posted on 2025-01-31, 09:29authored byDaqian Gao, William D. Shipman, Yaping Sun, Weijun Yang, Angelin Tresa Mathew, Leleda Beraki, Joshua Zev Glahn, Alejandro Kochen, Themis R. Kyriakides, Valerie Horsley, Henry C. Hsia
Encapsulating fibroblasts in alginate hydrogels is a
promising
strategy to promote wound healing. However, improving the cell function
within the alginate matrix remains a challenge. In this study, we
engineer an injectable hydrogel through mixing alginate function with
collagen and fibronectin, creating a better microenvironment for enhancing
fibroblast function and cytokine secretion. We systematically analyze
microstructure, mechanical properties, and fibroblast behavior of
the developed hydrogel and compare it to alginate control. Our results
demonstrate that inclusion collagen and fibronectin lead to the formation
of fibrils on macroporous structures with pore sizes ranging from
100 to 500 μm. Compared to collagen hydrogel, the composite
hydrogel shows approximately 12-fold increase in storage modulus.
After encapsulating fibroblasts into the modified hydrogels, we observed
increased fibroblast spreading, proliferation, and cytokine secretion
when compared to neat alginate hydrogel. In addition, VEGF secretion
of encapsulated fibroblasts is upregulated, indicating its pro-angiogenic
potential. These findings suggest that the alginate/collagen/fibronectin
hydrogel-encapsulated fibroblasts might serve as a promising therapeutic
approach for wound healing.