Ectopic induction of tendon and ligament in rats by growth and differentiation factors 5, 6, and 7, members of the TGF-beta gene family.

Neil M. Wolfman, Gary Hattersley(Pfizer (United States)), Karen Cox(Pfizer (United States)), Anthony Celeste(Pfizer (United States)), R. Nelson(Pfizer (United States)), Noboru Yamaji(Pfizer (United States)), Jennifer L. Dube(Pfizer (United States)), Elizabeth A. DiBlasio-Smith(Pfizer (United States)), John Nove(Pfizer (United States)), Jeffrey Song(Pfizer (United States)), John M. Wozney(Pfizer (United States)), Vicki Rosen(Pfizer (United States))
Journal of Clinical Investigation
July 15, 1997
Cited by 532Open Access
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Abstract

Little is known about the regulatory signals involved in tendon and ligament formation, and this lack of understanding has hindered attempts to develop biologically based therapies for tendon and ligament repair. Here we report that growth and differentiation factors (GDFs) 5, 6, and 7, members of the TGF-beta gene superfamily that are most related to the bone morphogenetic proteins, induce neotendon/ligament formation when implanted at ectopic sites in vivo. Analysis of tissue induced by GDF-5, 6, or 7, containing implants by currently available morphological and molecular criteria used to characterize tendon and ligament, adds further evidence to the idea that these GDFs act as signaling molecules during embryonic tendon/ligament formation. In addition, comparative in situ localizations of the GDF-5, 6, and 7 mRNAs suggest that these molecules are important regulatory components of synovial joint morphogenesis.


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