Nuclear lamin-A scales with tissue stiffness and enhances matrix-directed differentiation

Science. 2013 Aug 30;341(6149):1240104. doi: 10.1126/science.1240104.

Abstract

Tissues can be soft like fat, which bears little stress, or stiff like bone, which sustains high stress, but whether there is a systematic relationship between tissue mechanics and differentiation is unknown. Here, proteomics analyses revealed that levels of the nucleoskeletal protein lamin-A scaled with tissue elasticity, E, as did levels of collagens in the extracellular matrix that determine E. Stem cell differentiation into fat on soft matrix was enhanced by low lamin-A levels, whereas differentiation into bone on stiff matrix was enhanced by high lamin-A levels. Matrix stiffness directly influenced lamin-A protein levels, and, although lamin-A transcription was regulated by the vitamin A/retinoic acid (RA) pathway with broad roles in development, nuclear entry of RA receptors was modulated by lamin-A protein. Tissue stiffness and stress thus increase lamin-A levels, which stabilize the nucleus while also contributing to lineage determination.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adipogenesis
  • Animals
  • Cell Differentiation*
  • Collagen / analysis
  • Collagen / chemistry
  • Collagen / metabolism
  • Elasticity*
  • Extracellular Matrix / chemistry
  • Extracellular Matrix / metabolism
  • Gene Expression Regulation, Developmental
  • Humans
  • Lamin Type A / chemistry
  • Lamin Type A / genetics
  • Lamin Type A / metabolism*
  • Mesenchymal Stem Cells / cytology*
  • Mice
  • Models, Biological
  • Nuclear Lamina / metabolism
  • Osteogenesis* / genetics
  • Protein Conformation
  • Proteome
  • Stress, Mechanical*
  • Transcription, Genetic
  • Tretinoin / metabolism
  • Vitamin A / metabolism

Substances

  • Lamin Type A
  • Proteome
  • Vitamin A
  • Tretinoin
  • Collagen