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Pteridine modulation of lead inhibition of uroporphyrinogen synthesis in erythroid precursor cells

dc.contributor.authorKu, Warren W.en_US
dc.contributor.authorPiper, Walter N.en_US
dc.date.accessioned2006-04-10T13:48:51Z
dc.date.available2006-04-10T13:48:51Z
dc.date.issued1990-03en_US
dc.identifier.citationKu, Warren W., Piper, Walter N. (1990/03)."Pteridine modulation of lead inhibition of uroporphyrinogen synthesis in erythroid precursor cells." Toxicology Letters 51(1): 91-97. <http://hdl.handle.net/2027.42/28691>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TCR-477Y5VM-2M8/2/9f45e99e01229cf152914973d85bdefden_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28691
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2315962&dopt=citationen_US
dc.description.abstractThe role of nutritional factors on heme synthesis and their influence on the development of anemia in the bone marrow during lead exposure is unclear. Previous reports suggested that pteridines could regulate the formation of uroporphyrinogen, a step midway along the heme synthetic pathway. Studies were undertaken to determine if pteridines could modulate lead inhibition of uroporphyrinogen synthesis in erythroid precursor cells. Pteroylpolyglutamates of various glutamate chain lengths were tested for the ability to protect against lead inhibition of uroporphyrinogen I (URO) synthase prepared from murine erythroleukemia cells (MELC). Pteroylpentaglutamate, the major endogenous polyglutamate form by chain length found to be present in MELC, afforded rapid and specific protection of URO synthase against lead inhibition. MELC are expected to be a useful in vitro model for studying the role of endogenous folates on uroporphyrinogen synthesis and heme formation in erythroid precursor cells following lead exposure.en_US
dc.format.extent373856 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titlePteridine modulation of lead inhibition of uroporphyrinogen synthesis in erythroid precursor cellsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumToxicology Program, Department of Environmental and Industrial Health and Department of Pharmacology, Medical School, University of Michigan, Ann Arbor, MI, U.S.A.en_US
dc.contributor.affiliationumToxicology Program, Department of Environmental and Industrial Health and Department of Pharmacology, Medical School, University of Michigan, Ann Arbor, MI, U.S.A.en_US
dc.identifier.pmid2315962en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28691/1/0000511.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0378-4274(90)90228-Een_US
dc.identifier.sourceToxicology Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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