Interaction of alginate with nano-hydroxyapatite-collagen using strontium provides suitable osteogenic platform.
Interaction of alginate with nano-hydroxyapatite-collagen using strontium provides suitable osteogenic platform.
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DOI:
10.1186/s12951-022-01511-9
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发表时间:
2022-06-28
影响因子:
10.2
通讯作者:
Khoshfetrat, Ali Baradar
中科院分区:
文献类型:
--
作者:
Hassani, Ayla;Avci, Cigir Biray;Kerdar, Sajed Nazif;Amini, Hassan;Amini, Meisam;Ahmadi, Mahdi;Sakai, Shinji;Bagca, Bakiye Goker;Ozates, Neslihan Pinar;Rahbarghazi, Reza;Khoshfetrat, Ali Baradar
关键词:
Hydrogels based on organic/inorganic composites have been at the center of attention for the fabrication of engineered bone constructs. The establishment of a straightforward 3D microenvironment is critical to maintaining cell-to-cell interaction and cellular function, leading to appropriate regeneration. Ionic cross-linkers, Ca2+, Ba2+, and Sr2+, were used for the fabrication of Alginate-Nanohydroxyapatite-Collagen (Alg-nHA-Col) microspheres, and osteogenic properties of human osteoblasts were examined in in vitro and in vivo conditions after 21 days. Physicochemical properties of hydrogels illustrated that microspheres cross-linked with Sr2+ had reduced swelling, enhanced stability, and mechanical strength, as compared to the other groups. Human MG-63 osteoblasts inside Sr2+ cross-linked microspheres exhibited enhanced viability and osteogenic capacity indicated by mineralization and the increase of relevant proteins related to bone formation. PCR (Polymerase Chain Reaction) array analysis of the Wnt (Wingless-related integration site) signaling pathway revealed that Sr2+ cross-linked microspheres appropriately induced various signaling transduction pathways in human osteoblasts leading to osteogenic activity and dynamic growth. Transplantation of Sr2+ cross-linked microspheres with rat osteoblasts into cranium with critical size defect in the rat model accelerated bone formation analyzed with micro-CT and histological examination. Sr2+ cross-linked Alg-nHA-Col hydrogel can promote functionality and dynamic growth of osteoblasts. The online version contains supplementary material available at 10.1186/s12951-022-01511-9.
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影响因子:
5.5
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