Preparation
of Hydroxyapatite-Aligned Collagen Sheets
and Their Evaluation for Fibroblast Adhesion and Collagen Secretion
Posted on 2025-01-23 - 18:36
The structure of many native tissues
consists of aligned
collagen
(Col) fibrils, some of which are further composited with dispersed
hydroxyapatite (HAp) nanocrystals. Accurately mimicking this inherent
structure is a promising approach to enhance scaffold biocompatibility
in tissue engineering. In this study, biomimetic sheets composed of
highly aligned Col fibrils were fabricated using a plastic compression
and tension method, followed by the deposition of HAp nanocrystals
on the surface via an alternate soaking method. The fabricated Col
sheets exhibited high solid density, retained the native periodicity
(D-band) of Col fibrils, and displayed plate-like HAp nanocrystals
dispersed on their surface. In vitro experiments demonstrated that
these sheets could regulate fibroblasts adhesion, inducing more elongated
nuclei and oriented actin bundles on the aligned Col sheets. Analysis
of focal adhesion assembly revealed greater cell focal adhesions on
the aligned composite sheets compared to those with random Col fibril
structures. Fibroblasts cultured on aligned Col with partly HAp-mineralized
sheets exhibited the highest cell-extracellular matrix (ECM) protein
secretion, highlighting that HAp incorporation and fibroblast alignment
synergistically promote early ECM formation and wound healing. These
results suggest that highly aligned Col fibrils with dispersed HAp
nanocrystals, closely mimicking the microarchitecture of natural tissues,
have significant potential to control cell adhesion and protein secretion
for tissue engineering applications.
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Zhang, Yuxuan; Quindoza, Gerardo Martin; Mizuno, Hayato Laurence; Nakagawa, Yasuhiro; Tanaka, Toshiaki; Anraku, Yasutaka; et al. (2025). Preparation
of Hydroxyapatite-Aligned Collagen Sheets
and Their Evaluation for Fibroblast Adhesion and Collagen Secretion. ACS Publications. Collection. https://doi.org/10.1021/acsbiomaterials.4c01617Â