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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >The xenotransplantation of goat and human hematopoietic cells to sheep fetuses.
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The xenotransplantation of goat and human hematopoietic cells to sheep fetuses.

机译:山羊和人类造血细胞向绵羊胎儿的异种移植。

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摘要

Hematopoietic xenografts were carried out in three experiments using goat fetal liver (44-48 days, experiments I and II) or purified human CD 34+ cells (experiment III) as the donor cells. Recipients were sheep fetuses at 41-47 days of gestation. Goat fetal liver cells were either injected without any pretreatment or stimulated by preincubation in a culturing in goat phytohemagglutinin-stimulated lymphocyte supernatant. Human CD 34+ myeloid progenitor cells were purified from bone marrow by minimacs immunomagnetic purification and cultured in medium supplemented with stem cell factor, IL3, and IL6. Goat-sheep chimerism was assessed by flow cytometry analysis (FCA) of peripheral blood and bone marrow cells using a mouse anti-goat CD 45 monoclonal antibody and by karyotype analysis of peripheral blood from goat/sheep chimeras. Human cell engraftment was assessed by polymerase chain reaction amplification of the human DAX1 gene in blood and bone marrow DNA from sheep which had received human cells. In the three experiments, a mean of 76% (26 of 34) of injected fetuses were born alive without any clinical evidence of graft-versus-host disease. Three lambs were found to be goat/sheep chimeric after flow cytometry analysis (peripheral blood and bone marrow) and karyotype (peripheral blood) analysis. Both tissues continued to express goat cells at 6 or 12 months (last assessment) depending on the experiment. No human chimerism was detected using polymerase chain reaction amplification in peripheral blood and bone marrow of any of the six sheep grafted with human cells. These data and those also obtained on other species (human, pig/sheep) show that it is possible to carry out hematopoietic xenografts using the sheep fetus as recipient provided both donor and recipient fetal cells are processed during the period of tolerance to foreign antigens.
机译:在三个实验中使用山羊胎肝(44-48天,实验I和II)或纯化的人CD 34+细胞(实验III)作为供体细胞进行了造血异种移植。接收者是妊娠41-47天的绵羊胎儿。山羊胎儿肝细胞无需进行任何预处理就可以注射,或者通过在山羊植物血凝素刺激的淋巴细胞上清液中的培养进行预温育来刺激。通过minimacs免疫磁纯化从骨髓中纯化人CD 34+骨髓祖细胞,并在补充有干细胞因子,IL3和IL6的培养基中培养。通过使用小鼠抗山羊CD 45单克隆抗体对外周血和骨髓细胞进行流式细胞术分析(FCA)以及对来自山羊/绵羊嵌合体的外周血的核型分析来评估山羊绵羊的嵌合性。通过聚合酶链反应扩增人DAX1基因在已接受人细胞的绵羊的血液和骨髓DNA中的表达来评估人细胞的植入。在这三个实验中,平均有76%(34个中的26个)的被注射胎儿活着,没有任何移植物抗宿主病的临床证据。经过流式细胞仪分析(外周血和骨髓)和核型(外周血)分析后,发现三只羊是山羊/绵羊嵌合体。取决于实验,两种组织在6或12个月(最后评估)持续表达山羊细胞。使用聚合酶链反应扩增在移植有人类细胞的六只绵羊中的任何一只的外周血和骨髓中均未检测到人类嵌合现象。这些数据以及在其他物种(人类,猪/羊)上获得的数据表明,只要在对外源抗原的耐受期内对供体和受体胎儿细胞都进行了处理,就可以使用绵羊胎儿作为受体进行造血异种移植。

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