A non-transmembrane form of Jagged-1 regulates the formation of matrix-dependent chord-like structures

Biochem Biophys Res Commun. 2000 Feb 24;268(3):853-9. doi: 10.1006/bbrc.2000.2173.

Abstract

Jagged-Notch interactions regulate a transmembrane ligand-receptor signaling pathway involved in the regulation of cell fate determination as well as myoblast and endothelial cell differentiation. To further examine the role of the transmembrane ligand, Jagged-1, in the regulation of cell differentiation, we stably transfected NIH 3T3 cells with a truncated form of Jagged(J)-1, which results in the secretion of a soluble(s) form of the protein. Comparison of gene expression by serial analysis demonstrated that among the 227 transcripts differentially regulated in the sJ-1 transfectants, the expression of the pro-alpha-2(I) collagen transcript and pro-alpha-1(I) collagen translation product was predominantly repressed in sJ-1 transfectants. When plated on extracellular matrices, sJ-1 transfectants formed prominent chord-like structures on type I collagen but not on fibrin, fibronectin, or vitronectin. While the sJ-1 transfectants exhibited growth kinetics similar to control cells and were unable to grow in soft agar, the cells were less sensitive to contact inhibition of growth in vitro and sJ-1 allografts formed tissue masses in nude mice after a prolonged latency period and exhibited an abundance of host-derived microvascular endothelial cells. These data suggest that J-1 may be able to modulate, in a matrix-dependent manner, the organization of cell to cell interactions including its ability to promote the development of chord-like structures.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Animals
  • Base Sequence
  • Calcium-Binding Proteins
  • Cell Communication
  • Cell Differentiation
  • Cell Division
  • DNA Primers / genetics
  • Extracellular Matrix / metabolism
  • Gene Expression
  • Intercellular Signaling Peptides and Proteins
  • Jagged-1 Protein
  • Membrane Proteins
  • Mice
  • Mice, Nude
  • Neovascularization, Physiologic
  • Phenotype
  • Proteins / chemistry
  • Proteins / genetics
  • Proteins / metabolism*
  • Serrate-Jagged Proteins
  • Signal Transduction
  • Transfection

Substances

  • Calcium-Binding Proteins
  • DNA Primers
  • Intercellular Signaling Peptides and Proteins
  • Jag1 protein, mouse
  • Jagged-1 Protein
  • Membrane Proteins
  • Proteins
  • Serrate-Jagged Proteins