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人类干细胞植入的重症联合免疫缺陷(SCID)小鼠模型

SCID mouse models of human stem cell engraftment.

作者信息

Greiner D L, Hesselton R A, Shultz L D

机构信息

Department of Medicine, University of Massachusetts Medical School, Worcester, USA.

出版信息

Stem Cells. 1998;16(3):166-77. doi: 10.1002/stem.160166.

Abstract

The discovery of the severe combined immunodeficiency (scid) mouse mutation has provided a tool for establishment of small animal models as hosts for the in vivo analysis of normal and malignant human pluripotent hemopoietic stem cells. Intravenous injection of irradiated scid mice with human bone marrow, cord blood, or G-CSF cytokine-mobilized peripheral blood mononuclear cells, all rich in human hemopoietic stem cell activity, results in the engraftment of a human hemopoietic system in the murine recipient. This model has been used to identify a pluripotent stem cell, termed "scid-repopulating cell" (SRC) that is more primitive than any of the hemopoietic stem cell populations identified using the currently available in vitro methodology. In this review, we describe the development and use of this model system, termed Hu-SRC-SCID, and summarize the discoveries that have resulted from the investigation of human stem cells in this model. Finally, we detail the recent extension of the original Hu-SRC-SCID model system based on the C.B-17-scid mouse as the murine host to the Hu-SRC-NOD-SCID model based on the NOD-scid mouse as the host. The engraftment of human stem cells in the Hu-SRC-NOD-SCID model is enhanced over that observed in the Hu-SRC-SCID model and results in exceptionally high levels of human hemopoietic cells in the murine recipient. Future directions to further improve the Hu-SRC-NOD-SCID model system and the potential utility of this model in the preclinical and diagnostic arenas of hematology and oncology are discussed.

摘要

严重联合免疫缺陷(scid)小鼠突变的发现为建立小动物模型提供了一种工具,可作为体内分析正常和恶性人类多能造血干细胞的宿主。向经辐照的scid小鼠静脉注射富含人类造血干细胞活性的人类骨髓、脐带血或粒细胞集落刺激因子(G-CSF)细胞因子动员的外周血单个核细胞,会导致人类造血系统在小鼠受体中植入。该模型已用于鉴定一种多能干细胞,称为“scid重建造血细胞”(SRC),它比使用目前可用的体外方法鉴定的任何造血干细胞群体都更原始。在这篇综述中,我们描述了这个称为Hu-SRC-SCID的模型系统的开发和使用,并总结了在该模型中对人类干细胞进行研究所取得的发现。最后,我们详细介绍了最初基于C.B-17-scid小鼠作为小鼠宿主的Hu-SRC-SCID模型系统最近扩展为基于NOD-scid小鼠作为宿主的Hu-SRC-NOD-SCID模型。与Hu-SRC-SCID模型相比,人类干细胞在Hu-SRC-NOD-SCID模型中的植入得到增强,并导致小鼠受体中人类造血细胞水平异常高。本文还讨论了进一步改进Hu-SRC-NOD-SCID模型系统的未来方向以及该模型在血液学和肿瘤学临床前和诊断领域的潜在用途。

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