Bio-3D printer

生物 3D 打印机
  • 文章类型: Journal Article
    用于再生医学的干细胞疗法已经得到了真诚的研究,但仍然不受欢迎,尽管一些临床试验显示出希望的结果。该疗法被认为是由于事故导致的骨缺损等代表性候选,医源性肿瘤切除,先天性疾病,和口腔区域的严重牙周炎。最近,Bio-3D打印机“Regenova®”作为一种创新的三维文化系统被引入,配备无支架生物组装技术,无需任何生物材料。因此,我们预计,通过使用成骨潜能干细胞从Bio-3D打印机建立的结构,可以修复大量的骨缺损。
    从同意我们研究的患者的下智齿远端部分去除牙龈组织(1x1mm)。从该组织中分离人牙龈间充质干细胞(hGMSCs)并进行培养,由于我们证实了容易分离和加速增殖等特征,进一步,成骨分化的强大潜力。使用hGMSC在设计用于低细胞粘附的96孔板中形成球状体。测量球体的大小,用荧光免疫染色验证干细胞和凋亡标志物的表达,和细胞外基质。骨分化四周后,进行μCT成像。通过茜素红和vonKossa染色证实钙化。利用荧光免疫染色来评估指示晚期骨分化的标志物的表达。
    我们已经建立并证实了由人GMSCs(hGMSCs)构建的球体(直径约600μm)仍然保持干细胞潜能和成骨分化能力,结果CD73而不是CD34表达为干细胞阳性和阴性标记。分别。这些球体像圆柱形一样堆积到Bio-3D打印机的“Kenzan”平台上,并培养7天。尝试使用成骨诱导培养基将源自复合球体的圆柱形结构分化为骨骼4周。通过茜素红和VonKossa染色证实了生物3D打印的骨样结构的钙化。此外,μCT分析显示,钙化结构的HU(Hounsfield单位)几乎与小梁骨相同。免疫荧光染色检测骨钙蛋白的表达,晚期骨分化标志物。
    第一次,我们已经实现了无脚手架的建设,通过由这种hGMSC组成的球状体的组装形成骨样管腔结构。这一成功肯定会接近诱导针对再生医学的临床应用,特别是针对骨缺损疾病。
    UNASSIGNED: Stem cell therapy for regenerative medicine has been sincerely investigated, but not still popular although some clinical trials show hopeful results. This therapy is suggested to be a representative candidate such as bone defect due to the accident, iatrogenic resection oncological tumor, congenital disease, and severe periodontitis in oral region. Recently, the Bio-3D printer \"Regenova®\" has been introduced as an innovative three-dimensional culture system, equipped scaffold-free bio-assembling techniques without any biomaterials. Therefore, we expected a mount of bone defect could be repaired by the structure established from this Bio-3D printer using osteogenic potential stem cells.
    UNASSIGNED: The gingival tissue (1x1 mm) was removed from the distal part of the lower wisdom tooth of the patients who agreed our study. Human Gingival Mesenchymal Stem Cells (hGMSCs) were isolated from this tissue and cultured, since we confirmed the characteristics such as facile isolation and accelerated proliferation, further, strong potential of osteogenic-differentiation. Spheroids were formed using hGMSC in 96-well plates designed for low cell adhesion. The size of the spheroids was measured, and fluorescent immunostaining was employed to verify the expression of stem cell and apoptosis marker, and extracellular matrix. Following four weeks of bone differentiation, μCT imaging was performed. Calcification was confirmed by alizarin red and von Kossa staining. Fluorescent immunostaining was utilized to assess the expression of markers indicative of advanced bone differentiation.
    UNASSIGNED: We have established and confirmed the spheroids (∼600 μm in diameter) constructed from human GMSCs (hGMSCs) still maintain stem cell potentials and osteogenic differentiation abilities from the results that CD73 and not CD34 were expressed as stem cell positive and negative marker, respectively. These spheroids were pilled up like cylindal shape to the \"Kenzan\" platform of Bio-3D printer and cultured for 7days. The cylindal structure originated from compound spheroids were tried to differentiate into bone four weeks with osteogenic induction medium. The calcification of bio-3D printed bone-like structures was confirmed by alizarin red and Von Kossa staining. In addition, μCT analysis revealed that the HU (Hounsfield Unit) of the calcified structures was almost identical to that of trabecular bone. Immunofluorescent staining detected osteocalcin expression, a late-stage bone differentiation marker.
    UNASSIGNED: For the first time, we have achieved the construction of a scaffold-free, bone-like luminal structure through the assembly of spheroids comprised of this hGMSCs. This success is sure to be close to the induction of clinical application against regenerative medicine especially for bone defect disease.
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  • 文章类型: Journal Article
    胆管损伤或胆管-胆管重建后的胆道狭窄是严重的并发症,显著降低患者的生活质量,因为他们的治疗包括定期更换支架。这项研究旨在创建一种无支架的管状结构,作为治疗胆道并发症的介入移植物。
    同种异体猪成纤维细胞的无支架管状结构,也就是说,成纤维细胞管,使用Bio-3D打印机创建并植入猪作为导管到导管胆道重建的插入移植物。
    虽然成纤维细胞管弱于天然胆管,它足够坚固以进行缝合。实验期间猪血清肝胆酶水平保持稳定。显微计算机断层扫描显示无胆道狭窄,没有胆漏,肝内胆管没有扩张.管状结构保留在所有切除的标本中,成纤维细胞持续存在于移植部位。免疫组织化学分析显示成纤维细胞管中的血管生成,并且胆管上皮没有延伸到成纤维细胞管腔中。
    这项研究的发现证明了使用新型Bio-3D打印机从猪成纤维细胞产生的无支架管状结构成功重建肝外胆管。该构建体可以为肝胆疾病患者提供新的再生治疗。
    UNASSIGNED: Biliary strictures after bile duct injury or duct-to-duct biliary reconstruction are serious complications that markedly reduce patients\' quality of life because their treatment involves periodic stent replacements. This study aimed to create a scaffold-free tubular construct as an interposition graft to treat biliary complications.
    UNASSIGNED: Scaffold-free tubular constructs of allogeneic pig fibroblasts, that is, fibroblast tubes, were created using a Bio-3D Printer and implanted into pigs as interposition grafts for duct-to-duct biliary reconstruction.
    UNASSIGNED: Although the fibroblast tube was weaker than the native bile duct, it was sufficiently strong to enable suturing. The pigs\' serum hepatobiliary enzyme levels remained stable during the experimental period. Micro-computed tomography showed no biliary strictures, no biliary leakages, and no intrahepatic bile duct dilations. The tubular structure was retained in all resected specimens, and the fibroblasts persisted at the graft sites. Immunohistochemical analyses revealed angiogenesis in the fibroblast tube and absence of extensions of the biliary epithelium into the fibroblast tube\'s lumen.
    UNASSIGNED: This study\'s findings demonstrated successful reconstruction of the extrahepatic bile duct with a scaffold-free tubular construct created from pig fibroblasts using a novel Bio-3D Printer. This construct could provide a novel regenerative treatment for patients with hepatobiliary diseases.
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  • 文章类型: Journal Article
    背景:我们一直在尝试使用带有球体的生物3D打印机生产用于气道再生的无支架结构,以避免与支架相关的风险,如感染。先前的研究表明,人脐静脉内皮细胞(HUVECs)在此类结构中起着重要作用,但是HUVECs不能与成年人分离。这项研究的目的是确定用于无支架结构的HUVEC的替代品。
    方法:比较了三种结构类型,由软骨细胞和间充质干细胞与HUVECs,人肺微血管内皮细胞(HMVEC-Ls),和诱导多能干细胞(iPSC)衍生的内皮细胞。
    结果:三组之间的拉伸强度没有显着差异。组织学上,在所有组中都观察到一些包含CD31阳性细胞的小毛细管样导管形成.在iPSC衍生的内皮细胞组中,这种形成的数量和直径明显低于其他组。在iPSC来源的内皮细胞组中糖胺聚糖含量显著低于HUVEC组,而HUVEC和HMVEC-L组之间没有观察到显著差异。
    结论:HMVEC-Ls可以替代HUVEC作为无支架气管样结构的细胞来源。然而,一些局限性与iPSC来源的内皮细胞相关.
    BACKGROUND: We have been trying to produce scaffold-free structures for airway regeneration using a bio-3D-printer with spheroids, to avoid scaffold-associated risks such as infection. Previous studies have shown that human umbilical vein endothelial cells (HUVECs) play an important role in such structures, but HUVECs cannot be isolated from adult humans. The aim of this study was to identify alternatives to HUVECs for use in scaffold-free structures.
    METHODS: Three types of structure were compared, made of chondrocytes and mesenchymal stem cells with HUVECs, human lung microvascular endothelial cells (HMVEC-Ls), and induced pluripotent stem cell (iPSC)-derived endothelial cells.
    RESULTS: No significant difference in tensile strength was observed between the three groups. Histologically, some small capillary-like tube formations comprising CD31-positive cells were observed in all groups. The number and diameters of such formations were significantly lower in the iPSC-derived endothelial cell group than in other groups. Glycosaminoglycan content was significantly lower in the iPSC-derived endothelial cell group than in the HUVEC group, while no significant difference was observed between the HUVEC and HMVEC-L groups.
    CONCLUSIONS: HMVEC-Ls can replace HUVECs as a cell source for scaffold-free trachea-like structures. However, some limitations were associated with iPSC-derived endothelial cells.
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