One of the objectives of bone tissue
engineering is to produce
scaffolds that are biocompatible, osteoinductive, and mechanically
equivalent to the natural extracellular matrix of bone in terms of
structure and function. Reconstructing the osteoconductive bone microenvironment
into a scaffold can attract native mesenchymal stem cells and differentiate
them into osteoblasts at the defect site. The symbiotic relationship
between cell biology and biomaterial engineering could result in composite
polymers containing the necessary signals to recreate tissue- and
organ-specific differentiation. In the current work, drawing inspiration
from the natural stem cell niche to govern stem cell fate, the cell-instructive
hydrogel platforms were constructed by engineering the mineralized
microenvironment. This work employed two different hydroxyapatite
delivery strategies to create a mineralized microenvironment in an
alginate–PEGDA interpenetrating network (IPN) hydrogel. The
first approach involved coating of nano-hydroxyapatite (nHAp) on poly(lactide-co-glycolide) microspheres and then encapsulating the coated
microspheres in an IPN hydrogel for a sustained release of nHAp, whereas
the second approach involved directly loading nHAp into the IPN hydrogel.
This study demonstrate that both direct encapsulation and a sustained
release approach showed enhanced osteogenesis in target-encapsulated
cells; however, direct loading of nHAp into the IPN hydrogel increased
the mechanical strength and swelling ratio of the scaffold by 4.6-fold
and 1.14-fold, respectively. In addition, the biochemical and molecular
studies revealed improved osteoinductive and osteoconductive potential
of encapsulated target cells. Being less expensive and simple to perform,
this approach could be beneficial in clinical settings.