Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation

Joe Swift(University of Pennsylvania), Irena L. Ivanovska(University of Pennsylvania), Amnon Buxboim(University of Pennsylvania), Takamasa Harada(University of Pennsylvania), P.C. Dave P. Dingal(University of Pennsylvania), Joel Pinter(University of Pennsylvania), J. David Pajerowski(University of Pennsylvania), Kyle Spinler(University of Pennsylvania), Jae‐Won Shin(University of Pennsylvania), Manorama Tewari(University of Pennsylvania), Florian Rehfeldt(University of Pennsylvania), David W. Speicher(The Wistar Institute), Dennis E. Discher(The Wistar Institute)
Science
August 29, 2013
Cited by 2,002

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.


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