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体内小鼠胸腺中nbl基因表达与糖皮质激素诱导的细胞凋亡的关联

Association of nbl gene expression and glucocorticoid-induced apoptosis in mouse thymus in vivo.

作者信息

Naora H, Nishida T, Shindo Y, Adachi M, Naora H

机构信息

Research School of Biological Sciences, Australian National University, Canberra.

出版信息

Immunology. 1995 May;85(1):63-8.

Abstract

A gene of unknown biological function, nbl, was originally isolated by virtue of its abundance in a Namalwa Burkitt Lymphoma cDNA library. nbl expression was initially found to be higher in tissues which exhibited internucleosomal DNA cleavage characteristic of apoptosis, than in tissues which did not exhibit a 'DNA ladder'. nbl expression was therefore examined in mouse thymus in vivo, in which apoptosis is induced by the glucocorticoid, dexamethasone. nbl expression was markedly enhanced by dexamethasone treatment and then sharply decreased prior to the occurrence of maximal 'DNA ladder' formation. In contrast, expression of myc, which is believed to be involved in apoptosis in other cell systems, declined as thymic apoptosis increased. Thymic apoptosis was blocked by the transcriptional inhibitor actinomycin D, if administered when nbl expression was enhanced, but not before or after the peak of nbl expression. These results suggest that nbl expression is associated with thymic apoptosis.

摘要

一个生物学功能未知的基因nbl最初是因其在Namalwa伯基特淋巴瘤cDNA文库中的高丰度而被分离出来的。最初发现,nbl在表现出凋亡特征性核小体间DNA切割的组织中的表达,高于未表现出“DNA梯”的组织。因此,在体内对小鼠胸腺中的nbl表达进行了检测,在小鼠胸腺中,糖皮质激素地塞米松可诱导凋亡。地塞米松处理可使nbl表达显著增强,然后在最大程度的“DNA梯”形成之前急剧下降。相比之下,据信在其他细胞系统中参与凋亡的myc的表达,随着胸腺凋亡的增加而下降。如果在nbl表达增强时给予转录抑制剂放线菌素D,胸腺凋亡会被阻断,但在nbl表达峰值之前或之后给予则不会。这些结果表明,nbl表达与胸腺凋亡有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b4/1384025/57f27f77e668/immunology00067-0071-a.jpg

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