Physical Cues Drive Chondrogenic Differentiation

Curr Stem Cell Res Ther. 2018;13(7):576-582. doi: 10.2174/1574888X13666180102121455.

Abstract

Background: Cellular differentiation occurs in a complicated microenvironment containing multiple components including soluble factors and physical cues. In addition to biochemical composition, physical cues are also crucial in determining cellular behaviors.

Objective: To better understand the interaction between physical signals and cells, we discuss the effects of physical cues on cellular behaviors, especially chondrogenic differentiation in vitro. Furthermore, the mechanisms by which these physical signals are transmitted from the extracellular matrix into the cell are also considered.

Results: Physical cues can dramatically regulate specific cellular functions in cartilage tissue engineering. Integrin and FAs act as mechano-sensors to transmit physical cues from the ECM into cytoskeleton- signaling network. Meanwhile, the RhoA/ROCK signaling pathway and YAP/TAZ play indispensable roles in cell and ECM linkages.

Conclusion: The investigation of physical cues clarifies cellular behaviors. This information can be applied to tissue engineering scaffold and biological material production in the future.

Keywords: Cell differentiation; Chondrocytes/ physiology; articular cartilage; extracellular matrix; focal adhesions; tissue engineering; tissue scaffolds..

Publication types

  • Review

MeSH terms

  • Animals
  • Biopolymers / chemistry
  • Biopolymers / pharmacology*
  • Cartilage, Articular / drug effects*
  • Cartilage, Articular / growth & development
  • Cartilage, Articular / injuries
  • Cartilage, Articular / surgery
  • Cell Cycle Proteins
  • Cell Differentiation
  • Chondrocytes / cytology*
  • Chondrocytes / drug effects
  • Chondrocytes / physiology
  • Chondrogenesis / drug effects*
  • Chondrogenesis / genetics
  • Cytoskeleton / chemistry
  • Cytoskeleton / drug effects
  • Cytoskeleton / metabolism
  • Extracellular Matrix / chemistry
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism
  • Gene Expression Regulation
  • Humans
  • Intercellular Signaling Peptides and Proteins / pharmacology
  • Mechanotransduction, Cellular*
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / physiology
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Regeneration / drug effects
  • Regeneration / physiology
  • Tissue Engineering
  • Tissue Scaffolds
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • rho-Associated Kinases / genetics
  • rho-Associated Kinases / metabolism

Substances

  • Biopolymers
  • Cell Cycle Proteins
  • Intercellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Transcription Factors
  • YY1AP1 protein, human
  • rho-Associated Kinases