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SCID-ra小鼠:严重联合免疫缺陷小鼠中的大鼠T细胞分化

The SCID-ra mouse: rat T-cell differentiation in the severe combined immunodeficient mouse.

作者信息

De Heer C, Verlaan A P, Penninks A H, Schuurman H J, Van Loveren H

机构信息

National Institute of Public Health and Environmental Protection, Bilthoven, The Netherlands.

出版信息

APMIS. 1993 Jun;101(6):467-79. doi: 10.1111/j.1699-0463.1993.tb00135.x.

Abstract

The SCID-hu mouse model offers the possibility to study the human thymus in vivo in an isolated xenogeneic environment. Whilst studying the toxicology of the human thymus using the SCID-hu model, a "control" model to test for differences in toxicokinetics due to the different localization of the thymus is desirable when SCID-hu data have to be extrapolated to the normal human situation. For this reason, SCID-ra mice were constructed by implanting rat fetal or postnatal thymus and liver explants under the renal capsule of severe combined immunodeficient (SCID) mice. Implantation of rat fetal thymus in combination with fetal liver resulted in thymus grafts with a histological appearance that was virtually identical to that of normal age-matched rat thymus. T cells of rat origin were found in the circulating blood and lymphoid organs of the recipient mice. After implantation of postnatal thymus and liver, the thymus grafts showed a dysplastic morphology. These grafts were devoid of thymocytes and consisted mainly of thymic microenvironmental components and large numbers of thymic macrophages. Some SCID-ra mice showed signs of graft-versus-host (GVH) reactions in the skin. The incidence of GVH reactions was higher with increasing developmental stage of the donor material used for implantation.

摘要

SCID-hu小鼠模型提供了在隔离的异种环境中体内研究人类胸腺的可能性。在使用SCID-hu模型研究人类胸腺的毒理学时,当必须将SCID-hu数据外推至正常人类情况时,需要一个“对照”模型来测试由于胸腺不同定位导致的毒代动力学差异。出于这个原因,通过将大鼠胎儿或出生后胸腺及肝脏外植体植入严重联合免疫缺陷(SCID)小鼠的肾被膜下构建了SCID-ra小鼠。将大鼠胎儿胸腺与胎儿肝脏联合植入导致胸腺移植物的组织学外观与年龄匹配的正常大鼠胸腺几乎相同。在受体小鼠的循环血液和淋巴器官中发现了大鼠来源的T细胞。植入出生后胸腺和肝脏后,胸腺移植物呈现发育异常的形态。这些移植物缺乏胸腺细胞,主要由胸腺微环境成分和大量胸腺巨噬细胞组成。一些SCID-ra小鼠在皮肤中表现出移植物抗宿主(GVH)反应的迹象。随着用于植入的供体材料发育阶段的增加,GVH反应的发生率更高。

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