Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/111924
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dc.titleHuman tumour necrosis factors-α and -β: Differences in their structure, expression and biological properties
dc.contributor.authorPorter, A.G.
dc.date.accessioned2014-11-28T02:51:12Z
dc.date.available2014-11-28T02:51:12Z
dc.date.issued1990-11
dc.identifier.citationPorter, A.G. (1990-11). Human tumour necrosis factors-α and -β: Differences in their structure, expression and biological properties. FEMS Microbiology Letters 64 (4) : 193-199. ScholarBank@NUS Repository.
dc.identifier.issn03781097
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/111924
dc.description.abstractTumour necrosis factor-α (TNF-α) and lymphotoxin (LT or TNF-β) are cytokines, best known for their cytotoxic or cytostatic effects on some tumour cells. They are structurally related, compete for a common receptor, and are potent inducers of similar biological responses. TNF-α and LT appear to have distinct three-dimensional structures because they differ greatly in their sensitivity to various proteases and chemical agents, and antibodies raised against one cytokine do not cross-react with the other cytokine. The closely linked TNF-α and LT genes are independently regulated since many cell types produce only TNF-α or LT. Expression of the TNF-α gene can be controlled either at the transcriptional or at the post-transcriptional level. In some cell types, TNF-α and LT induce qualitatively or quantitatively different biological responses, and LT can antagonize the action of TNF-α. The disparate biological activities of TNF-α and LT may be related to their different interactions with a common receptor. It is possible that TNF-α and LT have different physiological roles. © 1990.
dc.sourceScopus
dc.subjectCytokines
dc.subjectCytotoxicity
dc.subjectGene transcription
dc.subjectImmune regulation
dc.subjectInflammation
dc.subjectLymphotoxin
dc.subjectReceptors
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.sourcetitleFEMS Microbiology Letters
dc.description.volume64
dc.description.issue4
dc.description.page193-199
dc.description.codenFMLED
dc.identifier.isiutNOT_IN_WOS
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