Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/111925
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dc.titleIdentification of a new receptor subtype for tumor necrosis factor-α
dc.contributor.authorSchwalb, D.M.
dc.contributor.authorHan, H.-M.
dc.contributor.authorMarino, M.
dc.contributor.authorWarren, R.
dc.contributor.authorPorter, A.
dc.contributor.authorGoh, C.
dc.contributor.authorFairt, W.R.
dc.contributor.authorDonner, D.B.
dc.date.accessioned2014-11-28T02:51:13Z
dc.date.available2014-11-28T02:51:13Z
dc.date.issued1993-05-15
dc.identifier.citationSchwalb, D.M.,Han, H.-M.,Marino, M.,Warren, R.,Porter, A.,Goh, C.,Fairt, W.R.,Donner, D.B. (1993-05-15). Identification of a new receptor subtype for tumor necrosis factor-α. Journal of Biological Chemistry 268 (14) : 9949-9952. ScholarBank@NUS Repository.
dc.identifier.issn00219258
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/111925
dc.description.abstractTwo distinct receptors, which bind both tumor necrosis factor-α and tumor necrosis factor-β (TNF-α and TNF-β), have been previously identified and cloned from transformed cells. The present study identifies a novel receptor subtype in normal human liver which binds TNF-α but not TNF-β. TNF-α but not TNF-β competes for 125I-TNF-α binding and incorporation into affinity-labeled complexes in human liver plasma membranes (HLPM). Antisera to the cloned receptors competed for 125I-TNF-α binding to plasma membranes isolated from various transformed cell lines but not to HLPM. However, mRNAs corresponding in size to both known TNF receptors were detected in liver RNA, making it likely that post-transcriptional modifications account for the TNF-α specificity of HLPM. These observations suggest that the effects of TNF-α and TNF-β on some normal tissues may be more distinct than previously realized.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.sourcetitleJournal of Biological Chemistry
dc.description.volume268
dc.description.issue14
dc.description.page9949-9952
dc.description.codenJBCHA
dc.identifier.isiutNOT_IN_WOS
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