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Macrophage plasticity deployed for efficient bone (re-) generation

Fachliche Zuordnung Orthopädie, Unfallchirurgie, rekonstruktive Chirurgie
Förderung Förderung von 2015 bis 2018
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 270576131
 
Macrophages (MPhi) achieve different activation states in response to environmental priming, the M1 ("classical" state involved in anti-microbial function) or M2 ("alternative" state involved in tissue repair). The potential to control MPhi skewing in an experimental system in vitro and in vivo by integrated bioresponsive drug delivery systems will open exciting new avenues to deploy the advantageous roles that M2-MPhi play in skeletal tissue formation - and more importantly angiogenesis - leading to superior host-implant integration in critical size bone defects. As a prerequisite to this endeavor, we will develop an experimental system composed of a column-like index compartment containing a three-dimensional bone-like tissue, engineered from human mesenchymal stem cells (hMSCs; TE-bone) which is inserted into a tube-like supply compartment within which M2-MPhi will be harbored. M2-MPhi status is controlled by a bioresponsive, IL-4 releasing drug delivery system, covalently attached to the supply compartment and releasing this M2 skewing cytokine in response to upregulated collagenase activity. The plans build off our extensive preliminary data and previous publication demonstrating functional bone-like tissue engineering, the genetic engineering of cytokine mutants with an integrated pyrrolysine analogue (propargyl pyrrolysine, plk) for site directed chemistry (including plk-IL-4), an array of more than 200 collagenase sensitive cleavable linker sequences and successful binding of these bioresponsive drug delivery systems to SF as a prerequisite for controlled, bioresponsive macrophage skewing, and relevant animal model systems for critical size bone defects.
DFG-Verfahren Sachbeihilfen
Internationaler Bezug China
 
 

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