Naringin-inlaid silk fibroin/hydroxyapatite scaffold enhances human umbilical cord-derived mesenchymal stem cell-based bone regeneration.
Naringin-inlaid silk fibroin/hydroxyapatite scaffold enhances human umbilical cord-derived mesenchymal stem cell-based bone regeneration.
复制标题
柚皮苷镶嵌丝素蛋白/羟基磷灰石支架增强人脐带间充质干细胞骨再生
DOI:
10.1111/cpr.13043
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发表时间:
2021-07
影响因子:
8.5
通讯作者:
Sun L
中科院分区:
文献类型:
--
作者:
Zhao ZH;Ma XL;Zhao B;Tian P;Ma JX;Kang JY;Zhang Y;Guo Y;Sun L
Large bone defects are a common, debilitating clinical condition that have substantial global health and economic burden. Bone tissue engineering technology has become one of the most promising approaches for regenerating defective bones. In this study, we fabricated a naringin‐inlaid composite silk fibroin/hydroxyapatite (NG/SF/HAp) scaffold to repair bone defects. The salt‐leaching technology was used to fabricate the NG/SF/HAp scaffold. The cytocompatibility of the NG/SF/HAp scaffold was assessed using scanning electron microscopy, live/dead cell staining and phalloidin staining. The osteogenic and angiogenic properties were assessed in vitro and in vivo. The porous NG/SF/HAp scaffold had a well‐designed biomimetic porous structure with osteoinductive and angiogenic activities. A gene microarray identified 854 differentially expressed genes between human umbilical cord‐derived mesenchymal stem cells (hUCMSCs) cultured on SF‐nHAp scaffolds and cells cultured on NG/SF/HAp scaffolds. The underlying osteoblastic mechanism was investigated using hUCMSCs in vitro. Naringin facilitated hUCMSC ingrowth into the SF/HAp scaffold and promoted osteogenic differentiation. The osteogenic and angiogenic capabilities of cells cultured in the NG/SF/HAp scaffold were superior to those of cells cultured in the SF/HAp scaffold. The data indicate the potential of the SF/HAp composite scaffold incorporating naringin for bone regeneration. Overall schematic illustration of naringin‐inlaid silk fibroin/hydroxyapatite scaffold enhances human umbilical cord‐derived mesenchymal stem cell‐based bone regeneration.
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影响因子:
9.8
作者:
Filipowska J;Tomaszewski KA;Niedźwiedzki Ł;Walocha JA;Niedźwiedzki T
通讯作者:
Niedźwiedzki T
影响因子:
3.3
作者:
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通讯作者:
Yao, Chun-Hsu
影响因子:
5.4
作者:
Maisani, Mathieu;Sindhu, K. R.;Chassande, Olivier
通讯作者:
Chassande, Olivier
影响因子:
8.2
作者:
Kim, Seung Hyun L.;Lee, Seunghun S.;Hwang, Nathaniel S.
通讯作者:
Hwang, Nathaniel S.
影响因子:
9.7
作者:
Feng, Chun;Xue, Jianmin;Wu, Chengtie
通讯作者:
Wu, Chengtie