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来自人血液的供体基质细胞可植入NOD/SCID小鼠体内。

Donor stromal cells from human blood engraft in NOD/SCID mice.

作者信息

Goan S R, Junghahn I, Wissler M, Becker M, Aumann J, Just U, Martiny-Baron G, Fichtner I, Henschler R

机构信息

Max Delbrück Center for Molecular Medicine, Berlin, Germany.

出版信息

Blood. 2000 Dec 1;96(12):3971-8.

Abstract

Little is known about the presence, frequency, and in vivo proliferative potential of stromal cells within blood-derived hematopoietic transplants. In this study, nonobese diabetic/severe combined immunodeficiency (NOD/SCID) mice were injected with human CD34(+) peripheral blood cells (PBCs) or cord blood cells (CBCs, either enriched for CD34 or density-gradient separated mononuclear cells). Flow cytometric analysis 5 to 11 weeks after transplantation revealed the presence of a human lymphomyeloid hematopoiesis within the murine bone marrow. Immunohistochemical staining of bone marrow cell suspensions using human-specific antibodies showed human cells staining positive for human fibroblast markers, human von Willebrand factor (vWF) and human KDR (vascular endothelial growth factor receptor-2) in mice transplanted with CD34(+) PBCs or CBCs, with mean frequencies between 0.6% and 2.4%. In stromal layers of bone marrow cultures established from the mice, immunohistochemical staining using human-specific antibodies revealed flattened reticular cells or spindle-shaped cells staining positive with human-specific antifibroblast antibodies (mean frequency, 2.2%). Cell populations of more rounded cells stained positive with human-specific antibodies recognizing CD34 (1.5%), vWF (2.2%), and KDR (1.6%). Reverse transcriptase-polymerase chain reaction (RT-PCR) analysis and subsequent complementary DNA sequencing detected transcripts of human KDR (endothelial specific) and human proline hydroxylase-alpha (fibroblast specific) within the bone marrow and spleen of transplanted mice. Analysis of nontransplanted control mice yielded negative results in immunocytochemistry and RT-PCR. Cells expressing endothelial and fibroblast markers were also detected in the grafts before transplantation, and their numbers increased up to 3 log in vivo after transplantation. These results indicate that stromal progenitor cells are present in human cytokine-mobilized peripheral blood or cord blood that engraft in NOD/SCID mice. (Blood. 2000;96:3971-3978)

摘要

关于血液来源的造血移植中基质细胞的存在、频率及体内增殖潜能,人们了解甚少。在本研究中,给非肥胖糖尿病/严重联合免疫缺陷(NOD/SCID)小鼠注射人CD34(+)外周血细胞(PBCs)或脐血细胞(CBCs,要么富集CD34,要么经密度梯度分离的单核细胞)。移植后5至11周的流式细胞术分析显示,小鼠骨髓内存在人淋巴髓系造血。使用人特异性抗体对骨髓细胞悬液进行免疫组化染色,结果显示,在移植了CD34(+) PBCs或CBCs的小鼠中,人细胞对人成纤维细胞标志物、人血管性血友病因子(vWF)和人KDR(血管内皮生长因子受体-2)呈阳性染色,平均频率在0.6%至2.4%之间。在用这些小鼠建立的骨髓培养物的基质层中,使用人特异性抗体进行免疫组化染色显示,扁平的网状细胞或梭形细胞对人特异性抗成纤维细胞抗体呈阳性染色(平均频率为2.2%)。更多圆形细胞的细胞群体对识别CD34(1.5%)、vWF(2.2%)和KDR(1.6%)的人特异性抗体呈阳性染色。逆转录聚合酶链反应(RT-PCR)分析及随后的互补DNA测序在移植小鼠的骨髓和脾脏中检测到了人KDR(内皮特异性)和人脯氨酸羟化酶-α(成纤维细胞特异性)的转录本。对未移植的对照小鼠进行分析,免疫细胞化学和RT-PCR结果均为阴性。在移植前的移植物中也检测到了表达内皮和成纤维细胞标志物的细胞,移植后其数量在体内增加了多达3个对数。这些结果表明,基质祖细胞存在于植入NOD/SCID小鼠体内的人细胞因子动员的外周血或脐血中。(《血液》。2000年;96:3971 - 3978)

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