Regulated Expression of PTPRJ/CD148 and an Antisense Long Noncoding RNA in Macrophages by Proinflammatory Stimuli

被引:37
作者
Dave, Richa K. [1 ,2 ,3 ]
Dinger, Marcel E. [4 ,5 ]
Andrew, Megan [3 ]
Askarian-Amiri, Marjan [1 ]
Hume, David A. [1 ,2 ,6 ]
Kellie, Stuart [1 ,2 ,3 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
[2] Univ Queensland, CRC CID, Brisbane, Qld, Australia
[3] Univ Queensland, Australian Infect Dis Res Ctr, Sch Chem & Mol Biosci, Brisbane, Qld, Australia
[4] Univ Queensland, Diamantina Inst, Brisbane, Qld, Australia
[5] St Vincents Hosp, Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
[6] Univ Edinburgh, Roslin Inst, Roslin, Midlothian, Scotland
来源
PLOS ONE | 2013年 / 8卷 / 06期
基金
澳大利亚国家健康与医学研究理事会;
关键词
PROTEIN-TYROSINE-PHOSPHATASE; PLASMINOGEN-ACTIVATOR GENE; TRANSCRIPTION FACTORS; INTERFERON-GAMMA; CELL; RECEPTOR; CD148; CSF-1; CANCER; GROWTH;
D O I
10.1371/journal.pone.0068306
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
PTPRJ/CD148 is a tyrosine phosphatase that has tumour suppressor-like activity. Quantitative PCR of various cells and tissues revealed that it is preferentially expressed in macrophage-enriched tissues. Within lymphoid tissues immunohistochemistry revealed that PTPRJ/CD148 co-localised with F4/80, indicating that macrophages most strongly express the protein. Macrophages express the highest basal level of ptprj, and this is elevated further by treatment with LPS and other Toll-like receptor ligands. In contrast, CSF-1 treatment reduced basal and stimulated Ptprj expression in human and mouse cells, and interferon also repressed Ptprj expression. We identified a 1006 nucleotide long noncoding RNA species, Ptprj-as1 that is transcribed antisense to Ptprj. Ptprj-as1 was highly expressed in macrophage-enriched tissue and was transiently induced by Toll-like receptor ligands with a similar time course to Ptprj. Finally, putative transcription factor binding sites in the promoter region of Ptprj were identified.
引用
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页数:13
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