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肝脏在体内清除经历抗原触发凋亡的T细胞。

The liver eliminates T cells undergoing antigen-triggered apoptosis in vivo.

作者信息

Huang L, Soldevila G, Leeker M, Flavell R, Crispe I N

机构信息

Section of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Immunity. 1994 Dec;1(9):741-9. doi: 10.1016/s1074-7613(94)80016-2.

Abstract

Deletion of mature peripheral T cells may result from TCR ligation by bacterial enterotoxins, endogenous provirus-encoded superantigens, and peptide antigens. But the ultimate fate of deleted T cells is not clear. Using a line of T cell receptor transgenic mice injected with antigenic peptide, we have documented that peripheral deletion is accompanied by the induction of abortive T cell activation followed by the disappearance of transgene-positive T cells. As these T cells disappear from the lymph nodes and spleen, they accumulate in the liver, where they undergo apoptosis. This is likely to be a general clearance pathway for T cells that are programmed to undergo apoptosis in vivo, and it may further explain the expansion of the intrahepatic T cell pool in mice with genetic defects in the T cell apoptosis mechanism, such as the lpr mutant.

摘要

成熟外周T细胞的缺失可能源于细菌肠毒素、内源性前病毒编码的超抗原和肽抗原与TCR的结合。但被删除的T细胞的最终命运尚不清楚。通过给一组注射了抗原肽的T细胞受体转基因小鼠进行实验,我们发现外周细胞缺失伴随着流产性T细胞激活的诱导,随后转基因阳性T细胞消失。随着这些T细胞从淋巴结和脾脏中消失,它们在肝脏中积聚,并在那里发生凋亡。这可能是体内被编程发生凋亡的T细胞的一种普遍清除途径,并且它可能进一步解释了在T细胞凋亡机制存在遗传缺陷的小鼠(如lpr突变体)中肝内T细胞池的扩张。

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