statusPublished - 2016 Nov 1

Fingerprint

Cell adhesion
Stem cells
Tissue engineering
Peptides
Nanofibers
Copolymers
Stars
Tissue regeneration
Biodegradable polymers
Cell proliferation
Electrospinning
Biocompatible Materials
Biomaterials
Hydroxyl Radical
Amino acids
Adhesives
Polymers
Repair
Cells
Nuclear magnetic resonance

Keywords

  • electrospinning
  • MSC-adhesive peptide
  • PLCL copolymer
  • scaffolds
  • stem cell adhesion
  • stem cell homing
  • tissue engineering

ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Polymers and Plastics
  • Organic Chemistry
  • Materials Chemistry

Cite this

Covalent immobilization of MSC-affinity peptide on poly(L-lactide-co-ε-caprolactone) copolymer to enhance stem cell adhesion and retention for tissue engineering applications. / Shafiq, Muhammad; Kim, Soo Hyun.

In: Macromolecular Research, Vol. 24, No. 11, 01.11.2016, p. 986-994.

Research output: Contribution to journalArticle

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AB - Electrospun nanofibers mimicking the extracellular microenvironment have tremendous potential for tissue regeneration applications. However, a lack of bioactive functionalities limits the effective utilization of nanofibers fabricated from synthetic biodegradable polymers. The objective of this study was to conjugate mesenchymal stem cell affinity peptide (EPLQLKM, E7) with star-shaped poly(L-lactide-co-ε-caprolactone) (PLCL) copolymer and to evaluate the potential of this modified polymer to enhance stem cell adhesion and proliferation in vitro. MSCadhesive peptide was covalently conjugated with the hydroxyl functionalities of the star-shaped PLCL copolymer and nanofibers were prepared by mixing appropriate proportions of linear PLCL and E7-conjugated star-shaped PLCL copolymers using electrospinning. Nuclear magnetic resonance and amino acid composition analysis revealed that E7 was successfully conjugated to PLCL copolymers. Nanofibers were smooth and homogenous as examined using scanning electron micrography. Nanofibrous meshes containing PLCL-E7 showed significantly higher cell viability and proliferation compared with the control group. In addition, cells spread well on meshes containing PLCL-E7 compared with the control group. The strategy adopted here may be very useful for designing stem cell adhesive polymeric biomaterials to enhance stem cell-based tissue repair. In addition, E7-immobilized PLCL copolymers can be fabricated into different shapes and structures as needed for various tissue engineering applications. [Figure not available: see fulltext.]

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