Hydroxyapatite Chitosan Gradient Pore Scaffold Activates Oxidative Phosphorylation Pathway to Induce Bone Formation

Background: In this study, we prepared a porous gradient scaffold with hydroxyapatite microtubules (HAMT) and chitosan (CHS) and investigated osteogenesis induced by these scaffolds. Methods: The arrangement of...

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Main Authors: Zeliang Zhang, Wei Shang, Lisong Lin
Format: Article
Language:English
Published: IMR Press 2025-01-01
Series:Frontiers in Bioscience-Landmark
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Online Access:https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL26299
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author Zeliang Zhang
Wei Shang
Lisong Lin
author_facet Zeliang Zhang
Wei Shang
Lisong Lin
author_sort Zeliang Zhang
collection DOAJ
description Background: In this study, we prepared a porous gradient scaffold with hydroxyapatite microtubules (HAMT) and chitosan (CHS) and investigated osteogenesis induced by these scaffolds. Methods: The arrangement of wax balls in the mold can control the size and distribution of the pores of the scaffold, and form an interconnected gradient pore structure. The scaffolds were systematically evaluated in vitro and in vivo for biocompatibility, biological activity, and regulatory mechanisms. Results: The porosity of the four scaffolds was more than 80%. The 50% and 70% HAMT-CHS scaffolds formed an excellent gradient pore structure, with interconnected pores. Furthermore, the 70% HAMT-CHS scaffold showed better anti-compressive deformation ability. In vitro experiments indicated that the scaffolds had good biocompatibility, promoted the expression of osteogenesis-related genes and proteins, and activated the oxidative phosphorylation pathway to promote bone regeneration. Eight weeks after implanting the HAMT-CHS scaffold in rat skull defects, new bone formation was observed in vivo by micro-computed tomographic (CT) staining. The obtained data were statistically analyzed, and the p-value < 0.05 was statistically significant. Conclusion: HAMT-CHS scaffolds can accelerate osteogenesis in bone defects, potentially through the activation of the oxidative phosphorylation pathway. These results highlight the potential therapeutic application of HAMT-CHS scaffolds.
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series Frontiers in Bioscience-Landmark
spelling doaj-art-b779b46393034691bc86679099dc6b1b2025-01-25T08:55:52ZengIMR PressFrontiers in Bioscience-Landmark2768-67012025-01-013012629910.31083/FBL26299S2768-6701(24)01565-XHydroxyapatite Chitosan Gradient Pore Scaffold Activates Oxidative Phosphorylation Pathway to Induce Bone FormationZeliang Zhang0Wei Shang1Lisong Lin2Department of Stomatology, The First Affiliated Hospital of Fujian Medical University, 350001 Fuzhou, Fujian, ChinaDepartment of Stomatology, The Affiliated Heping Hospital of Changzhi Medical College, 046000 Changzhi, Shanxi, ChinaDepartment of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Fujian Medical University, Fujian Provincial Key Laboratory of Stomatology, National Regional Medical Center, Binhai Campus of The First Affiliated Hospital, 350005 Fuzhou, Fujian, ChinaBackground: In this study, we prepared a porous gradient scaffold with hydroxyapatite microtubules (HAMT) and chitosan (CHS) and investigated osteogenesis induced by these scaffolds. Methods: The arrangement of wax balls in the mold can control the size and distribution of the pores of the scaffold, and form an interconnected gradient pore structure. The scaffolds were systematically evaluated in vitro and in vivo for biocompatibility, biological activity, and regulatory mechanisms. Results: The porosity of the four scaffolds was more than 80%. The 50% and 70% HAMT-CHS scaffolds formed an excellent gradient pore structure, with interconnected pores. Furthermore, the 70% HAMT-CHS scaffold showed better anti-compressive deformation ability. In vitro experiments indicated that the scaffolds had good biocompatibility, promoted the expression of osteogenesis-related genes and proteins, and activated the oxidative phosphorylation pathway to promote bone regeneration. Eight weeks after implanting the HAMT-CHS scaffold in rat skull defects, new bone formation was observed in vivo by micro-computed tomographic (CT) staining. The obtained data were statistically analyzed, and the p-value < 0.05 was statistically significant. Conclusion: HAMT-CHS scaffolds can accelerate osteogenesis in bone defects, potentially through the activation of the oxidative phosphorylation pathway. These results highlight the potential therapeutic application of HAMT-CHS scaffolds.https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL26299osteogenesishydroxyapatitechitosanpore scaffoldoxidative phosphorylation
spellingShingle Zeliang Zhang
Wei Shang
Lisong Lin
Hydroxyapatite Chitosan Gradient Pore Scaffold Activates Oxidative Phosphorylation Pathway to Induce Bone Formation
Frontiers in Bioscience-Landmark
osteogenesis
hydroxyapatite
chitosan
pore scaffold
oxidative phosphorylation
title Hydroxyapatite Chitosan Gradient Pore Scaffold Activates Oxidative Phosphorylation Pathway to Induce Bone Formation
title_full Hydroxyapatite Chitosan Gradient Pore Scaffold Activates Oxidative Phosphorylation Pathway to Induce Bone Formation
title_fullStr Hydroxyapatite Chitosan Gradient Pore Scaffold Activates Oxidative Phosphorylation Pathway to Induce Bone Formation
title_full_unstemmed Hydroxyapatite Chitosan Gradient Pore Scaffold Activates Oxidative Phosphorylation Pathway to Induce Bone Formation
title_short Hydroxyapatite Chitosan Gradient Pore Scaffold Activates Oxidative Phosphorylation Pathway to Induce Bone Formation
title_sort hydroxyapatite chitosan gradient pore scaffold activates oxidative phosphorylation pathway to induce bone formation
topic osteogenesis
hydroxyapatite
chitosan
pore scaffold
oxidative phosphorylation
url https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL26299
work_keys_str_mv AT zeliangzhang hydroxyapatitechitosangradientporescaffoldactivatesoxidativephosphorylationpathwaytoinduceboneformation
AT weishang hydroxyapatitechitosangradientporescaffoldactivatesoxidativephosphorylationpathwaytoinduceboneformation
AT lisonglin hydroxyapatitechitosangradientporescaffoldactivatesoxidativephosphorylationpathwaytoinduceboneformation