ABSTRACT
The red-crowned crane (Grus japonensis) is a critically endangered species. Three-dimensional-printed prosthetic beaks made of titanium alloy and polyether ether ketone (PEEK) were used to repair the beak of a red-crowned crane that had a complete fracture of the anterior maxillary bone and rhinotheca. The physical properties and stability of the prostheses and changes in the crane's behaviors after application of either beak were evaluated. The titanium alloy and PEEK prosthetic beaks weighed 30.81 g and 5.9 g, respectively. Scanning electron microscopy showed differences in microstructure between the 2 materials and the true beak; the true beak was softer than both materials from which the prostheses were made. The titanium beak frequently detached, and the residual natural beak showed significant cuticle softening with this prosthetic beak. The titanium beak detached within an approximately 3-month period after placement, whereas the PEEK prosthetic beak has remained secure for 2 years. Moreover, the crane's foraging times (P < .01) and grooming times (P < .05) with the titanium alloy false beak were lower than the normal, red-crowned crane. With the PEEK beak, no detachment or cuticle softening occurred, and foraging and grooming behaviors were evaluated by the investigators as natural (P > .05). Based on the results of this clinical case, the PEEK prosthetic beak was found to be superior to the titanium alloy prosthetic beak in color, weight, firmness, and postoperative effects.
Subject(s)
Beak , Titanium , Alloys , Animals , Beak/surgery , Benzophenones , Ethers , Ketones , Polymers , Printing, Three-DimensionalABSTRACT
BACKGROUND:The establishment of a good blood supply is a key mechanism for successful implantation of engineered tissues. OBJECTIVE:To observe the effect of basic fibroblast growth factor on the migration of human adipose-derived stem cells via implanting the human adipose-derived stem cells and sodium hyaluronate composite graft at the subcutaneous site of BALB/C mice, in order to explore an optimal scheme for soft tissue reconstruction. METHODS:Human adipose-derived stem cells were isolated from the adipose tissue of healthy cosmetic patients which received liposuction, and the cells were subcultured. Then 5×109/L passage 3 cellsuspension labeled by cm-dil was prepared. The working solution containing 2 mg/L basic fibroblast growth factor was prepared. Composite tissue al-lografts which were the mixtures of 0.25 mL sodium hyaluronate, 0.2 mL cellsuspension and 0.05 mL working solution or DMEM were implanted into the subcutaneous site of both sides of the mouse back. Specimens were taken at 6 weeks after operation and were evaluated histological y after hematoxylin-eosin and vascular immunofluorescent staining. RESULTS AND CONCLUSION:No necrosis, liquefaction, nodular tissue or gel remained in operated position. The hematoxylin-eosin staining showed the main components of the specimens were the adipose tissue and the loose connective tissue. The immunofluorescence staining showed the overlaps between the cm-dil fluorescence from human adipose-derived stem cells and the FITC fluorescence from the vascular endothelium in the experimental group were more than those in the control group (P<0.05). Basic fibroblast growth factor promotes the migration and the differentiation of human adipose-derived stem cells in the sodium hyaluronate scaffold into vascular endothelium.
ABSTRACT
BACKGROUND:Adipose-derived stem cels are a population of multilineage cels isolated from adipose tissue, which may have a positive effect on the treatment of ischemic diseases. OBJECTIVE:To explore the therapeutic and angiogenic effects of adipose-derived stem celsvia local transplantation on random pattern skin flaps in mice. METHODS: Human adipose-derived stem cels were isolated, cultured and passagedin vitro. On the back of the SPF mice, random pattern skin flaps were performed. After the operation, the adipose-derived stem cels were injected into the pedicle, central, and distal end of the flaps in the experimental group, while only PBS was injected into the control flaps. Seven days later, the survival rate of flaps was evaluated. Immunofluorescence assay was preformed to observe the distribution of microvessels in the flaps and trace the CM-Dil labeled adipose-derived stem cels, while the level of vascular endothelial growth factor was tested by ELISA and the protein expression of stromal cel-derived factor 1 tested by western blot at day 14 after adipose-derived stem cels transplantation. RESULTS AND CONCLUSION:Compared with the control group, there was a significant increase in the flap survival rate in the experimental group, and along with the sharply increased number of microvessels, the secretions of vascular endothelial growth factor and stromal cel-derived factor 1 were also obviously raised in the experimental group (P < 0.05). After local transplantation of adipose-derived stem cels into random skin flaps, it could intervene the secretion of vascular endothelial growth factor and stromal cel-derived factor 1 and promote angiogenesis of the skin flap.
ABSTRACT
BACKGROUND:Expanded polytetrafluoroethylene is a kind of porous polymer materials which is commonly used as clinical implants, and it has good biocompatibility, and is not easy to deformation or metamorphism. There is no existence of inflammation absorption reaction, and it al ows the cel migration and tissue ingrowth. OBJECTIVE:To study the biocompatibility of expanded polytetrafluoroethylene scaffold and human adipose-derived stem cel s. METHODS:The passage 4 human adipose-derived stem cel s were co-cultured with expanded polytetrafluoroethylene scaffold in vitro. The morphology and function of cel s adhered to the scaffold were observed by inverted phase contrast microscope, and cel adhesive rates and proliferation rates were also calculated by MTT assay. RESULTS AND CONCLUSION:The inoculated cel s were round and bright, distributed on the surface of scaffolds uniformly, with good cel viability. After 3 hours a large number of adherent cel s were observed from the micrograph;after 24 hours there were a smal amount of short-spindle adipose-derived stem cel s. After cultured for 3 days, the short fusiform or polygon cel s could be seen clearly. After cultured for 7 days, the number of cel s increased significantly, few cel s fel off from the scaffold, and cel adhesion rate was up to an average of 95.7%. Meanwhile, the cel s revealed normal splitting proliferation rate. These findings indicate that human adipose-derived stem cel s are able to attach, grow and proliferate wel on the scaffold. Expanded polytetrafluoroethylene reveals excel ent cel ular compatibility and can be used as a vehicle for adipose tissue engineering.
ABSTRACT
Objective To study the effect of the exogenous recombinant human FGF-basic with different concentrations upon inducing human adipose-derived stem cells (hASCs) to differentiate into adipose cells,and the optimum concentration of exogenous rh-bFGF by experimental research.Methods hASCs were isolated and extracted by enzymatic digestion from the liposuction aspirate.hASCs using adipogenic supplement were divided into experimental group and blank group:the experimental group of adipogenic supplement was divided into adding the exogenous rh-bFGF 10 ng/ml,20 ng/ml and 40 ng/ml,the blank group of adipogenic supplement was cultured without exogenous rh-bFGF.MTT method was used to detect the adipocytes proliferation.The oil red O staining was used in the qualitative analysis on the time of newly forming adipocyte cells.Western blot was used to detect the effects of rh-bFGF on the expression of lipid droplets surface protein CIDEC at different stages during the culture.Results The experimental group could obviously shorten the period of inducing hASCs to differentiate into adioicytes,and promote the proliferation of adipocytes.The formation rate and the proliferation of adipocytes in the group adding 40 ng/ml rh-bFGF were superior to those in the experimental group else and blank group.The average time of the newly formed lipid droplets by adding 40 ng/ml rh-bFGFwas (11.5±1.9)h.The average absorbance of cell proliferation by adding 40ml rh-bFGF was 0.52 ±0.10.The CIDEC expression quantity of adding 40 ng/ml rh-bFGF group was also superior to that in the experimental group and blank group.Conclusions rh-bFGF in hASCs adipogenic supplement could promote the proliferation of adipocytes and dramatically accelerates the program of hASCs differentiating to adipocytes,in which the optimum concentration of rh-bFGF is 40ng/ml.