Reciprocal influence of hMSCs/HaCaT cultivated on electrospun scaffolds

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Sirsendu Bhowmick - , State University of New York at Albany, TUD Dresden University of Technology, Indian Institute of Technology Delhi (IITD) (Author)
  • Sandra Rother - , Chair of Biomaterials (Author)
  • Heike Zimmermann - , TUD Dresden University of Technology (Author)
  • Poh S. Lee - , Chair of Biomaterials (Author)
  • Stephanie Moeller - , Innovent e.V. (Author)
  • Matthias Schnabelrauch - , Innovent e.V. (Author)
  • Veena Koul - , Indian Institute of Technology Delhi (IITD) (Author)
  • Dieter Scharnweber - , Chair of Biomaterials (Author)

Abstract

Abstract: Here, we investigated the synergistic effect of electrospun nanofibrous scaffolds made of gelatin /sulfated hyaluronan (sHA) or native hyaluronan (HA)/chondroitin sulfate (CS) and, keratinocytes (HaCaT)—human mesenchymal stem cells (hMSCs) contact co-culture on epithelial differentiation of hMSCs. The hMSCs were co-cultured in contact with HaCaT cells for 5 days on electrospun scaffold. Results show that electrospun scaffolds containing sulfated glycosaminoglycans (GAGs) stimulate epithelial differentiation in terms of various protein expression markers (keratin 14, ΔNp63α and Pan-cytokeratin) and gene expression of several dermal proteins (keratin 14, ΔNp63α). Electrospun scaffold independent of GAGs alone did not affect the epithelial differentiation of hMSCs but combination of keratinocyte-hMSC contact co-culture and electrospun scaffold promotes the epithelial differentiation of hMSCs. Graphical abstract: [InlineMediaObject not available: see fulltext.].

Details

Original languageEnglish
Article number128
JournalJournal of Materials Science: Materials in Medicine
Volume28
Issue number8
Publication statusPublished - 1 Aug 2017
Peer-reviewedYes

External IDs

PubMed 28721664
ORCID /0000-0003-2285-3621/work/181860171