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对移植到成年小鼠中枢神经系统中的神经胶质来源的小鼠细胞系的免疫反应。

Immune response to murine cell lines of glial origin transplanted into the central nervous system of adult mice.

作者信息

Terry L A, Usherwood E J, Lees S, MacIntyre N, Nash A A

机构信息

Department of Veterinary Pathology, Royal (Dick) School of Veterinary Studies, University of Edinburgh, UK.

出版信息

Immunology. 1997 Jul;91(3):436-43. doi: 10.1046/j.1365-2567.1997.00276.x.

Abstract

Temperature-sensitive simian virus 40 (SV40) T antigen-transformed central nervous system (CNS)-derived murine cell lines were used to analyse the host response to transplantation in the mouse adult brain. The cell lines were shown to be susceptible to immune recognition in vitro by cytotoxic effector cells indicating that tissue-specific privilege was not in operation. Histological examination at time points post-implantation showed characteristic responses similar to those seen during graft rejection. Astrocytosis and up-regulation of major histocompatibility complex (MHC) class I and MHC class II activation of resident microglia and recruitment of macrophages were observed in both allogeneic and syngeneic hosts 10 days post-implantation suggesting a trauma-induced response. However, the response in allogeneic hosts was more widespread and evident when the syngeneic responses had returned to normal levels. Evidence of T-cell infiltration was also more pronounced in the allogeneic hosts. Despite quite extensive host reactions to these cellular grafts at early time-points the implants appeared to survive in the host CNS long after the responses had abated and could be detected at the maximum time-point studied of 40 days.

摘要

利用温度敏感型猿猴病毒40(SV40)T抗原转化的中枢神经系统(CNS)来源的小鼠细胞系,分析小鼠成年大脑对移植的宿主反应。细胞系在体外显示对细胞毒性效应细胞的免疫识别敏感,表明组织特异性特权不起作用。植入后各时间点的组织学检查显示出与移植排斥反应中所见相似的特征性反应。植入后10天,在同种异体和同基因宿主中均观察到星形细胞增生以及主要组织相容性复合体(MHC)I类和MHC II类上调、驻留小胶质细胞活化和巨噬细胞募集,提示这是一种创伤诱导的反应。然而,当同基因反应恢复到正常水平时,同种异体宿主中的反应更为广泛和明显。T细胞浸润的证据在同种异体宿主中也更为明显。尽管在早期时间点宿主对这些细胞移植有相当广泛的反应,但在反应减弱后很长时间,植入物似乎仍存活于宿主中枢神经系统中,并且在研究的最长时间点40天时仍可检测到。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4de/1364014/02646f27fb11/immunology00056-0120-a.jpg

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