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大鼠的天然细胞介导细胞毒性。I. 组织和品系分布,以及IgG Fc部分膜受体的证明。

Natural cell-mediated cytotoxicity in rats. I. Tissue and strain distribution, and demonstration of a membrance receptor for the Fc portion of IgG.

作者信息

Oehler J R, Lindsay L R, Nunn M E, Herberman R B

出版信息

Int J Cancer. 1978 Feb 15;21(2):204-9. doi: 10.1002/ijc.2910210212.

DOI:10.1002/ijc.2910210212
PMID:627427
Abstract

Studies in mice and in humans have provided most of the available information concerning natural cell-mediated cytotoxicity. Rats represent a second experimental species which is well suited for the study of natural cytotoxicity. Our studies indicate that the distribution of natural killer (NK)3 cells in rat lymphoid tissues is similar to their tissue distribution in man, with high levels in the blood and spleen and low or undetectable levels in lymph node, thymus, thoracic duct or peritoneal exudate cells. The levels of NK activity varied considerably among various inbred strains of rats. However, the genetic control of levels of NK activity did not appear to be linked to the rat major histocompatibility complex. As recently demonstrated in mice by depletion experiments on antibody-erythrocyte monolayers, many or most rat natural killer cells were found to have surface receptors for the Fc portion of IgG.

摘要

对小鼠和人类的研究提供了有关天然细胞介导细胞毒性的大部分现有信息。大鼠是第二个非常适合用于天然细胞毒性研究的实验物种。我们的研究表明,大鼠淋巴组织中自然杀伤(NK)细胞的分布与其在人类组织中的分布相似,血液和脾脏中的水平较高,而淋巴结、胸腺、胸导管或腹腔渗出细胞中的水平较低或检测不到。不同近交系大鼠的NK活性水平差异很大。然而,NK活性水平的遗传控制似乎与大鼠主要组织相容性复合体无关。正如最近在小鼠中通过对抗体 - 红细胞单层的耗竭实验所证明的那样,发现许多或大多数大鼠自然杀伤细胞具有针对IgG Fc部分的表面受体。

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引用本文的文献

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2
Natural killer activity of Wistar rat spleen cells: blocking effect of homologous sera.Wistar大鼠脾细胞的自然杀伤活性:同源血清的阻断作用。
Immunology. 1980 Nov;41(3):541-5.
3
The in vitro discrimination of rat immune and natural cytotoxicity by serum choice.通过血清选择对大鼠免疫和自然细胞毒性进行体外鉴别。
Immunology. 1980 Aug;40(4):571-7.
4
The cell populations mediating natural killing-(NK) and antibody-dependent cell-mediated cytotoxicity are only partially identical.介导自然杀伤(NK)和抗体依赖性细胞介导的细胞毒性的细胞群体仅部分相同。
Clin Exp Immunol. 1981 Mar;43(3):534-9.
5
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J Cancer Res Clin Oncol. 1982;102(3):195-214. doi: 10.1007/BF00411340.
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