Temporal TGF-β Supergene Family Signalling Cues Modulating Tissue Morphogenesis: Chondrogenesis within a Muscle Tissue Model?

Int J Mol Sci

Department of Orthopedics, Physical Medicine and Rehabilitation, University Hospital, LMU Munich, 81377 Munich, Germany.

Published: July 2020

AI Article Synopsis

  • The study examines how different signaling molecules influence the development of muscle tissue and the potential induction of cartilage formation (chondrogenesis).
  • Researchers found that continuous exposure to the bone morphogenic protein 2 (rBMP-2) is crucial for triggering chondrogenesis, but its effectiveness decreases after the first week unless paired with specific other proteins (rBMP-7 and rTGF-β).
  • The research aims to create a model that can systematically predict the timing and combination of signals needed to engineer desired tissues, advancing tissue modeling and therapeutic strategies.

Article Abstract

Temporal translational signalling cues modulate all forms of tissue morphogenesis. However, if the rules to obtain specific tissues rely upon specific ligands to be active or inactive, does this mean we can engineer any tissue from another? The present study focused on the temporal effect of "multiple" morphogen interactions on muscle tissue to figure out if chondrogenesis could be induced, opening up the way for new tissue models or therapies. Gene expression and histomorphometrical analysis of muscle tissue exposed to rat bone morphogenic protein 2 (rBMP-2), rat transforming growth factor beta 3 (rTGF-β, and/or rBMP-7, including different combinations applied briefly for 48 h or continuously for 30 days, revealed that a continuous rBMP-2 stimulation seems to be critical to initiate a chondrogenesis response that was limited to the first seven days of culture, but only in the absence of rBMP-7 and/or rTGF-β. After day 7, unknown modulatory effects retard rBMP-2s' effect where only through the paired-up addition of rBMP-7 and/or rTGF-β a chondrogenesis-like reaction seemed to be maintained. This new tissue model, whilst still very crude in its design, is a world-first attempt to better understand how multiple morphogens affect tissue morphogenesis with time, with our goal being to one day predict the chronological order of what signals have to be applied, when, for how long, and with which other signals to induce and maintain a desired tissue morphogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402331PMC
http://dx.doi.org/10.3390/ijms21144863DOI Listing

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