Dysregulation of a lncRNA within the TNFRSF10A locus activates cell death pathways.

Dysregulation of a lncRNA within the TNFRSF10A locus activates cell death pathways.
复制标题

DOI:
10.1038/s41420-023-01544-5
复制
发表时间:
2023-07-13
影响因子:
7
通讯作者:
Farkas, Michael H. H.
Farkas, Michael H. H.
中科院分区:
医学2区
文献类型:
--
作者:
Kaczynski, Tadeusz J. J.;Husami, Nadine J. J.;Au, Elizabeth D. D.;Farkas, Michael H. H.

文献摘要

参考文献

相似文献

TNFRSF10A (tumor necrosis factor receptor superfamily member 10A) encodes a cell surface receptor protein involved in apoptotic, necroptotic, and inflammatory pathways. Dysregulation of TNFRSF10A has been implicated in sensitization to apoptosis and to the development of multiple diseases, yet little is known of the AC100861.1 long noncoding RNA (lncRNA) that lies head-to-head with TNFRSF10A. Given its genomic positioning, we sought to investigate the function of AC100861.1, focusing on its potential relationship with TNFRSF10A and the role it may play in death receptor signaling. Using knockdown and overexpression strategies, we probed cell viability and examined transcript and protein-level changes in key genes involved in apoptosis, necroptosis, and inflammation. Decreased cell viability was observed upon TNFRSF10A overexpression, regardless of whether the cells were subjected to the chemical stressor tunicamycin. Similarly, overexpression of AC100861.1 led to increased cell death, with a further increase observed under conditions of cellular stress. Knockdown of TNFRSF10A increased cell death only when the cells were stressed, and AC100861.1 knockdown exhibited no effect on cell death. Neither knockdown nor overexpression of either of these genes greatly affected the expression of the other. Manipulating AC100861.1, however, led to marked changes in the expression of genes involved in necroptosis and inflammatory cell-signaling pathways. Additionally, RNA fluorescence in situ hybridization (RNA-FISH) revealed that the AC100861.1 transcript is localized primarily to the cytoplasm. Together, these data suggest that AC100861.1 may have a role in regulating necroptotic and inflammatory signaling pathways and that this function is separate from changes in TNFRSF10A expression. Given the importance of this genomic locus for cell survival, these data provide insight into the function of a poorly understood lncRNA with potential implications regarding disease pathology and treatment.
DOI: 10.1016/s1074-7613(00)80400-8
发表时间: 1997-12-01
期刊: IMMUNITY
影响因子: 32.4
作者:
Chaudhary, PM;Eby, M;Hood, L
通讯作者: Hood, L
caspase-3在调节细胞存活,增殖和肿瘤发生中的悖论作用。
DOI: 10.1083/jcb.202201159
发表时间: 2022-06-06
期刊: The Journal of cell biology
影响因子: --
作者:
通讯作者: --
DDIT3 和 KAT2A 蛋白调节人肺癌细胞内质网应激介导的细胞凋亡中 TNFRSF10A 和 TNFRSF10B 的表达。
DOI: 10.1074/jbc.m115.645333
发表时间: 2015-04-24
影响因子: 4.8
作者:
Li, Tianliang;Su, Ling;Liu, Xiangguo
通讯作者: Liu, Xiangguo
DOI: 10.1126/science.1262110
发表时间: 2015-05-08
期刊: Science (New York, N.Y.)
影响因子: --
作者:
GTEx Consortium
通讯作者: GTEx Consortium
DOI: 10.1186/s12864-022-08777-1
发表时间: 2022-07-26
期刊: BMC GENOMICS
影响因子: 4.4
作者:
Kaczynski, Tadeusz J.;Au, Elizabeth D.;Farkas, Michael H.
通讯作者: Farkas, Michael H.