2023
DOI: 10.1016/j.bioactmat.2022.10.018
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A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis

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Cited by 27 publications
(29 citation statements)
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“…In addition, Parfejevs et al found that SCs could activate the TGFβ signaling pathway to promote skin wound healing by increasing paracrine signaling [ 61 ]. Similarly, Hao et al found that the GelMA-loaded SC-exos could promote the osteogenic differentiation of BMSCs by activating the TGF-β/Smad signaling pathway [ 26 ]. Therefore, the activation of the TGFβ signaling pathway may be an important mechanism in SC-regulated tissue repair.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In addition, Parfejevs et al found that SCs could activate the TGFβ signaling pathway to promote skin wound healing by increasing paracrine signaling [ 61 ]. Similarly, Hao et al found that the GelMA-loaded SC-exos could promote the osteogenic differentiation of BMSCs by activating the TGF-β/Smad signaling pathway [ 26 ]. Therefore, the activation of the TGFβ signaling pathway may be an important mechanism in SC-regulated tissue repair.…”
Section: Discussionmentioning
confidence: 99%
“…Su et al created a biomimetic periosteum loading SC-exos to enhance nerve repair for angiogenesis and bone regeneration [ 25 ]. Hao et al developed a multifunctional neuromodulation platform utilizing SC-exos that improved bone repair by regulating immunomodulation, angiogenesis, and osteogenesis [ 26 ]. These studies demonstrate that SC-exos are crucial paracrine signaling agents for SCs to regulate tissue repair and that the regulatory effects of SCs for bone repair in the microenvironment can be simulated via SC-exos.…”
Section: Introductionmentioning
confidence: 99%
“…All animal experiments reported here were performed under guidelines evaluated and approved by the Animal Ethical Committee of Tianjin Medical University (NKYY-DWLL-2022-098). Thirty male SD rats (5–6 weeks old, 200–250 g) were used to establish two critical-sized (ϕ = 5 mm) skull defects besides the sagittal suture. , All rats were randomly divided into five groups: (1) control group, (2) GM microspheres filled group, (3) GMH microspheres filled group, (4) GMC microspheres filled group, and (5) GMHC microspheres filled group. The sterilized microspheres (∼10 mg) were dispersed in saline and injected into the defects, followed by suturing the overlying tissue.…”
Section: Materials and Methodsmentioning
confidence: 99%
“…Similarly, CEVs derived from monocytes (MC-EVs) induced the up-regulated expression of osteogenic-related genes in MSCs [ 88 ]. Schwann cell-derived CEVs (SC-EVs) promoted BMMSC osteogenic differentiation through TGF-β1/SMAD2/3 signaling pathway, M2 macrophage polarization, vascularization, nerve repair, and ultimately bone defect restoration [ 89 ]. Inflammatory osteoclast (iOC)-derived CEVs (iOC-EVs) have been proved to reduce the Osterix ubiquitination in MC3T3-E1 cells by transferring lncRNA LIOCE, thus facilitating bone regeneration [ 90 ].…”
Section: Cevs and Periodontal Regenerationmentioning
confidence: 99%
“…The adverse effects of M-EVs on HUVEC function under certain conditions have ever been reported. However, M2-EVs could inhibit inflammation and apoptosis of HUVECs, and promote their functions by delivering miR-221-3p and miR-21 activating related signaling pathways [ 89 , 125 , 126 ]. Therefore, the degree of vascularization of tissues or scaffolds should be taken into consideration in a successful periodontal regeneration strategy.…”
Section: Cevs and Periodontal Regenerationmentioning
confidence: 99%