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- Publisher Website: 10.1016/S0024-3205(01)00997-3
- Scopus: eid_2-s2.0-0035937423
- PMID: 11324713
- WOS: WOS:000167852100003
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Article: Induction of tumor necrosis factor receptor type 2 gene expression by tumor necrosis factor-α in rat primary astrocytes
Title | Induction of tumor necrosis factor receptor type 2 gene expression by tumor necrosis factor-α in rat primary astrocytes |
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Authors | |
Keywords | Gene expression Rat primary astrocytes Receptor Tumor necrosis factor-α |
Issue Date | 2001 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/lifescie |
Citation | Life Sciences, 2001, v. 68 n. 18, p. 2081-2091 How to Cite? |
Abstract | Using reverse transcription-polymerase chain reaction (RT-PCR) technique, the messenger RNA (mRNA) for tumor necrosis factor receptor type 2 (TNF-R2, 75/80 kDa) was detected in rat primary astrocytes, with much lower level of expression when compared to that for tumor necrosis factor receptor type 1 (TNF-R1, 55/60 kDa). Upon exposure to TNF-α (100 U/ml), the TNF-R2 mRNA level was greatly enhanced at 8 h, while TNF-R1 mRNA remained unchanged even after 24 h. The induction of TNF-R2 gene expression by TNF-α was dose-dependent and seemed to be unique to TNF-α, as interleukin-6 (IL-6) had no significant effect on TNF-R2 expression. Since TNF-R2 was reported to mediate mitogenic and gene-inducing effects in many other cell types, it is likely that the reported proliferative effect of TNF-α on astrocytes was also mediated by this TNF receptor subtype. Upon exposure to TNF-α or lipopolysaccharide (LPS), the expression of TNF-α gene was induced, and the LPS-induced TNF-α seemed to selectively enhance the TNF-R2 gene expression. Collectively, our results suggest that the TNF-α or LPS-induced expression of both TNF-R2 and TNF-α may provide a positive control mechanism to further enhance the proliferative effect of TNF-α in astrocytes. © 2001 Elsevier Science Inc. |
Persistent Identifier | http://hdl.handle.net/10722/150762 |
ISSN | 2023 Impact Factor: 5.2 2023 SCImago Journal Rankings: 1.257 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lung, HL | en_US |
dc.contributor.author | Leung, KN | en_US |
dc.contributor.author | Stadlin, A | en_US |
dc.contributor.author | Ma, CM | en_US |
dc.contributor.author | Tsang, D | en_US |
dc.date.accessioned | 2012-06-26T06:10:00Z | - |
dc.date.available | 2012-06-26T06:10:00Z | - |
dc.date.issued | 2001 | en_US |
dc.identifier.citation | Life Sciences, 2001, v. 68 n. 18, p. 2081-2091 | en_US |
dc.identifier.issn | 0024-3205 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/150762 | - |
dc.description.abstract | Using reverse transcription-polymerase chain reaction (RT-PCR) technique, the messenger RNA (mRNA) for tumor necrosis factor receptor type 2 (TNF-R2, 75/80 kDa) was detected in rat primary astrocytes, with much lower level of expression when compared to that for tumor necrosis factor receptor type 1 (TNF-R1, 55/60 kDa). Upon exposure to TNF-α (100 U/ml), the TNF-R2 mRNA level was greatly enhanced at 8 h, while TNF-R1 mRNA remained unchanged even after 24 h. The induction of TNF-R2 gene expression by TNF-α was dose-dependent and seemed to be unique to TNF-α, as interleukin-6 (IL-6) had no significant effect on TNF-R2 expression. Since TNF-R2 was reported to mediate mitogenic and gene-inducing effects in many other cell types, it is likely that the reported proliferative effect of TNF-α on astrocytes was also mediated by this TNF receptor subtype. Upon exposure to TNF-α or lipopolysaccharide (LPS), the expression of TNF-α gene was induced, and the LPS-induced TNF-α seemed to selectively enhance the TNF-R2 gene expression. Collectively, our results suggest that the TNF-α or LPS-induced expression of both TNF-R2 and TNF-α may provide a positive control mechanism to further enhance the proliferative effect of TNF-α in astrocytes. © 2001 Elsevier Science Inc. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/lifescie | en_US |
dc.relation.ispartof | Life Sciences | en_US |
dc.subject | Gene expression | - |
dc.subject | Rat primary astrocytes | - |
dc.subject | Receptor | - |
dc.subject | Tumor necrosis factor-α | - |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Animals, Newborn | en_US |
dc.subject.mesh | Antigens, Cd - Biosynthesis - Genetics | en_US |
dc.subject.mesh | Astrocytes - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Cells, Cultured | en_US |
dc.subject.mesh | Dna Primers - Chemistry | en_US |
dc.subject.mesh | Dose-Response Relationship, Drug | en_US |
dc.subject.mesh | Gene Expression - Drug Effects | en_US |
dc.subject.mesh | Interleukin-6 - Pharmacology | en_US |
dc.subject.mesh | Lipopolysaccharides - Pharmacology | en_US |
dc.subject.mesh | Oligonucleotides, Antisense - Chemistry | en_US |
dc.subject.mesh | Rna, Messenger - Biosynthesis | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, Sprague-Dawley | en_US |
dc.subject.mesh | Receptors, Tumor Necrosis Factor - Biosynthesis - Genetics | en_US |
dc.subject.mesh | Receptors, Tumor Necrosis Factor, Type I | en_US |
dc.subject.mesh | Receptors, Tumor Necrosis Factor, Type Ii | en_US |
dc.subject.mesh | Recombinant Proteins - Pharmacology | en_US |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_US |
dc.subject.mesh | Tumor Necrosis Factor-Alpha - Genetics - Pharmacology | en_US |
dc.title | Induction of tumor necrosis factor receptor type 2 gene expression by tumor necrosis factor-α in rat primary astrocytes | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lung, HL:hllung2@hku.hk | en_US |
dc.identifier.authority | Lung, HL=rp00299 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/S0024-3205(01)00997-3 | en_US |
dc.identifier.pmid | 11324713 | - |
dc.identifier.scopus | eid_2-s2.0-0035937423 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035937423&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 68 | en_US |
dc.identifier.issue | 18 | en_US |
dc.identifier.spage | 2081 | en_US |
dc.identifier.epage | 2091 | en_US |
dc.identifier.isi | WOS:000167852100003 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Lung, HL=6603819904 | en_US |
dc.identifier.scopusauthorid | Leung, KN=7401860476 | en_US |
dc.identifier.scopusauthorid | Stadlin, A=6602676624 | en_US |
dc.identifier.scopusauthorid | Ma, CM=36986460800 | en_US |
dc.identifier.scopusauthorid | Tsang, D=7005609135 | en_US |
dc.identifier.issnl | 0024-3205 | - |