A fibronectin gradient remodels mixed-phase mesoderm

Author:

Zhu Min1ORCID,Gu Bin2ORCID,Thomas Evan C.1,Huang Yunyun13ORCID,Kim Yun-Kyo1ORCID,Tao Hirotaka1ORCID,Yung Theodora M.1ORCID,Chen Xin1ORCID,Zhang Kaiwen14,Woolaver Elizabeth K.15,Nevin Mikaela R.15,Huang Xi15ORCID,Winklbauer Rudolph4,Rossant Janet15ORCID,Sun Yu3ORCID,Hopyan Sevan156ORCID

Affiliation:

1. Program in Developmental and Stem Cell Biology, Research Institute, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.

2. Department of Obstetrics Gynecology and Reproductive Biology, and Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing, MI 48824, USA.

3. Department of Cell and Systems Biology, University of Toronto, Toronto, ON M5S 3G5, Canada.

4. Department of Mechanical and Industrial Engineering, University of Toronto, Toronto, ON M5S 3G8, Canada.

5. Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.

6. Division of Orthopaedic Surgery, The Hospital for Sick Children and University of Toronto, Toronto, ON M5G 1X8, Canada.

Abstract

Physical processes ultimately shape tissue during development. Two emerging proposals are that cells migrate toward stiffer tissue (durotaxis) and that the extent of cell rearrangements reflects tissue phase, but it is unclear whether and how these concepts are related. Here, we identify fibronectin-dependent tissue stiffness as a control variable that underlies and unifies these phenomena in vivo. In murine limb bud mesoderm, cells are either caged, move directionally, or intercalate as a function of their location along a stiffness gradient. A modified Landau phase equation that incorporates tissue stiffness accurately predicts cell diffusivity upon loss or gain of fibronectin. Fibronectin is regulated by WNT5A-YAP feedback that controls cell movements, tissue shape, and skeletal pattern. The results identify a key determinant of phase transition and show how fibronectin-dependent directional cell movement emerges in a mixed-phase environment in vivo.

Publisher

American Association for the Advancement of Science (AAAS)

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