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dc.contributor.author Horváth, Zsuzsanna
dc.contributor.author Pállinger, Éva
dc.contributor.author Horvath G
dc.contributor.author Jelinek I
dc.contributor.author Veszely G
dc.contributor.author Furesz J
dc.contributor.author Falus, András
dc.contributor.author Buzás, Edit Irén
dc.date.accessioned 2018-10-12T08:10:01Z
dc.date.available 2018-10-12T08:10:01Z
dc.date.issued 2010
dc.identifier 77953323274
dc.identifier.citation pagination=429-436; journalVolume=59; journalIssueNumber=6; journalTitle=INFLAMMATION RESEARCH;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4826
dc.identifier.uri doi:10.1007/s00011-009-0114-7
dc.description.abstract OBJECTIVE AND DESIGN: In this study we investigated the role of histamine on the extramedullary hematopoiesis. METHODS: Male histidine decarboxylase knockout (HDC(-/-)) mice and wild-type mice were used (n = 5/group). Groups of mice received sublethal total-body gamma irradiation at a single dose of 4 Gy. Spleen cells were studied at different time points post-irradiation by flow cytometry, colony forming unit (CFU) assay, and real-time PCR. For statistical analysis Student's t test, ANOVA, and Holm-Sidak post-hoc test were used. RESULTS: By day 14 after irradiation, spleen cell counts increased almost eightfold in wild-type and not even fourfold in HDC(-/-) mice (P < 0.01). The proliferative capacity and interleukin-3 signaling of stem cells were impaired in HDC(-/-) mice. STAT5 mRNA expression was decreased in granulocyte-myeloid colonies by 72.9 +/- 8.6% (P < 0.001), compared to the wild-type. CONCLUSIONS: The absence of histamine adversely affects splenic hematopoiesis via direct and indirect mechanisms.
dc.relation.ispartof urn:issn:1023-3830
dc.title Extramedullary hematopoiesis is dysregulated in histamine-free histidine decarboxylase knockout (HDC-/-) mice.
dc.type Journal Article
dc.date.updated 2018-02-16T13:46:29Z
dc.language.rfc3066 en
dc.identifier.mtmt 1392681
dc.identifier.wos 000277641200004
dc.identifier.pubmed 19921486
dc.contributor.department SE/AOK/I/Genetikai, Sejt- és Immunbiológiai Intézet
dc.contributor.institution Semmelweis Egyetem


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