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己酮可可碱抑制前B细胞中Ig κ基因的转录和重排。

Pentoxifylline inhibits Ig kappa gene transcription and rearrangements in pre-B cells.

作者信息

Wang W, Rath S, Durdik J M, Sen R

机构信息

Rosenstiel Research Center, Department of Biology, Brandeis University, Waltham, MA 02254, USA.

出版信息

J Immunol. 1998 Feb 15;160(4):1789-95.

PMID:9469438
Abstract

Pentoxifylline (PF) has been used in a wide variety of clinical situations; however, the molecular consequences of this drug are not well characterized. In this paper we assayed the effects of PF in two models of pre-B differentiation. In 70Z pre-B cells, transcriptional induction of rearranged Ig kappa-chain gene in response to LPS was suppressed by PF, without affecting the induction of Rel family proteins. In contrast, kappa induction by IFN-gamma was not suppressed by PF, indicating that the drug inhibited certain activation pathways. We also found that LPS-induced activation of germline kappa transcription and V kappa to J kappa recombination were inhibited by PF in the pre-B cell line 38B9. These observations suggest that PF may adversely affect B lymphopoiesis during chronic administration.

摘要

己酮可可碱(PF)已被用于多种临床情况;然而,这种药物的分子效应尚未得到充分表征。在本文中,我们检测了PF在两种前B细胞分化模型中的作用。在70Z前B细胞中,PF抑制了对脂多糖(LPS)作出反应的重排Ig κ链基因的转录诱导,而不影响Rel家族蛋白的诱导。相反,PF并未抑制γ干扰素(IFN-γ)诱导的κ链表达,这表明该药物抑制了某些激活途径。我们还发现,在38B9前B细胞系中,PF抑制了LPS诱导的胚系κ转录激活以及Vκ到Jκ的重组。这些观察结果表明,长期给药时PF可能对B淋巴细胞生成产生不利影响。

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