AI Article Synopsis

  • - The study focuses on creating nanofibrous scaffolds that mimic extracellular matrices (ECMs) through a technique called electrospinning, specifically using silk fibroin (SF) and halloysite nanotubes (HNT) composites.
  • - Adding 1 wt% HNT to SF scaffolds improved their hydrophilicity, water absorption, and thermal stability without compromising their mechanical strength or altering the SF's molecular structure.
  • - These improved scaffolds support better growth and differentiation of cells like fibroblasts and myoblasts, especially when coated with decellularized ECM from human fibroblasts, making them promising for soft tissue repair and skin regeneration.

Article Abstract

The production of nanofibrous materials for soft tissue repair that resemble extracellular matrices (ECMs) is challenging. Electrospinning uniquely produces scaffolds resembling the ultrastructure of natural ECMs. Herein, electrospinning was used to fabricate silk fibroin (SF) and SF/halloysite nanotube (HNT) composite scaffolds. Different HNT loadings were examined, but 1 wt% HNTs enhanced scaffold hydrophilicity and water uptake capacity without loss of mechanical strength. The inclusion of 1 wt% HNTs in SF scaffolds also increased the scaffold's thermal stability without altering the molecular structure of the SF, as revealed by thermogravimetric analyses and Fourier transform infrared spectroscopy (FTIR), respectively. SF/HNT 1 wt% composite scaffolds better supported the viability and spreading of 3T3 fibroblasts and the differentiation of C2C12 myoblasts into aligned myotubes. These scaffolds coated with decellularised ECM from 3T3 cells or primary human dermal fibroblasts (HDFs) supported the growth of primary human keratinocytes. However, SF/HNT 1 wt% composite scaffolds with HDF-derived ECM provided the best microenvironment, as on these, keratinocytes formed intact monolayers with an undifferentiated, basal cell phenotype. Our data indicate the merits of SF/HNT 1 wt% composite scaffolds for applications in soft tissue repair and the expansion of primary human keratinocytes for skin regeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9332275PMC
http://dx.doi.org/10.3390/polym14153004DOI Listing

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