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支原体污染的靶细胞产生的可溶性细胞毒性因子与自然杀伤细胞介导的杀伤作用的相关性。

Relevance of soluble cytotoxic factors generated by mycoplasma-contaminated targets to natural killer cell-mediated killing.

作者信息

Hommel-Berrey G A, Brahmi Z

机构信息

Department of Medicine, Indiana University School of Medicine, Riley Hospital, Indianapolis 46223.

出版信息

Hum Immunol. 1987 Sep;20(1):33-46. doi: 10.1016/0198-8859(87)90004-8.

Abstract

The possible involvement of soluble cytotoxic factors (SCF) in the lytic mechanism of natural killer (NK) cell-mediated cytotoxicity (CMC) was investigated. Tumor target cells (TC) were examined for their ability to stimulate the release of SCF from human peripheral blood lymphocytes (PBL). SCF were detected when effector cells (EC) were stimulated with mycoplasma-contaminated (MC)-TC and with concanavalin A (Con A), but mycoplasma-free (MF)-TC were unable to induce SCF. Pretreatment of EC with beta-interferon augmented the production of SCF with MC-K562 and Con A, but not with MF-K562. However, MF-K562 once infected with the culture supernatant from MC-K562, as well as mycoplasmas concentrated from culture supernatant, were able to induce SCF. Only Con A was capable of generating cytotoxic supernatants from EC that had been inactivated with MF-K562 and from EC depleted of Leu 11b positive cells. Moreover, when EC were evaluated for NK activity after coculture with MF-K562, their ability to kill fresh MF-K562 in the standard NK-CMC assay was greatly reduced. This loss of lytic potential was not accompanied by SCF release. Collectively, these data suggest that mycoplasma organisms play a crucial role in the induction of human SCF, and the implication that SCF, including NK cytotoxic factors (NKCF), are the lytic mediators in NK-CMC needs to be re-evaluated.

摘要

研究了可溶性细胞毒性因子(SCF)在自然杀伤(NK)细胞介导的细胞毒性(CMC)的溶解机制中的可能作用。检测肿瘤靶细胞(TC)刺激人外周血淋巴细胞(PBL)释放SCF的能力。当效应细胞(EC)用支原体污染(MC)的TC和伴刀豆球蛋白A(Con A)刺激时可检测到SCF,但无支原体(MF)的TC不能诱导SCF。用β-干扰素预处理EC可增加MC-K562和Con A刺激的SCF产生,但MF-K562刺激则不能。然而,一旦用MC-K562的培养上清液感染MF-K562,以及从培养上清液中浓缩的支原体,都能够诱导SCF。只有Con A能够从用MF-K562灭活的EC和去除Leu 11b阳性细胞的EC中产生细胞毒性上清液。此外,当评估EC与MF-K562共培养后的NK活性时,它们在标准NK-CMC试验中杀伤新鲜MF-K562的能力大大降低。这种溶解潜能的丧失并不伴随着SCF的释放。总体而言,这些数据表明支原体在人SCF的诱导中起关键作用,并且包括NK细胞毒性因子(NKCF)在内的SCF是NK-CMC中的溶解介质这一观点需要重新评估。

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