Effects of BDNF and PEC Nanoparticles on Osteocytes
Thomas Leonhard Loy1, David Vehlow2, Vivien Kauschke1
1Experimental Trauma Surgery, Justus-Liebig-University, 35392 Giessen, Germany.
Molecules (Basel, Switzerland)
|September 15, 2020
Summary
Brain-derived neurotrophic factor (BDNF) stimulates osteocyte proliferation for enhanced fracture healing. Polyelectrolyte complex nanoparticles (PECNP) show no negative effects, confirming their suitability for drug delivery in bone implants.
Area of Science:
- Biomaterials Science
- Orthopedic Surgery
- Cell Biology
Background:
- Bone substitute materials require mediators to enhance fracture healing in orthopedic and trauma surgery.
- Brain-derived neurotrophic factor (BDNF) promotes osteoblast differentiation from mesenchymal stem cells.
- Controlled drug delivery systems are needed to load implants with BDNF for improved functionality.
Purpose of the Study:
- To evaluate the biocompatibility of polyelectrolyte complex nanoparticles (PECNP) and BDNF with osteocytes.
- To determine if BDNF and PECNP loaded with BDNF (PECNP+BDNF) negatively impact osteocyte viability and proliferation in vitro.
- To confirm the suitability of PECNP as a drug delivery system for bone regeneration applications.
Main Methods:
- Murine osteocyte cell line (MLO-Y4) was treated with BDNF, PECNP+BDNF, and pure PECNP.
- Cell proliferation was assessed using the Bromodeoxyuridine (BrdU) test.
- In vitro study design with n=5 for statistical analysis.
Main Results:
- BDNF application significantly increased osteocyte proliferation at 24 hours.
- PECNP+BDNF treatment did not result in significant changes in proliferation.
- Pure PECNP did not adversely affect osteocyte viability, indicating good biocompatibility.
Conclusions:
- BDNF is an effective mediator for stimulating osteocytes, crucial for fracture healing.
- PECNP demonstrate suitability as a drug delivery system for bone implants due to their non-toxic nature.
- The combination of BDNF and PECNP holds promise for advanced bone regenerative therapies.
Keywords:
MLO-Y4brain-derived neurotrophic factordorsal root ganglianeurotrophinosteocytepolyelectrolyte complex nanoparticlesproliferationvitality

