Project Details
SFB 1444: Directed Cellular Self-Organisation for Advancing Bone Regeneration
Subject Area
Medicine
Term
since 2021
Website
Homepage
Project identifier
Deutsche Forschungsgemeinschaft (DFG) - Project number 427826188
Musculoskeletal diseases and disorders are on the continuous rise due to the epidemic of obesity resulting in reduced mobility, and the increased physical activity of the elderly in an increasingly aging population. The healing potential of bone varies greatly in the different patient groups, but there is a substantial lack of understanding how the endogenous healing processes are altered due to age, metabolic status or immune experience of the individuals. This Collaborative Research Center aims to unravel the basic mechanisms that differentiate between success and failure in bone regeneration. Since bone is one of the few tissues in the body that has the general capability of scar-less healing resulting in complete functional and structural reconstitution it is an ideal model system to understand the general principals of endogenous healing, which is relevant also for regeneration processes of other tissues. Bone healing is initiated by cellular self-organisation that guides the regenerative processes throughout all consecutive regeneration phases. The early phases of bone regeneration are essential for the long-term healing success, but also delays of healing or non-unions are already initiated during these very early stages. Central to all regenerative cascades driven by cellular self-organisation are (1) a well-controlled local inflammatory response, (2) well-balanced nutrition supply and consumption, and (3) a well-structured matrix re-organization by force transmission and sensing. These are the three key mechanism that need to be closely coordinated to achieve successful endogenous tissue regeneration in bone. To prove this hypothesis, we want to understand the interdependencies between these key mechanisms of healing, which have only been studied from a one-dimensional perspective so far. The aim of this CRC is to reveal (1) how the interplay between these three key mechanisms is controlled and regulated; (2) how their interdependencies are adjusted during healthy aging so that regeneration remains - in principle – possible; and (3) how each of the three key mechanisms are challenged by distinct stressors that are associated with delayed or non-healing conditions. Over the 12-year period of this Collaborative Research Center, we will concentrate in the beginning on the understanding of the interdependencies between these three key mechanisms of healing. Within the second funding period, we aim to understand the effect of stressors on the interdependencies of the three key mechanisms of healing. Finally, in the third funding period we aim at controlling and steering the three key mechanisms and their interdependencies, specifically in impaired healing cascades of challenged clinical settings. We will validate our understanding of the “control” mechanism in both pre-clinical and first-in-men clinical studies and thereby lay the foundation for personalized therapeutic approaches.
DFG Programme
Collaborative Research Centres
Current projects
- C01 - Central Service Project - Cell and Tissue Harvesting: supply of functionally and immunologically characterised human samples for the CRC research projects (Project Heads Perka, Carsten ; Reinke, Simon )
- C02 - Central tasks of the Collaborative Research Centre (Project Head Duda, Georg )
- P01 - Understand and reshape the impact of an experienced adaptive immunity on fracture healing (Project Heads Schmidt-Bleek, Katharina ; Volk, Hans-Dieter )
- P02 - Impact of epigenetic regulation on T subsets involved in bone fracture healing (Project Heads Polansky-Biskup, Julia ; Volk, Hans-Dieter )
- P03 - ECM coding and reading: alterations of ECM properties under compromised conditions and consequences for regeneration (Project Heads Knaus, Petra ; Petersen, Ansgar )
- P04 - The effects of mechano-biology on chromatin folding and gene regulation (Project Heads Knaus, Petra ; Mundlos, Stefan )
- P05 - Effects of implant-derived metal debris on bone formation and resorption (Project Heads Geißler, Sven ; Perka, Carsten )
- P06 - In vivo forces and musculoskeletal loading conditions in human fracture healing (Project Heads Trepczynski, Adam ; Zachow, Stefan )
- P07 - The role and the development of internal tissue tension in normal versus compromised healing bone (Project Heads Fratzl, Peter ; Zaslansky, Paul )
- P08 - Hydrogels with spatial patterning of biophysical and biochemical properties to guide osteogenesis (Project Heads Cipitria, Ph.D., Amaia ; Duda, Georg )
- P09 - Mechano-dependency of early bone healing and angiogenesis (Project Heads Duda, Georg ; Gerhardt, Holger )
- P10 - Outer-vascular mechanics as an age-dependent regulator of sprouting angiogenesis and vessel patterning (Project Heads Checa, Sara ; Petersen, Ansgar )
- P11 - Innate immune circuits for bone maintenance and regeneration (Project Heads Diefenbach, Andreas ; Triantafyllopoulou, Antigoni )
- P12 - Bone marrow adipose tissue: Nutrient metabolism and immunomodulation during bone maintenance and regeneration (Project Heads Schmidt-Bleek, Katharina ; Schulz, Tim J. )
- P13 - Understanding and shaping of bone regeneration by cellular metabolic adaption (Project Heads Duda, Georg ; Sawitzki, Birgit )
- P14 - Interactions between myeloid and stromal cells during bone healing under compromising conditions (Project Heads Hauser, Anja Erika ; Niesner, Raluca Aura )
- P15 - Effect of traumatic brain injury and traumatic spinal cord injury on energy distribution, alpha adrenergic signalling and bone regeneration (Project Heads Pumberger, Matthias ; Tsitsilonis, Ph.D., Serafeim )
- P16 - Promoting humeral head fracture healing by local immunomodulation - A phase I/IIa, prospective, mono-centre, randomized, open labelled, controlled study (Project Heads Geißler, Sven ; Winkler, Tobias )
Applicant Institution
shared FU Berlin and HU Berlin through:
Charité - Universitätsmedizin Berlin
Charité - Universitätsmedizin Berlin
Co-Applicant Institution
Humboldt-Universität zu Berlin
Participating Institution
Zuse-Institut Berlin (ZIB)
Mathematische Methoden für Lebens- u Materialwissenschaft
Department Visual and Data-centric Computing; Deutsches Institut für Ernährungsforschung Potsdam-Rehbrücke (DIfE); Max-Delbrück-Centrum für Molekulare Medizin (MDC)
Forschungsgruppe Integrative Vaskuläre Biologie; Max-Planck-Institut für Kolloid- und Grenzflächenforschung
Wissenschaftspark Potsdam-Golm
Mathematische Methoden für Lebens- u Materialwissenschaft
Department Visual and Data-centric Computing; Deutsches Institut für Ernährungsforschung Potsdam-Rehbrücke (DIfE); Max-Delbrück-Centrum für Molekulare Medizin (MDC)
Forschungsgruppe Integrative Vaskuläre Biologie; Max-Planck-Institut für Kolloid- und Grenzflächenforschung
Wissenschaftspark Potsdam-Golm
Participating University
Freie Universität Berlin
Spokesperson
Professor Dr.-Ing. Georg Duda