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MicroRNA-146a-loaded magnesium silicate nanospheres promote bone regeneration in an inflammatory microenvironment
by
Lu, Jingyi
, Yang, Jiakang
, Wang, Baixiang
, Sun, Miao
, Shuai, Jing
, Yu, Mengfei
, An, Wenyue
, Siow, Lixuen
, Chen, Qianming
in
Arthritis
/ Bone marrow
/ Bone surgery
/ Defects
/ Gum disease
/ Inflammation
/ Kinases
/ MicroRNAs
/ Microscopy
/ Morphology
/ Nanomaterials
/ Silica
/ Stem cells
2024
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MicroRNA-146a-loaded magnesium silicate nanospheres promote bone regeneration in an inflammatory microenvironment
by
Lu, Jingyi
, Yang, Jiakang
, Wang, Baixiang
, Sun, Miao
, Shuai, Jing
, Yu, Mengfei
, An, Wenyue
, Siow, Lixuen
, Chen, Qianming
in
Arthritis
/ Bone marrow
/ Bone surgery
/ Defects
/ Gum disease
/ Inflammation
/ Kinases
/ MicroRNAs
/ Microscopy
/ Morphology
/ Nanomaterials
/ Silica
/ Stem cells
2024
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Do you wish to request the book?
MicroRNA-146a-loaded magnesium silicate nanospheres promote bone regeneration in an inflammatory microenvironment
by
Lu, Jingyi
, Yang, Jiakang
, Wang, Baixiang
, Sun, Miao
, Shuai, Jing
, Yu, Mengfei
, An, Wenyue
, Siow, Lixuen
, Chen, Qianming
in
Arthritis
/ Bone marrow
/ Bone surgery
/ Defects
/ Gum disease
/ Inflammation
/ Kinases
/ MicroRNAs
/ Microscopy
/ Morphology
/ Nanomaterials
/ Silica
/ Stem cells
2024
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MicroRNA-146a-loaded magnesium silicate nanospheres promote bone regeneration in an inflammatory microenvironment
Journal Article
MicroRNA-146a-loaded magnesium silicate nanospheres promote bone regeneration in an inflammatory microenvironment
2024
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Overview
Reconstruction of irregular oral-maxillofacial bone defects with an inflammatory microenvironment remains a challenge, as chronic local inflammation can largely impair bone healing. Here, we used magnesium silicate nanospheres (MSNs) to load microRNA-146a-5p (miR-146a) to fabricate a nanobiomaterial, MSN+miR-146a, which showed synergistic promoting effects on the osteogenic differentiation of human dental pulp stem cells (hDPSCs). In addition, miR-146a exhibited an anti-inflammatory effect on mouse bone marrow-derived macrophages (BMMs) under lipopolysaccharide (LPS) stimulation by inhibiting the NF-κB pathway via targeting tumor necrosis factor receptor-associated factor 6 (TRAF6), and MSNs could simultaneously promote M2 polarization of BMMs. MiR-146a was also found to inhibit osteoclast formation. Finally, the dual osteogenic-promoting and immunoregulatory effects of MSN+miR-146a were further validated in a stimulated infected mouse mandibular bone defect model via delivery by a photocuring hydrogel. Collectively, the MSN+miR-146a complex revealed good potential in treating inflammatory irregular oral-maxillofacial bone defects.
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