Abstract:Scaffolds with the capacity to deliver signaling molecules are attractive for bone regeneration. Here, we developed bioactive siloxane-gelatin hybrid scaffolds via a sol gel process containing stromal derived factor-1 (SDF-1) to recruit osteoprogenitor/stem cells. The process was undertaken under room temperature aqueous conditions, which enabled therapeutic molecules to be effectively incorporated. After the sol-gel reaction and lyophilization process, well-crosslinked hybrid scaffolds were obtained with poro… Show more
“…As aforementioned, SDF-1 is a powerful chemokine, which directly induces cell migration in various cell types including NSC, MSC and so on. In our previous study, SDF-1 loaded scaffolds significantly enhanced cell migration (17). Similarly, SDF-1 significantly enhanced the migration of PC-12 cells in the present study.…”
Section: Discussionsupporting
confidence: 84%
“…Construction of expression plasmids. Recombinant SDF-1 protein was constructed as described previously (17). Briefly, the human SDF-1 sequence was amplified by PCR (Perkin Elmer, Inc.) using primers flanked with restriction sites for XhoI and KpnI (forward, 5'-XhoI-AACCTCGAGAGCGAT GGCAAACCGGTG-3'; reverse, 5'-KpnI-GTTGGTACCTTA TTTGTTCAGCGCT-3').…”
Section: Methodsmentioning
confidence: 99%
“…In the present study, it was hypothesized that a recombinant SDF-1 protein might induce neuronal differentiation of PC-12 cells. A recombinant SDF-1 protein constructed in our previous study was isolated and purified in Escherichia coli (E. coli) (17). Cell toxicity and the proliferative effect of SDF-1 protein in PC-12 cells were measured.…”
Stromal cell-derived factor-1 (SDF-1) is a chemokine involved in neuronal differentiation, as well as proliferation and migration. In the present study, the effects of recombinant SDF-1 on neurite outgrowth for nerve regeneration and engineering were evaluated in PC-12 cells. The effects of purified SDF-1 protein on cell toxicity, proliferation and migration were also assessed. SDF-1 significantly augmented cell proliferation in a dose-dependent manner, with low cytotoxicity in PC-12 cells. Cell migration also increased in the presence of SDF-1. SDF-1 significantly increased neurite number and length, compared with the control (untreated cells). Neurofilament mRNA levels, which are involved in neuronal differentiation, were also significantly upregulated in the presence of SDF-1. These results suggested that SDF-1 might prove useful for tissue engineering through induction of neuronal differentiation.
“…As aforementioned, SDF-1 is a powerful chemokine, which directly induces cell migration in various cell types including NSC, MSC and so on. In our previous study, SDF-1 loaded scaffolds significantly enhanced cell migration (17). Similarly, SDF-1 significantly enhanced the migration of PC-12 cells in the present study.…”
Section: Discussionsupporting
confidence: 84%
“…Construction of expression plasmids. Recombinant SDF-1 protein was constructed as described previously (17). Briefly, the human SDF-1 sequence was amplified by PCR (Perkin Elmer, Inc.) using primers flanked with restriction sites for XhoI and KpnI (forward, 5'-XhoI-AACCTCGAGAGCGAT GGCAAACCGGTG-3'; reverse, 5'-KpnI-GTTGGTACCTTA TTTGTTCAGCGCT-3').…”
Section: Methodsmentioning
confidence: 99%
“…In the present study, it was hypothesized that a recombinant SDF-1 protein might induce neuronal differentiation of PC-12 cells. A recombinant SDF-1 protein constructed in our previous study was isolated and purified in Escherichia coli (E. coli) (17). Cell toxicity and the proliferative effect of SDF-1 protein in PC-12 cells were measured.…”
Stromal cell-derived factor-1 (SDF-1) is a chemokine involved in neuronal differentiation, as well as proliferation and migration. In the present study, the effects of recombinant SDF-1 on neurite outgrowth for nerve regeneration and engineering were evaluated in PC-12 cells. The effects of purified SDF-1 protein on cell toxicity, proliferation and migration were also assessed. SDF-1 significantly augmented cell proliferation in a dose-dependent manner, with low cytotoxicity in PC-12 cells. Cell migration also increased in the presence of SDF-1. SDF-1 significantly increased neurite number and length, compared with the control (untreated cells). Neurofilament mRNA levels, which are involved in neuronal differentiation, were also significantly upregulated in the presence of SDF-1. These results suggested that SDF-1 might prove useful for tissue engineering through induction of neuronal differentiation.
“…Similar result had also been reported by another research group (Huang, Gronthos, & Shi, 2009). However, other studies using constructs with burst release of SDF-1α in the early stage demonstrated successfully the recruitment of BMSCs (Dashnyam et al, 2014;He, Ma, & Jabbari, 2010;Ji et al, 2013).…”
Section: Discussionmentioning
confidence: 97%
“…Similar result had also been reported by another research group (Huang, Gronthos, & Shi, ). However, other studies using constructs with burst release of SDF‐1α in the early stage demonstrated successfully the recruitment of BMSCs (Dashnyam et al., ; He, Ma, & Jabbari, ; Ji et al., ). Therefore, further investigation is needed to confirm the recruitment of GFP‐positive rat BMSCs in the periodontal defect, and higher dose of SDF‐1α might be considered.…”
AimChemoattractants, such as stromal cell‐derived factor‐1α (SDF‐1α), can offer an advantage for periodontal regeneration by recruiting the patient’s own stem cells to stimulate self‐repair. We here developed a chemoattractive construct for periodontal regeneration using SDF‐1α and evaluated its efficacy in vivo.Materials and MethodsSDF‐1α was loaded on gelatin sponge and tested in vitro for SDF‐1α release. Subsequently, SDF‐1α constructs were implanted into rat periodontal defects for 1 and 6 weeks, with unloaded materials and empty defects as controls. The regenerative efficacy was evaluated by micro‐CT, histological and histomorphometrical analyses.ResultsIn vitro results showed limited SDF‐1α release up to 35 days. In contrast, SDF‐1α constructs significantly improved periodontal defect regeneration in terms of alveolar bone height, new bone area and functional ligament length. Additionally, SDF‐1α constructs decreased the inflammatory response at Week 6.ConclusionChemoattractive constructs significantly improved periodontal regeneration in terms of alveolar bone height, new bone area and functional ligament length.
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