4.7 Article

Fibronectin mediates mesendodermal cell fate decisions

Journal

DEVELOPMENT
Volume 140, Issue 12, Pages 2587-2596

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.089052

Keywords

Fibronectin; Endoderm; Mesoderm; Integrin-beta 1; Wnt

Funding

  1. National Institutes of Health/National Heart, Lung, and Blood Institute (NIH/NHLBI) [U01 HL100406, R01 HL057181, P01 HL089707]
  2. California Institute for Regenerative Medicine
  3. William Younger Family Foundation
  4. Whittier Foundation
  5. Eugene Roddenberry Foundation
  6. NIH/NHLBI [R00 HL092234, R01 HL111198]
  7. Maryland Stem Cell Research Fund
  8. Magic That Matters Fund
  9. Lundbeck Foundation [R83-A8133]
  10. NIH/National Institute of General Medical Sciences (NIGMS) grant [T32 GM07618]
  11. NIH/National Center for Research Resources (NCRR) grant [C06 RR018928]

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Non-cell-autonomous signals often play crucial roles in cell fate decisions during animal development. Reciprocal signaling between endoderm and mesoderm is vital for embryonic development, yet the key signals and mechanisms remain unclear. Here, we show that endodermal cells efficiently promote the emergence of mesodermal cells in the neighboring population through signals containing an essential short-range component. The endoderm-mesoderm interaction promoted precardiac mesoderm formation in mouse embryonic stem cells and involved endodermal production of fibronectin. In vivo, fibronectin deficiency resulted in a dramatic reduction of mesoderm accompanied by endodermal expansion in zebrafish embryos. This event was mediated by regulation of Wnt signaling in mesodermal cells through activation of integrin-beta 1. Our findings highlight the importance of the extracellular matrix in mediating short-range signals and reveal a novel function of endoderm, involving fibronectin and its downstream signaling cascades, in promoting the emergence of mesoderm.

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