首页> 外文期刊>Journal of periodontal research >Graft of autologous fibroblasts in gingival tissue in vivo after culture in vitro. Preliminary study on rats.
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Graft of autologous fibroblasts in gingival tissue in vivo after culture in vitro. Preliminary study on rats.

机译:体外培养后,体内自体成纤维细胞在牙龈组织中的移植。对大鼠的初步研究。

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Several grafting techniques and guided tissue regeneration techniques (GTR) have been well-developed in periodontal surgery. However, these techniques could induce pain and side effects, such as a gingival recession during the healing period following the therapy. The graft of a small autologous connective tissue, using non-invasive surgical techniques could yield several benefits for the patients. Our preliminary study explores the feasibility of collecting healthy gingival tissues, culturing them in vitro to amplify rat gingival fibroblasts (RGF) and inoculating the obtained cells into autologous rat gingival tissues in vivo. Gingival tissues samples were cultured as explants as described by Freshney et al. and Adolphe. Confluent cells surrounding explants were detached after 7 d of culture from Petri dishes using 0.05% trypsin and designated "first transferred cells" (T1). At the third passage (T3), cells cultured as monolayer were either examined under microscopy--phase contrast, scanning, or transmission electron--or numerated after trypan blue exclusion test. Autologous RGF labelled with fluorochrome were inoculated at the vestibular and palatine site of gingival tissue close to the superior incisors. In this preliminary study, 12 Wistar rats were used; for each, 2 biopsies were dissected and fixed for phase contrast or fluorescence microscopy. On d 1, 3 and 7 after injection in rat gingival tissues, fluorochrome-labelled cells could be detected in all these.
机译:在牙周手术中已经发展了几种移植技术和引导组织再生技术(GTR)。但是,这些技术可能会在治疗后的愈合期间引起疼痛和副作用,例如牙龈萎缩。使用非侵入性手术技术移植小的自体结缔组织可以为患者带来多种益处。我们的初步研究探索了收集健康牙龈组织,在体外培养它们以扩增大鼠牙龈成纤维细胞(RGF)以及将获得的细胞接种到体内自体大鼠牙龈组织中的可行性。如Freshney等人所述,将牙龈组织样品作为外植体培养。和阿道夫培养后7天,使用0.05%胰蛋白酶从培养皿中分离出外植体周围的融合细胞,并命名为“首次转移细胞”(T1)。在第三次传代(T3),在显微镜下检查培养为单层的细胞-相差,扫描或透射电子-或在台盼蓝排除试验后进行计数。用荧光染料标记的自体RGF接种在靠近上门牙的牙龈组织的前庭和p骨部位。在这项初步研究中,使用了12只Wistar大鼠。对于每一个,解剖2个活组织检查并固定以进行相差或荧光显微镜检查。在大鼠牙龈组织中注射后第1、3和7天,所有这些中都可以检测到荧光染料标记的细胞。

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