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影响肠道单核细胞自发细胞介导细胞毒性的因素。

Factors affecting the spontaneous cell-mediated cytotoxicity of intestinal mononuclear cells.

作者信息

Gibson P R, Hermanowicz A, Jewell D P

出版信息

Immunology. 1984 Oct;53(2):267-74.

Abstract

This study was performed to determine what factors related to the enzymatic isolation technique and assay conditions may influence the measurement of spontaneous cell-mediated cytotoxicity (SCMC) of mononuclear cells (MNC) isolated from human intestinal mucosa. In 18 studies, the SCMC of freshly isolated cells was 1.8 +/- 0.4% but increased to 12 +/- 3% following 24 hr culture without a change in the proportion of cells with the NK phenotype (Leu-7+). The SCMC tended to plateau with more prolonged culture. Culturing peripheral blood (PB) MNC for 24 hr did not alter SCMC nor the proportion of Leu-7+ cells. However, the suppression of the SCMC of PBMNC preincubated with the supernatant of the collagenase digestion of intestinal mucosa was completely reversed by 24 hr culture. Intestinal MNC were found to suppress the SCMC of autologous PBMNC in mixing experiments. However, 24 hr culture did not affect the degree of suppression and the proportion of T cells of the suppressor-cytotoxic phenotype (Leu-2a+) was also unchanged. It is concluded that the SCMC of intestinal MNC may be accurately assessed following 24 hr culture of the cells to allow recovery from the suppressive influences of the isolation process and that this does not introduce other artefactual problems. However, suppression of cytotoxicity within the assay may result in an underestimation of the SCMC of intestinal MNC when compared to that of PBMNC.

摘要

本研究旨在确定与酶分离技术和检测条件相关的哪些因素可能影响从人肠黏膜分离的单核细胞(MNC)的自发细胞介导细胞毒性(SCMC)的测量。在18项研究中,新鲜分离细胞的SCMC为1.8±0.4%,但在无NK表型(Leu-7+)细胞比例变化的情况下培养24小时后,SCMC增加至12±3%。随着培养时间延长,SCMC趋于平稳。培养外周血(PB)MNC 24小时不会改变SCMC或Leu-7+细胞的比例。然而,用肠黏膜胶原酶消化上清预孵育的PBMNC的SCMC抑制作用在培养24小时后完全逆转。在混合实验中发现肠MNC可抑制自体PBMNC的SCMC。然而,24小时培养并不影响抑制程度,抑制性细胞毒性表型(Leu-2a+)的T细胞比例也未改变。得出结论,肠MNC的SCMC在细胞培养24小时后可得到准确评估,以便从分离过程的抑制性影响中恢复,且这不会引入其他人为问题。然而,与PBMNC相比,检测内的细胞毒性抑制可能导致对肠MNC的SCMC估计不足。

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