FAK- and YAP/TAZ dependent mechanotransduction pathways are required for enhanced immunomodulatory properties of adipose-derived mesenchymal stem cells induced by aligned fibrous scaffolds

Biomaterials. 2018 Jul:171:107-117. doi: 10.1016/j.biomaterials.2018.04.035. Epub 2018 Apr 16.

Abstract

Adipose-derived mesenchymal stem cells (ASCs) represent an excellent candidate for tissue engineering due to their multipotency and paracrine functions. Physical cues provided by the scaffolds have been shown to direct a variety of cellular behaviors of ASCs; however, their effects on the paracrine functions of ASCs, especially immunomodulatory functions, remain largely unexplored. Thus, PLLA electrospun fibrous scaffolds, with fibers oriented either randomly or aligned, were used as a model to investigate the effects of fiber orientation on the immunomodulatory paracrine secretion of ASCs. ASCs cultured on aligned fibers produced significantly higher levels of immunomodulatory factors than those cultured on random fibers. By using the conditioned media from ASCs cultured on aligned fibers, the enhanced immunomodulatory functions of ASCs were confirmed by the M2 phenotypic change seen in macrophages. The enhanced immunomodulation of ASCs correlated with the activation of FAK signaling, as evidenced by a decreased production of immunomodulatory factors in ASCs after treatment with inhibitors of the FAK pathway. In addition, aligned fibers promoted the activation of YAP signaling in ASCs. The inhibited immunomodulatory properties of ASCs by a YAP inhibitor indicated that YAP signaling was also involved in mediating the increased immunomodulatory functions of ASCs on aligned fibers. Our findings identify both FAK and YAP/TAZ signaling as required mechanotransduction pathways through which aligned fibers stimulate the immunomodulatory function of ASCs and highlight fiber orientation as a key design parameter for immunomodulatory fibrous engineered scaffolds.

Keywords: Adipose-derived mesenchymal stem cells (ASCs); FAK; Fiber orientation; Immunomodulatory factors; Mechanotransduction; YAP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Cell Shape / drug effects
  • Cells, Cultured
  • Culture Media, Conditioned / pharmacology
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism*
  • Humans
  • Immunomodulation* / drug effects
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Mechanotransduction, Cellular* / drug effects
  • Mesenchymal Stem Cells / cytology*
  • Phosphoproteins / metabolism*
  • Signal Transduction
  • Tissue Engineering / methods*
  • Tissue Scaffolds / chemistry*
  • Trans-Activators
  • Transcription Factors
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • YAP-Signaling Proteins

Substances

  • Adaptor Proteins, Signal Transducing
  • Culture Media, Conditioned
  • Intracellular Signaling Peptides and Proteins
  • Phosphoproteins
  • Trans-Activators
  • Transcription Factors
  • Transcriptional Coactivator with PDZ-Binding Motif Proteins
  • WWTR1 protein, human
  • YAP-Signaling Proteins
  • YAP1 protein, human
  • Focal Adhesion Protein-Tyrosine Kinases